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Article

High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.

Neuroscience - 17 Dec 2016

AlAyadhi Laila Y, Hashmi Jamil A, Iqbal Muhammad, Albalawi Alia M, Samman Mohammad I, Elamin Nadra E, Bashir Shahid, Basit Sulman

Abstract excerpt

Single nucleotide polymorphisms (SNPs)-based genotyping using microarray platform is now frequently used to detect copy number variants (CNVs) in the human genome. Here, we report CNVs identified using Illumina Human Omni 2.5M oligonucleotide microarrays in 11 multiplex families with autism spectrum disorder (ASD) referred to Autism Research and Treatment Center (ART) and Madinah Maternity and Children Hospital...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27771533
DOI: 10.1016/j.neuroscience.2016.10.030

Genes

CLSTN2

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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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