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WGC-2021

List of abstracts related to

86863 Reprogramming to recover youthful epigenetic information and restore vision
Lu Y; Brommer B; Tian X; Krishnan A; Meer M; Wang C; Vera DL; Zeng Q; Yu D; Bonkowski MS; Yang JH; Zhou S; Hoffmann EM; Karg MM; Schultz MB; Kane AE; Davidsohn N; Korobkina E; Chwalek K; Rajman LA; Church GM; Hochedlinger K; Gladyshev VN; Horvath S; Levine ME; Gregory-Ksander MS; Ksander BR; He Z; Sinclair DA
Nature 2020; 588: 124-129

Listed by Classification


3.4.2 Gene studies (4546 abstracts found)


91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Senthil S
Ophthalmic Genetics 2021; 42: 28-34 (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Yang X
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91504 Predicting the Future of Genetic Risk Profiling of Glaucoma: A Narrative Review
Han X
JAMA ophthalmology 2021; 139: 224-231 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Shi H
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91727 A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma
Huang FR
European review for medical and pharmacological sciences 2021; 25: 1447-1454 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Neroev V
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Yaman D
Molecular Biology Reports 2020; 47: 9337-9344 (IGR: 21-4)


91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Tjandra I
International Journal of Ophthalmology 2020; 13: 1872-1879 (IGR: 21-4)


91693 Clinical and genetic analysis of Ser341Pro variant in a Korean family with primary open angle glaucoma
Moon S
International Journal of Ophthalmology 2020; 13: 1689-1696 (IGR: 21-4)


91382 Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife)
Neustaeter A
BMC Ophthalmology 2021; 21: 18 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Bonet-Fernández JM
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Canut MI
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Occhiutto ML
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Yamamoto Y
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Wang L
Current Eye Research 2020; 0: 1-9 (IGR: 21-4)


91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Alghamdi A
PLoS ONE 2020; 15: e0241902 (IGR: 21-4)


91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Thakur N
BMC Medical Genomics 2021; 14: 1 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Silva F
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Qassim A
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91259 Prevalence of MYOC risk variants for glaucoma in different populations
Liuska PJ
Acta Ophthalmologica 2021; 0: (IGR: 21-4)


91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Jee D
Nutrients 2020; 12: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Mullany S
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
de Melo MB
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Takmaz T
Molecular Biology Reports 2020; 47: 9337-9344 (IGR: 21-4)


91504 Predicting the Future of Genetic Risk Profiling of Glaucoma: A Narrative Review
Hewitt AW
JAMA ophthalmology 2021; 139: 224-231 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Ferreira F
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Villa O
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Huang S
Nutrients 2020; 12: (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Sun NN
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Soeharso P
International Journal of Ophthalmology 2020; 13: 1872-1879 (IGR: 21-4)


91259 Prevalence of MYOC risk variants for glaucoma in different populations
Harju M
Acta Ophthalmologica 2021; 0: (IGR: 21-4)


91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Sharma S
Ophthalmic Genetics 2021; 42: 28-34 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Mukai A
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Gong J
Current Eye Research 2020; 0: 1-9 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Chen Y
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Malishevskaya T
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Aldossary W
PLoS ONE 2020; 15: e0241902 (IGR: 21-4)


91727 A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma
Zhang AM
European review for medical and pharmacological sciences 2021; 25: 1447-1454 (IGR: 21-4)


91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Kupani M
BMC Medical Genomics 2021; 14: 1 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Aroca-Aguilar JD
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91693 Clinical and genetic analysis of Ser341Pro variant in a Korean family with primary open angle glaucoma
Kim N
International Journal of Ophthalmology 2020; 13: 1689-1696 (IGR: 21-4)


91382 Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife)
Nolte I
BMC Ophthalmology 2021; 21: 18 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Ikushima T
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Yüksel N
Molecular Biology Reports 2020; 47: 9337-9344 (IGR: 21-4)


91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Albahkali S
PLoS ONE 2020; 15: e0241902 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Weinert D
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Artini W
International Journal of Ophthalmology 2020; 13: 1872-1879 (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Zhao ZN
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Wang J
Current Eye Research 2020; 0: 1-9 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Lu H
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91259 Prevalence of MYOC risk variants for glaucoma in different populations
Kivelä TT
Acta Ophthalmologica 2021; 0: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Awadalla MS
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91693 Clinical and genetic analysis of Ser341Pro variant in a Korean family with primary open angle glaucoma
Lee J
International Journal of Ophthalmology 2020; 13: 1689-1696 (IGR: 21-4)


91382 Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife)
Snieder H
BMC Ophthalmology 2021; 21: 18 (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Cabral de Vasconcellos JP
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Kang S
Nutrients 2020; 12: (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Faria P
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91727 A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma
Xu J
European review for medical and pharmacological sciences 2021; 25: 1447-1454 (IGR: 21-4)


91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Mannan R
BMC Medical Genomics 2021; 14: 1 (IGR: 21-4)


91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Vishwakarma S
Ophthalmic Genetics 2021; 42: 28-34 (IGR: 21-4)


91504 Predicting the Future of Genetic Risk Profiling of Glaucoma: A Narrative Review
Macgregor S
JAMA ophthalmology 2021; 139: 224-231 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Kudsieh B
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Corton M
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Sobral I
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Park S
Nutrients 2020; 12: (IGR: 21-4)


91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Alotaibi B
PLoS ONE 2020; 15: e0241902 (IGR: 21-4)


91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Kaur I
Ophthalmic Genetics 2021; 42: 28-34 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Urata Y
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Ramírez AI
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Hassall MM
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91727 A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma
Huang L
European review for medical and pharmacological sciences 2021; 25: 1447-1454 (IGR: 21-4)


91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Pruthi A
BMC Medical Genomics 2021; 14: 1 (IGR: 21-4)


91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Dinçer SA
Molecular Biology Reports 2020; 47: 9337-9344 (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
He SX
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Mattlin H
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Rodrigues TAR
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Dan J
Current Eye Research 2020; 0: 1-9 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Astakhov S
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Siregar NC
International Journal of Ophthalmology 2020; 13: 1872-1879 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Zhu R
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91382 Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife)
Jansonius NM
BMC Ophthalmology 2021; 21: 18 (IGR: 21-4)


91259 Prevalence of MYOC risk variants for glaucoma in different populations
Turunen JA
Acta Ophthalmologica 2021; 0: (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Bajano FF
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Kolomeichuk S
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Mehrotra S
BMC Medical Genomics 2021; 14: 1 (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Zhang M
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Banchs I
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Alexandre-Moreno S
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Zhang J
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Kinoshita S
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Şahin Fİ
Molecular Biology Reports 2020; 47: 9337-9344 (IGR: 21-4)


91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Alrfaei BM
PLoS ONE 2020; 15: e0241902 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Nguyen T
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Wang P
Current Eye Research 2020; 0: 1-9 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Rodrigues M
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Victor AA
International Journal of Ophthalmology 2020; 13: 1872-1879 (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Zhang DD
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Pratas J
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Cornelissen G
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
García-Antón MT
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Costa FF
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Hamuro J
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
González JR
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
He M
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Marshall H
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Ueno M
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Kabitskaya Y
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Yu XW
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Guan H
Experimental Eye Research 2021; 202: 108350 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Silva JF
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Costa VP
Ophthalmic Genetics 2021; 42: 53-61 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Kolovos A
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Armengol L
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Salazar JJ
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Kolovos A
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Ferre-Fernández JJ
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Casaroli-Marano RP
Scientific reports 2021; 11: 1583 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Schulz AM
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Sotozono C
Scientific reports 2020; 10: 20936 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Boiko E
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Grazina M
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Zhang JM
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Atienzar-Aroca R
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Nemtsova I
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Han X
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Moura Pereira J
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Fan ZG
World journal of clinical cases 2021; 9: 697-706 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Girão H
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Gubin D
International journal of molecular sciences 2020; 22: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Gharahkhani P
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Villaverde C
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Galanopoulos A
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Iancu I
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Pereira P
Acta medica portuguesa 2020; 0: (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Agar A
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Tamayo A
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Healey PR
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Méndez-Hernández CD
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Hewitt AW
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Morales-Fernández L
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Landers J
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Rojas B; Ayuso C
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Casson RJ
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Coca-Prados M
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Graham SL
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Martinez-de-la-Casa JM
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Macgregor S; Souzeau E
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
García-Feijoo J; Escribano J
Human Genetics 2020; 139: 1209-1231 (IGR: 21-4)


91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Siggs OM; Craig JE
Ophthalmology. Glaucoma 2020; 0: (IGR: 21-4)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Moschos MM
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90178 Insights into the regulatory molecules involved in glaucoma pathogenesis
Moazzeni H
American journal of medical genetics. Part C, Seminars in medical genetics 2020; 184: 782-827 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Chai X
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Minyaylo O
Data in brief 2020; 31: 106004 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Adachi K
Scientific reports 2020; 10: 15036 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Liu X
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Wu CL
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Lu H
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Fan W
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
VanderWall KB
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Ling C
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Lee JS
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90268 Lack of correlation between S1 RNA binding domain 1 SNP rs3213787/rs11884064 and normal-tension glaucoma in a population from the Republic of Korea
Jung SH
Medicine 2020; 99: e20066 (IGR: 21-3)


89975 A comprehensive map of disease networks and molecular drug discoveries for glaucoma
Wang H
Scientific reports 2020; 10: 9719 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Kondkar AA
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


90090 Expression profile analysis to predict potential biomarkers for glaucoma: BMP1, DMD and GEM
Zhang DW
PeerJ 2020; 8: e9462 (IGR: 21-3)


90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Trivli A
Molecular medicine reports 2020; 22: 1103-1110 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
VanderWall KB
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Yanagisawa M
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Or L
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Qiao C
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Jeoung JW
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Chen Y
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Jia H
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Sultan T
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Low KY
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90268 Lack of correlation between S1 RNA binding domain 1 SNP rs3213787/rs11884064 and normal-tension glaucoma in a population from the Republic of Korea
Lee YC
Medicine 2020; 99: e20066 (IGR: 21-3)


90090 Expression profile analysis to predict potential biomarkers for glaucoma: BMP1, DMD and GEM
Zhang S
PeerJ 2020; 8: e9462 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Starikova D
Data in brief 2020; 31: 106004 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Asada Y
Scientific reports 2020; 10: 15036 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Zhang D
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Zervou MI
Molecular medicine reports 2020; 22: 1103-1110 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Dettoraki M
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Huang KC
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Namekata K
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Li J
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Li W
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


89975 A comprehensive map of disease networks and molecular drug discoveries for glaucoma
Deng Y
Scientific reports 2020; 10: 9719 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Barkana Y
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


90178 Insights into the regulatory molecules involved in glaucoma pathogenesis
Khani M
American journal of medical genetics. Part C, Seminars in medical genetics 2020; 184: 782-827 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Yang YT
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Hirakata T
Scientific reports 2020; 10: 15036 (IGR: 21-3)


