advertisement

WGC-2021

List of abstracts related to

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

Listed by Classification


3.4.2 Gene studies (4399 abstracts found)


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)


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


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


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


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


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)


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


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


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


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


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


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


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)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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)


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


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


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


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


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


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


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


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


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


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


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


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


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)


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)


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


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


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


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


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


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


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


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


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)


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)


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)


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


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)


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


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


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


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


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


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


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


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


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


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


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)


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)


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


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


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


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


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)


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


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


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


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)


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)


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)


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)


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


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


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
Zhang S
Genomics 2020; 112: 5129-5135 (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)


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)


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)


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


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


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


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


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


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


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)


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)


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)


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)


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


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


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


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


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


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


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


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


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


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


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)


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


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


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


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


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


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)


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


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


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)


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


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


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


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)


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)


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)


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)


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


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


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


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


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


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


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)


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)


86201 Lysyl Oxidase Like 1: Biological roles and regulation
Eivers SB
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
Larsen MC
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
Somarajan BI
Eye 2020; 0: (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)


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


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


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


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


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


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


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


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


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


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)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Jeoung JW
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
Kurata K
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)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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)


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)


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)


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)


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)


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


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


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


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


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


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


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


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


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


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


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


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


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)


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


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)


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


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


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


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


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 2020; 0: (IGR: 21-2)


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


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


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


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


86222 Genomic Characterization of TBK1 Duplication in Korean Normal-tension Glaucoma Patients
Song JY
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
Yamamoto T
Ophthalmic Genetics 2020; 41: 175-182 (IGR: 21-2)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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)


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


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


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


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


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


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


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


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


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


86081 Novel PXDN biallelic variants in patients with microphthalmia and anterior segment dysgenesis
Ragge N; 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)


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


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


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


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)


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)


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)


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)


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Rauf B
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
Kondkar AA
PLoS ONE 2020; 15: e0227417 (IGR: 21-1)


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


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


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


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


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


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)


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)


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)


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)


85194 Systems Genetics of Optic Nerve Axon Necrosis During Glaucoma
Stiemke AB
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
Liu H
Journal of Gene Medicine 2020; 22: e3139 (IGR: 21-1)


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


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


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)


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)


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


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


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


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


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


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


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


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


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


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


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)


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


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


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


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


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


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


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


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


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)


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


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


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)


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


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


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


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


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


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


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


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


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


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


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


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


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


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)


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)


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)


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)


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)


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)


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)


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)


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)


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


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


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


85188 Novel mutations in identified in familial cases of primary congenital glaucoma
Riazuddin S
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
Song YJ
Scientific reports 2020; 10: 221 (IGR: 21-1)


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


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


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)


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)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
van der Heide C
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


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


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wiggs JL; Fingert JH
JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


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


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


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


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


80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma

JAMA ophthalmology 2019; 137: 559-563 (IGR: 20-3)


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


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


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


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


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


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


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


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


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


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


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


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


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


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


80886 Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis
Wu Y; Zhou T; Shuai P; Tham CC; Weisschuh N; Krishnadas SR; Mardin C; Reis A; Yang J
Genetics in Medicine 2019; 21: 2345-2354 (IGR: 20-3)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Waryah YM
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Marques AM
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
Umali J
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Coêlho REA
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Gudiseva HV
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Lei L
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Morlino S
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Svidnicki PV
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Siggs OM
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Rong SS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Zhuang W
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lahola-Chomiak AA
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Park DY
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Huang L
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Medina-Trillo C
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Souzeau E
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Alesi V
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Pistilli M
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Wang S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Ananina G
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
Hawkey-Noble A
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Chen Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Footz T
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Aroca-Aguilar JD
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Braghini CA
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Sena DR
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Li S
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Iqbal M
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Lu SY
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Cho SY
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pasutto F
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Santa Cruz F
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Liu X
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
Costa VP
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Sheikh SA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Ferre-Fernández JJ
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Jin DK
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Matsushita K
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Calì F
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Hao J
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Lin Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79876 Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
French CR
Vision Research 2019; 156: 66-72 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Nguyen-Phuoc K
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Salowe R
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Costa VP
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Neil GJ
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Baig MA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


80023 Clinical Characteristics of Autosomal Dominant GJA1 Missense Mutation Linked to Oculodentodigital Dysplasia in a Korean Family
Kee C
Journal of Glaucoma 2019; 28: 357-362 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Singh LN
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Moura BCFS
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


80059 The clinical feature of myocilin Y437H mutation in a Chinese family with primary open-angle glaucoma
Zhang C
British Journal of Ophthalmology 2019; 103: 1524-1529 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
Schimiti RB
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
De Vasconcellos JPC
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Lepri FR
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Xu M
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Tam POS
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Alexandre-Moreno S
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Dubowsky A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Huang C; Leung CKS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Fan B
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
De Vasconcellos JPC
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Chi H
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Smith JEH
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Narsani AK
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Morales L
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Cheng Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Collins DW
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Secinaro A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79433 Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma
de Melo MB
PLoS ONE 2018; 13: e0207409 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Han CC
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Cole B
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Méndez-Hernández CD
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Kawashima R
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79339 Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients
de Melo MB
Ophthalmic Genetics 2018; 39: 717-724 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Shi Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Atif M
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Andrade FN
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Taranath D
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Piao S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allen KF
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Grammatico P; Novelli A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Usui S
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pater J
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
García-Feijoo J
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Greenfield DS
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
He J
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Gong B
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79794 CYP1B1 Gene and Phenotypic Correlation in Patients From Northeastern Brazil With Primary Congenital Glaucoma
Lira RPC
Journal of Glaucoma 2019; 28: 161-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Bhinder MA
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Ma J
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Merriam S
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Rait JL
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Lu F
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Ur Rahman A
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Drago F
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79951 Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
Escribano J
PLoS ONE 2019; 14: e0211029 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Parrish RK
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Zhang X
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tam POS
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79497 Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China
Ha S
PLoS ONE 2018; 13: e0206935 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Linkroum K
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Castori M
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yang J
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Young AL
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Khachataryan N
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Memon AI
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Narita A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tsujikawa M
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Mauri L
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Pirzado MS
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Henderer J
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Pasquale LR
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79696 LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant
Baban A
American Journal of Medical Genetics, Part A 2019; 179: 104-112 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Wang H
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79945 Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients
Waryah AM
International Journal of Ophthalmology 2019; 12: 8-15 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yin Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Zhang M
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Leonhardt RM
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Addis V
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Del Longo A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Ritch R
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Nishida K
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Reis A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Cui QN
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Cao Y
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Chappell A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Jiang D
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Javadiyan S
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Chappell A
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Sankar PS
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Wiggs JL
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Zhong L
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Craig JE
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Tham CC
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Kearns LS
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Miller-Ellis E
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Staffieri SE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allison WT
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Chavali VRM
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Xue B
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Pang CP
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Wang J
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Ying GS
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79575 Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese
Chen LJ
Experimental Eye Research 2019; 180: 129-136 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Elder JE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lehmann OJ; Walter MA
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Ruddle JB
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
Wallace D
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Hao F; Lee DY
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Hewitt AW
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Wiggs JL
Human Molecular Genetics 2019; 28: 1298-1311 (IGR: 20-2)


79960 The association of mitochondrial DNA haplogroups with POAG in African Americans
O'Brien JM
Experimental Eye Research 2019; 181: 85-89 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Pang CP
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Burdon KP
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Sun X
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Mackey DA
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


79556 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Yang Z
Science China Life Sciences 2019; 62: 153-164 (IGR: 20-2)


79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Craig JE
JAMA ophthalmology 2019; 137: 348-355 (IGR: 20-2)


78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Lin Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Tan Y
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Wubben TJ
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


79084 Transcriptional profiling analysis predicts potential biomarkers for glaucoma: HGF, AKR1B10 and AKR1C3
Nie Q
Experimental and therapeutic medicine 2018; 16: 5103-5111 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Qashqai M
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Takitani GEDS
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


