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GWAS Study

Genetic architecture reconciles linkage and association studies of complex traits.

Sidorenko J, Couvy-Duchesne B, Kemper KE et al.

39375568 PubMed ID
GWAS Study Type
650000 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SJ
Sidorenko J
CB
Couvy-Duchesne B
KK
Kemper KE
MG
Moen GH
BL
Bhatta L
ÅB
Åsvold BO
MR
Mägi R
AA
Ani A
WR
Wang R
NI
Nolte IM
GS
Gordon S
HC
Hayward C
CA
Campbell A
BD
Benjamin DJ
CD
Cesarini D
ED
Evans DM
GM
Goddard ME
HC
Haley CS
PD
Porteous D
MS
Medland SE
MN
Martin NG
SH
Snieder H
MA
Metspalu A
HK
Hveem K
BB
Brumpton B
VP
Visscher PM
YL
Yengo L
Chapter II

Abstract

Summary of the research findings

Linkage studies have successfully mapped loci underlying monogenic disorders, but mostly failed when applied to common diseases. Conversely, genome-wide association studies (GWASs) have identified replicable associations between thousands of SNPs and complex traits, yet capture less than half of the total heritability. In the present study we reconcile these two approaches by showing that linkage signals of height and body mass index (BMI) from 119,000 sibling pairs colocalize with GWAS-identified loci. Concordant with polygenicity, we observed the following: a genome-wide inflation of linkage test statistics; that GWAS results predict linkage signals; and that adjusting phenotypes for polygenic scores reduces linkage signals. Finally, we developed a method using recombination rate-stratified, identity-by-descent sharing between siblings to unbiasedly estimate heritability of height (0.76 ± 0.05) and BMI (0.55 ± 0.07). Our results imply that substantial heritability remains unaccounted for by GWAS-identified loci and this residual genetic variation is polygenic and enriched near these loci.

650,000 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

650000
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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