89975 A comprehensive map of disease networks and molecular drug discoveries for glaucoma
Wan L
Scientific reports 2020; 10: 9719 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Kong Y
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Zhang H
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Wang YH
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Hecht I
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Lin S
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90178 Insights into the regulatory molecules involved in glaucoma pathogenesis
Elahi E
American journal of medical genetics. Part C, Seminars in medical genetics 2020; 184: 782-827 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Aida T
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Tham YC
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Karekla A
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Duan C
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Pan Y
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Moskalenko M
Data in brief 2020; 31: 106004 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Oh S
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90268 Lack of correlation between S1 RNA binding domain 1 SNP rs3213787/rs11884064 and normal-tension glaucoma in a population from the Republic of Korea
Lee MY
Medicine 2020; 99: e20066 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Zhang J
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Azad TA
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


90090 Expression profile analysis to predict potential biomarkers for glaucoma: BMP1, DMD and GEM
Wu J
PeerJ 2020; 8: e9462 (IGR: 21-3)


90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Goulielmos GN
Molecular medicine reports 2020; 22: 1103-1110 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Lin TY
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Zhang W
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Xiao X
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Spandidos DA
Molecular medicine reports 2020; 22: 1103-1110 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Lavekar SS
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90268 Lack of correlation between S1 RNA binding domain 1 SNP rs3213787/rs11884064 and normal-tension glaucoma in a population from the Republic of Korea
Shin HY
Medicine 2020; 99: e20066 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Lamprinakis I
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


89975 A comprehensive map of disease networks and molecular drug discoveries for glaucoma
Huang L
Scientific reports 2020; 10: 9719 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Chee ML
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Onoue M
Scientific reports 2020; 10: 15036 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Osman EA
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Weiner C
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Ponomarenko I
Data in brief 2020; 31: 106004 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Sun H
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Wang H
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Chee ML
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Kim DM
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Liu X
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Katou S
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Einan-Lifshitz A
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Takeda T
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Damaskos C
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Thakur S
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Ahn JH
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Liang J
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Almobarak FA
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Reshetnikov E
Data in brief 2020; 31: 106004 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Fligor CM
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Detorakis ET
Molecular medicine reports 2020; 22: 1103-1110 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Luo J
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Iwamoto S
Scientific reports 2020; 10: 15036 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Li N
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Lin IC
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Du Q
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Guo Y
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Harada T
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Kim MJ
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Li X
Experimental and therapeutic medicine 2020; 20: 968-977 (IGR: 21-3)


90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Chen F
Molecular medicine reports 2020; 22: 3263-3270 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Wei W
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Allsop AR
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Al-Obeidan SA
BMC Medical Genetics 2020; 21: 145 (IGR: 21-3)


89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Sung CW
European Journal of Ophthalmology 2020; 0: 1120672120940198 (IGR: 21-3)


90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Pras E
Experimental Eye Research 2020; 200: 108220 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Kasuga T
Scientific reports 2020; 10: 15036 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Zhang S
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Zhang L
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Dvornyk V
Data in brief 2020; 31: 106004 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Song J
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Gouliopoulos N
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Lentsch KA
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Tan NY
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Tibilis M
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Xu H
Genomics 2020; 112: 5129-5135 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Li L
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Ling Y
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Seong MW
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90247 Alteration of gene expression in mice after glaucoma filtration surgery
Matsuda A
Scientific reports 2020; 10: 15036 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Fuse N
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Churnosov M
Data in brief 2020; 31: 106004 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Park SS
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Fang L
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
The Glaucoma Gene Research Group
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Gazouli M
PLoS ONE 2020; 15: e0233692 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Dang P
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Khor CC
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Duan X
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Aung T
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Cao K
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


89943 EAAT1 variants associated with glaucoma
Tanaka K
Biochemical and Biophysical Research Communications 2020; 529: 943-949 (IGR: 21-3)


90582 No association between polymorphisms and normal-tension glaucoma
Kim JY
Ophthalmic Genetics 2020; 41: 427-431 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Zhang C
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Xiao H; Chen L
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Tseng HC
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Hu J
DNA and cell biology 2020; 39: 949-957 (IGR: 21-3)


90638 Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study
Wong TY; Cheng CY
Investigative Ophthalmology and Visual Science 2020; 61: 37 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Huang J
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Cummins TR; Meyer JS
Stem cell reports 2020; 15: 52-66 (IGR: 21-3)


90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Zhong Y; Zhang Q
Experimental Eye Research 2020; 197: 108118 (IGR: 21-3)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Greene AG
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Sun L
Ophthalmic Research 2020; 0: (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim MJ
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86154 Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
Fakhraie G
BMC Medical Genetics 2020; 21: 32 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Gupta V
Eye 2020; 0: (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Mabuchi F
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Falero-Perez J
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Greene AG
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86764 Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review
Boysen KB
Ophthalmic Genetics 2020; 41: 223-234 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Hosono K
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Lu SY
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Eivers SB
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86337 Clinical practice guidelines for single gene glaucoma disorder
Writing Group For Practice Guidelines For Diagnosi
Chinese Journal of Medical Genetics 2020; 37: 329-333 (IGR: 21-2)


86409 Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran
Hozhabri H
American Journal of Medical Genetics, Part A 2020; 182: 957-961 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Li K
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Schmitt HM
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Eivers SB
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Thanikachalam S
Genes 2020; 11: (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Zazo-Seco C
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Larsen MC
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Greene AG
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Somarajan BI
Eye 2020; 0: (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Rong SS
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86409 Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran
Talebi M
American Journal of Medical Genetics, Part A 2020; 182: 957-961 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Hodapp E
Genes 2020; 11: (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Greene AG
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86154 Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
Parvini F
BMC Medical Genetics 2020; 21: 32 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Yang C
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86337 Clinical practice guidelines for single gene glaucoma disorder
Yang Z
Chinese Journal of Medical Genetics 2020; 37: 329-333 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Mabuchi N
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Johnson WM
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Cui R
Ophthalmic Research 2020; 0: (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim YW
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Plaisancié J
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Eivers SB
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Kawase K
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Eivers SB
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86764 Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review
la Cour M
Ophthalmic Genetics 2020; 41: 223-234 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Wan X
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Aboobakar IF
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Sakurada Y
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Dervan E
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86337 Clinical practice guidelines for single gene glaucoma disorder
Yang J
Chinese Journal of Medical Genetics 2020; 37: 329-333 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Wu Z
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Dervan EWJ
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Gupta S
Eye 2020; 0: (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Bitoun P
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86409 Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran
Mehrjardi MYV
American Journal of Medical Genetics, Part A 2020; 182: 957-961 (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Teixeira LBC
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86154 Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
Ghanavi J
BMC Medical Genetics 2020; 21: 32 (IGR: 21-2)


86764 Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review
Kessel L
Ophthalmic Genetics 2020; 41: 223-234 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Jeoung JW
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Chang TC
Genes 2020; 11: (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Meng H
Ophthalmic Research 2020; 0: (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Kurata K
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Yoneyama S
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86154 Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
Saif S
BMC Medical Genetics 2020; 21: 32 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Liu X
Ophthalmic Research 2020; 0: (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Corton M
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Xu J
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86409 Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran
De Luca A
American Journal of Medical Genetics, Part A 2020; 182: 957-961 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Seong MW
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Strickland S
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Swols DM
Genes 2020; 11: (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Niimi Y
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Huang C
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
O'Brien C
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
O'brien CJ
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Walia GK
Eye 2020; 0: (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Zhang HF
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86337 Clinical practice guidelines for single gene glaucoma disorder
Gong B
Chinese Journal of Medical Genetics 2020; 37: 329-333 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Saitsu H
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Cengiz FB
Genes 2020; 11: (IGR: 21-2)


86291 Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population
Wallace D
Journal of Glaucoma 2020; 29: 417-422 (IGR: 21-2)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Wallace DM
Experimental Eye Research 2020; 193: 107975 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Kashiwagi K
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Lee JS
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Arteche A
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86337 Clinical practice guidelines for single gene glaucoma disorder
Zhang Q
Chinese Journal of Medical Genetics 2020; 37: 329-333 (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Lindner V
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Gomez-Caraballo M
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Luo Q
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86154 Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucoma
Farnia P
BMC Medical Genetics 2020; 21: 32 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Singh A
Eye 2020; 0: (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Matsushita K
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86409 Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran
Dehghani M
American Journal of Medical Genetics, Part A 2020; 182: 957-961 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Cheng Y
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Sorenson CM
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Sofi R
Eye 2020; 0: (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Parker M
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Minoshima S
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Ng TK
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim DM
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Guo S
Genes 2020; 11: (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Iijima H
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Lu Y
Ophthalmic Research 2020; 0: (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Ayuso C
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Schneider A
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Ohnishi H
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Ahn JH
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Liu K
Ophthalmic Research 2020; 0: (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Jefcoate CR
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Chaudhary RS
Eye 2020; 0: (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Leung CKS
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Zafeer MF
Genes 2020; 11: (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Yamagata Z
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Finnegan L
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Peng J
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Yamamoto T
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Corcoran DL
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Zafeiropoulou D
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Jia L
Ophthalmic Research 2020; 0: (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Takamoto M
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Gong B
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Sharma A
Eye 2020; 0: (IGR: 21-2)


86634 Targeted deletion of Cyp1b1 in pericytes results in attenuation of retinal neovascularization and trabecular meshwork dysgenesis
Sheibani N
Trends in developmental biology 2019; 12: 1-12 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Seyhan S
Genes 2020; 11: (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Kawashima R
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Song JY
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Jiang L
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Bademci G
Genes 2020; 11: (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Skiba NP
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Usui S
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Hikoya A
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Aihara M
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Cho SI
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Gilissen C
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86603 Gene suppression of the ClC-2 chloride channel suppressed TGF-β1-induced proliferation, collagen synthesis, and collagen gel contraction mediated by conjunctival fibroblasts
Zheng Y
Ophthalmic Research 2020; 0: (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Tachibana N
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Iwata T
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Tam POS
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Allingham RR
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Roche O
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Liu Y
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Scott WK
Genes 2020; 11: (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Park SS
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Frémont F
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Hauser MA
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Fukao T
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim JY
Journal of Glaucoma 2020; 29: 331-336 (IGR: 21-2)


86686 Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population
Shuai P
Ophthalmic Genetics 2020; 41: 252-256 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Grajewski A
Genes 2020; 11: (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Hashimoto K
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Tsujikawa M; Young AL
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Tekin M
Genes 2020; 11: (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Calvas P
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Sato K
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86128 Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1
Stamer WD
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Zhang M
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86573 A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation
Hotta Y
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Shiga Y
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Slavotinek A
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Wiggs JL
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Nishiguchi KM
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Ragge N
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Nakazawa T
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Nishida K
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Chassaing N
Journal of Human Genetics 2020; 65: 487-491 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Tham CC
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Akiyama M
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Kawase K
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Pang CP
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Chen LJ
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma
Ozaki M; Araie M
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


86550 Genetic Variants Associated With the Onset and Progression of Primary Open-Angle Glaucoma

American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Nandeesh BN
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Rauf B
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Quist TS
American Journal of Ophthalmology 2020; 214: 52-62 (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Yousefian A
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Siggs OM
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Liu H
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


84521 Role of matrix metalloproteinase-9 gene polymorphisms in glaucoma: A hospital-based study in Chinese patients
Zhao F
Journal of Clinical Laboratory Analysis 2020; 34: e23105 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim YW
Scientific reports 2020; 10: 221 (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Stiemke AB
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Criscione J
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Kondkar AA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Simcoe MJ
JAMA ophthalmology 2020; 0: (IGR: 21-1)


