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

Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Jun 2008

Speed William C, O'Roak Brian J, Tárnok Zsanett, Barta Csaba, Pakstis Andrew J, State Matthew W, Kidd Kenneth K

Abstract excerpt

Gilles de la Tourette syndrome (GTS) is a complex disorder with a clear genetic component but no clearly identified genes with variation of etiologic relevance. Various candidate regions and genes show some evidence of affecting risk, though clearly not all patients/families can be explained by any one of them. Resequencing one candidate gene, SLITRK1, has identified four new variants. Including them, we have...

Read the complete abstract on PubMed

Topics

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

Share to DNA Mutational Analysis
Share to Evolution, Molecular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Membrane Proteins

Share to Molecular Epidemiology

Share to Nerve Tissue Proteins

Share to Sequence Analysis, DNA

Share to Tourette Syndrome

Source

Identifiers

PMID: 18004766
DOI: 10.1002/ajmg.b.30641

Genes

SLITRK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.PMID 18004766Read ↗

Association of SLITRK1 to Gilles de la Tourette Syndrome.Semantic proximity Read ↗

A new gene for Tourette's syndrome: a window into causal mechanisms?Semantic proximity Read ↗

Analysis of SLITRK1 in Japanese patients with Tourette syndrome using a next-generation sequencer.Semantic proximity Read ↗

Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.Semantic proximity Read ↗

The genetic basis of Gilles de la Tourette Syndrome.Semantic proximity Read ↗

The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population.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 ↗

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.Semantic proximity Read ↗

Sequence variants in SLITRK1 are associated with Tourette's syndrome.Semantic proximity Read ↗

Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population.Semantic proximity Read ↗

Genetic association signal near NTN4 in Tourette syndrome.Semantic proximity Read ↗

A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene.Semantic proximity Read ↗

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