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List of abstracts related to

Listed by Classification

3.4.2 Gene studies (4889 abstracts found)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Currant H
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Raga-Cervera J
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94483 Mendelian randomization analysis identified genes pleiotropically associated with central corneal thickness
Yang Z
BMC Genomics 2021; 22: 517 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Sayyad Z
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Li X
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94967 Overexpression and Activation of αvβ3 Integrin Differentially Affects TGFβ2 Signaling in Human Trabecular Meshwork Cells
Filla MS
Cells 2021; 10: (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Emamalizadeh B
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Thakur N
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94464 The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis
Salari N
International Ophthalmology 2021; 41: 2747-2763 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
van der Heide C
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94937 Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data
Scelsi HF
Human Mutation 2021; 42: 903-946 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Alipanahi B
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94384 Meta-analysis of gene mutations in primary congenital glaucoma patients
Haddad A
European Journal of Ophthalmology 2021; 0: 11206721211016308 (IGR: 22-2)

94482 Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature
Al Motawa MNA
American Journal of Case Reports 2021; 22: e930824 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Liuska PJ
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Kong N
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94923
Eliseeva N
Molecular Vision 2021; 27: 262-269 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Li X
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Zukerman R
Genes 2021; 12: (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Liu X
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94923
Ponomarenko I
Molecular Vision 2021; 27: 262-269 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Wang Q
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Sun W
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Kumar Pandey R
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94937 Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data
Barlow BM
Human Mutation 2021; 42: 903-946 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Lemmelä S
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Harris A
Genes 2021; 12: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Hormozdiari F
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94464 The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis
Bokaee S
International Ophthalmology 2021; 41: 2747-2763 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Goar W
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94384 Meta-analysis of gene mutations in primary congenital glaucoma patients
Ait Boujmia OK
European Journal of Ophthalmology 2021; 0: 11206721211016308 (IGR: 22-2)

94482 Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature
Al Shehri MSS
American Journal of Case Reports 2021; 22: e930824 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Bolarin JM
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94967 Overexpression and Activation of αvβ3 Integrin Differentially Affects TGFβ2 Signaling in Human Trabecular Meshwork Cells
Meyer KK
Cells 2021; 10: (IGR: 22-2)

94483 Mendelian randomization analysis identified genes pleiotropically associated with central corneal thickness
Yang J
BMC Genomics 2021; 22: 517 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Vishwakarma S
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Hysi P
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Daneshmandpour Y
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Xiao X
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Bao Y
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94464 The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis
Farshchian N
International Ophthalmology 2021; 41: 2747-2763 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Kazeminasb S
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Zhao H
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94923
Reshetnikov E
Molecular Vision 2021; 27: 262-269 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Behsaz B
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Xiao X
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Kumar V
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Shao Z
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94483 Mendelian randomization analysis identified genes pleiotropically associated with central corneal thickness
Liu D
BMC Genomics 2021; 22: 517 (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Li S
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Dave TV
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Millan JM
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94967 Overexpression and Activation of αvβ3 Integrin Differentially Affects TGFβ2 Signaling in Human Trabecular Meshwork Cells
Faralli JA
Cells 2021; 10: (IGR: 22-2)

94384 Meta-analysis of gene mutations in primary congenital glaucoma patients
El Maaloum L
European Journal of Ophthalmology 2021; 0: 11206721211016308 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Havulinna AS
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Fitzgerald TW
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94482 Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature
Al Buali MJ
American Journal of Case Reports 2021; 22: e930824 (IGR: 22-2)

94937 Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data
Saccuzzo EG
Human Mutation 2021; 42: 903-946 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Meyer KJ
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Oddone F
Genes 2021; 12: (IGR: 22-2)

94967 Overexpression and Activation of αvβ3 Integrin Differentially Affects TGFβ2 Signaling in Human Trabecular Meshwork Cells
Peters DM
Cells 2021; 10: (IGR: 22-2)