84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
AlSaad R
American Journal of Case Reports 2020; 21: e918128 (IGR: 21-1)


84752 Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Gauthier AC
Experimental Eye Research 2020; 190: 107893 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Bashir R
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Mocan MC
Turkish journal of ophthalmology 2019; 49: 347-355 (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Azad TA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Ji W
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Qi S
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Bindu PS
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


84752 Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Wiggs JL
Experimental Eye Research 2020; 190: 107893 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Souzeau E
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Mehta AA
Turkish journal of ophthalmology 2019; 49: 347-355 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim YJ
Scientific reports 2020; 10: 221 (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Sah E
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Irfan B
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
ElMansoury J
American Journal of Case Reports 2020; 21: e918128 (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Shokoohi-Rad S
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Johnson CA
American Journal of Ophthalmology 2020; 214: 52-62 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Irum B
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Weisschuh N
JAMA ophthalmology 2020; 0: (IGR: 21-1)


84521 Role of matrix metalloproteinase-9 gene polymorphisms in glaucoma: A hospital-based study in Chinese patients
Fan Z
Journal of Clinical Laboratory Analysis 2020; 34: e23105 (IGR: 21-1)


85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Robin AL
American Journal of Ophthalmology 2020; 214: 52-62 (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Simpson RN
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Taranath DA
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Khalid M
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
AlHazzaa SAF
American Journal of Case Reports 2020; 21: e918128 (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Sultan T
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
He W
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Cheong HS
Scientific reports 2020; 10: 221 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Jeffries L
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Abbaszadegan MR
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Wissinger B
JAMA ophthalmology 2020; 0: (IGR: 21-1)


84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Aref AA
Turkish journal of ophthalmology 2019; 49: 347-355 (IGR: 21-1)


84521 Role of matrix metalloproteinase-9 gene polymorphisms in glaucoma: A hospital-based study in Chinese patients
Huang X
Journal of Clinical Laboratory Analysis 2020; 34: e23105 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Narayanappa G
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Khan SY
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Hysi PG
JAMA ophthalmology 2020; 0: (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Lu L
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


84918 Chromosome 1q Terminal Deletion and Congenital Glaucoma: A Case Report
Dirar QS
American Journal of Case Reports 2020; 21: e918128 (IGR: 21-1)


85034 Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree
Fingert JH
American Journal of Ophthalmology 2020; 214: 52-62 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
McGrath JM
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Chang C
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Rad DM
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Kabir F
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Osman EA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Shiga Y
Scientific reports 2020; 10: 221 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Chickabasaviah Yasha T
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Dubowsky A
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Zargari S
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Mahadevan A
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Naeem MA
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


85057 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes
Hammond CJ
JAMA ophthalmology 2020; 0: (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Hashimoto K
Scientific reports 2020; 10: 221 (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Williams RW
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Almobarak FA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Saleem F
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Chappell A
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Chen Y
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Chappell A
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Soloway S
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Milanizadeh S
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Song YJ
Scientific reports 2020; 10: 221 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Pusztai L
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


84895 Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohort
Al-Obeidan SA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Riazuddin S
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Kulanthaivelu K
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Zhou T
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Nouman U
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


84490 Association of single-nucleotide polymorphisms in TLR4 gene and gene-environment interaction with primary open angle glaucoma in a Chinese northern population
Yu J
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Jablonski MM
Frontiers in genetics 2020; 11: 31 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim SH
Scientific reports 2020; 10: 221 (IGR: 21-1)


84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Santosh V
Neuropathology 2020; 40: 93-98 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Javadiyan S
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


85125 Association of hepatocyte growth factor gene polymorphisms with primary angle closure glaucoma from Lahore, Pakistan
Naz S
Journal of the Pakistan Medical Association 2020; 70: 208-212 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Ayyagari R
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


84439 Identification of a novel variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
Lakhani S
Cold Spring Harbor molecular case studies 2019; 5: (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Morovatdar N
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Choi HJ
Scientific reports 2020; 10: 221 (IGR: 21-1)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Riazuddin SA
Molecular Vision 2020; 26: 14-25 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Nicholl J
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


85145 Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran
Daneshvar R
Journal of ophthalmic & vision research 2020; 15: 45-52 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Nishiguchi KM
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Kearns LS
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kawai Y
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Staffieri SE; Narita A
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Nagasaki M
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Smith JEH
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Nakazawa T; Park KH
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Pater J; Hewitt AW
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Kim DM
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Ruddle JB
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


84941 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study
Jeoung JW
Scientific reports 2020; 10: 221 (IGR: 21-1)


85135 Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma
Elder JE; Mackey DA; Burdon KP; Craig JE
Ophthalmology 2020; 127: 758-766 (IGR: 21-1)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Han X
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Kondkar AA
BMC research notes 2019; 12: 453 (IGR: 20-4)


82326 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Chernyshova K
Investigative Ophthalmology and Visual Science 2019; 60: 3625-3635 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Hadrami M
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Moazzeni H
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82761 NEW GENETIC MARKERS ASSOCIATED WITH SUSCEPTIBILITY TO EXFOLIATION SYNDROME AMONG GEORGIAN POPULATION
Kobakhidze N
Georgian Medical News 2019; 0: 41-45 (IGR: 20-4)


82398 Association of HK2 and NCK2 with normal-tension glaucoma in a population from the Republic of Korea
Jung SH
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2717-2721 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wu X
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82859 LOXL1 folding in exfoliation glaucoma
Bernstein AM
Advances in protein chemistry and structural biology 2019; 118: 273-288 (IGR: 20-4)


82079 Identification of Gene Changes Induced by Dexamethasone in the Anterior Segment of the Human Eye Using Bioinformatics Analysis
Zhang Y
Medical Science Monitor 2019; 25: 5501-5509 (IGR: 20-4)


82502 The role of lysyl oxidase-like 1 (LOXL1) in exfoliation syndrome and glaucoma
Schlötzer-Schrehardt U
Experimental Eye Research 2019; 189: 107818 (IGR: 20-4)


82427 Update on the genetics of primary open-angle glaucoma
Youngblood H
Experimental Eye Research 2019; 188: 107795 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Wang SL
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82881 Investigation of Gene Involvement in Primary Congenital Glaucoma in Iraqi Children
Jubair S
Middle East African Journal of Ophthalmology 2019; 26: 203-209 (IGR: 20-4)


82668 Association between interleukin-10 genetic polymorphisms and risk of primary open angle glaucoma in a Chinese Han population: a case-control study
Zhang YH
International Journal of Ophthalmology 2019; 12: 1605-1611 (IGR: 20-4)


82417 Lack of Correlation between ASB10 and Normal-tension Glaucoma in a Population from the Republic of Korea
Jung SH
Current Eye Research 2020; 45: 521-525 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Kosior-Jarecka E
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Hill SE
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Zhang X
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Fan BJ
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82255 Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis
Lin Z
BioMed research international 2019; 2019: 6707650 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Xiao X
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Alkhatib R
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


82689 Clinical implications of recent advances in primary open-angle glaucoma genetics
Choquet H
Eye 2020; 34: 29-39 (IGR: 20-4)


82186 HLA-DPA1 gene polymorphism in primary glaucoma
Li JH
European review for medical and pharmacological sciences 2019; 23: 24-30 (IGR: 20-4)


82841 Association of Gene Polymorphisms with Exfoliation Glaucoma Patients
Taghavi E
Iranian journal of public health 2019; 48: 1827-1837 (IGR: 20-4)


82659 The genetics of angle closure glaucoma
Wang J
Experimental Eye Research 2019; 189: 107835 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Can Demirdöğen B
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Nongpiur ME
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Nikhalashree S
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82841 Association of Gene Polymorphisms with Exfoliation Glaucoma Patients
Daneshvar R
Iranian journal of public health 2019; 48: 1827-1837 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Bonnet C
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82659 The genetics of angle closure glaucoma
Yusufu M
Experimental Eye Research 2019; 189: 107835 (IGR: 20-4)


82417 Lack of Correlation between ASB10 and Normal-tension Glaucoma in a Population from the Republic of Korea
Lee YC
Current Eye Research 2020; 45: 521-525 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Bailey JC
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82186 HLA-DPA1 gene polymorphism in primary glaucoma
Shao JF
European review for medical and pharmacological sciences 2019; 23: 24-30 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Abudhaim N
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Azad TA
BMC research notes 2019; 12: 453 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Zhang D
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82689 Clinical implications of recent advances in primary open-angle glaucoma genetics
Wiggs JL
Eye 2020; 34: 29-39 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Khor CC
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Huang C
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Kwon MS
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Koçan Akçin C
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Xie HN
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Qassim A
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82859 LOXL1 folding in exfoliation glaucoma
Ritch R
Advances in protein chemistry and structural biology 2019; 118: 273-288 (IGR: 20-4)


82326 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Inoue K
Investigative Ophthalmology and Visual Science 2019; 60: 3625-3635 (IGR: 20-4)


82079 Identification of Gene Changes Induced by Dexamethasone in the Anterior Segment of the Human Eye Using Bioinformatics Analysis
Yang A
Medical Science Monitor 2019; 25: 5501-5509 (IGR: 20-4)


82502 The role of lysyl oxidase-like 1 (LOXL1) in exfoliation syndrome and glaucoma
Zenkel M
Experimental Eye Research 2019; 189: 107818 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Mirrahimi M
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Karthikkeyan G
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Koçan Akçin C
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Piao SY
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82398 Association of HK2 and NCK2 with normal-tension glaucoma in a population from the Republic of Korea
Lee YC
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2717-2721 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Sagan M
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82881 Investigation of Gene Involvement in Primary Congenital Glaucoma in Iraqi Children
N Al-Rubae'i SH
Middle East African Journal of Ophthalmology 2019; 26: 203-209 (IGR: 20-4)


82668 Association between interleukin-10 genetic polymorphisms and risk of primary open angle glaucoma in a Chinese Han population: a case-control study
Xing YQ
International Journal of Ophthalmology 2019; 12: 1605-1611 (IGR: 20-4)


82255 Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis
Huang S
BioMed research international 2019; 2019: 6707650 (IGR: 20-4)


82761 NEW GENETIC MARKERS ASSOCIATED WITH SUSCEPTIBILITY TO EXFOLIATION SYNDROME AMONG GEORGIAN POPULATION
Tabagari S
Georgian Medical News 2019; 0: 41-45 (IGR: 20-4)


82427 Update on the genetics of primary open-angle glaucoma
Hauser MA
Experimental Eye Research 2019; 188: 107795 (IGR: 20-4)


82186 HLA-DPA1 gene polymorphism in primary glaucoma
Sui ZG
European review for medical and pharmacological sciences 2019; 23: 24-30 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Wróbel-Dudzińska D
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Al-Eitan L
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Göksoy E
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82859 LOXL1 folding in exfoliation glaucoma
Wolosin JM
Advances in protein chemistry and structural biology 2019; 118: 273-288 (IGR: 20-4)


