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Article

Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.

Journal of human genetics - 1 Mar 2016

Hashimoto Ryota, Nakazawa Takanobu, Tsurusaki Yoshinori, Yasuda Yuka, Nagayasu Kazuki, Matsumura Kensuke, Kawashima Hitoshi, Yamamori Hidenaga, Fujimoto Michiko, Ohi Kazutaka, Umeda-Yano Satomi, Fukunaga Masaki, Fujino Haruo, Kasai Atsushi, Hayata-Takano Atsuko, Shintani Norihito, Takeda Masatoshi, Matsumoto Naomichi, Hashimoto Hitoshi

Abstract excerpt

Autism spectrum disorder (ASD) is a complex group of clinically heterogeneous neurodevelopmental disorders with unclear etiology and pathogenesis. Genetic studies have identified numerous candidate genetic variants, including de novo mutated ASD-associated genes; however, the function of these de novo mutated genes remains unclear despite extensive bioinformatics resources. Accordingly, it is not easy to assign...

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Identifiers

PMID: 26582266
DOI: 10.1038/jhg.2015.141
PMCID: PMC4819764

Genes

HERC1
PLEKHA4
PRKD2

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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