94384 Meta-analysis of gene mutations in primary congenital glaucoma patients
Dehbi H
European Journal of Ophthalmology 2021; 0: 11206721211016308 (IGR: 22-2)

94482 Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature
Al Agnam AAM
American Journal of Case Reports 2021; 22: e930824 (IGR: 22-2)

94483 Mendelian randomization analysis identified genes pleiotropically associated with central corneal thickness
Yu W
BMC Genomics 2021; 22: 517 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Naik MN
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Mannan R
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Gharahkhani P
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Aghaei Moghadam E
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Kang X
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94937 Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data
Lieberman RL
Human Mutation 2021; 42: 903-946 (IGR: 22-2)

94464 The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis
Mohammadi M
International Ophthalmology 2021; 41: 2747-2763 (IGR: 22-2)

94923
Dvornyk V
Molecular Vision 2021; 27: 262-269 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Zhang S
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Ouyang J
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Alward WLM
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Siesky B
Genes 2021; 12: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Cosentino J
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Kaarniranta K
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Fang L
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Garcia-Medina JJ
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Pruthi A
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
McCaw ZR
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Li S
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Uusitalo H
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Tai X
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Verticchio Vercellin A
Genes 2021; 12: (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Bonnemaijer PWM
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Bahmanpour Z
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Pedrola L
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Hou M
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Sun W
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Hou M
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94464 The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis
Kazeminia M
International Ophthalmology 2021; 41: 2747-2763 (IGR: 22-2)

94923
Churnosov M
Molecular Vision 2021; 27: 262-269 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Boese EA
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Radha V
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Alehabib E
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Sears NC
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Schorsch E
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Jiang M
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Liu X
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Senabouth A
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Kaur I
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94283 Glaucoma Heritability: Molecular Mechanisms of Disease
Ciulla TA
Genes 2021; 12: (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Laivuori H
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94884 Suggestive evidence of genetic association of -572G > C polymorphism with primary open angle glaucoma in a North Indian Punjabi population
Mehrotra S
Human immunology 2021; 82: 791-797 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Abellán-Abenza J
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Liu X
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Chen X
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Valero-Vello M
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94897 Heterozygous variants with ocular phenotype: Missense in domain but truncation out of domain
Zhang Q
Molecular Vision 2021; 27: 309-322 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Roos BR
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Guo W
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Kiiskinen T
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Hewitt AW
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94296 Biallelic variants in are associated with primary open-angle glaucoma and primary angle-closure glaucoma
Zhang Q
British Journal of Ophthalmology 2022; 106: 1710-1715 (IGR: 22-2)

94820 Human primary retinal cells as an in-vitro model for investigating defective signalling caused by OPTN mutants associated with glaucoma
Swarup G
Neurochemistry International 2021; 148: 105075 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Valero-Vello M
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Alinaghi S
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Sculley D
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Du M
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Daly MJ
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Kwon YH
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Sanz-González SM
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Li J
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Dorfman EH
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94900 Long Noncoding RNA LINC01518 Modulates Proliferation and Migration in TGF-β1-Treated Human Tenon Capsule Fibroblast Cells Through the Regulation of hsa-miR-216b-5p
Shen Y
NeuroMolecular Medicine 2022; 24: 88-96 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Doozandeh A
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Palotie A
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
DeLuca AP
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Atakhorrami M
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
O'Connor JE
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Foster PJ
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94895 Proteomic analysis of aged and OPTN E50K retina in the development of normal tension glaucoma
Yuan H
Human Molecular Genetics 2021; 30: 1030-1044 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images

PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Galarreta-Mira D
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Peng LH
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94564 Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations
Darvish H
International Ophthalmology 2021; 41: 3269-3276 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Siggs OM
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Atan D
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Galarreta-Mira D
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
Turunen JA
JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Gonzaga-Jauregui C
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94728 Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population

