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Article

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.

BMC medical genetics - 21 Jun 2010

Delorme Richard, Moreno-De-Luca Daniel, Gennetier Aurélie, Maier Wolfgang, Chaste Pauline, Mössner Rainald, Grabe Hans Jörgen, Ruhrmann Stephan, Falkai Peter, Mouren Marie-Christine, Leboyer Marion, Wagner Michael, Betancur Catalina

Abstract excerpt

BACKGROUND: Obsessive-compulsive disorder (OCD) is a clinically and etiologically heterogeneous syndrome. The high frequency of obsessive-compulsive symptoms reported in subjects with the 22q11.2 deletion syndrome (DiGeorge/velocardiofacial syndrome) or Prader-Willi syndrome (15q11-13 deletion of the paternally derived chromosome), suggests that gene dosage effects in these chromosomal regions could increase risk...

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Identifiers

PMID: 20565924
DOI: 10.1186/1471-2350-11-100
PMCID: PMC2909937

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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