78902
Stamenkovic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Shihadeh W
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Pandav SS
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Wang S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Saeedi O
Genes 2018; 9: (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Restrepo NA
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Kondkar AA
BMC research notes 2018; 11: 733 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yaz Y
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Afzal R
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Yu-Wai-Man C
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Khawaja AP
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Singh LN
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Abu-Amero KK
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen Y
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Oliveira MB
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Sultan T
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Qiu C
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Sultan T
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Azevedo AGB
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Zhang D
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Laper SM
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Firasat S
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Arno G
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Chan MPY
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Zhuang W
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
De Vasconcellos JPC
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Branham KH
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


78902
Lukic V
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Gao H
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Khabour O
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


79084 Transcriptional profiling analysis predicts potential biomarkers for glaucoma: HGF, AKR1B10 and AKR1C3
Zhang X
Experimental and therapeutic medicine 2018; 16: 5103-5111 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Chakma P
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yıldırım N
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Yousaf S
Genes 2018; 9: (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Suri F
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Crowston JG
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Ma J
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Khera A
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Aydın Yaz Y
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Ananina G
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Khalil MB
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Almobarak FA
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Qian S
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Kaul H
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Yaseri M
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Al-Obeidan SA
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Gong B
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Tsai J
Genes 2018; 9: (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Besirli CG
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


78902
Suvakov S
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Zhu Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Farber-Eger E
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Motta FL
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Brookes J
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Yip JLY
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Lopez Sanchez MIG
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
Costa VP
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78449 Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutations
Bohnsack BL
Ophthalmic Genetics 2018; 39: 615-618 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Al-Dabbagh A
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Chen C
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78847 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records
Crawford DC
BMC Medical Genomics 2018; 11: 70 (IGR: 20-1)


78776 P.Gly61Glu and P.Arg368His Mutations in CYP1B1 that Cause Congenital Glaucoma may be Relatively Frequent in Certain Regions of Gilan Province, Iran
Elahi E
Journal of ophthalmic & vision research 2018; 13: 403-410 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Palmer K
Genes 2018; 9: (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Ahmed B
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Bahabri IM
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78451 Analysis of sequence alterations in patients with primary open-angle glaucoma of Saudi origin
Kondkar AA
Clinical Ophthalmology 2018; 12: 1413-1416 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Chugh N
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Broadway DC
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Teixeira SH
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Çilingir O
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Zhang X
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Van Bergen NJ
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78902
Simic T
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Kalantan H
BMC research notes 2018; 11: 733 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen J
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Garcia-Feijoo J
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Xu M
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Riazuddin S
Genes 2018; 9: (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Abu-Amero KK
BMC research notes 2018; 11: 733 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Jiang L
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Kearns LS
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Chen X
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Li T
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Khaw PT
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Sallum JMF
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78902
Sencanic I
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78325 Association between IL1A and IL1B polymorphisms and primary open angle glaucoma in a Brazilian population
de Melo MB
Experimental biology and medicine (Maywood, N.J.) 2018; 243: 1083-1091 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Siddiqui SN
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79151 Association of gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma
Al-Hashimi M
International Journal of Ophthalmology 2018; 11: 1583-1587 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Gupta PC
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Yüksel Z
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Garway-Heath DF
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Piao S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78781 Three Single Nucleotide Polymorphisms of ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Mutlu F
Turkish journal of ophthalmology 2018; 48: 215-220 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Zafar SN
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Wang L
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


78902
Pljesa-Ercegovac M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Liu B
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78511 Primary congenital glaucoma including next-generation sequencing-based approaches: clinical utility gene card
Moosajee M
European Journal of Human Genetics 2018; 26: 1713-1718 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Thattaruthody F
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Viswanathan AC
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Hao J
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Hewitt AW
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78362 Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
Vessani RM
Arquivos Brasileiros de Oftalmologia 2018; 81: 437-439 (IGR: 20-1)


79210 Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort
Al-Obeidan SA
BMC research notes 2018; 11: 733 (IGR: 20-1)


79253 Association of ZP4 gene polymorphism with primary open-angle glaucoma in an ethnic Chinese population from Sichuan province
Lin Y
Chinese Journal of Medical Genetics 2018; 35: 737-740 (IGR: 20-1)


79129 Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma
Ahmed ZM
Genes 2018; 9: (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Yazar S
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Shahzadi M
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Luben R
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79110 Lack of Association of rs1192415 in With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients
Sun X
Frontiers in genetics 2018; 9: 488 (IGR: 20-1)


79089 Lack of Association between Variant rs7916697 in and Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetics research international 2018; 2018: 2148056 (IGR: 20-1)


78902
Jaksic V
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Lyu C
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Zhang W
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Seth NG
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78902
Babovic S
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Mackey DA
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Raj S
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Chi H
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Huang Y
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Hayat S
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78827 Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3' splice acceptor site of intron 2
Afshan K
Congenital anomalies 2019; 59: 152-161 (IGR: 20-1)


78902
Matic M
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Li H
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Wallace DC
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Kaushik S
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Xue Z
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Hauser MA
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


79180 Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population
Ha S
BMC Ophthalmology 2018; 18: 271 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Wareham NJ
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78902
Radosavljevic A
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Khullar M
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78872 Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma
Trounce IA
Investigative Ophthalmology and Visual Science 2018; 59: 4598-4602 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Wu Q
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78952 Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
Ram J
European Journal of Ophthalmology 2018; 0: 1120672118795405 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Khaw KT
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Jin C
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78902
Savic-Radojevic A
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Liang X
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Fortune B
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78902
Djukic T
International Journal of Ophthalmology 2018; 11: 1514-1520 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Allingham RR
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78904 Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract
Huang X; Lu L
Molecular medicine reports 2018; 18: 4439-4445 (IGR: 20-1)


78564 A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study
Foster PJ
Journal of Glaucoma 2018; 27: 743-749 (IGR: 20-1)


78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Swarup G
Frontiers in immunology 2018; 9: 1287 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Pasquale LR
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Ou Z
Bioscience reports 2018; 38: (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Horita S
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Ayala M
Clinical Ophthalmology 2018; 12: 1155-1162 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Wang X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Syrimis A
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Aung T
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Choquet H
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Macgregor S
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Bashir R
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Gao XR
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Tong L
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


78197 Indistinguishable gene expression between healthy eyes and eyes with unilateral exfoliative glaucoma
Cuklev F
Clinical Ophthalmology 2018; 12: 1155-1162 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Liu X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Ong JS
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Paylakhi S
Nature communications 2018; 9: 2278 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Nicolaou N
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Hou AH
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Huang H
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Simsek E
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78026 Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin
Sayyad Z
Frontiers in immunology 2018; 9: 1287 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Yousaf K
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Kang JH
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Chan AS
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Liu G
Bioscience reports 2018; 38: (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Alexandrou A
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Nannini DR
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Tahir H
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77990 Altered expression level of inflammation-related genes and long-term changes in ocular surface after trabeculectomy, a prospective cohort study
Wong TT
Ocular Surface 2018; 16: 441-447 (IGR: 19-4)


78047 Genetics of Exfoliation Syndrome
Khor CC
Journal of Glaucoma 2018; 27: S12-S14 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Simsek T
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Fan B
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Kneeland SC
Nature communications 2018; 9: 2278 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Huang L
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Liu W
Bioscience reports 2018; 38: (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
An J
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Yildirim N
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Han X
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Sanai M
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Thai KK
Nature communications 2018; 9: 2278 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Fang S
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Fan F
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Deng Y
Bioscience reports 2018; 38: (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Levkovitch-Verbin H
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Papaevripidou I
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Hoffmann TJ
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Zhou T
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Jia X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Zheng L
Bioscience reports 2018; 38: (IGR: 19-4)


78048 LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome
Wiggs JL
Journal of Glaucoma 2018; 27: S20-S23 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Nicolaou M
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Qayyum S
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Ishiura H
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77585 Genome-wide association analyses identify new loci influencing intraocular pressure
Kim H
Human Molecular Genetics 2018; 27: 2205-2213 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Yin J
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Siggs OM
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Loukianou E
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Zhang S
Bioscience reports 2018; 38: (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Nakamura M
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Xiao X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Kvale MN
Nature communications 2018; 9: 2278 (IGR: 19-4)


