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Article

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Molecular psychiatry - 1 Nov 2015

Merikangas A K, Segurado R, Heron E A, Anney R J L, Paterson A D, Cook E H, Pinto D, Scherer S W, Szatmari P, Gill M, Corvin A P, Gallagher L

Abstract excerpt

Significant evidence exists for the association between copy number variants (CNVs) and Autism Spectrum Disorder (ASD); however, most of this work has focused solely on the diagnosis of ASD. There is limited understanding of the impact of CNVs on the 'sub-phenotypes' of ASD. The objective of this paper is to evaluate associations between CNVs in differentially brain expressed (DBE) genes or genes previously...

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Identifiers

PMID: 25421404
DOI: 10.1038/mp.2014.150
PMCID: PMC4759095

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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.

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