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

Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22.

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

Cuker Adam, State Matthew W, King Robert A, Davis Nicole, Ward David C

Abstract excerpt

Gilles de la Tourette syndrome (GTS), obsessive compulsive disorder (OCD), and chronic tic disorder (CTD) are chronic, potentially debilitating neuropsychiatric disorders that often cluster in families. Comorbidity data and family and linkage studies support the hypothesis that these phenotypes, in some cases, share a common etiology. Studies of chromosomal abnormalities associated with this phenotypic spectrum...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Chromosomes, Human, Pair 18

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comorbidity

Share to Obsessive-Compulsive Disorder

Share to Phenotype

Share to Tourette Syndrome

Share to Translocation, Genetic

Source

Identifiers

PMID: 15368493
DOI: 10.1002/ajmg.a.30066

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

Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22.PMID 15368493Read ↗

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.Semantic proximity Read ↗

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.Semantic proximity Read ↗

Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.Semantic proximity Read ↗

The genetics of Tourette syndrome: a review.Semantic proximity Read ↗

Chromosomal rearrangements in Tourette syndrome: implications for identification of candidate susceptibility genes and review of the literature.Semantic proximity Read ↗

Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region.Semantic proximity Read ↗

Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.Semantic proximity Read ↗

Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13Semantic proximity Read ↗

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.Semantic proximity Read ↗

Tourette syndrome and chronic tics in a sample of children and adolescents.Semantic proximity Read ↗

[Genetic linkage analysis of Gilles de la Tourette Syndrome in a Colombian family].Semantic proximity Read ↗

Brain-derived neurotrophic factor: a genetic risk factor for obsessive-compulsive disorder and Tourette syndrome?Semantic proximity Read ↗

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