JAMA ophthalmology 2021; 139: 762-768 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Bendala-Tufanisco E
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Aung T
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Phene S
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Sheffield VC
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Charng J
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Hammel N
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Mayordomo-Febrer A
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Carroll A
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Choquet H
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Pinazo-Durán MD
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Wang K
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Craig J
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94833 miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks
Zanón-Moreno V
Journal of clinical medicine 2021; 10: (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
Khawaja AP
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Stone EM
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94538 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology
McLean CY
American Journal of Human Genetics 2021; 108: 1217-1230 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Khaw PT
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Mullins RF; Anderson MG
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Klaver CCW; Kubo M
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Fan BJ
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Ong JS
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Ritch R; Craig JE
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Pasquale LR; Reisman CA
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Wiggs JL
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Daniszewski M
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Scheetz TE
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Powell JE
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

94491 Exome-based investigation of the genetic basis of human pigmentary glaucoma
Fingert JH
BMC Genomics 2021; 22: 477 (IGR: 22-2)

94622 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Pébay A; Simcoe MJ; Thiadens AAHJ; Van Duijn CM; Yazar S; Jorgenson E; Macgregor S; Hammond CJ; Mackey DA; Wiggs JL; Foster PJ; Patel PJ; Birney E; Khawaja AP
PLoS Genetics 2021; 17: e1009497 (IGR: 22-2)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Kim YW
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Gharahkhani P
Nature communications 2021; 12: 1258 (IGR: 22-1)

92538 An Assessment of GUCA1C Variants in Primary Congenital Glaucoma
Souzeau E
Genes 2021; 12: (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Ding RF
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92731 LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis
Li X
PLoS ONE 2021; 16: e0250772 (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Dada T
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92425 Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review
Jemmeih S
Ophthalmic Epidemiology 2021; 0: 1-12 (IGR: 22-1)

92041 Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype
Atanasovska Velkovska M
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Zebardast N
Ophthalmology 2021; 0: (IGR: 22-1)

92543 Analysis of risk allele frequencies of single nucleotide polymorphisms related to open-angle glaucoma in different ethnic groups
Shin HT
BMC Medical Genomics 2021; 14: 80 (IGR: 22-1)

92160 Updates on Genes and Genetic Mechanisms Implicated in Primary Angle-Closure Glaucoma
Kondkar AA
The application of clinical genetics 2021; 14: 89-112 (IGR: 22-1)

92672 Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
Gołaszewska K
BMC Ophthalmology 2021; 21: 154 (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Hu D
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

92477 A glaucoma- and ALS-associated mutant of OPTN induces neuronal cell death dependent on Tbk1 activity, autophagy and ER stress
Medchalmi S
FEBS Journal 2021; 288: 4576-4595 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Wu Y
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Knight LSW
Ophthalmology 2021; 0: (IGR: 22-1)

91921 Pseudoexfoliation syndrome and glaucoma: from genes to disease mechanisms
Schlötzer-Schrehardt U
Current Opinions in Ophthalmology 2021; 32: 118-128 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Tolman NG
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Papadopoulou MK
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Zhou Z
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

92833 Acute Angle Closure in Knobloch Syndrome
Wawrzynski J
Journal of Glaucoma 2021; 30: e265-e268 (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Koenighofer M
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92731 LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis
He J
PLoS ONE 2021; 16: e0250772 (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Gao Z
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

92425 Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review
Malik S
Ophthalmic Epidemiology 2021; 0: 1-12 (IGR: 22-1)

92538 An Assessment of GUCA1C Variants in Primary Congenital Glaucoma
Weisschuh N
Genes 2021; 12: (IGR: 22-1)

91921 Pseudoexfoliation syndrome and glaucoma: from genes to disease mechanisms
Khor CC
Current Opinions in Ophthalmology 2021; 32: 118-128 (IGR: 22-1)

92543 Analysis of risk allele frequencies of single nucleotide polymorphisms related to open-angle glaucoma in different ethnic groups
Yoon BW
BMC Medical Genomics 2021; 14: 80 (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Parzefall T
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Chatziralli I
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Bak E
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92833 Acute Angle Closure in Knobloch Syndrome
Than J
Journal of Glaucoma 2021; 30: e265-e268 (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Jiang J
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Jorgenson E
Nature communications 2021; 12: 1258 (IGR: 22-1)

