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GWAS Study

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.

Perry JR, Day F, Elks CE et al.

25231870 PubMed ID
GWAS Study Type
182413 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PJ
Perry JR
DF
Day F
EC
Elks CE
SP
Sulem P
TD
Thompson DJ
FT
Ferreira T
HC
He C
CD
Chasman DI
ET
Esko T
TG
Thorleifsson G
AE
Albrecht E
AW
Ang WQ
CT
Corre T
CD
Cousminer DL
FB
Feenstra B
FN
Franceschini N
GA
Ganna A
JA
Johnson AD
KS
Kjellqvist S
LK
Lunetta KL
MG
McMahon G
NI
Nolte IM
PL
Paternoster L
PE
Porcu E
SA
Smith AV
SL
Stolk L
TA
Teumer A
TN
Tšernikova N
TE
Tikkanen E
US
Ulivi S
WE
Wagner EK
AN
Amin N
BL
Bierut LJ
BE
Byrne EM
HJ
Hottenga JJ
KD
Koller DL
MM
Mangino M
PT
Pers TH
YL
Yerges-Armstrong LM
ZJ
Zhao JH
AI
Andrulis IL
AH
Anton-Culver H
AF
Atsma F
BS
Bandinelli S
BM
Beckmann MW
BJ
Benitez J
BC
Blomqvist C
BS
Bojesen SE
BM
Bolla MK
BB
Bonanni B
BH
Brauch H
BH
Brenner H
BJ
Buring JE
CJ
Chang-Claude J
CS
Chanock S
CJ
Chen J
CG
Chenevix-Trench G
CJ
Collée JM
CF
Couch FJ
CD
Couper D
CA
Coveillo AD
CA
Cox A
CK
Czene K
DA
D'adamo AP
SG
Smith GD
DV
De Vivo I
DE
Demerath EW
DJ
Dennis J
DP
Devilee P
DA
Dieffenbach AK
DA
Dunning AM
EG
Eiriksdottir G
EJ
Eriksson JG
FP
Fasching PA
FL
Ferrucci L
FD
Flesch-Janys D
FH
Flyger H
FT
Foroud T
FL
Franke L
GM
Garcia ME
GM
García-Closas M
GF
Geller F
DG
de Geus EE
GG
Giles GG
GD
Gudbjartsson DF
GV
Gudnason V
GP
Guénel P
GS
Guo S
HP
Hall P
HU
Hamann U
HR
Haring R
HC
Hartman CA
HA
Heath AC
HA
Hofman A
HM
Hooning MJ
HJ
Hopper JL
HF
Hu FB
HD
Hunter DJ
KD
Karasik D
KD
Kiel DP
KJ
Knight JA
KV
Kosma VM
KZ
Kutalik Z
LS
Lai S
LD
Lambrechts D
LA
Lindblom A
MR
Mägi R
MP
Magnusson PK
MA
Mannermaa A
MN
Martin NG
MG
Masson G
MP
McArdle PF
MW
McArdle WL
MM
Melbye M
MK
Michailidou K
ME
Mihailov E
ML
Milani L
MR
Milne RL
NH
Nevanlinna H
NP
Neven P
NE
Nohr EA
OA
Oldehinkel AJ
OB
Oostra BA
PA
Palotie A
PM
Peacock M
PN
Pedersen NL
PP
Peterlongo P
PJ
Peto J
PP
Pharoah PD
PD
Postma DS
PA
Pouta A
PK
Pylkäs K
RP
Radice P
RS
Ring S
RF
Rivadeneira F
RA
Robino A
RL
Rose LM
RA
Rudolph A
SV
Salomaa V
SS
Sanna S
SD
Schlessinger D
SM
Schmidt MK
SM
Southey MC
SU
Sovio U
SM
Stampfer MJ
SD
Stöckl D
SA
Storniolo AM
TN
Timpson NJ
TJ
Tyrer J
VJ
Visser JA
VP
Vollenweider P
VH
Völzke H
WG
Waeber G
WM
Waldenberger M
WH
Wallaschofski H
WQ
Wang Q
WG
Willemsen G
WR
Winqvist R
WB
Wolffenbuttel BH
WM
Wright MJ
BD
Boomsma DI
EM
Econs MJ
KK
Khaw KT
LR
Loos RJ
MM
McCarthy MI
MG
Montgomery GW
RJ
Rice JP
SE
Streeten EA
TU
Thorsteinsdottir U
VD
van Duijn CM
AB
Alizadeh BZ
BS
Bergmann S
BE
Boerwinkle E
BH
Boyd HA
CL
Crisponi L
GP
Gasparini P
GC
Gieger C
HT
Harris TB
IE
Ingelsson E
JM
Järvelin MR
KP
Kraft P
LD
Lawlor D
MA
Metspalu A
PC
Pennell CE
RP
Ridker PM
SH
Snieder H
ST
Sørensen TI
ST
Spector TD
SD
Strachan DP
UA
Uitterlinden AG
WN
Wareham NJ
WE
Widen E
ZM
Zygmunt M
MA
Murray A
ED
Easton DF
SK
Stefansson K
MJ
Murabito JM
OK
Ong KK
Chapter II

Abstract

Summary of the research findings

Age at menarche is a marker of timing of puberty in females. It varies widely between individuals, is a heritable trait and is associated with risks for obesity, type 2 diabetes, cardiovascular disease, breast cancer and all-cause mortality. Studies of rare human disorders of puberty and animal models point to a complex hypothalamic-pituitary-hormonal regulation, but the mechanisms that determine pubertal timing and underlie its links to disease risk remain unclear. Here, using genome-wide and custom-genotyping arrays in up to 182,416 women of European descent from 57 studies, we found robust evidence (P < 5 × 10(-8)) for 123 signals at 106 genomic loci associated with age at menarche. Many loci were associated with other pubertal traits in both sexes, and there was substantial overlap with genes implicated in body mass index and various diseases, including rare disorders of puberty. Menarche signals were enriched in imprinted regions, with three loci (DLK1-WDR25, MKRN3-MAGEL2 and KCNK9) demonstrating parent-of-origin-specific associations concordant with known parental expression patterns. Pathway analyses implicated nuclear hormone receptors, particularly retinoic acid and γ-aminobutyric acid-B2 receptor signalling, among novel mechanisms that regulate pubertal timing in humans. Our findings suggest a genetic architecture involving at least hundreds of common variants in the coordinated timing of the pubertal transition.

Up to 182,413 European ancestry females

Chapter III

Study Statistics

Key metrics and study information

182413
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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