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GWAS Study

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S et al.

18849994 PubMed ID
GWAS Study Type
1361 Participants
1,035 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HA
Hillmer AM
BF
Brockschmidt FF
HS
Hanneken S
ES
Eigelshoven S
SM
Steffens M
FA
Flaquer A
HS
Herms S
BT
Becker T
KA
Kortüm AK
ND
Nyholt DR
ZZ
Zhao ZZ
MG
Montgomery GW
MN
Martin NG
MT
Mühleisen TW
AM
Alblas MA
MS
Moebus S
JK
Jöckel KH
BM
Bröcker-Preuss M
ER
Erbel R
RR
Reinartz R
BR
Betz RC
CS
Cichon S
PP
Propping P
BM
Baur MP
WT
Wienker TF
KR
Kruse R
NM
Nöthen MM
Chapter II

Abstract

Summary of the research findings

We carried out a genome-wide association study in 296 individuals with male-pattern baldness (androgenetic alopecia) and 347 controls. We then investigated the 30 best SNPs in an independent replication sample and found highly significant association for five SNPs on chromosome 20p11 (rs2180439 combined P = 2.7 x 10(-15)). No interaction was detected with the X-chromosomal androgen receptor locus, suggesting that the 20p11 locus has a role in a yet-to-be-identified androgen-independent pathway.

296 European ancestry cases, 347 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1361
Total Participants
GWAS
Study Type
Yes
Replicated
319 European ancestry cases, 234 European ancestry controls
Replication Participants
European
Ancestry
Chapter IV

AI-Generated Summary

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