92477 A glaucoma- and ALS-associated mutant of OPTN induces neuronal cell death dependent on Tbk1 activity, autophagy and ER stress
Tare P
FEBS Journal 2021; 288: 4576-4595 (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Sekimitsu S
Ophthalmology 2021; 0: (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Bak E
Journal of clinical medicine 2021; 10: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Bhai N
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92041 Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype
Goričar K
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Balasubramanian R
Disease models & mechanisms 2021; 14: (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Ruddle JB
Ophthalmology 2021; 0: (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Yu Q
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Peng C
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Bak E
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92672 Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
Dub N
BMC Ophthalmology 2021; 21: 154 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Bak E
Journal of clinical medicine 2021; 10: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Midha N
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92672 Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
Saeed E
BMC Ophthalmology 2021; 21: 154 (IGR: 22-1)

92041 Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype
Blagus T
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Lin Z
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Liu K
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Frohne A
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Taranath DA
Ophthalmology 2021; 0: (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Yan W
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Tzika K
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Huang L
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92833 Acute Angle Closure in Knobloch Syndrome
Gillam M
Journal of Glaucoma 2021; 30: e265-e268 (IGR: 22-1)

92543 Analysis of risk allele frequencies of single nucleotide polymorphisms related to open-angle glaucoma in different ethnic groups
Seo JH
BMC Medical Genomics 2021; 14: 80 (IGR: 22-1)

92731 LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis
Sun J
PLoS ONE 2021; 16: e0250772 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Wy S
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92425 Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review
Okashah S
Ophthalmic Epidemiology 2021; 0: 1-12 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
MacAlinao DG
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92538 An Assessment of GUCA1C Variants in Primary Congenital Glaucoma
Craig JE
Genes 2021; 12: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Hysi P
Nature communications 2021; 12: 1258 (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Wang J
Ophthalmology 2021; 0: (IGR: 22-1)

92477 A glaucoma- and ALS-associated mutant of OPTN induces neuronal cell death dependent on Tbk1 activity, autophagy and ER stress
Sayyad Z
FEBS Journal 2021; 288: 4576-4595 (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Chiras D
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Kearney AL
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Zhang Y
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

92477 A glaucoma- and ALS-associated mutant of OPTN induces neuronal cell death dependent on Tbk1 activity, autophagy and ER stress
Swarup G
FEBS Journal 2021; 288: 4576-4595 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Goldberg I
Ophthalmology 2021; 0: (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Lee SC
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92425 Genetic Epidemiology of Primary Congenital Glaucoma in the 22 Arab Countries: A Systematic Review
Zayed H
Ophthalmic Epidemiology 2021; 0: 1-12 (IGR: 22-1)

92538 An Assessment of GUCA1C Variants in Primary Congenital Glaucoma
Pasutto F
Genes 2021; 12: (IGR: 22-1)

92672 Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
Mariak Z
BMC Ophthalmology 2021; 21: 154 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Khawaja AP
Nature communications 2021; 12: 1258 (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Shakrawal J
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92833 Acute Angle Closure in Knobloch Syndrome
Foster PJ
Journal of Glaucoma 2021; 30: e265-e268 (IGR: 22-1)

92041 Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype
Dolžan V
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Elze T
Ophthalmology 2021; 0: (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Frei E
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Xu L
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Du J
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Zhang C
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Ding X
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Gharahkhani P
Ophthalmology 2021; 0: (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Macnicoll KH
Disease models & mechanisms 2021; 14: (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Smith JEH
Ophthalmology 2021; 0: (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Kitsos G
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92672 Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report
Konopińska J
BMC Ophthalmology 2021; 21: 154 (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Huang J
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Kumar M
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Pendergrass S
Nature communications 2021; 12: 1258 (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Waldstein SM
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92041 Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype
Cvenkel B
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Moonasar N
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Yin HJ
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Kim YJ
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92538 An Assessment of GUCA1C Variants in Primary Congenital Glaucoma
Koch KW
Genes 2021; 12: (IGR: 22-1)

