Genome|wide association study of the common retinal disorder ...

Genome-wide association study of the common retinal disorder ...

Epiretinal membrane (ERM) is a common retinal condition characterized by the presence of fibrocellular tissue on the retinal surface, ...

Significant risk loci in each of three American populations - Cell Press

Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations.

Genome-wide association study of the common retinal disorder ...

Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American ...

Significant risk loci in each of three American populations

Genome-wide association study of the common retinal disorder epiretinal ... We completed a genome-wide association study (GWAS) in each ...

Cell Genomics on X: "Genome-wide association study of the ...

Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American ...

Genome-wide association study and polygenic risk scores of retinal ...

Alzheimer's disease (AD) is the most common form of dementia in the elderly, responsible for 60–80% of cases. AD is a slowly progressive ...

Genome-wide Association Studies of Retinal Vessel Tortuosity ...

... disease variants and risk factors ... Conclusions: Several alleles associated with retinal vessel tortuosity suggest a common genetic ...

Genomewide Association Study of Retinal Traits in the Amish ... - IOVS

More recent genomewide association studies (GWASs) have revealed as many as 34 independent loci associated with AMD status across both common and rare variants.

Common and rare variation both contribute to the onset of retinal ...

The researchers carried out genome-wide association studies (GWAS) of PRC thickness using the UK Biobank data. The first stage of the work ...

Latest Development on Genetics of Common Retinal Diseases

To understand their genetic basis, candidate gene mutational and association analyses, linkage analysis, genome-wide association studies, transcriptome analysis ...

Genome-wide Association Studies of Retinal Vessel Tortuosity ...

Several alleles associated with retinal vessel tortuosity suggest a common genetic architecture of this trait with ocular diseases (glaucoma, ...

Genome-wide association study identifies genetic risk underlying ...

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment ... study of 14,000 cases of seven common diseases ...

Genome-wide association meta-analysis of 88250 individuals ...

... associations among several common ocular diseases ... Risk of retinal detachment after cataract extraction, 1980-2004: a population-based study.

Genome-wide association study of the common retinal disorder ...

Genome-wide association study of the common retinal disorder epiretinal membrane: Significant risk loci in each of three American populations ... Authors: Joel ...

Large-scale study enables new insights into rare eye disorders | EMBL

... study and enabled us to identify genetic links to rare retinal dystrophies. ... The researchers conducted genome-wide association studies (GWAS) ...

Genetic epidemiology of inherited retinal diseases in a large patient ...

... genetic etiology of IRDs and reveals the high prevalence of ABCA4 and USH2A mutations. This study also uncovers genetic associations with a ...

Genetic architecture of retinal and macular degenerative diseases

Candidate gene and genome-wide association studies (GWAS) have been successful in identifying susceptibility loci for complex RDDs. A recent ...

retinopathy - GWAS Catalog

GWAS Catalog. The NHGRI-EBI Catalog of human genome-wide association studies. Examples: Parkinson disease, ...

Genome-wide association meta-analysis of 88250 ... - The Lancet

4 These studies demonstrated that the coexistence of myopia and other ocular diseases is frequent. Some phenotypic and genetic overlap have been ...

Insights into the genetic basis of retinal detachment - Oxford Academic

The proportion of RRD liability contributed by common genetic variants was estimated at 27% in the very first RRD genome-wide association study (GWAS), which we ...