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GWAS Study

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.

Lasky-Su J, Anney RJ, Neale BM et al.

18937294 PubMed ID
GWAS Study Type
2790 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LJ
Lasky-Su J
AR
Anney RJ
NB
Neale BM
FB
Franke B
ZK
Zhou K
MJ
Maller JB
VA
Vasquez AA
CW
Chen W
AP
Asherson P
BJ
Buitelaar J
BT
Banaschewski T
ER
Ebstein R
GM
Gill M
MA
Miranda A
MF
Mulas F
OR
Oades RD
RH
Roeyers H
RA
Rothenberger A
SJ
Sergeant J
SE
Sonuga-Barke E
SH
Steinhausen HC
TE
Taylor E
DM
Daly M
LN
Laird N
LC
Lange C
FS
Faraone SV
Chapter II

Abstract

Summary of the research findings

A time-to-onset analysis for family-based samples was performed on the genomewide association (GWAS) data for attention deficit hyperactivity disorder (ADHD) to determine if associations exist with the age at onset of ADHD. The initial dataset consisted of 958 parent-offspring trios that were genotyped on the Perlegen 600,000 SNP array. After data cleaning procedures, 429,981 autosomal SNPs and 930 parent-offspring trios were used found suitable for use and a family-based logrank analysis was performed using that age at first ADHD symptoms as the quantitative trait of interest. No SNP achieved genome-wide significance, and the lowest P-values had a magnitude of 10(-7). Several SNPs among a pre-specified list of candidate genes had nominal associations including SLC9A9, DRD1, ADRB2, SLC6A3, NFIL3, ADRB1, SYT1, HTR2A, ARRB2, and CHRNA4. Of these findings SLC9A9 stood out as a promising candidate, with nominally significant SNPs in six distinct regions of the gene.

930 European ancestry trios

Chapter III

Study Statistics

Key metrics and study information

2790
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Israel, Netherlands, Belgium, Germany, U.K., Switzerland, Spain, Republic of Ireland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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