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GWAS Study

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.

Meguro A, Inoko H, Ota M et al.

20363506 PubMed ID
GWAS Study Type
660 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MA
Meguro A
IH
Inoko H
OM
Ota M
MN
Mizuki N
BS
Bahram S
Chapter II

Abstract

Summary of the research findings

Purpose: Factors contributing to the development of normal tension glaucoma (NTG), degenerative optic neuropathy characterized by the progressive loss of retinal ganglion cells, optic nerve axons, and visual fields, have not been determined. To identify genetic risk factors for NTG, we performed a genome-wide association study of NTG.

305 Japanese ancestry cases, 355 Japanese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

660
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Japan
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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