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3.4.2 Gene studies (149)
Showing records 1 to 25
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies72164 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
73070 Genetics of Glaucoma
Wiggs JL
Human Molecular Genetics 2017; 26: R21-R27
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
73045 Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Iglesias AI
Human Mutation 2017; 38: 1025-1032
72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu MY
BMC Ophthalmology 2017; 17: 48
73061 Major review: Molecular genetics of primary open-angle glaucoma
Liu Y
Experimental Eye Research 2017; 160: 62-84
72836 LADD syndrome with glaucoma is caused by a novel gene
Simpson A
Molecular Vision 2017; 23: 179-184
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
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
73035 Nicotinamide and WLD(S) Act Together to Prevent Neurodegeneration in Glaucoma
Williams PA
Frontiers in neuroscience 2017; 11: 232
72869 CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma
Hu Z
Oncotarget 2017; 8: 21167-21176
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
72965 Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye
Swierkowska J
Ophthalmic Genetics 2017; 0: 1-10
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:
73002 Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis
Song E
Scientific reports 2017; 7: 1442
73021 Gene Expression Profiling of the Optic Nerve Head of Patients with Primary Open-Angle Glaucoma
Wang X
Journal of Ophthalmology 2017; 2017: 6896390
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
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
73161 Primary Congenital and Developmental Glaucomas
Lewis C
Human Molecular Genetics 2017; 26: R28-R36
72857 Association analysis between LOXL1 gene and exfoliation syndrome
Chen L
Chinese Journal of Ophthalmology 2017; 53: 294-299
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
72903 Associations between matrix metalloproteinase gene polymorphisms and glaucoma susceptibility: a meta-analysis
Wu Y
BMC Ophthalmology 2017; 17: 48
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
72836 LADD syndrome with glaucoma is caused by a novel gene
Avdic A
Molecular Vision 2017; 23: 179-184
72857 Association analysis between LOXL1 gene and exfoliation syndrome
Wang NL
Chinese Journal of Ophthalmology 2017; 53: 294-299