78263 Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families
Naz S
Journal of the Pakistan Medical Association 2018; 68: 1205-1211 (IGR: 19-4)


77936 Bioinformatics analysis of mutation hotspots in Chinese primary congenital glaucoma patients
Feng G
Bioscience reports 2018; 38: (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Sismani C
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Satoh N
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Li S
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Law MH
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Malas S
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Souzeau E
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77994 Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome
Guo X
Current Eye Research 2018; 43: 1334-1341 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Suzuki A
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Banda Y
Nature communications 2018; 9: 2278 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Tsukada H
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Sharma S
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Christophidou-Anastasiadou V
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Tolman NG
Nature communications 2018; 9: 2278 (IGR: 19-4)


77931 Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation
Tanteles GA
Molecular medicine reports 2018; 18: 1623-1627 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Lynn DJ
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Mizuno T
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Williams PA
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Beesley J
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Seki G
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Schaefer C; Melles RB
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Sheldrick B
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77951 SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case report
Tsuji S; Nangaku M
BMC Medical Genetics 2018; 19: 103 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Mills RA
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Risch N; John SWM
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Landers J; Ruddle JB
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Nair KS
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Graham SL
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77911 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Jorgenson E
Nature communications 2018; 9: 2278 (IGR: 19-4)


78212 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Healey PR; White AJR; Casson RJ; Best S; Grigg JR; Goldberg I; Powell JE; Whiteman DC; Radford-Smi
Nature Genetics 2018; 50: 1067-1071 (IGR: 19-4)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wang GM
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Mohanty K
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Struebing FL
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khawaja AP
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wang GM
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Collins DW
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Shiga Y
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
King R
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Gharahkhani P
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Doucette LP
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Ouyang P
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Rangachari K
Genomics 2019; 111: 696-699 (IGR: 19-3)


76943 Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutations
Khan AO
Ophthalmic Genetics 2018; 39: 425-427 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Karmiris E
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alsaif HS
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Huang C
Scientific reports 2018; 8: 4498 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Wang HW
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Cooke Bailey JN
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Gudiseva HV
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Akiyama M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Prasov L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
King R
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Sun P
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Bankoti N
Genomics 2019; 111: 696-699 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Xie L
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Dada R
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


76943 Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutations
Basamh OS
Ophthalmic Genetics 2018; 39: 425-427 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Kourtis N
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Burdon KP
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Li Y
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Khan AO
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Footz T
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Prasov L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Li Y
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Wang J
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


77203 FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost
Walter MA
Investigative Ophthalmology and Visual Science 2018; 59: 2548-2554 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Chavali VRM
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Cooke Bailey JN
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Patel N
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Wu Z
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Li Y
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76435 Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma
Dada T
Ophthalmic Genetics 2018; 39: 366-372 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Al-Hasani H
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhang F
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Chen Y
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Nishiguchi KM
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wareham NJ
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
P Pantou M
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Shyamala N
Genomics 2019; 111: 696-699 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alkuraya H
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Degiannis D
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Cao Y
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Sato K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Cooke Bailey JN
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Marrs CER
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhu C
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Jiang LP
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Trachtman B
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Scott RA
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Michael D
Genomics 2019; 111: 696-699 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Hewitt AW
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Struebing FL
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Georgalas I
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zou B
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76605 Genomic Locus Modulating IOP in the BXD RI Mouse Strains
Geisert EE
G3 (Bethesda, Md.) 2018; 8: 1571-1578 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Law MH
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Wu HP
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Sameer Ahmed Z
Genomics 2019; 111: 696-699 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Tolia S
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Hashem M
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse

Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Zheng Y
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Ramakrishnan M
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Shimozawa N
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Simcoe M
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Chandrasekaran P
Genomics 2019; 111: 696-699 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Pang CP
Scientific reports 2018; 8: 4498 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Zhang W
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Merritt WT
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76910 The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study
Papaconstantinou D
Medical hypothesis, discovery and innovation in ophthalmology 2018; 7: 25-31 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Abdulwahab F
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Igo RP
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Takahashi A
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Pasquale LR
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Wiinikka-Buesser L
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Wiggs JL
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Le J
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Kang JH
Scientific reports 2018; 8: 3124 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Song YE
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76936 Glaucoma Pred: Glaucoma prediction based on Myocilin genotype and phenotype information
Sekar K
Genomics 2019; 111: 696-699 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Richards JE
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76865 A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
Zhang L
Molecular medicine reports 2018; 17: 7918-7924 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Ibrahim N
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


77192 Research progress on human genes involved in the pathogenesis of glaucoma (Review)
Gao F
Molecular medicine reports 2018; 18: 656-674 (IGR: 19-3)


76697 Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing
Zhang M
Scientific reports 2018; 8: 4498 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Pistilli M
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76454 Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse
Geisert EE
Experimental Eye Research 2018; 169: 61-67 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Momozawa Y
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Aldahmesh MA
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Haines JL
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Rossi RA
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Hirata M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wojciechowski R
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


77211 Phenotypic Variation in a Four-Generation Family with Aniridia Carrying a Novel Mutation
Bohnsack BL
Journal of Ophthalmology 2018; 2018: 5978293 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Blachon S
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Cheng CY
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Matsuda K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Souzeau E
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76731 Congenital glaucoma and CYP1B1: an old story revisited
Alkuraya FS
Human Genetics 2019; 138: 1043-1049 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Zhou T
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Sankar PS
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khaw PT
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yamaji T
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Pasquale LR
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Iwasaki M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Siggs OM
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Miller-Ellis E
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Haines JL
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Tsugane S
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Landers J
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Lehman A
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Oze I
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Awadalla M
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
Addis V
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Foster PJ
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Mikami H
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Wiggs JL
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Sharma S
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76845 The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men
O'Brien JM
Investigative Ophthalmology and Visual Science 2018; 59: 1751-1759 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Mills RA
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Naito M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Hammond CJ; Hysi PG
Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Wakai K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Ridge B
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yoshikawa M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Lynn D; Casson R
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Miyake M
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


77154 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma

Nature Genetics 2018; 50: 778-782 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yamashiro K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Graham SL; Goldberg I
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
; Kashiwagi K
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
White A; Healey PR
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Iwata T; Mabuchi F
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


76513 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Grigg J; Lawlor M,
Scientific reports 2018; 8: 3124 (IGR: 19-3)


76522 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Takamoto M; Oz
Human Molecular Genetics 2018; 27: 1486-1496 (IGR: 19-3)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Chintalapudi SR
Nature communications 2017; 8: 1755 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Karaca I
International Ophthalmology 2017; 0: (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Choquet H
Nature communications 2017; 8: 2108 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Winegarner A
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Nunes HF
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
DeLuca AP
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Fang Kho P
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta V
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Zagajewska K
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Gupta S
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Jeoung JW
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Shiga Y
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Molasy M
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Burdon KP
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Li J
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Suh W
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Oie Y
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Alward WLM
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Ananina G
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Nishiguchi KM
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Yilmaz SG
International Ophthalmology 2017; 0: (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Piątkowska M
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Somarajan BI
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Walczak A
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Maria D
Nature communications 2017; 8: 1755 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Awadalla MS
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Ko JH
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Feng Y
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Won HH
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Lea RA
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Thai KK
Nature communications 2017; 8: 2108 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Sung MS
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Przybyłowska-Sygut K
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Mitchell P
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Di Wang X
Nature communications 2017; 8: 1755 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Chandra A
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Costa VP
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75446 The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma
Kee C
Current Eye Research 2018; 43: 534-538 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Benton MC
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Palamar M
International Ophthalmology 2017; 0: (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Kawasaki S
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kawai Y
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Kim YJ
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Liebmann J
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Yin J
Nature communications 2017; 8: 2108 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Goryca K
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Walia GK
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Maurya OPS
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Eccles D
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Kim YW
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Hoffmann TJ
Nature communications 2017; 8: 2108 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kojima K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Zaleska-Żmijewska A
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Ritch R
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Bałabas A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Nishida N
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Bailey JNC
Nature communications 2017; 8: 1755 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Lee TH
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
Zanchin NIT
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kaur J
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Onay H
International Ophthalmology 2017; 0: (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Wang JJ
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Haupt LM
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Park KH
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Kawase K
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Szaflik J
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kumar S
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75376 Association of Interleukin-1 gene clusters polymorphisms with primary open-angle glaucoma: a meta-analysis
Park SW
BMC Ophthalmology 2017; 17: 218 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Kluska A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Sato K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
De Vasconcellos JPC
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Kvale MN
Nature communications 2017; 8: 2108 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Akgun B
International Ophthalmology 2017; 0: (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mishra RN
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75513 Novel mutation reported in an aniridia patient
Nishida K
Human genome variation 2017; 4: 17053 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
White A
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Paziewska A
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Fujita K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74906 Microarray-based analysis of gene expression profiles in peripheral blood of patients with acute primary angle closure
Oh JY
Ophthalmic Genetics 2017; 38: 520-526 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Banda Y
Nature communications 2017; 8: 2108 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Aytacoglu B
International Ophthalmology 2017; 0: (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Hewitt AW
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Alsabaani NA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility

