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GWAS Study

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.

van der Lee SJ, Knol MJ, Chauhan G et al.

31396565 PubMed ID
GWAS Study Type
24058 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

VD
van der Lee SJ
KM
Knol MJ
CG
Chauhan G
SC
Satizabal CL
SA
Smith AV
HE
Hofer E
BJ
Bis JC
HD
Hibar DP
HS
Hilal S
VD
van den Akker EB
AK
Arfanakis K
BM
Bernard M
YL
Yanek LR
AN
Amin N
CF
Crivello F
CJ
Cheung JW
HT
Harris TB
SY
Saba Y
LO
Lopez OL
LS
Li S
VD
van der Grond J
YL
Yu L
PT
Paus T
RG
Roshchupkin GV
AP
Amouyel P
JN
Jahanshad N
TK
Taylor KD
YQ
Yang Q
MR
Mathias RA
BS
Boehringer S
MB
Mazoyer B
RK
Rice K
CC
Cheng CY
MP
Maillard P
VH
van Heemst D
WT
Wong TY
NW
Niessen WJ
BA
Beiser AS
BM
Beekman M
ZW
Zhao W
NP
Nyquist PA
CC
Chen C
LL
Launer LJ
PB
Psaty BM
IM
Ikram MK
VM
Vernooij MW
SH
Schmidt H
PZ
Pausova Z
BD
Becker DM
DJ
De Jager PL
TP
Thompson PM
VD
van Duijn CM
BD
Bennett DA
SP
Slagboom PE
SR
Schmidt R
LW
Longstreth WT
IM
Ikram MA
SS
Seshadri S
DS
Debette S
GV
Gudnason V
AH
Adams HHH
DC
DeCarli C
Chapter II

Abstract

Summary of the research findings

Brain lobar volumes are heritable but genetic studies are limited. We performed genome-wide association studies of frontal, occipital, parietal and temporal lobe volumes in 16,016 individuals, and replicated our findings in 8,789 individuals. We identified six genetic loci associated with specific lobar volumes independent of intracranial volume. Two loci, associated with occipital (6q22.32) and temporal lobe volume (12q14.3), were previously reported to associate with intracranial and hippocampal volume, respectively. We identified four loci previously unknown to affect brain volumes: 3q24 for parietal lobe volume, and 1q22, 4p16.3 and 14q23.1 for occipital lobe volume. The associated variants were located in regions enriched for histone modifications (DAAM1 and THBS3), or close to genes causing Mendelian brain-related diseases (ZIC4 and FGFRL1). No genetic overlap between lobar volumes and neurological or psychiatric diseases was observed. Our findings reveal part of the complex genetics underlying brain development and suggest a role for regulatory regions in determining brain volumes.

15,269 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

24058
Total Participants
GWAS
Study Type
Yes
Replicated
8,789 European ancestry individuals
Replication Participants
European, East Asian, South East Asian, African American or Afro-Caribbean
Ancestry
U.K., Canada, U.S., Austria, France, Netherlands, Iceland, Singapore
Recruitment Country
Chapter IV

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