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Article

New copy number variations in schizophrenia.

PloS one - 13 Oct 2010

Magri Chiara, Sacchetti Emilio, Traversa Michele, Valsecchi Paolo, Gardella Rita, Bonvicini Cristian, Minelli Alessandra, Gennarelli Massimo, Barlati Sergio

Abstract excerpt

Genome-wide screenings for copy number variations (CNVs) in patients with schizophrenia have demonstrated the presence of several CNVs that increase the risk of developing the disease and a growing number of large rare CNVs; the contribution of these rare CNVs to schizophrenia remains unknown. Using Affymetrix 6.0 arrays, we undertook a systematic search for CNVs in 172 patients with schizophrenia and 160 healthy...

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Identifiers

PMID: 20967226
DOI: 10.1371/journal.pone.0013422
PMCID: PMC2954184

Genes

NRXN1

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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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