Nature communications 2017; 8: 1755 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Kwon YH
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Keane MC
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta S
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Szaflik JP
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mukherjee A
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75258 Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil
de Melo MB
Ophthalmic Genetics 2018; 39: 194-199 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Schaefer C
Nature communications 2017; 8: 2108 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Souzeau E
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75563 TP53 codon 72 polymorphism and the risk of glaucoma in a north Indian cohort: A genetic association study
Mutsuddi M
Ophthalmic Genetics 2018; 39: 228-235 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Takahashi M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Chaurasia AK
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Aykut A
International Ophthalmology 2017; 0: (IGR: 19-2)


75219 Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish population
Majsterek I
Ophthalmic Genetics 2018; 39: 180-188 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Hysi PG
Nature communications 2017; 8: 1755 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Pośpiech E
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Sherwin JC
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Robin AL
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Risch N
Nature communications 2017; 8: 2108 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Mackey DA
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Stone EM
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75562 Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome
Ozkinay FF
International Ophthalmology 2017; 0: (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Gupta D
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Wiggs JL
Nature communications 2017; 8: 1755 (IGR: 19-2)


75416 Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2018; 22: 74-78 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Graham SL
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Grabska-Liberek I
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Omodaka K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Goldberg I
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Williams RW
Nature communications 2017; 8: 1755 (IGR: 19-2)


75606 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma
Hennig EE
Experimental Eye Research 2018; 168: 138-148 (IGR: 19-2)


75472 Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size
Griffiths LR
Journal of Human Genetics 2018; 63: 83-87 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Nair KS
Nature communications 2017; 8: 2108 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Kaushik A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Scheetz TE
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Araie M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Mehta A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kashiwagi K
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75367 Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
Jablonski MM
Nature communications 2017; 8: 1755 (IGR: 19-2)


75131 Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients
Fingert JH
Journal of Glaucoma 2017; 26: 1063-1067 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Healey PR
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Melles R
Nature communications 2017; 8: 2108 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Landers J
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Aihara M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75506 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure
Jorgenson E
Nature communications 2017; 8: 2108 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Mills RAD
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Iwata T
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75349 Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma
Sharma A
Graefe's Archive for Clinical and Experimental Ophthalmology 2018; 256: 355-362 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Best S
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Mabuchi F; Takamoto M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Hewitt AW
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Ozaki M
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


75574 DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
Sharma S; Craig JE
Ophthalmic Genetics 2018; 39: 221-227 (IGR: 19-2)


75566 Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7
Kawase K; Fuse N; Yamamoto M; Yasuda J; Nagasaki M; Nakazawa T;
PLoS ONE 2017; 12: e0186678 (IGR: 19-2)


74479 RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
Lu C
Frontiers in genetics 2017; 8: 118 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Chhunchha B
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Zanon-Moreno V
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Tikunova E
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Syc-Mazurek SB
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Mabuchi F
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Lee MC
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Qiu H
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Matovinovic E
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74503 Axenfeld-Rieger syndrome
Seifi M
Clinical Genetics 2018; 93: 1123-1130 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Ghanbari M
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tang FY
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vande Perre P
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Taskiran EZ
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Su HA
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil A
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Jeoung JW
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Li Y
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74249 RNA expression in human retina
Li M
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Ghorbanpour E
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Abbas S
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhang L
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Chen X
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Yu-Wai-Man C
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Gong B
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Wang J
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Mabuchi F
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Protas ME
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74827 Primary Open-Angle Glaucoma Genetics in African Americans
Restrepo NA
Current genetic medicine reports 2017; 5: 167-174 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Narooie-Nejad M
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Mabuchi N
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Ma L
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Xu J
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Karaosmanoglu B
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Qu D
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Tagalakis AD
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Raza ST
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74827 Primary Open-Angle Glaucoma Genetics in African Americans
Cooke Bailey JN
Current genetic medicine reports 2017; 5: 167-174 (IGR: 19-1)


74479 RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
MacDougall M
Frontiers in genetics 2017; 8: 118 (IGR: 19-1)


74249 RNA expression in human retina
Zauhar RJ
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Li SY
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Kim DM
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Rasouli A
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Pasalar P
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Zhu B
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Ortega-Azorin C
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Wang QL
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74503 Axenfeld-Rieger syndrome
Walter MA
Clinical Genetics 2018; 93: 1123-1130 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Mabuchi N
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Singh P
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Fernandes KA
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Al-Haddad C
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Shi Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Kho PF
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Shei W
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Weh E
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Jin L
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Iglesias AI
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Zazo Seco C
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Ovtcharova V
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Chandra A
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Qu C
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Yang JJ
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Footz T
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Dong A
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Takamoto M
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Springelkamp H
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Zhang MH
Experimental and therapeutic medicine 2017; 14: 3651-3657 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Meng J
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Liu R
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Reshetnikov E
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
An J
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Sakurada Y
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Lea RA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Oh S
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tam POS
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Yazdani S
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Ni S
International Ophthalmology 2018; 38: 19-28 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Mousavi M
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Patat O
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Koşukcu C
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Asensio-Marquez EM
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Wilson MP
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chan AS
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Almobarak FA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Hariri H
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74249 RNA expression in human retina
Grazal C
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Stamer WD
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Moazzeni H
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74123 Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran
Rohani MR
Clinical laboratory 2017; 63: 1283-1291 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Dvornyk V
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Kasberger J
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Lee JS
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chua BT
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Kalantan H
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Doğan ÖA
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Singh DP
Cell death discovery 2017; 3: 17060 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Shrager P
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74249 RNA expression in human retina
Curcio CA
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Chen W
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Yoneyama S
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Bouremel Y
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Van Duijn CM
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Benton MC
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Garcia-Medina JJ
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Sakurada Y
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Shibbani K
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Ye Z
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Yen YC
International journal of medical sciences 2017; 14: 1251-1256 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Yuan G
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Pang CP
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Bouneau L
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Singh L
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Zhou X
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Ikram MA
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74249 RNA expression in human retina
DeAngelis MM
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Bitar F
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vigouroux A
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Taylan-Şekeroğlu H
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Kashiwagi K
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tham CCY
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Elahi E
Journal of ophthalmic & vision research 2017; 12: 407-412 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Eccles DA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Pinazo-Duran MD
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Yuan H
Molecular medicine reports 2017; 16: 1255-1261 (IGR: 19-1)


