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Research Database

Health & Traits Publications

Explore scientific publications on genetic research, GWAS studies, and genomic discoveries.

7659 Publications
7659 GWAS Studies
916 Journals
3388 Replicated
10 of 7659 publications
Active: Ophthalmology Clear all
Title
Author
Journal
Disease/Trait
Date
Actions
GWAS of age-related macular degeneration reveals two new loci implying shared genetic components with central serous chorioretinopathy.
Akiyama M
Ophthalmology
Age-related macular degeneration
2022-11-21
Genome-wide Survival Analysis for Macular Neovascularization Development in Central Serous Chorioretinopathy Revealed Shared Genetic Susceptibility with Polypoidal Choroidal Vasculopathy.
Mori Y, Miyake M et al.
Ophthalmology
Macular neovascularization in central serous chorioretinopathy
2022-04-28
GWAS identifies two common loci associated with pigment dispersion syndrome/pigmentary glaucoma and implicate myopia in its development.
Simcoe MJ, Shah A et al.
Ophthalmology
Pigment dispersion syndrome or pigmentary glaucoma
2022-01-11
High-density lipoprotein 3 cholesterol and primary open-angle glaucoma: metabolomics and mendelian randomization analyses.
Nusinovici S, Li H et al.
Ophthalmology
High-density lipoprotein 3 cholesterol levels
2021-09-27
Genome-wide association study in Asians identifies novel loci for high myopia and highlights a nervous system role in its pathogenesis.
Meguro A, Yamane T et al.
Ophthalmology
High myopia
2020-05-16
Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration.
Lorés-Motta L, Paun CC et al.
Ophthalmology
Serum C3d:C3 ratio (systemic complement activation)
2018-02-01
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Sobrin L, Ripke S et al.
Ophthalmology
Age-related macular degeneration (choroidal neovascularisation)
2012-06-15
Genome-wide association study of diabetic retinopathy in a Taiwanese population.
Huang YC, Lin JM et al.
Ophthalmology
Diabetic retinopathy
2011-02-08
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.
Li YJ, Goh L et al.
Ophthalmology
Myopia (pathological)
2010-11-20
Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.
Meguro A, Inoko H et al.
Ophthalmology
Glaucoma
2010-04-02
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