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Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.A genome-wide association study of optic disc parameters.The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR GeneVariations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people.Comprehensive analysis of the candidate genes CCL2, CCR2, and TLR4 in age-related macular degeneration.Progressive loss of cones in Achromatopsia: an imaging study using spectral-domain optical coherence tomography.Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.Clinical characteristics and natural history of rho-associated retinitis pigmentosa.Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia.The SERPING1 gene and age-related macular degeneration.The complement component 5 gene and age-related macular degeneration.Clinical course of cone dystrophy caused by mutations in the RPGR gene.Genome-wide meta-analyses of multi-ethnic cohorts identify multiple new susceptibility loci for refractive error and myopia.Reducing the geneetic risk of age-related macular degeneration with dietary antioxidants, zinc, and omega-3 fatty acids.A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.Common genetic determinants of intraocular pressure and primary open-angle glaucoma.Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration.Epidemiology of AMD.The ERCC6 gene and age-related macular degeneration.A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology.Genetic architecture of open angle glaucoma and related determinants.Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip.Clinical implications of old and new genes for open-angle glaucoma.Geographic atrophy in age-related macular degeneration and TLR3.The vast complexity of primary open angle glaucoma: disease genes, risks, molecular mechanisms and pathobiology.Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal DystrophiesComplement component C3 and risk of age-related macular degeneration.Cone-rod dystrophy can be a manifestation of Danon disease.Common genetic variants associated with open-angle glaucoma.The SERPING1 gene and age-related macular degeneration.Three genome-wide association studies ans a linkage analysis identify HERC2 as a human iris color gene.Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies.