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GWAS Study

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.

Demontis D, Walters GB, Athanasiadis G et al.

36702997 PubMed ID
GWAS Study Type
225534 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DD
Demontis D
WG
Walters GB
AG
Athanasiadis G
WR
Walters R
TK
Therrien K
NT
Nielsen TT
FL
Farajzadeh L
VG
Voloudakis G
BJ
Bendl J
ZB
Zeng B
ZW
Zhang W
GJ
Grove J
AT
Als TD
DJ
Duan J
SF
Satterstrom FK
BJ
Bybjerg-Grauholm J
BM
Bækved-Hansen M
GO
Gudmundsson OO
MS
Magnusson SH
BG
Baldursson G
DK
Davidsdottir K
HG
Haraldsdottir GS
AE
Agerbo E
HG
Hoffman GE
DS
Dalsgaard S
MJ
Martin J
RM
Ribasés M
BD
Boomsma DI
SA
Soler Artigas M
RM
Roth Mota N
HD
Howrigan D
MS
Medland SE
ZT
Zayats T
RV
Rajagopal VM
NM
Nordentoft M
MO
Mors O
HD
Hougaard DM
MP
Mortensen PB
DM
Daly MJ
FS
Faraone SV
SH
Stefansson H
RP
Roussos P
FB
Franke B
WT
Werge T
NB
Neale BM
SK
Stefansson K
BA
Børglum AD
Chapter II

Abstract

Summary of the research findings

Attention-deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder with a major genetic component. Here, we present a genome-wide association study meta-analysis of ADHD comprising 38,691 individuals with ADHD and 186,843 controls. We identified 27 genome-wide significant loci, highlighting 76 potential risk genes enriched among genes expressed particularly in early brain development. Overall, ADHD genetic risk was associated with several brain-specific neuronal subtypes and midbrain dopaminergic neurons. In exome-sequencing data from 17,896 individuals, we identified an increased load of rare protein-truncating variants in ADHD for a set of risk genes enriched with probable causal common variants, potentially implicating SORCS3 in ADHD by both common and rare variants. Bivariate Gaussian mixture modeling estimated that 84-98% of ADHD-influencing variants are shared with other psychiatric disorders. In addition, common-variant ADHD risk was associated with impaired complex cognition such as verbal reasoning and a range of executive functions, including attention.

38,691 European ancestry cases, 186,843 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

225534
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada, U.S., Norway, Denmark, U.K., Germany, Spain
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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