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17-3
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Classification #3.4.2
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3.4.2 Gene studies
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3.4.2 Gene studies
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66332
A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17
Forman OP
PLoS ONE
2015; 10: e0143546
65962
CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients
Do T
Journal of Glaucoma
2016; 25: e491-e498
66512
Roles of CYP2C19 Gene Polymorphisms in Susceptibility to POAG and Individual Differences in Drug Treatment Response
Liu XL
Medical Science Monitor
2016; 22: 310-315
66250
Risk Factors for Normal and High-Tension Glaucoma in Poland in Connection with Polymorphisms of the Endothelial Nitric Oxide Synthase Gene
Kosior-Jarecka E
PLoS ONE
2016; 11: e0147540
66584
LOXL1 gene analysis in Turkish patients with exfoliation glaucoma
Yilmaz SG
International Ophthalmology
2016; 36: 629-635
65867
Candidate genes involved in the susceptibility of primary open angle glaucoma
Kumar S
Gene
2016; 577: 119-131
65791
Identification of an Alu-repeat-mediated deletion of OPTN upstream region in a patient with a complex ocular phenotype
Schilter KF
Molecular genetics & genomic medicine
2015; 3: 490-499
66258
Analysis of functional polymorphisms in apoptosis-related genes in primary open angle glaucoma
Lindner E
Molecular Vision
2015; 21: 1340-1344
65810
Risk Factors in Normal-Tension Glaucoma and High-Tension Glaucoma in relation to Polymorphisms of Endothelin-1 Gene and Endothelin-1 Receptor Type A Gene
Wróbel-Dudzińska D
Journal of Ophthalmology
2015; 2015: 368792
66357
Construction of CYP1B1 gene haplotypes predisposing to primary congenital glaucoma through allele-specific PCR/restriction fragment length polymorphism analysis
Zhang A
Chinese Journal of Medical Genetics
2015; 32: 780-784
66311
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation Sequencing
Ma AS
Human Mutation
2016; 37: 371-384
66288
Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma
Micheal S
PLoS ONE
2015; 10: e0145005
66339
Association of single nucleotide polymorphisms in the CYP1B1 gene with the risk of primary open-angle glaucoma: a meta-analysis
Wang Z
Genetics and Molecular Research
2015; 14: 17262-17272
66325
An Updated Review on the Genetics of Primary Open Angle Glaucoma
Abu-Amero K
International journal of molecular sciences
2015; 16: 28886-28911
66288
Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma
Ayub H
PLoS ONE
2015; 10: e0145005
66258
Analysis of functional polymorphisms in apoptosis-related genes in primary open angle glaucoma
Glatz W
Molecular Vision
2015; 21: 1340-1344
66311
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation Sequencing
Grigg JR
Human Mutation
2016; 37: 371-384
65867
Candidate genes involved in the susceptibility of primary open angle glaucoma
Malik MA
Gene
2016; 577: 119-131
66339
Association of single nucleotide polymorphisms in the CYP1B1 gene with the risk of primary open-angle glaucoma: a meta-analysis
Li M
Genetics and Molecular Research
2015; 14: 17262-17272
65962
CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients
Shei W
Journal of Glaucoma
2016; 25: e491-e498
66357
Construction of CYP1B1 gene haplotypes predisposing to primary congenital glaucoma through allele-specific PCR/restriction fragment length polymorphism analysis
Li S
Chinese Journal of Medical Genetics
2015; 32: 780-784
66325
An Updated Review on the Genetics of Primary Open Angle Glaucoma
Kondkar AA
International journal of molecular sciences
2015; 16: 28886-28911
66584
LOXL1 gene analysis in Turkish patients with exfoliation glaucoma
Palamar M
International Ophthalmology
2016; 36: 629-635
66332
A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17
Pettitt L
PLoS ONE
2015; 10: e0143546
66250
Risk Factors for Normal and High-Tension Glaucoma in Poland in Connection with Polymorphisms of the Endothelial Nitric Oxide Synthase Gene
Łukasik U
PLoS ONE
2016; 11: e0147540
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