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Article

Exome array analysis suggests an increased variant burden in families with schizophrenia.

Schizophrenia research - 1 Jul 2017

McCarthy Nina S, Melton Phillip E, Ward Sarah V, Allan Spencer M, Dragovic Milan, Clark Melanie L, Morar Bharti, Rubio Justin P, Blangero John, Badcock Johanna C, Morgan Vera A, Moses Eric K, Jablensky Assen

Abstract excerpt

The exome array assays rare-but-recurrent, likely deleterious, exonic variants and represents an intermediary between single nucleotide polymorphism (SNP) arrays and sequencing for genetic association studies. Multiplex families with multiple affected individuals may be enriched for disease-associated variants of this class compared to unrelated populations. We present an exome array study of schizophrenia in 99...

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Identifiers

PMID: 27939555
DOI: 10.1016/j.schres.2016.12.007

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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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