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3.4.2 Gene studies (91)

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Display all abstracts in classification 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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