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GWAS Study

A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model.

Nassan M, Li Q, Croarkin PE et al.

27769005 PubMed ID
GWAS Study Type
4257 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

NM
Nassan M
LQ
Li Q
CP
Croarkin PE
CW
Chen W
CC
Colby CL
VM
Veldic M
MS
McElroy SL
JG
Jenkins GD
RE
Ryu E
CJ
Cunningham JM
LM
Leboyer M
FM
Frye MA
BJ
Biernacka JM
Chapter II

Abstract

Summary of the research findings

Although multiple genes have been implicated in bipolar disorder (BD), they explain only a small proportion of its heritability. Identifying additional BD risk variants may be impaired by phenotypic heterogeneity, which is usually not taken into account in genome-wide association studies (GWAS). BD with early age at onset is a more homogeneous familial form of the disorder associated with greater symptom severity.

600 European ancestry cases, 1,811 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

4257
Total Participants
GWAS
Study Type
Yes
Replicated
142 European ancestry cases, 746 European ancestry controls
Replication Participants
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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