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Article

Association and mutation analyses of 16p11.2 autism candidate genes.

PloS one - 1 Jan 2009

Kumar Ravinesh A, Marshall Christian R, Badner Judith A, Babatz Timothy D, Mukamel Zohar, Aldinger Kimberly A, Sudi Jyotsna, Brune Camille W, Goh Gerald, Karamohamed Samer, Sutcliffe James S, Cook Edwin H, Geschwind Daniel H, Dobyns William B, Scherer Stephen W, Christian Susan L

Abstract excerpt

BACKGROUND: Autism is a complex childhood neurodevelopmental disorder with a strong genetic basis. Microdeletion or duplication of a approximately 500-700-kb genomic rearrangement on 16p11.2 that contains 24 genes represents the second most frequent chromosomal disorder associated with autism. Th...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19242545
DOI: 10.1371/journal.pone.0004582
PMCID: PMC2644762

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19242545-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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