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

The BTBD9 gene polymorphisms in Polish patients with Gilles de la Tourette syndrome.

Acta neurobiologiae experimentalis - 1 Jan 2014

Janik Piotr, Berdyński Mariusz, Safranow Krzysztof, Zekanowski Cezary

Abstract excerpt

Gilles de la Tourette syndrome (GTS) is a neurodevelopmental disorder characterized by motor and vocal tics. The etiology of the disorder is unknown, although the predominant role of genetic factors has been established. Variants of the BTBD9 gene (rs4714156, rs9296249 and rs9357271) have been reported to be associated with GTS in French Canadian and Chinese Han populations. Therefore, we decided to test the...

Read the complete abstract on PubMed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Topics

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

Share to Attention Deficit Disorder with Hyperactivity
Share to Child, Preschool
Share to Cohort Studies
Share to Nerve Tissue Proteins
Share to Poland
Share to Tourette Syndrome
Share to Transcription Factors
Share to Young Adult

Source

Identifiers

PMID: 24993631
DOI: 10.55782/ane-2014-1987

Genes

BTBD9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The BTBD9 gene polymorphisms in Polish patients with Gilles de la Tourette syndrome.PMID 24993631Read ↗

Association of intronic variants of the BTBD9 gene with Tourette syndrome.Semantic proximity Read ↗

Association of ADORA1 rs2228079 and ADORA2A rs5751876 Polymorphisms with Gilles de la Tourette Syndrome in the Polish Population.Semantic proximity Read ↗

Genetics of Tourette Syndrome.Semantic proximity Read ↗

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

Oligogenic risk model for Gilles de la Tourette syndrome reveals a genetic continuum of tic disordersSemantic proximity Read ↗

Biallelic ZBTB11 variants associated with complex neuropsychiatric phenotype featuring Tourette syndrome.Semantic proximity Read ↗

Tourette Syndrome and Chronic Tic Disorders.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 ↗

Whole-exome sequencing identifies high-confidence genes for tic disorders in a Chinese Han population.Semantic proximity Read ↗

The Gilles de la Tourette syndrome: the current status.Semantic proximity Read ↗

A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population.Semantic proximity Read ↗

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