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Article

An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.

Molecular psychiatry - 1 Nov 2019

Williams Sarah M, An Joon Yong, Edson Janette, Watts Michelle, Murigneux Valentine, Whitehouse Andrew J O, Jackson Colin J, Bellgrove Mark A, Cristino Alexandre S, Claudianos Charles

Abstract excerpt

A number of genetic studies have identified rare protein-coding DNA variations associated with autism spectrum disorder (ASD), a neurodevelopmental disorder with significant genetic etiology and heterogeneity. In contrast, the contributions of functional, regulatory genetic variations that occur in the extensive non-protein-coding regions of the genome remain poorly understood. Here we developed a genome-wide...

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Share to Autism Spectrum Disorder
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Intergenic

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Share to Promoter Regions, Genetic

Share to Regulatory Elements, Transcriptional

Source

Identifiers

PMID: 29703944
DOI: 10.1038/s41380-018-0049-x

Genes

CNTNAP2
NRXN1
NRXN2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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