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GWAS Study

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.

Anney RJ

25087078 PubMed ID
GWAS Study Type
34853 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AR
Anney RJ
Chapter II

Abstract

Summary of the research findings

The epilepsies are a clinically heterogeneous group of neurological disorders. Despite strong evidence for heritability, genome-wide association studies have had little success in identification of risk loci associated with epilepsy, probably because of relatively small sample sizes and insufficient power. We aimed to identify risk loci through meta-analyses of genome-wide association studies for all epilepsy and the two largest clinical subtypes (genetic generalised epilepsy and focal epilepsy).

405 European ancestry cases, 127 African American cases, 248 cases, 2,330 European ancestry genetic generalised epilepsy cases, 81 African American genetic generalised epilepsy cases, 195 genetic generalised epilepsy cases, 3,277 European ancestry focal epilepsy cases, 222 African American focal epilepsy cases, 487 Han Chinese ancestry focal epilepsy cases, 1,324 focal epilepsy cases, up to 17,441 European ancestry controls, up to 2,843 African American controls, up to 2,875 Han Chinese ancestry controls, up to 2,998 controls

Chapter III

Study Statistics

Key metrics and study information

34853
Total Participants
GWAS
Study Type
No
Replicated
NR, European, East Asian, African American or Afro-Caribbean, European, African American or Afro-Caribbean, European
Ancestry
U.K., China, Hong Kong SAR, U.S., Canada, Finland, Australia, Belgium, Republic of Ireland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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