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Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic Maculopathy.

Investigative ophthalmology & visual science - 3 Mar 2025

Gurung Rajya L, Nangia Charvi, Cai Tengda, FitzGerald Liesel M, McComish Bennet J, Liu Ebony, Kaidonis Georgia, Ridge Bronwyn, Hewitt Alex W, Vote Brendan, Verma Nitin, Craig Jamie E, Palmer Colin N A, Burdon Kathryn P, Meng Weihua

Abstract excerpt

Purpose: Diabetic maculopathy (including diabetic macular edema [DME]) is the leading cause of vision loss in people with diabetes. We aimed to identify the genetic determinants of diabetic maculopathy. Methods: We conducted a genome-wide association study (GWAS) in two cohorts with a meta-analysis. The Australian cohort comprised 551 cases of DME and 599 controls recruited from the states of South Australia and...

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Australia
Case-Control Studies
Chromosomes, Human, Pair 7
Diabetic Retinopathy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Genetic Predisposition to Disease

Genome-Wide Association Study

Polymorphism, Single Nucleotide

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Identifiers

PMID: 40136285
DOI: 10.1167/iovs.66.3.55
PMCID: PMC11951052

Genes

ERICH6B

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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