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GWAS Study

Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma.

Nieuwenhuis MA, Siedlinski M, van den Berge M et al.

27439200 PubMed ID
GWAS Study Type
13556 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

NM
Nieuwenhuis MA
SM
Siedlinski M
VD
van den Berge M
GR
Granell R
LX
Li X
NM
Niens M
VD
van der Vlies P
AJ
Altmüller J
NP
Nürnberg P
KM
Kerkhof M
VS
van Schayck OC
RR
Riemersma RA
VD
van der Molen T
DM
de Monchy JG
BY
Bossé Y
SA
Sandford A
BC
Bruijnzeel-Koomen CA
GV
Gerth van Wijk R
TH
Ten Hacken NH
TW
Timens W
BH
Boezen HM
HJ
Henderson J
KM
Kabesch M
VJ
Vonk JM
PD
Postma DS
KG
Koppelman GH
Chapter II

Abstract

Summary of the research findings

Genomewide association studies (GWASs) of asthma have identified single-nucleotide polymorphisms (SNPs) that modestly increase the risk for asthma. This could be due to phenotypic heterogeneity of asthma. Bronchial hyperresponsiveness (BHR) is a phenotypic hallmark of asthma. We aim to identify susceptibility genes for asthma combined with BHR and analyse the presence of cis-eQTLs among replicated SNPs. Secondly, we compare the genetic association of SNPs previously associated with (doctor's diagnosed) asthma to our GWAS of asthma with BHR.

920 Dutch ancestry cases, 980 Dutch ancestry controls

Chapter III

Study Statistics

Key metrics and study information

13556
Total Participants
GWAS
Study Type
Yes
Replicated
2,589 European ancestry cases, 473 cases, 6,702 European ancestry controls, 1,892 controls
Replication Participants
European
Ancestry
U.S., Germany, U.K., Austria, Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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