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

Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.

Genes - 5 Oct 2022

Mahjani Behrang, Birnbaum Rebecca, Buxbaum Grice Ariela, Cappi Carolina, Jung Seulgi, Avila Marina Natividad, Reichenberg Abraham, Sandin Sven, Hultman Christina M, Buxbaum Joseph D, Grice Dorothy E

Abstract excerpt

BACKGROUND: Recent studies report an important-and previously underestimated-role of rare variation in risk of obsessive-compulsive disorder (OCD) and chronic tic disorders (CTD). Using data from a large epidemiological study, we evaluate the distribution of potentially damaging copy number variation (pdCNV) in OCD and CTD, examining associations between pdCNV and the phenotypes of probands, including a...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Obsessive-Compulsive Disorder

Share to Phenotype

Share to Tourette Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 36292681
DOI: 10.3390/genes13101796
PMCID: PMC9601402

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

Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.PMID 36292681Read ↗

De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.Semantic proximity Read ↗

Characterizing Rare DNA Copy-Number Variants in Pediatric Obsessive-Compulsive Disorder.Semantic proximity Read ↗

A burden of rare copy number variants in obsessive-compulsive disorder.Semantic proximity Read ↗

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.Semantic proximity Read ↗

Rare coding variation in OCD implicates shared genes with other psychiatric disordersSemantic proximity Read ↗

A Burden of Rare Copy Number Variants in Obsessive-Compulsive DisorderSemantic proximity Read ↗

De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autismSemantic proximity Read ↗

Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants.Semantic proximity Read ↗

Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorderSemantic proximity Read ↗

Genome-wide association study identifies new loci associated with OCDSemantic proximity Read ↗

The OCD collaborative genetics study: methods and sample description.Semantic proximity Read ↗

Genetics of obsessive-compulsive disorder.Semantic proximity Read ↗

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