Article

Converging pathways found in copy number variation syndromes with high schizophrenia risk

2022-02-10

Abstract excerpt

Schizophrenia genetics is complex, and the contribution of common and rare variants are not fully understood. Several specific copy number variations (CNVs) confer increased risk for schizophrenia, and the study of their effects is central to molecular models of mental illness. However, these CNVs – microdeletions or -duplications – are spread across the genome and differ in the number of genes affected and classe...

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Literature Corpus work: ca82018d-28b6-54c5-95a4-664554fdedf6
DOI: 10.1101/2022.02.07.479370

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