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GWAS Study

A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies <i>ANXA1</i> as a susceptibility locus for persistent wheezing.

Granell R, Curtin JA, Haider S et al.

37227431 PubMed ID
GWAS Study Type
8427 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GR
Granell R
CJ
Curtin JA
HS
Haider S
KN
Kitaba NT
MS
Mathie SA
GL
Gregory LG
YL
Yates LL
TM
Tutino M
HJ
Hankinson J
PM
Perretti M
VJ
Vonk JM
AH
Arshad HS
CP
Cullinan P
FS
Fontanella S
RG
Roberts GC
KG
Koppelman GH
SA
Simpson A
TS
Turner SW
MC
Murray CS
LC
Lloyd CM
HJ
Holloway JW
CA
Custovic A
Chapter II

Abstract

Summary of the research findings

Many genes associated with asthma explain only a fraction of its heritability. Most genome-wide association studies (GWASs) used a broad definition of 'doctor-diagnosed asthma', thereby diluting genetic signals by not considering asthma heterogeneity. The objective of our study was to identify genetic associates of childhood wheezing phenotypes.

943 European ancestry cases, 5,887 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

8427
Total Participants
GWAS
Study Type
Yes
Replicated
40 cases, 1,557 controls
Replication Participants
European
Ancestry
U.K., Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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