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Article

Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Mar 2014

Wang Zhenling, Hong Yuan, Zou Li, Zhong Rong, Zhu Beibei, Shen Na, Chen Wei, Lou Jiao, Ke Juntao, Zhang Ti, Wang Weipeng, Miao Xiaoping

Abstract excerpt

Autism spectrum disorder (ASD) is a severe neurological disorder with a high degree of heritability. Reelin gene (RELN), which plays a crucial role in the migration and positioning of neurons during brain development, has been strongly posed as a candidate gene for ASD. Genetic variants in RELN have been investigated as risk factors of ASD in numerous epidemiologic studies but with inconclusive results. To...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24453138
DOI: 10.1002/ajmg.b.32222

Genes

RELN

Provenance

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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