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Article

Schizophrenia copy number variants and associative learning.

Molecular psychiatry - 1 Feb 2017

Clifton N E, Pocklington A J, Scholz B, Rees E, Walters J T R, Kirov G, O'Donovan M C, Owen M J, Wilkinson L S, Thomas K L, Hall J

Abstract excerpt

Large-scale genomic studies have made major progress in identifying genetic risk variants for schizophrenia. A key finding from these studies is that there is an increased burden of genomic copy number variants (CNVs) in schizophrenia cases compared with controls. The mechanism through which these CNVs confer risk for the symptoms of schizophrenia, however, remains unclear. One possibility is that schizophrenia...

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Identifiers

PMID: 27956746
DOI: 10.1038/mp.2016.227
PMCID: PMC5285462

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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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