74600 Association of fatty acid-binding protein 2 and fat mass and obesity-associated gene polymorphism with primary open-angle glaucoma
Mahdi F
Taiwan journal of ophthalmology 2017; 7: 138-142 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Yin Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Baraban SC
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Goh SR
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Chen Q
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Polonikov A
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Liu Y
Molecular medicine reports 2017; 16: 8735-8746 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Lee RMH
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Park SS
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Yoneyama S
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Libby RT
Molecular Neurodegeneration 2017; 12: 71 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Virasami A
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Haupt LM
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74095 The Relation Between Endothelial Nitric Oxide Synthase Polymorphisms and Normal Tension Glaucoma
Kim JY
Journal of Glaucoma 2017; 26: 1030-1035 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Levin AV
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Dehghan A
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Kurban M
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Kashiwagi K
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Iijima H
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Chong YF
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74249 RNA expression in human retina
Stambolian D
Human Molecular Genetics 2017; 26: R68-R74 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Bourgeois D
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Tan C
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Chen LJ
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Bushueva O
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Şimşek-Kiper PÖ
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Coltell O
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Hu W
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Nemer G
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
El Hout S
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Iijima H
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Hilmy MH
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Shuai P
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Hart SL
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Utine EG
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74659 Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia
Churnosov M
International Journal of Ophthalmology 2017; 10: 1490-1494 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Erkeland SJ
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Ordovas JM
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Hewitt AW
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhou L
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Yamagata Z
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Katz LJ
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2017; 21: 754-758 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Sherwin JC
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Corella D
International journal of molecular sciences 2017; 18: (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Chassaing N
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Arabi M
Frontiers in cardiovascular medicine 2017; 4: 58 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhang R
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Ritch R
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Yamagata Z
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Boduroğlu K
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Nongpiur ME
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Klaver CCW
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Takamoto M
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Li J
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Khaw PT
JAMA ophthalmology 2017; 135: 1147-1155 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Meester-Smoor MA
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Xu H
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Calvas P
European Journal of Medical Genetics 2018; 61: 72-78 (IGR: 19-1)


74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Alikaşifoğlu M
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Baskaran M
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Mackey DA
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Aihara M
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Guo X
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Walter MA
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Aihara M; Iwata T
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Cheng Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Iwata T
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Semina EV
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Khor CC
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma

Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377 (IGR: 19-1)


74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Griffiths LR
Molecular Vision 2017; 23: 660-665 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Lin D; Li X
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Yang Z
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Kawase K
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Aung T
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Gould DB
Human Molecular Genetics 2017; 26: 3630-3638 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Araie M
Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Lin Y
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Hunziker W
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Tang Z
Scientific reports 2017; 7: 10716 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Shiga Y
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74437 Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population

Journal of Glaucoma 2017; 26: 963-966 (IGR: 19-1)


74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Liu X
Ophthalmic Genetics 2018; 39: 35-40 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Nishiguchi KM
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


74570 Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function
Vithana EN
Human Molecular Genetics 2017; 26: 4011-4027 (IGR: 19-1)


74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Nakazawa T; Ozaki M; Araie M;
PLoS ONE 2017; 12: e0183709 (IGR: 19-1)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Zhou T
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Nannini DR
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73061 Major review: Molecular genetics of primary open-angle glaucoma
Liu Y
Experimental Eye Research 2017; 160: 62-84 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Song E
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Firasat S
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72869 CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma
Hu Z
Oncotarget 2017; 8: 21167-21176 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Zeng K
Bioscience reports 2017; 37: (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Chen L
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Wang X
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Williams PA
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72965 Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye
Swierkowska J
Ophthalmic Genetics 2017; 0: 1-10 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Kim WJ
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Simpson A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Yang Y
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Ferre-Fernández JJ
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Iglesias AI
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yoshikawa M
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Dabbagh N
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


73070 Genetics of Glaucoma
Wiggs JL
Human Molecular Genetics 2017; 26: R21-R27 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Lewis C
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu MY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Aroca-Aguilar JD
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Kim JH
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
van der Lee SJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Gong K
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Zhang L
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Kaul H
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Zhong B
Bioscience reports 2017; 37: (IGR: 18-4)


73061 Major review: Molecular genetics of primary open-angle glaucoma
Allingham RR
Experimental Eye Research 2017; 160: 62-84 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Shahrani H
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Avdic A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Torres M
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Hedberg-Buenz A
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Souzeau E
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73070 Genetics of Glaucoma
Pasquale LR
Human Molecular Genetics 2017; 26: R21-R27 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Wang NL
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu Y
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Harder JM
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72965 Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye
Gajecka M
Ophthalmic Genetics 2017; 0: 1-10 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Luo N
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Nakanishi H
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72869 CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma
He C
Oncotarget 2017; 8: 21167-21176 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamashiro K
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Bonnemaijer PWM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Li S
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Fang M
Bioscience reports 2017; 37: (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Foxworth NE
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
DeLuca AP
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Dohayan N
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Roos BR
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Chen YI
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Zhang Y
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Ashfaq UA
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Siggs OM
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Rong SS
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72653 Newly identified paired box 6 mutation of variant familial aniridia: Congenital iris ectropion with foveal hypoplasia
Cho NC
Indian Journal of Ophthalmology 2017; 65: 55-56 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Alvarado JA
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Medina-Trillo C
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Stone EM
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Lim M
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Huang LN
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
DeLuca A
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Cardozo BH
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Höhn R
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Taylor KD
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Shen XL
Bioscience reports 2017; 37: (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Miyake M
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Zhu X
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Wang C
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Liu CY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Bonet-Fernández JM
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Mustafa M
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72803 In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma
Idrees S
International Ophthalmology 2018; 38: 807-814 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Landers J
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Nag A
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Akagi T
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Arfin M
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Méndez-Hernández CD
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72794 Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma
Sundaresan P
Genetic testing and molecular biomarkers 2017; 21: 252-258 (IGR: 18-4)


72857 Association analysis between LOXL1 gene and exfoliation syndrome
Cheng HB
Chinese Journal of Ophthalmology 2017; 53: 294-299 (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Qu C
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Deng CY
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Walnuss C
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Mills R
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Miller K
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Alward WLM
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Cochran KE
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Rotter JI
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72824 Common polymorphisms of the hOGG1, APE1 and XRCC1 genes correlate with the susceptibility and clinicopathological features of primary angle-closure glaucoma
Huang LN
Bioscience reports 2017; 37: (IGR: 18-4)


73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Li H
Journal of Ophthalmology 2017; 2017: 6896390 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Morales-Fernández L
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72746 The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study
Al-Asmari AK
Clinical Ophthalmology 2017; 11: 549-555 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Peng L
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


73161 Primary Congenital and Developmental Glaucomas
Fingert JH
Human Molecular Genetics 2017; 26: R28-R36 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Neely D
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Gharahkhani P
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Gotoh N
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Varma R
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Goldberg I
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Schnieders MJ
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
John SWM
Frontiers in neuroscience 2017; 11: 232 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Scheetz TE
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Zhou L
BMC Ophthalmology 2017; 17: 48 (IGR: 18-4)


72164 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population
Gao X
Investigative Ophthalmology and Visual Science 2017; 58: 87-95 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Healey PR
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Corton M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Khawaja AP
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Ikeda HO
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Spandau D
Scientific reports 2017; 7: 1442 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Suda K
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Broer L
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Ghaffarieh A
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Graham S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Cabañero-Valera MJ
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Alward WL
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamada H
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72836 LADD syndrome with glaucoma is caused by a novel gene
Fingert JH
Molecular Vision 2017; 23: 179-184 (IGR: 18-4)


73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Sun Y
Scientific reports 2017; 7: 1442 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Gut M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Hewitt AW
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels

Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Mackey DA
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Foster PJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Tonda R
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Hasegawa T; Iida Y
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Galanopoulos A
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Hammond CJ
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Ayuso C
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yamada R
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Casson RJ
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Coca-Prados M
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Hysi PG
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Ruddle JB
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
García-Feijoo J
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Matsuda F
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
van Leeuwen EM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72826 Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
Es
Scientific reports 2017; 7: 46175 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Macgregor S
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects
Yoshimura N
Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Ellis J
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Mackey DA
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


73000 Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects

Investigative Ophthalmology and Visual Science 2017; 58: 2510-2519 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Leo P; Brown MA
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Mazur J; Nickels S
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Macgregor S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Uitterlinden AG
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Sharma S
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Klaver CCW
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


72616 Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma
Burdon KP; Craig JE
Investigative Ophthalmology and Visual Science 2017; 58: 1537-1544 (IGR: 18-4)