82689 Clinical implications of recent advances in primary open-angle glaucoma genetics
Khawaja AP
Eye 2020; 34: 29-39 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Martin MD
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Xu MY
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82881 Investigation of Gene Involvement in Primary Congenital Glaucoma in Iraqi Children
M Al-Sharifi AN
Middle East African Journal of Ophthalmology 2019; 26: 203-209 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Cao Y
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Igo RP
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82659 The genetics of angle closure glaucoma
Khor CC
Experimental Eye Research 2019; 189: 107835 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
George R
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82255 Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis
Sun J
BioMed research international 2019; 2019: 6707650 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Moghadam A
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82841 Association of Gene Polymorphisms with Exfoliation Glaucoma Patients
Noormohammadi Z
Iranian journal of public health 2019; 48: 1827-1837 (IGR: 20-4)


82326 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Yamashita SI
Investigative Ophthalmology and Visual Science 2019; 60: 3625-3635 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Zeitz C
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82761 NEW GENETIC MARKERS ASSOCIATED WITH SUSCEPTIBILITY TO EXFOLIATION SYNDROME AMONG GEORGIAN POPULATION
Chichua G
Georgian Medical News 2019; 0: 41-45 (IGR: 20-4)


82398 Association of HK2 and NCK2 with normal-tension glaucoma in a population from the Republic of Korea
Lee MY
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2717-2721 (IGR: 20-4)


82427 Update on the genetics of primary open-angle glaucoma
Liu Y
Experimental Eye Research 2019; 188: 107795 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
An J
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Sultan T
BMC research notes 2019; 12: 453 (IGR: 20-4)


82668 Association between interleukin-10 genetic polymorphisms and risk of primary open angle glaucoma in a Chinese Han population: a case-control study
Chen Z
International Journal of Ophthalmology 2019; 12: 1605-1611 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Huang L
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82417 Lack of Correlation between ASB10 and Normal-tension Glaucoma in a Population from the Republic of Korea
Lee MY
Current Eye Research 2020; 45: 521-525 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Cheng CY
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wu T
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82079 Identification of Gene Changes Induced by Dexamethasone in the Anterior Segment of the Human Eye Using Bioinformatics Analysis
Huang J
Medical Science Monitor 2019; 25: 5501-5509 (IGR: 20-4)


82255 Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis
Xie B
BioMed research international 2019; 2019: 6707650 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Liu W
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82659 The genetics of angle closure glaucoma
Aung T
Experimental Eye Research 2019; 189: 107835 (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Al-Mobarak FA
BMC research notes 2019; 12: 453 (IGR: 20-4)


82417 Lack of Correlation between ASB10 and Normal-tension Glaucoma in a Population from the Republic of Korea
Shin HY
Current Eye Research 2020; 45: 521-525 (IGR: 20-4)


82326 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Fukuchi T
Investigative Ophthalmology and Visual Science 2019; 60: 3625-3635 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Zhang W
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Chen S
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82186 HLA-DPA1 gene polymorphism in primary glaucoma
Qin YX
European review for medical and pharmacological sciences 2019; 23: 24-30 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Abdo N
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


82668 Association between interleukin-10 genetic polymorphisms and risk of primary open angle glaucoma in a Chinese Han population: a case-control study
Ma XC
International Journal of Ophthalmology 2019; 12: 1605-1611 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Kang JH
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Łukasik U
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82841 Association of Gene Polymorphisms with Exfoliation Glaucoma Patients
Modarresi SM
Iranian journal of public health 2019; 48: 1827-1837 (IGR: 20-4)


82881 Investigation of Gene Involvement in Primary Congenital Glaucoma in Iraqi Children
Jabbar Suleiman AA
Middle East African Journal of Ophthalmology 2019; 26: 203-209 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Veten F
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Shantha B
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Marshall H
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Suntharalingam A
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Yakar G
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Hao F
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Banaei-Esfahani A
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Husain R
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82398 Association of HK2 and NCK2 with normal-tension glaucoma in a population from the Republic of Korea
Shin HY
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2717-2721 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Hazel A
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Ma JQ
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Chen LL
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82841 Association of Gene Polymorphisms with Exfoliation Glaucoma Patients
Sedaghat MR
Iranian journal of public health 2019; 48: 1827-1837 (IGR: 20-4)


82668 Association between interleukin-10 genetic polymorphisms and risk of primary open angle glaucoma in a Chinese Han population: a case-control study
Lu Q
International Journal of Ophthalmology 2019; 12: 1605-1611 (IGR: 20-4)


82255 Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis
Zhong Y
BioMed research international 2019; 2019: 6707650 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Biya M
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Kalantan H
BMC research notes 2019; 12: 453 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Lin Y
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Zhou T
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82659 The genetics of angle closure glaucoma
Wang N
Experimental Eye Research 2019; 189: 107835 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Öztepe T
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Vijaya L
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Boey PY
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Yazdani S
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Boumenna T
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82326 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy
Kanki T
Investigative Ophthalmology and Visual Science 2019; 60: 3625-3635 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Aung T
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Alqudah A
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Xu Y
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Ong JS
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Chen H
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Chew A
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Hao J
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Gong B
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Ratra V
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Khor CC
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Dickey CA
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Demirkaya-Budak S
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82411 Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies
Elahi E
Human Molecular Genetics 2019; 28: 3637-3663 (IGR: 20-4)


82652 Genetic Analysis Of Gene Of Primary Glaucoma In Jordanian Arab Population
Aman H
The application of clinical genetics 2019; 12: 181-189 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Brilliant MH
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82075 Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control study
Al-Obeidan SA
BMC research notes 2019; 12: 453 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Li ZH
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Hamed CT
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82003 Analysis of MYOC gene variants among sporadic patients with primary open-angle glaucoma
Yang Z
Chinese Journal of Medical Genetics 2019; 36: 662-665 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Sulochana KN
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Ho CL
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Pang C
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


81990 Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk
Oflaz S
Graefe's Archive for Clinical and Experimental Ophthalmology 2019; 257: 2257-2270 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Budenz DL
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Hassall MM
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Kocki J
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Condroyer C
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Chi H
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wang DJ
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


81955 Stable calcium-free myocilin olfactomedin domain variants reveal challenges in differentiating between benign and glaucoma-causing mutations
Gumbart JC; Lieberman RL
Journal of Biological Chemistry 2019; 294: 12717-12728 (IGR: 20-4)


82030 Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucoma
Żarnowski T
Ophthalmic Genetics 2019; 40: 323-328 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Fingert JH
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Wong TT
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Hysi PG
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82791 Lowered Decorin With Aberrant Extracellular Matrix Remodeling in Aqueous Humor and Tenon's Tissue From Primary Glaucoma Patients
Coral K
Investigative Ophthalmology and Visual Science 2019; 60: 4661-4669 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Wang Y
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Wang P
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82622 Exome Sequencing Reveals a Heterozygous OAS3 Mutation in a Chinese Family With Juvenile-Onset Open-Angle Glaucoma
Zhang M
Investigative Ophthalmology and Visual Science 2019; 60: 4277-4284 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Xue ZQ
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Sidi MM
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Foster PJ
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Perera S
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Ha SP
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82223 A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome
Huang HB
Experimental and therapeutic medicine 2019; 18: 2255-2261 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Gaasterland T
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Khaw PT
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Wong TY
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Cheikh S
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Gaasterland D
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82311 Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China
Zhuang WJ
International Journal of Ophthalmology 2019; 12: 1317-1322 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Hauser MA
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Zhang Q
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Vithana EN
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Mackey DA
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82146 Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma
Aung T
American Journal of Ophthalmology 2019; 208: 160-165 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Gharahkhani P
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Audo I
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Kraft P
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Petit C
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Khawaja AP
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Lee RK; Lichter PR
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Hewitt AW
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82125 Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma
Houmeida A
Molecular Vision 2019; 25: 373-381 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Liu Y
JAMA ophthalmology 2019; 0: (IGR: 20-4)


82838 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Craig JE; Macgregor S
Human Molecular Genetics 2019; 28: 3680-3690 (IGR: 20-4)


82271 Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis
Moroi SE; Myers JS; Pericak-Vance MA; Realini A; Rhee DJ; Richards JE; Ritch R; Schuman JS; S
JAMA ophthalmology 2019; 0: (IGR: 20-4)


80594 Correlation between MTHFR polymorphisms and glaucoma: A meta-analysis
Zhang L
Molecular genetics & genomic medicine 2019; 7: e00538 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
He JN
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


81103 Identification of pathogenic genes and transcription factors in glaucoma
Feng J
Molecular medicine reports 2019; 20: 216-224 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Alward WLM
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Xu J
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Yi H
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


81368 Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
Souzeau E
Molecular genetics & genomic medicine 2019; 7: e774 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Gong B
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Cui QN
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
Shen T
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Liesenborghs I
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Chen M
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Berner D
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Patel A
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80839 Polygenic Risk Score Is Associated With Intraocular Pressure and Improves Glaucoma Prediction in the UK Biobank Cohort
Gao XR
Translational vision science & technology 2019; 8: 10 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Zhang L
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Verkuil L
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Wang Y
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Hubens WHG
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
He JN
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


80897 How does a protein's structure spell the difference between health and disease? Our journey to understand glaucoma-associated myocilin
Lieberman RL
PLoS biology 2019; 17: e3000237 (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
Khafagy MM
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


81421 Correlations of TIMP2 and TIMP3 gene polymorphisms with primary open-angle glaucoma
Ji ML
European review for medical and pharmacological sciences 2019; 23: 5542-5547 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Wu Z
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Derakhshan A
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


81337 Mendelian genes in primary open angle glaucoma
Sears NC
Experimental Eye Research 2019; 186: 107702 (IGR: 20-3)


80639 The association of toll-like receptor 4 gene polymorphisms with primary open angle glaucoma susceptibility: a meta-analysis
Chaiwiang N
Bioscience reports 2019; 39: (IGR: 20-3)


81260 Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population
Ma YN
Journal of Ophthalmology 2019; 2019: 9687823 (IGR: 20-3)


80615 Association between rs4938723 polymorphism and the risk of primary open-angle glaucoma (POAG) in a Chinese population
Zhang J
Journal of Cellular Biochemistry 2019; 120: 12875-12886 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
Lu SY
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Gohari M
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Lu Y
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


81148 Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
Passan S
Gene 2019; 709: 25-35 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Huang C
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Hoja U
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
El-Guendy N
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


81421 Correlations of TIMP2 and TIMP3 gene polymorphisms with primary open-angle glaucoma
Jia J
European review for medical and pharmacological sciences 2019; 23: 5542-5547 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Mirjalili SA
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Lu S
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


81148 Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
Goyal S
Gene 2019; 709: 25-35 (IGR: 20-3)


80639 The association of toll-like receptor 4 gene polymorphisms with primary open angle glaucoma susceptibility: a meta-analysis
Poyomtip T
Bioscience reports 2019; 39: (IGR: 20-3)


80615 Association between rs4938723 polymorphism and the risk of primary open-angle glaucoma (POAG) in a Chinese population
Wang L
Journal of Cellular Biochemistry 2019; 120: 12875-12886 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Zha X
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Zhang H
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
van der Heide C
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81103 Identification of pathogenic genes and transcription factors in glaucoma
Xu J
Molecular medicine reports 2019; 20: 216-224 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Peng Y
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


