Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Biological psychiatry - 1 Apr 2009

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

Abstract excerpt

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...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DRD3 gene
Share to Adolescent

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Attention Deficit Disorder with Hyperactivity

Share to Autistic Disorder

Share to Genome-Wide Association Study

Share to Polymorphism, Single Nucleotide

Share to Receptors, Dopamine D3

Source

Identifiers

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

Genes

DRD3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A common variant in DRD3 receptor is associated with autism spectrum disorder.PMID 19058789Read ↗

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

DRD3 gene and striatum in autism spectrum disorder.Semantic proximity Read ↗

Polymorphisms in GPCR genes: Their role in schizophrenia, autism diseases and response to antipsychotic treatment - A systematic review.Semantic proximity Read ↗

Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors.Semantic proximity Read ↗

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.Semantic proximity Read ↗

ADGRL3 rs6551665 as a Common Vulnerability Factor Underlying Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder.Semantic proximity Read ↗

Functional SLC6A3 polymorphisms differentially affect autism spectrum disorder severity: a study on Indian subjects.Semantic proximity Read ↗

Allelic variants in HTR3C show association with autism.Semantic proximity Read ↗

Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific.Semantic proximity Read ↗

An exploration of common dopaminergic variants and behavior problems in siblings at high risk for autism spectrum disorder.Semantic proximity Read ↗

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.Semantic proximity Read ↗

Meta-analysis of the dopamine D3 receptor gene (DRD3) Ser9Gly variant and schizophrenia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.