92287 Gene network analyses unveil possible molecular basis underlying drug-induced glaucoma
Ji ZL
BMC Medical Genomics 2021; 14: 109 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Montgomery CL
Disease models & mechanisms 2021; 14: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Chaurasia P
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Cole BS
Ophthalmology 2021; 0: (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Kim YK
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Han X
Nature communications 2021; 12: 1258 (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Mitulovic G
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Liu Y
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92745 Adenosine A3 receptor activated in HO oxidative stress of primary open-angle glaucoma
Xiong K
Annals of translational medicine 2021; 9: 526 (IGR: 22-1)

92567 Correlation of the intronic polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population
Kroupis C
Ophthalmic Genetics 2021; 0: 1-7 (IGR: 22-1)

92126 Identification of key genes and pathways in scleral extracellular matrix remodeling in glaucoma: Potential therapeutic agents discovered using bioinformatics analysis
Qian S
International journal of medical sciences 2021; 18: 1554-1565 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Gole G
Ophthalmology 2021; 0: (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Park KH
Journal of clinical medicine 2021; 10: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Gupta S
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Zeng C
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Chiang MY
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Ong JS
Nature communications 2021; 12: 1258 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
de Vries WN
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Lin MM
Ophthalmology 2021; 0: (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Schoefer C
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Hewitt AW
Nature communications 2021; 12: 1258 (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Angmo D
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Sun H
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

92417 Genetic Risk and Phenotype Correlation of Primary Open-Angle Glaucoma Based on Rho-Kinase Gene Polymorphisms
Jeoung JW
Journal of clinical medicine 2021; 10: (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Frei K
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Jackson IJ
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Segrè AV
Ophthalmology 2021; 0: (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Willett F
Ophthalmology 2021; 0: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank
Segrè AV; Wiggs JL
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Segrè AV
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
d'Mellow G
Ophthalmology 2021; 0: (IGR: 22-1)

92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Lucas T
Experimental Eye Research 2021; 205: 108497 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Segrè AV
Nature communications 2021; 12: 1258 (IGR: 22-1)

92366 Somatic GNAQ R183Q mutation is located within the sclera and episclera in patients with Sturge-Weber syndrome
Guo W
British Journal of Ophthalmology 2022; 106: 1006-1011 (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Yadav R
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Cross SH; Kizhatil K
Disease models & mechanisms 2021; 14: (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Breen J
Ophthalmology 2021; 0: (IGR: 22-1)

92116 Characteristics of Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank

Ophthalmology 2021; 0: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Dada R
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Rouhana JM
Nature communications 2021; 12: 1258 (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Nair KS
Disease models & mechanisms 2021; 14: (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Qassim A
Ophthalmology 2021; 0: (IGR: 22-1)

91995 Effect of Mindfulness Meditation on Intraocular Pressure and Trabecular Meshwork Gene Expression: A Randomized Controlled Trial
Sihota R
American Journal of Ophthalmology 2021; 223: 308-321 (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Hamel AR
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Mullany S
Ophthalmology 2021; 0: (IGR: 22-1)

92849 Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
John SWM
Disease models & mechanisms 2021; 14: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Igo RP
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Elder JE
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Choquet H; Qassim A
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Vincent AL
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Josyula NS
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Staffieri SE; Kearns LS
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Cooke Bailey JN; Bonnemaijer PWM
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Mackey DA; Luu S
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Iglesias A
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Siggs OM
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Siggs OM; Young TL
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Souzeau E
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Vitart V
Nature communications 2021; 12: 1258 (IGR: 22-1)

91972 Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry
Craig JE
Ophthalmology 2021; 0: (IGR: 22-1)