81337 Mendelian genes in primary open angle glaucoma
Boese EA
Experimental Eye Research 2019; 186: 107702 (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
Gupta VK
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Luo H
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Wang C
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Hayward JD
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Tavakkol-Afshari J
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Breddels EM
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


80839 Polygenic Risk Score Is Associated With Intraocular Pressure and Improves Glaucoma Prediction in the UK Biobank Cohort
Huang H
Translational vision science & technology 2019; 8: 10 (IGR: 20-3)


81260 Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population
Xie TY
Journal of Ophthalmology 2019; 2019: 9687823 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Eijssen LMT
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
He ZZ
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


80594 Correlation between MTHFR polymorphisms and glaucoma: A meta-analysis
Chen B
Molecular genetics & genomic medicine 2019; 7: e00538 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Ramakrishnan MS
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


81368 Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
Dubowsky A
Molecular genetics & genomic medicine 2019; 7: e774 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Zhou D
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Danford I
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Yu X
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Sadeghi Allah Abadi J
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
Klistorner A
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Tailor V
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


81260 Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population
Chen XY
Journal of Ophthalmology 2019; 2019: 9687823 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Lu H
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Xu C
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Zhu Y
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


81368 Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
Ruddle JB
Molecular genetics & genomic medicine 2019; 7: e774 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Walid Y
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
Xu JX
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


81148 Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
Bhat MA
Gene 2019; 709: 25-35 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Ouyang P
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Kutmon M
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
Tantawy MA
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Chen LJ
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Huang L
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


81337 Mendelian genes in primary open angle glaucoma
Miller MA
Experimental Eye Research 2019; 186: 107702 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Qi S
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Xu J
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Akbarian-Bafghi MJ
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Khanna CL
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Yu M
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80839 Polygenic Risk Score Is Associated With Intraocular Pressure and Improves Glaucoma Prediction in the UK Biobank Cohort
Kim H
Translational vision science & technology 2019; 8: 10 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Zenkel M
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Pistilli M
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Gudiseva HV
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Liang Y
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Chen Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Gorgels TGMF
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Ross JJ
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Ansari-Astaneh MR
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


81337 Mendelian genes in primary open angle glaucoma
Fingert JH
Experimental Eye Research 2019; 186: 107702 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Yang C
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Nyanhete R
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Xie L
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Jarahzadeh MH
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Roos BR
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
Chitranshi N
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Collins DW
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Ma J
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Xu F
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Collins DW
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81368 Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion
Craig JE
Molecular genetics & genomic medicine 2019; 7: e774 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Tam POS
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


81148 Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
Singh D
Gene 2019; 709: 25-35 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Lv J
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Ramdas WD
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
Yang C
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Gorgels TGMF
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
Eldaly MA
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Liu Z
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Uebe S
Human Molecular Genetics 2019; 0: (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Pistilli M
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Webers CAB
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Shu Y
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Su G
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Sivaprasad S
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Zare-Shehneh M
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Gudiseva HV
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Evelo CT
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Chen X
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Liang JJ
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Zhang BN
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
Chen LJ
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Ahlfors H
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Derakhshan AR
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
Graham SL
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
Elhilali HM
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Yue J
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


81148 Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
Vanita V
Gene 2019; 709: 25-35 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Zeng H
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Shi Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Hu S
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Paoli D
Human Molecular Genetics 2019; 0: (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Beckers HJM
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80836 Interaction between XRCC 1 gene polymorphisms and diabetes on susceptibility to primary open-angle glaucoma
Zheng Y
Experimental biology and medicine (Maywood, N.J.) 2019; 244: 588-592 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Gorgels TGMF
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81412 Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma
Gong B
Investigative Ophthalmology and Visual Science 2019; 60: 2914-2924 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Tam PO
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Nikpoor AR
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Lee R
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80923 Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma
Abdel Wahab AHA
International Journal of Ophthalmology 2019; 12: 607-614 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Tong J
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Kong Y
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Kam J
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81434 Association of MTHFR C677T and A1298C Polymorphisms with Glaucoma Risk: a Systematic Review Meta-Analysis based 42 Case-Control Studies
Neamatzadeh H
Romanian journal of ophthalmology 2019; 63: 107-118 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Liu L
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Gong B
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Gabriel C
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Trachtman BT
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80696 Sex-Specific Effect of BDNF Val66Met Genotypes on the Progression of Open-Angle Glaucoma
You Y
Investigative Ophthalmology and Visual Science 2019; 60: 1069-1075 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Chen B
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Leung CKS
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Wang N
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80857 Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Gorgels TGMF
Current Eye Research 2019; 44: 1006-1017 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Chavali VM
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Gu Y
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Pang CP
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80994 Investigating a downstream gene of using the systems genetics method
Lu L
Molecular Vision 2019; 25: 222-236 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Duan X
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
He J
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Ritch R
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Webers CAB
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Zhu X
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Wu G
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80763 Association of the Myocilin Gene Polymorphism With Primary Open Angle Glaucoma
Shokoohi Rad S
Medical hypothesis, discovery and innovation in ophthalmology 2019; 8: 28-33 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Jannini TB
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Lin Y
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Pang CP
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Frezzotti P
Human Molecular Genetics 2019; 0: (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Lehman A
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Tham CCY
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
Yang Y
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Rathi S
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81399 Association of polymorphism rs11656696 in with primary open-Angle Glaucoma in a Chinese Population
Wang J
Ophthalmic Genetics 2019; 40: 237-241 (IGR: 20-3)


81244 A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing
Shi J
BMC Medical Genetics 2019; 20: 105 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Rautenbach RM
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Ng TK
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Abbou-Rayyah Y
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Lotery A
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


81278 Comprehensive bioinformatics analysis of trabecular meshwork gene expression data to unravel the molecular pathogenesis of primary open-angle glaucoma
Schouten JSAG
Acta Ophthalmologica 2020; 98: 48-57 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Huang Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80710 Association of Gene Polymorphisms With Primary Open Angle Glaucoma: A Systematic Review and Meta-Analysis
Wang K
Investigative Ophthalmology and Visual Science 2019; 60: 1105-1121 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Lei B
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Henderson R
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80908 A novel nonsense mutation in ADAMTS17 caused autosomal recessive inheritance Weill-Marchesani syndrome from a Chinese family
He Y
Journal of Human Genetics 2019; 64: 681-687 (IGR: 20-3)


81280 Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients
Chu WK
Disease markers 2019; 2019: 5820537 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Ziskind A
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80736 Caveolin-1 regulates human trabecular meshwork cell adhesion, endocytosis, and autophagy
Zhang M
Journal of Cellular Biochemistry 2019; 120: 13382-13391 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Haider N
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
Addis VM
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Igo RP; Cooke Bailey JN
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Ying GS
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


81261 Mitochondrial haplogroup L1c2 is associated with increased disease severity in African American patients with primary open-angle glaucoma
O'Brien JM
Journal of clinical & experimental ophthalmology 2019; 10: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Nischal KK
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Williams SE
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Sundaresan P; Li X
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
Chavali VRM
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Stone EM
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Islam L
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Carmichael TR
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80621 SNP located in an repeat downstream of rs4657473, is protective for POAG in African Americans
O'Brien JM
British Journal of Ophthalmology 2019; 103: 1530-1536 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Ramsay M
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Scheetz TE
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Bitner-Glindzicz M
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Jiang L
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Topouzis F
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Hurst J
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Kwon YH
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Valdivia LE
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Pasquale LR
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Lin Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Chatzikyriakidou A
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Lu F
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Lambropoulos A
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Zanolli M
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wiggs JL
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Moosajee M
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Chen L
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Sundaresan P
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Fingert JH;
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Li Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Ayub H
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Brookes J; Papadopoulos M
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Akhtar F
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Leung CK; Guo X
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Qamar R
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Khaw PT; Cullup T
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Zenteno JC
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Zhang S
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Cruz-Aguilar M
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Huang G
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Jenkins L
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80866 The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
Astakho
Human Molecular Genetics 2019; 0: (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Wu Y
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


80402 The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders
Dahlma
Ophthalmology 2019; 126: 888-907 (IGR: 20-3)


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Zhou T; Shuai P; Tham CC; Weisschuh N; Krishnadas SR; Mardin C; Reis A; Yang J
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Waryah YM
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Svidnicki PV
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Zhuang W
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
Umali J
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lahola-Chomiak AA
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Gudiseva HV
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Lei L
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Huang L
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Siggs OM
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Rong SS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Marques AM
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Park DY
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Coêlho REA
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Medina-Trillo C
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Morlino S
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Chen Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Souzeau E
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Pistilli M
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Footz T
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Braghini CA
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Sena DR
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
Hawkey-Noble A
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Alesi V
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Aroca-Aguilar JD
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Wang S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Li S
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Iqbal M
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Ananina G
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Cho SY
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Lu SY
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pasutto F
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Hao J
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Calì F
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Liu X
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Lin Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Sheikh SA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Ferre-Fernández JJ
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Nguyen-Phuoc K
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Jin DK
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Costa VP
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Santa Cruz F
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
French CR
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Costa VP
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Salowe R
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Matsushita K
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Baig MA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Schimiti RB
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
De Vasconcellos JPC
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Xu M
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Kee C
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Lepri FR
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Singh LN
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Tam POS
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Zhang C
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Neil GJ
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Dubowsky A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Alexandre-Moreno S
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Huang C
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Moura BCFS
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Cheng Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Secinaro A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Han CC
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
de Melo MB
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Smith JEH
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Narsani AK
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Leung CKS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Fan B
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Morales L
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
De Vasconcellos JPC
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Collins DW
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Chi H
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Cole B
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Méndez-Hernández CD
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Andrade FN
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Kawashima R
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Piao S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Atif M
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allen KF
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Grammatico P
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Taranath D
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Shi Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
de Melo MB
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Gong B
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
García-Feijoo J
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pater J
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Lira RPC
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
He J
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Ma J
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Usui S
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Novelli A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Greenfield DS
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Bhinder MA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Merriam S
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Parrish RK
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Rait JL
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Ur Rahman A
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Zhang X
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tam POS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Escribano J
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Lu F
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Drago F
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yang J
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Young AL
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Ha S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Memon AI
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Linkroum K
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Khachataryan N
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Castori M
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Narita A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tsujikawa M
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Mauri L
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Pasquale LR
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Baban A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Wang H
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Pirzado MS
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Henderer J
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Waryah AM
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Addis V
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yin Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Del Longo A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Zhang M
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Leonhardt RM
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Cao Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Reis A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Cui QN
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Ritch R
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Nishida K
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Chappell A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Wiggs JL
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Chappell A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Sankar PS
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Jiang D
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Javadiyan S; Craig JE
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tham CC
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Zhong L
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Kearns LS
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Miller-Ellis E
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allison WT
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Xue B
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Staffieri SE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Pang CP
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Chavali VRM; Ying GS
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Chen LJ
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lehmann OJ
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Wang J
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Elder JE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Hao F
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Ruddle JB
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Wallace D
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Walter MA; Wiggs JL
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Hewitt AW
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Lee DY
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
O'Brien JM
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Pang CP
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Burdon KP; Mackey DA
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Sun X
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Craig JE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yang Z
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Oliveira MB
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen Y
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Lin Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Tan Y
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Wubben TJ
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