73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Amin N; Van Duijn CM
Human Mutation 2017; 38: 1025-1032 (IGR: 18-4)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Danford ID
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Mohanty K
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Zhao D
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Kondkar AA
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Springelkamp H
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Dulle JE
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Salehi Z
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Asfuroglu M
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71510 Epigenetics and Signaling Pathways in Glaucoma
Gauthier AC
BioMed research international 2017; 2017: 5712341 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhao J
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Micheal S
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Zhou T
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Maes ME
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Mao M
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Alghamdi KA
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Williams AL
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Navarro-Partida J
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Prat C
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhou H
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Cavdarli B
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Martinez-Rizo AB
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Souzeau E
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Nguyen CT
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Kiss M
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Dada R
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Alsaedi AB
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Belville C
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Liang CY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71510 Epigenetics and Signaling Pathways in Glaucoma
Liu J
BioMed research international 2017; 2017: 5712341 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Verkuil LD
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Iglesias AI
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Rübsam A
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Gholaminia M
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Eason J
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Saksens NT
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Schlamp CL
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Edward NB
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Chawla B
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71241 BAX to basics: How the BCL2 gene family controls the death of retinal ganglion cells
Nickells RW
Progress in Retinal and Eye Research 2017; 57: 1-25 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Aljasser A
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Sharma S
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Ramirez-Barrera P
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Mishra A
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Comptour A
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Wong VH
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Hogewind BF
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Choi DJ
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Garnai SJ
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Ou Y
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71358 Oxidative DNA damage and reduced expression of DNA repair genes: Role in primary open angle glaucoma (POAG)
Dada T
Ophthalmic Genetics 2017; 0: 1-5 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Koz OG
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Gholaminia Z
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Kalantan H
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Sun L
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Feng SC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Marceau G
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71575 Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation
Gould DB
Disease models & mechanisms 2017; 10: 475-485 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Collins DW
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Lin KH
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Panjtanpanah M
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Al-Kharashi AS
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71488 Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway
Bohnsack BL
Investigative Ophthalmology and Visual Science 2017; 58: 1084-1097 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Landers J
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Velazquez-Fernandez JB
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Pawar HS
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Lim JK
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Khan MI
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
A Yarangumeli A
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Höhn R
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Yang B
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Altawil A
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
Hoyng CB
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71618 The GG genotype of the HSPA1B gene is associated with increased risk of glaucoma in northern Iran
Qazvini MG
Molekuliarnaia biologiia 2017; 51: 31-36 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Altuwaijri S
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Mills R
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Lee HN
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71085 Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Ozdemir EY
Journal of Glaucoma 2017; 26: e54-e57 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zhang L
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71620 Extended clinical features associated with novel Glis3 mutation: a case report
Kamal NM
BMC endocrine disorders 2017; 17: 14 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
He Z
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Clairefond G
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71365 BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons
Fort PE
Experimental Eye Research 2017; 155: 85-90 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wojciechowski R
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Gudiseva HV
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Mondragon-Jaimes VA
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Chiambaretta F
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Uyhazi KE
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Shi H
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71403 Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family
den Hollander AI
Molecular Neurobiology 2018; 55: 1387-1395 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Goldberg I
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Shen YC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Jobling AI
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Khawaja AP
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Santos-Garcia A
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Mohamed G
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Wei LC
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71295 Selection of suitable reference genes for quantitative real-time PCR in trabecular meshwork cells under oxidative stress
Zheng Y
Free radical research 2017; 51: 103-111 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Nag A
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71522 Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma
Benites-Godinez V
Graefe's Archive for Clinical and Experimental Ophthalmology 2017; 255: 995-1001 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Sapin V
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Sultan T
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Healey PR
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Lau MK
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Fletcher EL
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Graham S
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71413 Myocilin expression is regulated by retinoic acid in the trabecular meshwork-derived cellular environment
Blanchon L
Experimental Eye Research 2017; 155: 91-98 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wang YX
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Azad TA
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Chinnery HR
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Kanu LN
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Chang CJ; Hsu MY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Wang JJ
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Grant GR
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Hewitt AW
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Vingrys AJ
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71412 Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients
Abu-Amero KK
Journal of negative results in biomedicine 2017; 16: 3 (IGR: 18-3)


71577 Characterization of the Circumlimbal Suture Model of Chronic IOP Elevation in Mice and Assessment of Changes in Gene Expression of Stretch Sensitive Channels
Bui BV
Frontiers in neuroscience 2017; 11: 41 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
Chavali VR
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Mackey DA
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Yang YY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Cuellar-Partida G
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Chiu CH
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71546 Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma
O'Brien JM
Progress in Retinal and Eye Research 2017; 58: 89-114 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Galanopoulos A
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Gibson J
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Casson RJ
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Cooke Bailey JN
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71461 Analysis of the Interleukin-6 (-174) Locus Polymorphism and Serum IL-6 Levels with the Severity of Normal Tension Glaucoma
Wang CY
Ophthalmic Research 2017; 57: 224-229 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Vithana EN
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Ruddle JB
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Gharahkhani P
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Ellis J; Leo P
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Boutin T; Ramdas WD
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Brown MA
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Zeller T
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Macgregor S; Lynn DJ
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Luben RN
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Burdon KP
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Yonova-Doing E; Viswanathan AC
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


71655 Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma
Craig JE
PLoS ONE 2017; 12: e0172427 (IGR: 18-3)


71253 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Yaz
Human Molecular Genetics 2017; 26: 438-453 (IGR: 18-3)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Reis LM
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zhong Y
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Kondkar AA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Rauf B
Human genome variation 2016; 3: 16021 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Scheetz TE
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Fingert JH
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Peotter JL
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Verma SS
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Moazzeni H
Gene 2016; 593: 76-83 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Zhou T
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Holt R
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Shahrani H
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Elliott MH
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Struebing FL
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
de Juan-Marcos L
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Navarro-Partida J
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Song C
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Souzeau E
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Kosior-Jarecka E
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Grønskov K
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Orssaud C
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Shi H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Mookherjee S
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Mauri L
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Morrison JC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Minegishi Y
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Miller MA
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70688 Dataset of eye disease-related proteins analyzed using the unfolding mutation screen
McCafferty CL
Scientific data 2016; 3: 160112 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Cui XJ
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Khawaja AP
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70928 The Pathway From Genes to Gene Therapy in Glaucoma: A Review of Possibilities for Using Genes as Glaucoma Drugs
Borrás T
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) 2017; 6: 80-93 (IGR: 18-2)


70150 A single gene connects stiffness in glaucoma and the vascular system
Borrás T
Experimental Eye Research 2017; 158: 13-22 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Gohari M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Kumar S
Genomics 2017; 109: 27-35 (IGR: 18-2)


70707 Systems Genetics Analysis to Identify the Genetic Modulation of a Glaucoma-Associated Gene
Chintalapudi SR
Methods in molecular biology (Clifton, N.J.) 2017; 1488: 391-417 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Nag A
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Alvarado Castillo B
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Wróbel-Dudzińska D
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Redó-Riveiro A
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ugur Iseri SA
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Neámatzadeh H
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Ashpole NE
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Escudero-Domínguez FA
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Min X
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Tram KH
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70707 Systems Genetics Analysis to Identify the Genetic Modulation of a Glaucoma-Associated Gene
Jablonski MM
Methods in molecular biology (Clifton, N.J.) 2017; 1488: 391-417 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Zhao AG
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Lee RK
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Robert MP
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Nakayama M
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Fingert JH
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Malik MA
Genomics 2017; 109: 27-35 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Guo X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Cooke Bailey JN
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Dabbagh N
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70688 Dataset of eye disease-related proteins analyzed using the unfolding mutation screen
Sergeev YV
Scientific data 2016; 3: 160112 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Banerjee D
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Cooke Bailey JN
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Lu H
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Phillips J
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Tyler RC
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Souzeau E
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Zhang J
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Faga B
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Cepurna WO
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Irum B
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Mousa A
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Akbari MT
Gene 2016; 593: 76-83 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Uebe S
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Robin AL
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Tehrani S
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Mousa A
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Iejima D
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70634 Genetics and genetic testing for glaucoma
Bettis DI
Current Opinions in Ophthalmology 2017; 28: 133-138 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
K S
Genomics 2017; 109: 27-35 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Zhu R
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Sharma S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Arno M
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Scheetz TE
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Azad TA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Lucas A
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Kang JH
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Wyatt AW
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70587 Correlations of AFAP1, GMDS and PTGFR gene polymorphisms with intra-ocular pressure response to latanoprost in patients with primary open-angle glaucoma
Wang XL
Journal of Clinical Pharmacy and Therapeutics 2017; 42: 87-92 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Ortega L
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Sticht H
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Tong T
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Xiao H
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Kabir F
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Jafari MA
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Gu X
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Martinez-Rizo AB
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Łukasik U
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Sandfeld L
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Dohayan N
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70885 THE SCREENING AND RANKING ALGORITHM FOR CHANGE-POINTS DETECTION IN MULTIPLE SAMPLES
Zhang H
The annals of applied statistics 2016; 10: 2102-2129 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Yazdani S
Gene 2016; 593: 76-83 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Chakraborty S
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Hernández-Galilea E
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Weh E
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70497 Relevance of Identifying JAG1 Mutations in Patients With Isolated Posterior Embryotoxon
Roche O
Journal of Glaucoma 2016; 25: 923-925 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Witney M
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Williams RW
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Rosales-Diaz R
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Hendee KE
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Zibrandtsen N
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Sihota R
Genomics 2017; 109: 27-35 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Vossmerbaeumer U
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Mukhopadhyay I
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Choe TE
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Herrnberger L
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Luo J
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Mazaheri M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Arfin M
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


