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Article

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

PloS one - 1 Jan 2013

Tropeano Maria, Ahn Joo Wook, Dobson Richard J B, Breen Gerome, Rucker James, Dixit Abhishek, Pal Deb K, McGuffin Peter, Farmer Anne, White Peter S, Andrieux Joris, Vassos Evangelos, Ogilvie Caroline Mackie, Curran Sarah, Collier David A

Abstract excerpt

Copy number variants (CNVs) at chromosome 16p13.11 have been associated with a range of neurodevelopmental disorders including autism, ADHD, intellectual disability and schizophrenia. Significant sex differences in prevalence, course and severity have been described for a number of these conditions but the biological and environmental factors underlying such sex-specific features remain unclear. We tested the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Chromosomes, Human, Pair 16

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Source

Open in PubMed Open full text

Identifiers

PMID: 23637818
DOI: 10.1371/journal.pone.0061365
PMCID: PMC3630198

Genes

ABCC1
ABCC6
MYH11
NDE1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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