79084 Transcriptional profiling analysis predicts potential biomarkers for glaucoma: HGF, AKR1B10 and AKR1C3
Nie Q
Experimental and therapeutic medicine 2018; 16: 5103-5111 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Takitani GEDS
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Pandav SS
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Qashqai M
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Shihadeh W
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Wang S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Saeedi O
Genes 2018; 9: (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Restrepo NA
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Yu-Wai-Man C
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Kondkar AA
BMC research notes 2018; 11: 733 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yaz Y
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Afzal R
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Singh LN
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Khawaja AP
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Abu-Amero KK
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Suri F
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Crowston JG
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Sultan T
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Sultan T
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Qiu C
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Azevedo AGB
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Zhang D
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Laper SM
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Arno G
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Firasat S
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Branham KH
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Gao H
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Zhuang W
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Chan MPY
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79084 Transcriptional profiling analysis predicts potential biomarkers for glaucoma: HGF, AKR1B10 and AKR1C3
Zhang X
Experimental and therapeutic medicine 2018; 16: 5103-5111 (IGR: 20-1)


78902
Lukic V
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
De Vasconcellos JPC
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Khabour O
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Chakma P
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yıldırım N
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Yousaf S
Genes 2018; 9: (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Brookes J
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Lopez Sanchez MIG
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Yip JLY
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Khera A
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Ma J
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Ananina G
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Aydın Yaz Y
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Khalil MB
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Almobarak FA
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Qian S
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Kaul H
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Al-Obeidan SA
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Yaseri M
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Gong B
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Besirli CG
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Tsai J
Genes 2018; 9: (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Zhu Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Motta FL
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78902
Suvakov S
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Farber-Eger E
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Xu M
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Bohnsack BL
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Costa VP
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Crawford DC
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Al-Dabbagh A
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Chen C
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Elahi E
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Ahmed B
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Palmer K
Genes 2018; 9: (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Kondkar AA
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Chugh N
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Bahabri IM
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Teixeira SH
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Broadway DC
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Zhang X
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Çilingir O
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Van Bergen NJ
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78902
Simic T
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Garcia-Feijoo J
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Kalantan H
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen J
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Garway-Heath DF
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yüksel Z
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Piao S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Riazuddin S
Genes 2018; 9: (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Abu-Amero KK
BMC research notes 2018; 11: 733 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Jiang L
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Kearns LS
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Khaw PT
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen X
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Sallum JMF
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Li T
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78902
Sencanic I
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Gupta PC
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
de Melo MB
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Siddiqui SN
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Al-Hashimi M
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Al-Obeidan SA
BMC research notes 2018; 11: 733 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Lin Y
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Ahmed ZM
Genes 2018; 9: (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Mutlu F
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Zafar SN
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Moosajee M
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Thattaruthody F
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Viswanathan AC
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Wang L
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78902
Pljesa-Ercegovac M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Liu B
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Vessani RM
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Hao J
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Hewitt AW
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Lyu C
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Seth NG
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78902
Jaksic V
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Zhang W
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Yazar S
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Shahzadi M
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Luben R
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Sun X
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Hayat S
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Afshan K
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78902
Babovic S
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Mackey DA
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Raj S
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Chi H
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Huang Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78902
Matic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Li H
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Wallace DC
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Kaushik S
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Xue Z
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Hauser MA
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Trounce IA
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Wu Q
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Ha S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Wareham NJ
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78902
Radosavljevic A
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Khullar M
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78902
Savic-Radojevic A
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Ram J
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Khaw KT
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Jin C; Liang X
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Fortune B
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78902
Djukic T
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Allingham RR
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Huang X; Lu L
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Foster PJ
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Gao XR
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Tong L
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Ou Z
Bioscience reports 2018; 38: (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Horita S
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Swarup G
Frontiers in immunology 2018; 9: 1287 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Pasquale LR
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Ayala M
Clinical Ophthalmology 2018; 12: 1155-1162 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Syrimis A
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Wang X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Aung T
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Macgregor S
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Choquet H
Nature communications 2018; 9: 2278 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Bashir R
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Sayyad Z
Frontiers in immunology 2018; 9: 1287 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Kang JH
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Yousaf K
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Liu G
Bioscience reports 2018; 38: (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Chan AS
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Cuklev F
Clinical Ophthalmology 2018; 12: 1155-1162 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Liu X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Ong JS
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Nicolaou N
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Paylakhi S
Nature communications 2018; 9: 2278 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Simsek E
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Hou AH
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Huang H
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
An J
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Alexandrou A
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Nannini DR
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Tahir H
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Simsek T
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Wong TT
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Khor CC
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Fan B
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Liu W
Bioscience reports 2018; 38: (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Kneeland SC
Nature communications 2018; 9: 2278 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Huang L
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Papaevripidou I
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Yildirim N
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Han X
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Sanai M
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Deng Y
Bioscience reports 2018; 38: (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Thai KK
Nature communications 2018; 9: 2278 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Fan F
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Fang S
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Levkovitch-Verbin H
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Kim H
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Hoffmann TJ
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Zhou T
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Zheng L
Bioscience reports 2018; 38: (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Jia X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Wiggs JL
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Nicolaou M
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Ishiura H
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Qayyum S
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Xiao X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Yin J
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Siggs OM
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Loukianou E
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Zhang S
Bioscience reports 2018; 38: (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Nakamura M
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Kvale MN
Nature communications 2018; 9: 2278 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Naz S
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Feng G
Bioscience reports 2018; 38: (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Sismani C
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Satoh N
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Law MH
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Li S
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Malas S
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Souzeau E
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Suzuki A
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Guo X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Banda Y; Tolman NG
Nature communications 2018; 9: 2278 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Tsukada H
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Sharma S
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Christophidou-Anastasiadou V; Tanteles GA
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Lynn DJ
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Mizuno T
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Williams PA
Nature communications 2018; 9: 2278 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Seki G
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Beesley J
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Schaefer C; Melles RB
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Sheldrick B
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Tsuji S; Nangaku M
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Mills RA
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Risch N
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Landers J
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
John SWM; Nair KS
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Ruddle JB; Graham SL
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Jorgenson E
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Healey PR; White AJR; Casson RJ; Best S; Grigg JR; Goldberg I; Powell JE; Whiteman DC; Radford-Smi
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Huang C
Scientific reports 2018; 8: 4498 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Wang HW
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Mohanty K
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Struebing FL
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wang GM
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khawaja AP
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Collins DW
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wang GM
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Shiga Y
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Gharahkhani P
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
King R
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Doucette LP
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Ouyang P
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Rangachari K
Genomics 2019; 111: 696-699 (IGR: 19-3)


76943 Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutations
Khan AO
Ophthalmic Genetics 2018; 39: 425-427 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alsaif HS
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Karmiris E
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Footz T
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Prasov L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Li Y
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Cooke Bailey JN
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Gudiseva HV
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Akiyama M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
King R
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Prasov L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Sun P
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Dada R
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Xie L
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Bankoti N
Genomics 2019; 111: 696-699 (IGR: 19-3)


76943 Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutations
Basamh OS
Ophthalmic Genetics 2018; 39: 425-427 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Kourtis N
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Khan AO
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Burdon KP
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Li Y
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
P Pantou M
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Shyamala N
Genomics 2019; 111: 696-699 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Chavali VRM
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Wang J
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Walter MA
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Cooke Bailey JN
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Patel N
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Li Y
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Wu Z
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Dada T
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhang F
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Al-Hasani H
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wareham NJ
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Chen Y
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Nishiguchi KM
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Struebing FL
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alkuraya H
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Degiannis D
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Cao Y
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Sato K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Cooke Bailey JN
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Marrs CER
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhu C
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Trachtman B
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Scott RA
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Jiang LP
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Michael D
Genomics 2019; 111: 696-699 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Hewitt AW
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Shimozawa N
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Georgalas I
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zou B
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Law MH
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Geisert EE
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Wu HP
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Sameer Ahmed Z
Genomics 2019; 111: 696-699 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Hashem M
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse

Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Tolia S
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Ramakrishnan M
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Zheng Y
Scientific reports 2018; 8: 4498 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Simcoe M
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Le J
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Chandrasekaran P
Genomics 2019; 111: 696-699 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Pang CP
Scientific reports 2018; 8: 4498 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Zhang W
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Merritt WT
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Abdulwahab F
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Papaconstantinou D
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Igo RP
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Takahashi A
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Wiggs JL
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Pasquale LR
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wiinikka-Buesser L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Geisert EE
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Momozawa Y
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Song YE
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Kang JH
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhang L
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Sekar K
Genomics 2019; 111: 696-699 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Richards JE
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Ibrahim N
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Gao F
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Pistilli M
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Zhang M
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Hirata M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wojciechowski R
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Bohnsack BL
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Aldahmesh MA
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Rossi RA
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Haines JL; Souzeau E
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Blachon S
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Cheng CY
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Matsuda K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alkuraya FS
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Zhou T
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Sankar PS
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khaw PT
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yamaji T
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Miller-Ellis E
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Siggs OM
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Pasquale LR
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Iwasaki M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Lehman A
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Landers J
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Haines JL
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Tsugane S
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Awadalla M
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Oze I
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Addis V
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Foster PJ
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Mikami H
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wiggs JL
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Sharma S
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
O'Brien JM
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Mills RA
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Hammond CJ
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Naito M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Hysi PG
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Wakai K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Ridge B
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yoshikawa M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Lynn D; Casson R
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Miyake M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma

Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yamashiro K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Graham SL; Goldberg I
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
; Kashiwagi K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
White A
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Iwata T
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Healey PR; Grigg J
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Mabuchi F
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Lawlor M,
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Takamoto M; Oz
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Jeoung JW
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Gupta S
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Molasy M
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Li J
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Suh W
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Chintalapudi SR
Nature communications 2017; 8: 1755 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Karaca I
International Ophthalmology 2017; 0: (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Choquet H
Nature communications 2017; 8: 2108 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Winegarner A
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Zagajewska K
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Nunes HF
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Fang Kho P
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
DeLuca AP
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Shiga Y
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta V
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Burdon KP
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Feng Y
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Won HH
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Lea RA
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Nishiguchi KM
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Thai KK
Nature communications 2017; 8: 2108 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Oie Y
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Piątkowska M
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Alward WLM
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Ananina G
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Yilmaz SG
International Ophthalmology 2017; 0: (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Awadalla MS
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Somarajan BI
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Walczak A
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Chatterjee S
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Maria D
Nature communications 2017; 8: 1755 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Ko JH
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Goryca K
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Kim YJ
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Mitchell P
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Liebmann J
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Yin J
Nature communications 2017; 8: 2108 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Walia GK
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Przybyłowska-Sygut K
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Sung MS
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Di Wang X
Nature communications 2017; 8: 1755 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Costa VP
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Chandra A
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Kee C
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Benton MC
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kawai Y
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Palamar M
International Ophthalmology 2017; 0: (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Kawasaki S
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Wang JJ
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Nishida N
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Ritch R
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Bailey JNC
Nature communications 2017; 8: 1755 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Lee TH
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Maurya OPS
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Zanchin NIT
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kaur J
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Onay H
International Ophthalmology 2017; 0: (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Eccles D
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kojima K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Kim YW
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Hoffmann TJ
Nature communications 2017; 8: 2108 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Bałabas A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Zaleska-Żmijewska A
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Kvale MN
Nature communications 2017; 8: 2108 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
De Vasconcellos JPC
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
White A
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Nishida K
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Akgun B
International Ophthalmology 2017; 0: (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Haupt LM
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Park KH
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Kluska A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Kawase K
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Szaflik J
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kumar S
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Sato K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Park SW
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mishra RN
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Kwon YH
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility

Nature communications 2017; 8: 1755 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta S
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Paziewska A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Szaflik JP
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mukherjee A
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
de Melo MB
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Fujita K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Oh JY
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Banda Y
Nature communications 2017; 8: 2108 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Hewitt AW
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Keane MC
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Aytacoglu B
International Ophthalmology 2017; 0: (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Alsabaani NA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Chaurasia AK
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Pośpiech E
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Majsterek I
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Aykut A
International Ophthalmology 2017; 0: (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Sherwin JC
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Hysi PG
Nature communications 2017; 8: 1755 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Souzeau E
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Robin AL
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Schaefer C
Nature communications 2017; 8: 2108 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mutsuddi M
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Takahashi M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Grabska-Liberek I
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Omodaka K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Risch N
Nature communications 2017; 8: 2108 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Mackey DA
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Stone EM
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Ozkinay FF
International Ophthalmology 2017; 0: (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta D
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Wiggs JL
Nature communications 2017; 8: 1755 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Graham SL
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Araie M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Griffiths LR
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Nair KS
Nature communications 2017; 8: 2108 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kaushik A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Scheetz TE
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Goldberg I
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Williams RW
Nature communications 2017; 8: 1755 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Hennig EE
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kashiwagi K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Mehta A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Healey PR
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Jablonski MM
Nature communications 2017; 8: 1755 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Fingert JH
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Melles R; Jorgenson E
Nature communications 2017; 8: 2108 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Landers J
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Aihara M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Sharma A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Mills RAD
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Iwata T; Mabuchi F
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Best S
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Takamoto M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Hewitt AW
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Ozaki M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Sharma S; Craig JE
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kawase K; Fuse N; Yamamoto M; Yasuda J; Nagasaki M; Nakazawa T;
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Abbas S
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Jeoung JW
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Li Y
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Ghorbanpour E
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74249 RNA expression in human retina
Li M
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhang L
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Chen X
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Yu-Wai-Man C
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Protas ME
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Gong B
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Mabuchi F
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Wang J
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Chhunchha B
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74827 Primary Open-Angle Glaucoma Genetics in African Americans
Restrepo NA
Current genetic medicine reports 2017; 5: 167-174 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Narooie-Nejad M
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Mabuchi F
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74479 RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
Lu C
Frontiers in genetics 2017; 8: 118 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Zanon-Moreno V
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Syc-Mazurek SB
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Qiu H
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Tikunova E
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Lee MC
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Matovinovic E
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74503 Axenfeld-Rieger syndrome
Seifi M
Clinical Genetics 2018; 93: 1123-1130 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Ghanbari M
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tang FY
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vande Perre P
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Taskiran EZ
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Su HA
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil A
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Fernandes KA
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Shei W
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Al-Haddad C
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Weh E
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Shi Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Kho PF
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Jin L
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Zazo Seco C
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Iglesias AI
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Ovtcharova V
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Ma L
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Mabuchi N
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Xu J
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Raza ST
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Karaosmanoglu B
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Qu D
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Tagalakis AD
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74827 Primary Open-Angle Glaucoma Genetics in African Americans
Cooke Bailey JN
Current genetic medicine reports 2017; 5: 167-174 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74479 RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
MacDougall M
Frontiers in genetics 2017; 8: 118 (IGR: 19-1)


74249 RNA expression in human retina
Zauhar RJ
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Zhu B
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Li SY
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Kim DM
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Rasouli A
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Pasalar P
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Ortega-Azorin C
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74503 Axenfeld-Rieger syndrome
Walter MA
Clinical Genetics 2018; 93: 1123-1130 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Singh P
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Wang QL
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Mabuchi N
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Ni S
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Mousavi M
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Patat O
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Asensio-Marquez EM
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Koşukcu C
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Wilson MP
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Stamer WD
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chan AS
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Hariri H
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74249 RNA expression in human retina
Grazal C
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Chandra A
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Footz T
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Qu C
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Yang JJ
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Dong A
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Takamoto M
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Springelkamp H
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Zhang MH
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Meng J
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Liu R
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Reshetnikov E
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
An J
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Sakurada Y
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Lea RA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Oh S
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Yazdani S
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tam POS
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Garcia-Medina JJ
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Benton MC
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Sakurada Y
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Shibbani K
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Ye Z
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Singh L
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Yen YC
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Yuan G
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Pang CP
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Bouneau L
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Zhou X
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Moazzeni H
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Rohani MR
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chua BT
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Kasberger J
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Dvornyk V
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Singh DP
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Lee JS
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Doğan ÖA
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Shrager P
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74249 RNA expression in human retina
Curcio CA
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Chen W
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Van Duijn CM
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Bouremel Y
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Yoneyama S
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Chen Q
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Polonikov A
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Liu Y
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Lee RMH
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Park SS
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Yoneyama S
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Libby RT
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Ikram MA
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Bitar F
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74249 RNA expression in human retina
DeAngelis MM
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vigouroux A
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Kashiwagi K
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Taylan-Şekeroğlu H
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Elahi E
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tham CCY
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Pinazo-Duran MD
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Mahdi F
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Eccles DA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Yuan H
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Baraban SC
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Yin Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Goh SR
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Tan C
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Chen LJ
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Bushueva O
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Şimşek-Kiper PÖ
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Hu W
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Coltell O
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Virasami A
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Haupt LM
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Kim JY
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Levin AV
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Dehghan A
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Kurban M
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Kashiwagi K
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chong YF
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Iijima H
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Bourgeois D
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74249 RNA expression in human retina
Stambolian D
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Erkeland SJ
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Ordovas JM
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Hewitt AW
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhou L
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Yamagata Z
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Katz LJ
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
El Hout S
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Nemer G
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Hilmy MH
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Iijima H
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Shuai P
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Hart SL
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Utine EG
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Churnosov M
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Boduroğlu K
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Klaver CCW
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Nongpiur ME
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Takamoto M
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Li J
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Khaw PT
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Sherwin JC
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Corella D
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Chassaing N
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Ritch R
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Arabi M
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhang R
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Yamagata Z
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Xu H
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Meester-Smoor MA
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Calvas P
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Alikaşifoğlu M
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Baskaran M
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Mackey DA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Aihara M
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Walter MA
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Guo X
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Aihara M
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Griffiths LR
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Lin D
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Iwata T
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Cheng Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Iwata T
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Semina EV
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Khor CC
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma

Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Gould DB
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Araie M
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Li X
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Yang Z
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Kawase K
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Aung T; Hunziker W
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Lin Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Tang Z
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Shiga Y
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population

Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Nishiguchi KM
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Vithana EN
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Liu X
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Nakazawa T; Ozaki M; Araie M;
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Iglesias AI
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yoshikawa M
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73070 Genetics of Glaucoma
Wiggs JL
Human Molecular Genetics 2017; 26: R21-R27 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Kim WJ
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Yang Y
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Lewis C
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu MY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Dabbagh N
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


73061 Major review: Molecular genetics of primary open-angle glaucoma
Liu Y
Experimental Eye Research 2017; 160: 62-84 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Zeng K
Bioscience reports 2017; 37: (IGR: 18-4)


72869 CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma
Hu Z
Oncotarget 2017; 8: 21167-21176 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Song E
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Zhou T
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Chen L
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Nannini DR
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Wang X
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72965 Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye
Swierkowska J
Ophthalmic Genetics 2017; 0: 1-10 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Williams PA
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Firasat S
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Ferre-Fernández JJ
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Simpson A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Wang NL
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu Y
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Zhang L
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72965 Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye
Gajecka M
Ophthalmic Genetics 2017; 0: 1-10 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Kaul H
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Harder JM
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Torres M
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Luo N
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Shahrani H
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Nakanishi H
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Souzeau E
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72869 CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma
He C
Oncotarget 2017; 8: 21167-21176 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Aroca-Aguilar JD
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
van der Lee SJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Gong K
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Zhong B
Bioscience reports 2017; 37: (IGR: 18-4)


73061 Major review: Molecular genetics of primary open-angle glaucoma
Allingham RR
Experimental Eye Research 2017; 160: 62-84 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Hedberg-Buenz A
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Avdic A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Kim JH
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


73070 Genetics of Glaucoma
Pasquale LR
Human Molecular Genetics 2017; 26: R21-R27 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Dohayan N
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Chen YI
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Rong SS
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Medina-Trillo C
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Alvarado JA
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Bonnemaijer PWM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Ashfaq UA
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamashiro K
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Siggs OM
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Foxworth NE
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Cho NC
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
DeLuca AP
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Roos BR
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Zhang Y
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Li S
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Fang M
Bioscience reports 2017; 37: (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Miyake M
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Bonet-Fernández JM
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Liu CY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Wang C
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Taylor KD
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Stone EM
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Lim M
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Huang LN
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Zhu X
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
DeLuca A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Mustafa M
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Idrees S
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Landers J
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Höhn R
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Cardozo BH
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Shen XL
Bioscience reports 2017; 37: (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Walnuss C
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Alward WLM
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Miller K
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Sundaresan P
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Huang LN
Bioscience reports 2017; 37: (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Cochran KE
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Nag A
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Mills R
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Akagi T
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Rotter JI
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Méndez-Hernández CD
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Arfin M
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Cheng HB
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Deng CY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Qu C
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Schnieders MJ
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
John SWM
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Morales-Fernández L
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Varma R
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Li H
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Goldberg I
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Peng L
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Fingert JH
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Gharahkhani P
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Neely D
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Gotoh N
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Asmari AK
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Spandau D
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Scheetz TE
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Zhou L
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Khawaja AP
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Corton M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Gao X
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Healey PR
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Ikeda HO
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Alward WL
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Graham S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Broer L
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Suda K
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Cabañero-Valera MJ
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Ghaffarieh A; Sun Y
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Gut M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels

Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Fingert JH
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Hewitt AW
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamada H; Hasegawa T
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Foster PJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Tonda R
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Mackey DA
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Ayuso C
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Iida Y
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Hammond CJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Galanopoulos A; Casson RJ
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamada R
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Coca-Prados M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Hysi PG; van Leeuwen EM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
García-Feijoo J
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Ruddle JB
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Matsuda F
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Es
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Ellis J
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Macgregor S
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yoshimura N
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Leo P
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Mackey DA
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects

Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Mazur J
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Brown MA; Macgregor S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Nickels S
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Sharma S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Uitterlinden AG
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Burdon KP
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Klaver CCW
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Craig JE
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Amin N; Van Duijn CM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Asfuroglu M
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhao J
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71510 Epigenetics and Signaling Pathways in Glaucoma
Gauthier AC
BioMed research international 2017; 2017: 5712341 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Micheal S
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Zhou T
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Maes ME
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Alghamdi KA
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Mao M
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Williams AL
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Navarro-Partida J
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Prat C
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Zhao D
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Danford ID
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Mohanty K
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Kondkar AA
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Salehi Z
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Springelkamp H
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Dulle JE
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Alsaedi AB
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Belville C
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Liang CY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71510 Epigenetics and Signaling Pathways in Glaucoma
Liu J
BioMed research international 2017; 2017: 5712341 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Verkuil LD
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Iglesias AI
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Gholaminia M
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhou H
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Rübsam A
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Saksens NT
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Schlamp CL
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Eason J
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Edward NB
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Cavdarli B
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Nguyen CT
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Martinez-Rizo AB
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Souzeau E
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Kiss M
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Dada R
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Hogewind BF
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Choi DJ
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Ou Y
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Garnai SJ
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Dada T
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Gholaminia Z
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Sun L
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Koz OG
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Kalantan H
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Feng SC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Aljasser A
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Mishra A
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Nickells RW
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Wong VH
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Chawla B
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Sharma S
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Ramirez-Barrera P
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Comptour A
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Lin KH
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Al-Kharashi AS
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Bohnsack BL
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Landers J
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Velazquez-Fernandez JB
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Pawar HS
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Lim JK
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Khan MI
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
A Yarangumeli A
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Yang B
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Höhn R
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Altawil A
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Marceau G
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Gould DB
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Collins DW
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Panjtanpanah M
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Lee HN
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhang L
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Ozdemir EY
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
He Z
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Kamal NM
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Clairefond G
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Fort PE
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wojciechowski R
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Gudiseva HV
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Qazvini MG
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Mondragon-Jaimes VA
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Hoyng CB
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Altuwaijri S
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Mills R; Goldberg I
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Shen YC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Jobling AI
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Khawaja AP
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Santos-Garcia A
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Mohamed G
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Shi H
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Chiambaretta F
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Uyhazi KE
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
den Hollander AI
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Benites-Godinez V
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Sapin V
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Sultan T
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Fletcher EL
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Healey PR
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Lau MK
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Wei LC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zheng Y
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Nag A
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Azad TA
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Chinnery HR
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Kanu LN
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Chang CJ
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Graham S
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Blanchon L
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wang YX
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Grant GR
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Vingrys AJ
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Hewitt AW
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Abu-Amero KK
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Hsu MY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wang JJ
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Mackey DA
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Cuellar-Partida G
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Bui BV
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Yang YY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Chavali VR; O'Brien JM
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Galanopoulos A
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Gibson J
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Chiu CH; Wang CY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Cooke Bailey JN
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Casson RJ
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Vithana EN
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Ruddle JB
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Gharahkhani P
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Ellis J; Leo P
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Boutin T; Ramdas WD
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Brown MA
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Zeller T
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Macgregor S; Lynn DJ
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Luben RN; Yonova-Doing E
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Burdon KP
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Viswanathan AC
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Craig JE
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Yaz
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Elliott MH
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Struebing FL
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
de Juan-Marcos L
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Navarro-Partida J
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Kosior-Jarecka E
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Song C
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Souzeau E
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Grønskov K
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Orssaud C
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Morrison JC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Shi H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Miller MA
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Mookherjee S
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70688 Dataset of eye disease-related proteins analyzed using the unfolding mutation screen
McCafferty CL
Scientific data 2016; 3: 160112 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Mauri L
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Minegishi Y
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Cui XJ
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Khawaja AP
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70150 A single gene connects stiffness in glaucoma and the vascular system
Borrás T
Experimental Eye Research 2017; 158: 13-22 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Gohari M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70707 Systems Genetics Analysis to Identify the Genetic Modulation of a Glaucoma-Associated Gene
Chintalapudi SR
Methods in molecular biology (Clifton, N.J.) 2017; 1488: 391-417 (IGR: 18-2)


70928 The Pathway From Genes to Gene Therapy in Glaucoma: A Review of Possibilities for Using Genes as Glaucoma Drugs
Borrás T
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) 2017; 6: 80-93 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Kumar S
Genomics 2017; 109: 27-35 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Nag A
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Reis LM
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zhong Y
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Kondkar AA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Scheetz TE
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Zhou T
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Rauf B
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Shahrani H
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Fingert JH
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Verma SS
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Peotter JL
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Holt R
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Moazzeni H
Gene 2016; 593: 76-83 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Nakayama M
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Cooke Bailey JN
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Malik MA
Genomics 2017; 109: 27-35 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Dabbagh N
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Guo X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70688 Dataset of eye disease-related proteins analyzed using the unfolding mutation screen
Sergeev YV
Scientific data 2016; 3: 160112 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Cooke Bailey JN
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Banerjee D
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Lu H
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Souzeau E
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Tyler RC
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Phillips J
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Zhang J
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Faga B
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Cepurna WO
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Mousa A
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Wróbel-Dudzińska D
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Irum B
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Redó-Riveiro A
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Akbari MT
Gene 2016; 593: 76-83 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Robin AL
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Alvarado Castillo B
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Neámatzadeh H
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Uebe S
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ugur Iseri SA
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Ashpole NE
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Escudero-Domínguez FA
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70707 Systems Genetics Analysis to Identify the Genetic Modulation of a Glaucoma-Associated Gene
Jablonski MM
Methods in molecular biology (Clifton, N.J.) 2017; 1488: 391-417 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Min X
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Tram KH
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Lee RK
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Fingert JH
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Zhao AG
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Robert MP
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Lucas A
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Azad TA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Kang JH
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Wyatt AW
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Ortega L
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Wang XL
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Jafari MA
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Sticht H
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Xiao H
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Tong T
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Łukasik U
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Kabir F
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Sandfeld L
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Gu X
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Martinez-Rizo AB
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Zhang H
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Dohayan N
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Yazdani S
Gene 2016; 593: 76-83 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Roche O
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Chakraborty S
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Hernández-Galilea E
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Weh E
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Witney M
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Williams RW
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Bettis DI
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Tehrani S
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Iejima D
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Zhu R
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
K S
Genomics 2017; 109: 27-35 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Sharma S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Arno M
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Scheetz TE
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Mukhopadhyay I
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Vossmerbaeumer U
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Luo J
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Arfin M
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Elahi E
Gene 2016; 593: 76-83 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Cruz-González F
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Firasat S
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Roos BR
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Geisert EE
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Iglesias AI
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Aung T
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Sultan T
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Allingham RR
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Ruddle JB
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Hu N
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Siggs OM
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Kwon YH
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Bradford Y
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Bax DA
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Dimeo K
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Kawase K
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Almobarak FA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Zibrandtsen N
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Rosales-Diaz R
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Hendee KE
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Sihota R
Genomics 2017; 109: 27-35 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Herrnberger L
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Mazaheri M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Choe TE
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Goldberg I
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Alawad A
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Naeem MA
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Bonnemaijer P
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Zare-Shehneh M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Liebmann JM
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Sen A
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Kariminejad A
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Gonzalez JM
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Graham SL
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Gold Diaz D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Alawad A
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Lu H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Jayaram H
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Linneman JG
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Velazquez-Fernandez JB
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Iwata T
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Kaur J
Genomics 2017; 109: 27-35 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Asmari M
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Weisschuh N
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zuo C
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Gordon MO
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
McClellan ME
Scientific reports 2016; 6: 37127 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Follana-Neira I
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Almobarak FA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Khor CC
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Hauser MA
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Harris P
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
González-Sarmiento R
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Santos C
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Kocki J
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Osman EA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Manfredini E
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Griffith GL
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Alawad A
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Ritch R
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Lozano DC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Healey PR
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Hauser MA
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Khan SN
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Bach-Holm D
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Santos A
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Huang X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Yang M
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Brilliant M
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Peters DM
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Altuwaijri S
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Broer L
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Abbasi-Shavazi E
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Ray K
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Healey PR
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Altuwaijri S
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Kass MA
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Rizvi S
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Abdul-Rahman O
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Altuwaijri S
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Goldberg I
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Qin B
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Wang K
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Tümer Z
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Fortune B
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Pasquale LR
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Alward WL
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Broadgate S
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Ben-Omran T
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Al-Obeidan SA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Budenz DL
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Reagan AM
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Uitterlinden AG
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Asmari A
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Graham S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Żarnowski T
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Huang J
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Maselli E
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Husnain T
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Hewitt AW
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Riazuddin S
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Fingert JH
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Mackey DA
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Boyce TM
Scientific reports 2016; 6: 37127 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Patrosso M
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Christen WG
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Peissig PL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Dunn R
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Manning MA
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Mi L
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Klaver CC
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Johnson EC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Abu-Amero KK
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Shi J
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Bruty J
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Akram J
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Tanito M
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zhang Q
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Mackey DA
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Fingert J
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Hewitt AW
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
van Duijn C
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Guan H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Weinreb RN
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
McCarty CA
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Brilliant MH
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Gaasterland D
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Hysi PG
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Kitchner TE
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Wallis Y
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Penco S
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Tamm ER
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Casson RJ
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Burdon KP
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Riazuddin SA
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
McCarty CA
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Liu X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Costakos D
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Hammond CJ
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Landers J
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Craig JE
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Haines JL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Gaasterland T
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Reis A
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
McMullan D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Stamer WD
Scientific reports 2016; 6: 37127 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Pasutto F
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Mills R
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Kraft P
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Semina EV
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ogilvie C
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Wiggs JL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Lee RK
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Gerrelli D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Ellis J
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Vrabec TR
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Zhang Y
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Tromp G
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Leo P
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Lichter PR
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Brown MA
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ragge N
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Ritchie MD
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Liu Y; Medeiros F
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium

PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Macgregor S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Moroi SE
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Burdon KP; Craig JE
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Richards JE; Realini T; Ritch R; Schuman JS; Scott WK; S
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Ng SK
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Collins DW
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Chen X
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Gao Y
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Khor CC
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Scheetz TE
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Lv Y
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69288 A global test for gene-gene interactions based on random matrix theory
Frost HR
Genetic epidemiology 2016; 40: 689-701 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Cuellar-Partida G
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Liu Y
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Kader MA
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Chen X
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Arunrut T
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Xiang Y
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Kuehn MH
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Sang J
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


69384 Smad-independent TGF-β2 signaling pathways in human trabecular meshwork cells
Pervan CL
Experimental Eye Research 2017; 158: 137-145 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Yi QY
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park J
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Rong SS
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Banerjee A
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Reis LM
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Tan C
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Bermudez JY
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Hull S
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Zhang P
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Nishisako M
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Sabbadini M
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Huang L
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Kim M
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Chen Y
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Jia L
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Deng G
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Bailey JC
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Chen LJ
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Burdon KP
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Chakraborty S
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Meguro A
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Tyler RC
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Craig JE
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69288 A global test for gene-gene interactions based on random matrix theory
Amos CI
Genetic epidemiology 2016; 40: 689-701 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Webber HC
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Jiang B
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Lipsett KA
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Namburi P
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Gudiseva HV
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Chen Y
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Arno G
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Roos BR
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Li W
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Do T
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Dong Y
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Yao Q
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Ramugade S
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Jain M
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Zafar SN
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Xie L
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Chakraborty A
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Fitzgerald JT
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park CK
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Wiggs JL
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Patel GC
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Leung CK
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Zhao B
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Menotti-Raymond M
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Yang Z
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


68573 Mitochond