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 between 7q31 markers and Tourette syndrome.

American journal of medical genetics. Part A - 15 May 2004

Díaz-Anzaldúa Adriana, Joober Ridha, Rivière Jean-Baptiste, Dion Yves, Lespérance Paul, Chouinard Sylvain, Richer Francois, Rouleau Guy Armand

Abstract excerpt

Tourette syndrome (TS) is a complex neuropychiatric disorder with a strong genetic basis. Although no specific susceptibility genes have been identified for TS, cytogenetic studies in selected cases suggest the existence of a predisposing gene located in the 7q31 chromosomal region. In order to test the hypothesis of a possible relationship between this region and TS at the population level, we undertook a family...

Read the complete abstract on PubMed

Topics

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

Share to Attention Deficit Disorder with Hyperactivity
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comorbidity

Share to DNA Fingerprinting

Share to Endopeptidases

Share to Obsessive-Compulsive Disorder

Share to Quebec

Share to Tourette Syndrome

Source

Identifiers

PMID: 15103711
DOI: 10.1002/ajmg.a.20631

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

Association between 7q31 markers and Tourette syndrome.PMID 15103711Read ↗

Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred.Semantic proximity Read ↗

Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population.Semantic proximity Read ↗

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree.Semantic proximity Read ↗

Genetics of Tourette Syndrome.Semantic proximity Read ↗

The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods.Semantic proximity Read ↗

Genome-wide association study of Tourette's syndrome.Semantic proximity Read ↗

Genetics of Tourette syndrome and tic disorders.Semantic proximity Read ↗

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.Semantic proximity Read ↗

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndromeSemantic proximity Read ↗

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndromeSemantic proximity Read ↗

Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting.Semantic proximity Read ↗

Familial Risks of Tourette Syndrome and Chronic Tic Disorders. A Population-Based Cohort Study.Semantic proximity Read ↗

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