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GWAS Study

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.

Davies RW, Wells GA, Stewart AF et al.

22319020 PubMed ID
GWAS Study Type
24981 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DR
Davies RW
WG
Wells GA
SA
Stewart AF
EJ
Erdmann J
SS
Shah SH
FJ
Ferguson JF
HA
Hall AS
AS
Anand SS
BM
Burnett MS
ES
Epstein SE
DS
Dandona S
CL
Chen L
NJ
Nahrstaedt J
LC
Loley C
KI
König IR
KW
Kraus WE
GC
Granger CB
EJ
Engert JC
HC
Hengstenberg C
WH
Wichmann HE
SS
Schreiber S
TW
Tang WH
ES
Ellis SG
RD
Rader DJ
HS
Hazen SL
RM
Reilly MP
SN
Samani NJ
SH
Schunkert H
RR
Roberts R
MR
McPherson R
Chapter II

Abstract

Summary of the research findings

Recent genome-wide association studies (GWAS) have identified several novel loci that reproducibly associate with coronary artery disease (CAD) and/or myocardial infarction risk. However, known common CAD risk variants explain only 10% of the predicted genetic heritability of the disease, suggesting that important genetic signals remain to be discovered.

7,123 European ancestry cases, 6,826 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

24981
Total Participants
GWAS
Study Type
Yes
Replicated
5,211 European ancestry cases, 5,821 European ancestry controls
Replication Participants
European
Ancestry
U.S., Canada, Germany, Australia, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.