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Article

Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia.

Psychiatric genetics - 1 Aug 2012

Lee Yohan, Mattai Anand, Long Robert, Rapoport Judith L, Gogtay Nitin, Addington Anjené M

Abstract excerpt

Childhood-onset schizophrenia (COS) is a rare severe form of schizophrenia that may have greater salient genetic risk. Despite evidence for high heritability, conclusive genetic causes of schizophrenia remain elusive. Recent genomic technologies in concert with large case-control cohorts have led to several associations of highly penetrant rare copy number variants (CNVs) and schizophrenia. We previously reported...

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Identifiers

PMID: 22547139
DOI: 10.1097/YPG.0b013e328353ae3d
PMCID: PMC3384746

Genes

PXDN

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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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