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Article

Gene and miRNA expression profiles in autism spectrum disorders.

Brain research - 22 Mar 2011

Ghahramani Seno Mohammad M, Hu Pingzhao, Gwadry Fuad G, Pinto Dalila, Marshall Christian R, Casallo Guillermo, Scherer Stephen W

Abstract excerpt

Accumulating data indicate that there is significant genetic heterogeneity underlying the etiology in individuals diagnosed with autism spectrum disorder (ASD). Some rare and highly-penetrant gene variants and copy number variation (CNV) regions including NLGN3, NLGN4, NRXN1, SHANK2, SHANK3, PTCH...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20868653
DOI: 10.1016/j.brainres.2010.09.046

Genes

HEY1
NLGN3
NRXN1
PTCHD1
SOX9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20868653-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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