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GWAS Study

Male-pattern baldness susceptibility locus at 20p11.

Richards JB, Yuan X, Geller F et al.

18849991 PubMed ID
GWAS Study Type
4961 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RJ
Richards JB
YX
Yuan X
GF
Geller F
WD
Waterworth D
BV
Bataille V
GD
Glass D
SK
Song K
WG
Waeber G
VP
Vollenweider P
AK
Aben KK
KL
Kiemeney LA
WB
Walters B
SN
Soranzo N
TU
Thorsteinsdottir U
KA
Kong A
RT
Rafnar T
DP
Deloukas P
SP
Sulem P
SH
Stefansson H
SK
Stefansson K
ST
Spector TD
MV
Mooser V
Chapter II

Abstract

Summary of the research findings

We conducted a genome-wide association study for androgenic alopecia in 1,125 men and identified a newly associated locus at chromosome 20p11.22, confirmed in three independent cohorts (n = 1,650; OR = 1.60, P = 1.1 x 10(-14) for rs1160312). The one man in seven who harbors risk alleles at both 20p11.22 and AR (encoding the androgen receptor) has a sevenfold-increased odds of androgenic alopecia (OR = 7.12, P = 3.7 x 10(-15)).

578 European ancestry cases, 547 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

4961
Total Participants
GWAS
Study Type
Yes
Replicated
1,351 European ancestry cases, 2,485 European ancestry controls
Replication Participants
European
Ancestry
Iceland, Netherlands, U.K., Switzerland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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