Literature DB >> 19058789

A common variant in DRD3 receptor is associated with autism spectrum disorder.

Mariken de Krom1, Wouter G Staal, Roel A Ophoff, Judith Hendriks, Jan Buitelaar, Barbara Franke, Maretha V de Jonge, Patrick Bolton, David Collier, Sarah Curran, Herman van Engeland, Jan M van Ree.   

Abstract

BACKGROUND: The presence of specific and common genetic etiologies for autism spectrum disorders (ASD) and attention-deficit/hyperactivity disorder (ADHD) was investigated for 132 candidate genes in a two-stage design-association study.
METHODS: 1,536 single nucleotide polymorphisms (SNPs) covering these candidate genes were tested in ASD (n = 144) and ADHD (n = 110) patients and control subjects (n = 404) from The Netherlands. A second stage was performed with those SNPs from Stage I reaching a significance threshold for association of p < .01 in an independent sample of ASD patients (n = 128) and controls (n = 124) from the United Kingdom and a Dutch ADHD (n = 150) and control (n = 149) sample.
RESULTS: No shared association was found between ASD and ADHD. However, in the first and second ASD samples and in a joint statistical analysis, a significant association between SNP rs167771 located in the DRD3 gene was found (joint analysis uncorrected: p = 3.11 x 10(-6); corrected for multiple testing and potential stratification: p = .00162).
CONCLUSIONS: The DRD3 gene is related to stereotyped behavior, liability to side effects of antipsychotic medication, and movement disorders and may therefore have important clinical implications for ASD.

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Year:  2008        PMID: 19058789     DOI: 10.1016/j.biopsych.2008.09.035

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  27 in total

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4.  Full-field electroretinogram in autism spectrum disorder.

Authors:  Paul A Constable; Sebastian B Gaigg; Dermot M Bowler; Herbert Jägle; Dorothy A Thompson
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Review 5.  The potential role of dopamine D₃ receptor neurotransmission in cognition.

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Review 6.  Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.

Authors:  Nanda N J Rommelse; Barbara Franke; Hilde M Geurts; Catharina A Hartman; Jan K Buitelaar
Journal:  Eur Child Adolesc Psychiatry       Date:  2010-02-11       Impact factor: 4.785

Review 7.  Glutamatergic candidate genes in autism spectrum disorder: an overview.

Authors:  Andreas G Chiocchetti; Hanna S Bour; Christine M Freitag
Journal:  J Neural Transm (Vienna)       Date:  2014-02-04       Impact factor: 3.575

8.  De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder.

Authors:  P J Hamilton; N G Campbell; S Sharma; K Erreger; F Herborg Hansen; C Saunders; A N Belovich; M A Sahai; E H Cook; U Gether; H S McHaourab; H J G Matthies; J S Sutcliffe; A Galli
Journal:  Mol Psychiatry       Date:  2013-08-27       Impact factor: 15.992

9.  Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors.

Authors:  Jun Liu; Huamei Fu; Jiangying Kong; Hong Yu; Zengyu Zhang
Journal:  Metab Brain Dis       Date:  2021-03-01       Impact factor: 3.584

10.  Brief report: the dopamine-3-receptor gene (DRD3) is associated with specific repetitive behavior in autism spectrum disorder (ASD).

Authors:  Wouter G Staal; Mariken de Krom; Maretha V de Jonge
Journal:  J Autism Dev Disord       Date:  2012-05
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