92322 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Thiadens AAHJ; Karjalainen J; Uebe S; Melles RB; Nair KS; Luben R; Simcoe M; Amersinghe N; Cree AJ; Hohn R; Poplawski A; Chen LJ; Rong SS; Aung T; Vithana EN; ; Tamiya G; Shiga Y; Yamamoto M; Nakazawa T; Currant H; Birney E; Wang X; Auton A; Lupton MK; Martin NG; Ashaye A; Olawoye O; Williams SE; Akafo S; Ramsay M; Hashimoto K; Kamatani Y; Akiyama M; Momozawa Y; Foster PJ; Khaw PT; Morgan JE; Strouthidis NG; Kraft P; Kang JH; Pang CP; Pasutto F; Mitchell P; Lotery AJ; Palotie A; van Duijn C; Haines JL; Hammond C; Pasquale LR; Klaver CCW; Hauser M; Khor CC; Mackey DA; Kubo M; Cheng CY; Craig JE; Macgregor S; Wiggs JL
Nature communications 2021; 12: 1258 (IGR: 22-1)

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 2021; 4: 411-420 (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)

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)

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)

91259 Prevalence of MYOC risk variants for glaucoma in different populations
Liuska PJ
Acta Ophthalmologica 2021; 99: e1090-e1097 (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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

91259 Prevalence of MYOC risk variants for glaucoma in different populations
Harju M
Acta Ophthalmologica 2021; 99: e1090-e1097 (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)

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 2021; 4: 411-420 (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)

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

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)

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)

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)

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)

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)

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)

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)

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)

91259 Prevalence of MYOC risk variants for glaucoma in different populations
Kivelä TT
Acta Ophthalmologica 2021; 99: e1090-e1097 (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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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)

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 2021; 4: 411-420 (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)

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)

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)

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)

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)

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)

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)

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)

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

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)

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)

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

91259 Prevalence of MYOC risk variants for glaucoma in different populations
Turunen JA
Acta Ophthalmologica 2021; 99: e1090-e1097 (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 2021; 4: 411-420 (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)

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)

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)

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)

91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Kinoshita S
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 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)

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 2021; 4: 411-420 (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)

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)

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)

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)

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

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)

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)

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)

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)

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

91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Costa FF
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
Marshall H
Ophthalmology. Glaucoma 2021; 4: 411-420 (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)

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)

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 2021; 4: 411-420 (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 2021; 4: 411-420 (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)

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)

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)

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)

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)

91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Costa VP
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
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
Ferre-Fernández 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
Schulz AM
Ophthalmology. Glaucoma 2021; 4: 411-420 (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)

91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Sotozono C
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
Atienzar-Aroca R
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
Moura Pereira 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
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 2021; 4: 411-420 (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)

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 2021; 4: 411-420 (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)

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)

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)

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)

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)

91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Galanopoulos A; Agar A
Ophthalmology. Glaucoma 2021; 4: 411-420 (IGR: 21-4)

91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Tamayo A; 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
Healey PR; Hewitt AW
Ophthalmology. Glaucoma 2021; 4: 411-420 (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 2021; 4: 411-420 (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; Graham SL
Ophthalmology. Glaucoma 2021; 4: 411-420 (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
Macgregor S
Ophthalmology. Glaucoma 2021; 4: 411-420 (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; García-Feijoo 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
Souzeau E
Ophthalmology. Glaucoma 2021; 4: 411-420 (IGR: 21-4)

91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
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 2021; 4: 411-420 (IGR: 21-4)

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)

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)

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)

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

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)

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)

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)

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

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)

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

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

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)

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)

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)

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)

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)

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)

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

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

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)

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

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

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)

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)

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)

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

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

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

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)

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

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)

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)

89943 EAAT1 variants associated with glaucoma
Aida 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
Karekla A
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
Tham YC
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 MY
Medicine 2020; 99: e20066 (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)

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)

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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

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

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)

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)

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

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

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)

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

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)

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)

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

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

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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

89943 EAAT1 variants associated with glaucoma
Tanaka K
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
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)

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)

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
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
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)

90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Cummins TR
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
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; Zhong Y
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
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
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)

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)

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

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Gupta V
Eye 2021; 35: 400-408 (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)

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

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)