69993 Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2
Elahi E
Gene 2016; 593: 76-83 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Firasat S
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Cruz-González F
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Roos BR
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70356 Genetic Networks in Mouse Retinal Ganglion Cells
Geisert EE
Frontiers in genetics 2016; 7: 169 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Iglesias AI
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Sultan T
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Allingham RR
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Ruddle JB
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Hu N
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Kwon YH
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Aung T
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Dimeo K
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Bradford Y
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Bax DA
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Almobarak FA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Kawase K
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Siggs OM
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
McClellan ME
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
Follana-Neira I
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Hauser MA
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Almobarak FA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Khor CC
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Alawad A
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Naeem MA
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Harris P
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Goldberg I
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Sen A
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Liebmann JM
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Gonzalez JM
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Bonnemaijer P
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Kariminejad A
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Alawad A
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Graham SL
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Gold Diaz D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Lu H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Zare-Shehneh M
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Jayaram H
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Linneman JG
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Velazquez-Fernandez JB
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70308 Significance of optineurin mutations in glaucoma and other diseases
Iwata T
Progress in Retinal and Eye Research 2016; 55: 149-181 (IGR: 18-2)


70561 Genetic variants associated with primary open angle glaucoma in Indian population
Kaur J
Genomics 2017; 109: 27-35 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Weisschuh N
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zuo C
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Asmari M
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Gordon MO
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Brilliant M
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Altuwaijri S
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Yang M
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70006 Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma Pathogenesis
Ray K
Genetic testing and molecular biomarkers 2016; 20: 633-636 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Broer L
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Altuwaijri S
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Rizvi S
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Healey PR
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Kass MA
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70651 Association between the p53 codon 72 polymorphism and primary open-angle glaucoma risk: Meta-analysis based on 11 case-control studies
Abbasi-Shavazi E
Indian Journal of Ophthalmology 2016; 64: 756-761 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Abdul-Rahman O
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70746 Investigation of Association between Autophagy-Related Gene Polymorphisms and Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma in a Spanish Population
González-Sarmiento R
Seminars in Ophthalmology 2016; 0: 1-6 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Osman EA
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Santos C
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Manfredini E
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Kocki J
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Griffith GL
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Alawad A
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Ritch R
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Khan SN
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Lozano DC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Healey PR
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Hauser MA
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Huang X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70616 Association of single-nucleotide polymorphisms in non-coding regions of the TLR4 gene with primary open angle glaucoma in a Mexican population
Santos A
Ophthalmic Genetics 2016; 0: 1-5 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Bach-Holm D
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70032 Involvement of Tiam1, RhoG and ELMO2/ILK in Rac1-mediated phagocytosis in human trabecular meshwork cells
Peters DM
Experimental Cell Research 2016; 347: 301-311 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Graham S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Maselli E
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Huang J
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Husnain T
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70418 Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma
Żarnowski T
Molecular Vision 2016; 22: 1256-1266 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Goldberg I
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Qin B
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Wang K
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Altuwaijri S
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Fortune B
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70495 CYP1B1 Mutations in Individuals With Primary Congenital Glaucoma and Residing in Denmark
Tümer Z
Journal of Glaucoma 2016; 25: 926-930 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Pasquale LR
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70606 Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis)
Alward WL
Transactions of the American Ophthalmological Society 2016; 114: T6 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Al-Obeidan SA
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Sultan T
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Broadgate S
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Ben-Omran T
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Budenz DL
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


69999 Lack of Association Between Polymorphism rs4986791 in TLR4 and Primary Open-Angle Glaucoma in a Saudi Cohort
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 556-559 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Reagan AM
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Uitterlinden AG
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70133 Association of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with primary glaucoma in Saudi population
Al-Asmari A
BMC Ophthalmology 2016; 16: 156 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Mi L
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Peissig PL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Dunn R
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Klaver CC
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70731 A Period of Controlled Elevation of IOP (CEI) Produces the Specific Gene Expression Responses and Focal Injury Pattern of Experimental Rat Glaucoma
Johnson EC
Investigative Ophthalmology and Visual Science 2016; 57: 6700-6711 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Manning MA
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70298 Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort
Abu-Amero KK
Journal of negative results in biomedicine 2016; 15: 17 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Shi J
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Riazuddin S
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Hewitt AW
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Azad TA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70328 Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study
Fingert JH
Ophthalmology 2016; 123: 2527-2536 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Mackey DA
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Patrosso M
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Boyce TM
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Christen WG
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
McCarty CA
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Brilliant MH
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Bruty J
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Akram J
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Tanito M
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Zhang Q
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Mackey DA
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70196 Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma
Abu-Amero KK
Genetic testing and molecular biomarkers 2016; 20: 715-718 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Fingert J
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70035 Analysis of Cyclin-Dependent Kinase Inhibitor-2B rs1063192 Polymorphism in Saudi Patients with Primary Open-Angle Glaucoma
Al-Obeidan SA
Genetic testing and molecular biomarkers 2016; 20: 637-641 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Hewitt AW
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
van Duijn C
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70508 Primary Angle Closure and Sequence Variants within MicroRNA Binding Sites of Genes Involved in Eye Development
Guan H
PLoS ONE 2016; 11: e0166055 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Weinreb RN
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Riazuddin SA
Human genome variation 2016; 3: 16021 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Casson RJ
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Burdon KP
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
McCarty CA
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70867 Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
Liu X
PLoS ONE 2017; 12: e0169395 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Gaasterland D
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Hysi PG
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Kitchner TE
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Wallis Y
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Penco S
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Tamm ER
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Haines JL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Reis A
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Gaasterland T
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
McMullan D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70535 Caveolin-1 modulates intraocular pressure: implications for caveolae mechanoprotection in glaucoma
Stamer WD
Scientific reports 2016; 6: 37127 (IGR: 18-2)


70857 Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations
Hammond CJ
Ophthalmology 2017; 124: 547-553 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Costakos D
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Landers J
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70791 Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals
Craig JE
Ophthalmology 2017; 124: 303-309 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Wiggs JL
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Pasutto F
Orphanet Journal of Rare Diseases 2016; 11: 108 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Mills R
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Kraft P
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70417 Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes
Semina EV
Molecular Vision 2016; 22: 1229-1238 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ogilvie C
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Lee RK
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Gerrelli D
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Ellis J
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Vrabec TR
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Zhang Y
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Tromp G
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Leo P
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Lichter PR
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Brown MA
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70547 Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders
Ragge N
Human Genetics 2017; 136: 119-127 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium
Ritchie MD
PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Liu Y
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Macgregor S
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Medeiros F
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70210 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium

PLoS Genetics 2016; 12: e1006186 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Moroi SE
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Burdon KP
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Richards JE
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


70630 Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma
Craig JE
Molecular genetics & genomic medicine 2016; 4: 624-633 (IGR: 18-2)


