Article

Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes

2020-06-24

Abstract excerpt

<h4>ABSTRACT</h4> Deletions and duplications of the multigenic 16p11.2 and 22q11.2 copy number variants (CNVs) are associated with brain-related disorders including schizophrenia, intellectual disability, obesity, bipolar disorder, and autism spectrum disorder (ASD). The contribution of individual CNV genes to each of these phenotypes is unknown, as is the contribution of CNV genes to subtler health impacts. Hypo...

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Literature Corpus work: 4783845b-7231-5415-968a-b40318b3c9c3
DOI: 10.1101/2020.06.23.166181

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