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Lu Y
Nature 2020; 588: 124-129 (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)

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)

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)

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)

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)

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Brommer B
Nature 2020; 588: 124-129 (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)

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)

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)

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)

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)

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)

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)

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

86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim YW
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
Johnson WM
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)

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

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)

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)

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)

86201 Lysyl Oxidase Like 1: Biological roles and regulation
Eivers SB
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
Somarajan BI
Eye 2021; 35: 400-408 (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)

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)

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)

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

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Tian X
Nature 2020; 588: 124-129 (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)

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Gupta S
Eye 2021; 35: 400-408 (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)

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)

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)

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)

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)

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

86863 Reprogramming to recover youthful epigenetic information and restore vision
Krishnan A
Nature 2020; 588: 124-129 (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)

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)

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)

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)

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)

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)

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Walia GK
Eye 2021; 35: 400-408 (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)

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

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

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)

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

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)

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)

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

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)

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)

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Meer M
Nature 2020; 588: 124-129 (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)

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

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Singh A
Eye 2021; 35: 400-408 (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)

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)

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)

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Sofi R
Eye 2021; 35: 400-408 (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)

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)

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)

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)

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)

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Wang C
Nature 2020; 588: 124-129 (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)

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)

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

86729 The mutational spectrum of Myocilin gene among familial versus sporadic cases of Juvenile onset open angle glaucoma
Chaudhary RS
Eye 2021; 35: 400-408 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Vera DL
Nature 2020; 588: 124-129 (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)

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)

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)

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)

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

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)

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

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)

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)

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)

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)

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)

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)

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 2021; 35: 400-408 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Zeng Q
Nature 2020; 588: 124-129 (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)

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)

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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Yu D
Nature 2020; 588: 124-129 (IGR: 21-2)

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

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)

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

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)

86581 Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
Scott WK
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
Tachibana N
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Bonkowski MS
Nature 2020; 588: 124-129 (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)

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)

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)

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)

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)

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

86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Kim JY
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
Hauser MA
Human Molecular Genetics 2020; 29: 1986-1995 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Yang JH
Nature 2020; 588: 124-129 (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)

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)

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

86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
Tsujikawa M
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
Sato K
American Journal of Ophthalmology 2020; 215: 135-140 (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)

86404 Association of the CAV1-CAV2 locus with normal-tension glaucoma in Chinese and Japanese
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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Zhou S
Nature 2020; 588: 124-129 (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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Hoffmann EM
Nature 2020; 588: 124-129 (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)

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)

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
Ragge 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
Wiggs JL
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Karg MM
Nature 2020; 588: 124-129 (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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Schultz MB
Nature 2020; 588: 124-129 (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)

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; Tham CC
Clinical and Experimental Ophthalmology 2020; 48: 658-665 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Kane AE
Nature 2020; 588: 124-129 (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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Davidsohn N
Nature 2020; 588: 124-129 (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)

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

86863 Reprogramming to recover youthful epigenetic information and restore vision
Korobkina E
Nature 2020; 588: 124-129 (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
Araie M
American Journal of Ophthalmology 2020; 215: 135-140 (IGR: 21-2)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Chwalek K; Rajman LA
Nature 2020; 588: 124-129 (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)

86863 Reprogramming to recover youthful epigenetic information and restore vision
Church GM; Hochedlinger K; Gladyshev VN; Horvath S; Levine ME; Gregory-Ksander MS; Ksander BR; He Z; Sinclair DA
Nature 2020; 588: 124-129 (IGR: 21-2)

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)

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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)

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

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

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

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

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)

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

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)

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)

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)

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

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)

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)

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)

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)

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

84848 Update in Genetics and Surgical Management of Primary Congenital Glaucoma
Aref 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
Cheong HS
Scientific reports 2020; 10: 221 (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)

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

85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Lu L
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
Shiga Y
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
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)

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

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)

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)

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

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)

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
Zargari S
Journal of ophthalmic & vision research 2020; 15: 45-52 (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)

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)

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)

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)

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)

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)

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