70262 Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses
Realini T; Ritch R; Schuman JS; Scott WK; S
Investigative Ophthalmology and Visual Science 2016; 57: 5046-5052 (IGR: 18-2)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Liu Y
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Chen X
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Kader MA
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69384 Smad-independent TGF-β2 signaling pathways in human trabecular meshwork cells
Pervan CL
Experimental Eye Research 2017; 158: 137-145 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Sang J
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Xiang Y
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Yi QY
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Arunrut T
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park J
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Kuehn MH
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Tan C
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Rong SS
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Reis LM
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Banerjee A
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Bermudez JY
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Hull S
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Nishisako M
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Ng SK
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Zhang P
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Collins DW
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Chen X
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Gao Y
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Khor CC
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Scheetz TE
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Lv Y
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69288 A global test for gene-gene interactions based on random matrix theory
Frost HR
Genetic epidemiology 2016; 40: 689-701 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Cuellar-Partida G
Scientific reports 2016; 6: 26885 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Meguro A
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Tyler RC
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Chakraborty S
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69288 A global test for gene-gene interactions based on random matrix theory
Amos CI
Genetic epidemiology 2016; 40: 689-701 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Webber HC
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Craig JE
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Jiang B
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Chen Y
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Lipsett KA
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Namburi P
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Roos BR
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Arno G
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Gudiseva HV
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Li W
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Do T
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Yao Q
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Dong Y
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Huang L
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Sabbadini M
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Kim M
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Chen Y
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Jia L
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Deng G
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Bailey JC
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Burdon KP
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Chen LJ
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Menotti-Raymond M
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Nomura E
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Burdon KP
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Ma W
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Li X
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Jia H
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Ku CA
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Zafar SN
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Fan BJ
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Trachtman B
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69288 A global test for gene-gene interactions based on random matrix theory
Moore JH
Genetic epidemiology 2016; 40: 689-701 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Weh E
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Solivan-Timpe F
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Helwa I
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Yin Z
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Ramugade S
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Zafar SN
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Fitzgerald JT
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Jain M
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Chakraborty A
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park CK
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Xie L
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Wiggs JL
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Patel GC
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69387 Association of PLEKHA7, COL11A1 and PCMTD1-ST18 gene polymorphisms with primary angle closure glaucoma in ethnic Han Chinese from Sichuan
Yang Z
Chinese Journal of Medical Genetics 2016; 33: 545-549 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Leung CK
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Zhao B
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Zhou HJ
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Pasquale LR
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Dismuke WM
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Ma Y
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nakano M
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69206 PTGFR and SLCO2A1 Gene Polymorphisms Determine Intraocular Pressure Response to Latanoprost in Han Chinese Patients with Glaucoma
Huang W
Current Eye Research 2016; 0: 1-5 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Chae H
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Whitmore SS
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Miller K
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Iqbal A
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Xia M
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Yamane T
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Zhou T
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Liu X
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Villanueva-Mendoza C
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Wang JJ
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Bowman AS
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Wang H
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Wu GH
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Matsushita K
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Hendee KE
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Liu H
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Ramakrishnan R
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Ge Z
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69057 Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis
Tang X
Journal of Ophthalmology 2016; 2016: 1348347 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Chakrabarti S
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Machol K
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Wang L
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


68573 Mitochondrial transfer RNA variants and primary congenital glaucoma
Tang L
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis 2016; 27: 2405-2407 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Cai J
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Jia L
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Cai H
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Zhang N
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Scaglia F
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Lee S
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Khan MI
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Waseem N
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Takeuchi M
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Vote BJ
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69058 Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases
Ray K
PLoS ONE 2016; 11: e0156252 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Cortés-González V
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Fogarty R
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Sun X
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Cheng YQ
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Scheetz TE
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
George R
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Schilter KF
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Krishnadas SR
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
DeLuca AP
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Ji J
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Sagaser A
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Chandra A
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Kim Y
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
den Hollander AI
PLoS ONE 2016; 11: e0159259 (IGR: 18-1)


69087 Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population
Wang N
Science China Life Sciences 2016; 59: 694-699 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Khan MI
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Souzeau E
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Souzeau E
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Phillips JA
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Ota M
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69358 Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma
Li X
BMC Ophthalmology 2016; 16: 116 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Miki A
Scientific reports 2016; 6: 27837 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Abu-Amero K
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69144 Screening of the LTBP2 gene in 214 Chinese sporadic CYP1B1-negative patients with primary congenital glaucoma
Sun X
Molecular Vision 2016; 22: 528-535 (IGR: 18-1)


69194 Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes
Slavotinek A
American Journal of Medical Genetics, Part A 2016; 170: 2711-2718 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Clark AF
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69102 Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma
Fan BJ
PLoS ONE 2016; 11: e0157093 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Roos BR
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Stone EM
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Sankar P
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69008 Association between Genetic Polymorphisms of the Beta Adrenergic Receptor and Diurnal Intraocular Pressure in Chinese Volunteers and Glaucoma Patients
Tang X
Current Eye Research 2016; 0: 1-8 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Drewry M
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
David VA
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69309 HDAC Inhibitor-Mediated Epigenetic Regulation of Glaucoma-Associated TGFβ2 in the Trabecular Meshwork
Mao W
Investigative Ophthalmology and Visual Science 2016; 57: 3698-3707 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Periasamy S
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Landers J
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Kwon YH
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Brilliant MH
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Kashiwagi K
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
den Hollander AI
PLoS ONE 2016; 11: e0160016 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Duvesh R
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Jang W
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Chiang SW
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Sequeira S
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
O'Brien SJ
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
McAllister IL
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Webster AR
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Miller-Ellis E
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Zhao Z
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Robin AL
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Mabuchi F
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Lehman A
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Budenz DL
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Isaacs T
Scientific reports 2016; 6: 26885 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Chen LJ
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Mills RA
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Alward WL
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Chi HY
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Robson AG
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Tam PO
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Schinzel A
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Wang K
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Hashida N
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park HY
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Michaelides M
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Christen WG
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69230 Clinical and genetic characterization of a large primary open angle glaucoma pedigree
Fingert JH
Ophthalmic Genetics 2016; 0: 1-4 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Iijima H
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Li Z
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Jens JK
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Lake S
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69100 Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Semina EV
Clinical Genetics 2016; 90: 378-382 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
Addis V
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Casson RJ
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nongpiur ME
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69013 Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans
O'Brien JM
Molecular Vision 2016; 22: 454-471 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Chasman DI
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Young AL
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69123 SQSTM1 Mutations and Glaucoma
Fingert JH
PLoS ONE 2016; 11: e0156001 (IGR: 18-1)


69445 Molecular analysis of myocilin and optineurin genes in Korean primary glaucoma patients
Park SH
Molecular medicine reports 2016; 14: 2439-2448 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Kawase K
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Snella EM
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Weleber RG
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Mackey DA
Scientific reports 2016; 6: 26885 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Ridge B
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Davagnanam I
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
Ellinwood NM
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Perera SA
Nature Genetics 2016; 48: 556-562 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Constable IJ
Scientific reports 2016; 6: 26885 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Yamamoto T
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Graham SL
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Tsujikawa M
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69468 A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium
Fingert JH
Investigative Ophthalmology and Visual Science 2016; 57: 3974-3981 (IGR: 18-1)


69086 Molecular and Clinical Findings in Patients With Knobloch Syndrome
Chen R
JAMA ophthalmology 2016; 134: 753-762 (IGR: 18-1)


68909 A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)
McLellan GJ
PLoS ONE 2016; 11: e0154412 (IGR: 18-1)


69256 Genetic Association at the 9p21 Glaucoma Locus Contributes to Sex Bias in Normal-Tension Glaucoma
Hewitt AW
Investigative Ophthalmology and Visual Science 2016; 57: 3416-3421 (IGR: 18-1)


69153 Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
Zhang M
Scientific reports 2016; 6: 27837 (IGR: 18-1)


69053 Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration
Mitchell P
Scientific reports 2016; 6: 26885 (IGR: 18-1)


68715 SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study
Nakamura M
Ophthalmic Genetics 2016; 37: 194-200 (IGR: 18-1)


68845 Genome-wide association study identifies five new susceptibility loci for primary angle c