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GWAS Study

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.

Lesch KP, Timmesfeld N, Renner TJ et al.

18839057 PubMed ID
GWAS Study Type
647 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LK
Lesch KP
TN
Timmesfeld N
RT
Renner TJ
HR
Halperin R
RC
Röser C
NT
Nguyen TT
CD
Craig DW
RJ
Romanos J
HM
Heine M
MJ
Meyer J
FC
Freitag C
WA
Warnke A
RM
Romanos M
SH
Schäfer H
WS
Walitza S
RA
Reif A
SD
Stephan DA
JC
Jacob C
Chapter II

Abstract

Summary of the research findings

A genome-wide association (GWA) study with pooled DNA in adult attention-deficit/hyperactivity disorder (ADHD) employing approximately 500K SNP markers identifies novel risk genes and reveals remarkable overlap with findings from recent GWA scans in substance use disorders. Comparison with results from our previously reported high-resolution linkage scan in extended pedigrees confirms several chromosomal loci, including 16q23.1-24.3 which also reached genome-wide significance in a recent meta-analysis of seven linkage studies (Zhou et al. in Am J Med Genet Part B, 2008). The findings provide additional support for a common effect of genes coding for cell adhesion molecules (e.g., CDH13, ASTN2) and regulators of synaptic plasticity (e.g., CTNNA2, KALRN) despite the complex multifactorial etiologies of adult ADHD and addiction vulnerability.

343 European ancestry cases, 250 European ancestry controls, 54 controls

Chapter III

Study Statistics

Key metrics and study information

647
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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