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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, PTCHD1, 1q21.1, maternally-inherited duplication of 15q11-q13, 16p11.2, amongst others, have been identified to be involved...

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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 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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