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Article

Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.

Molecular autism - 1 Jan 2016

Yin Chia-Lin, Chen Hsin-I, Li Ling-Hui, Chien Yi-Ling, Liao Hsiao-Mei, Chou Miao Chun, Chou Wen-Jiun, Tsai Wen-Che, Chiu Yen-Nan, Wu Yu-Yu, Lo Chen-Zen, Wu Jer-Yuarn, Chen Yuan-Tsong, Gau Susan Shur-Fen

Abstract excerpt

BACKGROUND: Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder with complex genetic underpinning in its etiology. Copy number variations (CNVs) as one of the genetic factors associated with ASD have been addressed in recent genome-wide association studies (GWAS). However, the significance of CNV has not been well investigated in non-Caucasian ASD population. METHODS: To identify the...

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Identifiers

PMID: 27042285
DOI: 10.1186/s13229-016-0087-7
PMCID: PMC4818409

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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