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Article

Clinical evaluation of patients with a neuropsychiatric risk copy number variant.

Current opinion in genetics & development - 1 Jun 2021

Chawner Samuel Jra, Watson Cameron J, Owen Michael J

Abstract excerpt

Several copy number variants (CNVs) have been identified to confer high risk for a range of neuropsychiatric conditions. Because of advances in genetic testing within clinical settings, patients are increasingly receiving diagnoses of copy number variant genomic disorders. However, clinical guidelines surrounding assessment and management are limited. This review synthesises recent research and makes preliminary...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33461126
DOI: 10.1016/j.gde.2020.12.012
PMCID: PMC8219523

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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