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

Association analysis between a VNTR intron 8 polymorphism of the dopamine transporter gene (SLC6A3) and obsessive- compulsive disorder in a Brazilian sample.

Arquivos de neuro-psiquiatria - 1 Dec 2007

Miguita Karen, Cordeiro Quirino, Siqueira-Roberto Jacqueline, Shavitt Roseli Gedanke, Castillo José Carlos Ramos, Castillo Ana Regina, Miguel Euripedes Constantino, Vallada Homero

Abstract excerpt

Family, twin and segregation analysis have provided evidences that genetic factors are implicated in the susceptibility for obsessive-compulsive disorder (OCD). Several lines of research suggest that the dopaminergic system may be involved in the pathophysiology of OCD. Thus, the aim of the present study was to investigate a possible association between a polymorphism located in intron 8 of the dopamine...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Dopamine Plasma Membrane Transport Proteins

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Introns

Share to Obsessive-Compulsive Disorder

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 18094849
DOI: 10.1590/s0004-282x2007000600002

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association analysis between a VNTR intron 8 polymorphism of the dopamine transporter gene (SLC6A3) and obsessive- compulsive disorder in a Brazilian sample.PMID 18094849Read ↗

Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder.Semantic proximity Read ↗

Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.Semantic proximity Read ↗

Association study between the dopamine receptor D(4) gene and obsessive-compulsive disorder.Semantic proximity Read ↗

Molecular genetics of obsessive-compulsive disorder: a comprehensive meta-analysis of genetic association studies.Semantic proximity Read ↗

Genetic Polymorphism of the Serotonin Transporter Gene, SLC6A4 rs16965628, Is Associated with Obsessive Compulsive Disorder.Semantic proximity Read ↗

Correlations between single nucleotide polymorphisms in obsessive-compulsive disorder with the clinical features or response to therapy.Semantic proximity Read ↗

Association study between BDNF gene variants and Mexican patients with obsessive-compulsive disorder.Semantic proximity Read ↗

A large case-control study of common functional SLC6A4 and BDNF variants in obsessive-compulsive disorder.Semantic proximity Read ↗

Association of the functional serotonin transporter haplotype with familial form of obsessive compulsive disorder in Iranian patients.Semantic proximity Read ↗

The genetics of obsessive-compulsive disorder: a review.Semantic proximity Read ↗

Disorder-specific genetic factors in obsessive-compulsive disorder: A comprehensive meta-analysis.Semantic proximity Read ↗

COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.Semantic proximity Read ↗

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