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Article

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.

Human molecular genetics - 15 Nov 2013

Costain Gregory, Lionel Anath C, Merico Daniele, Forsythe Pamela, Russell Kathryn, Lowther Chelsea, Yuen Tracy, Husted Janice, Stavropoulos Dimitri J, Speevak Marsha, Chow Eva W C, Marshall Christian R, Scherer Stephen W, Bassett Anne S

Abstract excerpt

Individually rare, large copy number variants (CNVs) contribute to genetic vulnerability for schizophrenia. Unresolved questions remain, however, regarding the anticipated yield of clinical microarray testing in schizophrenia. Using high-resolution genome-wide microarrays and rigorous methods, we investigated rare CNVs in a prospectively recruited community-based cohort of 459 unrelated adults with schizophrenia...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23813976
DOI: 10.1093/hmg/ddt297
PMCID: PMC3889806

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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.

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