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Article

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.

Lancet (London, England) - 23 Oct 2010

Williams Nigel M, Zaharieva Irina, Martin Andrew, Langley Kate, Mantripragada Kiran, Fossdal Ragnheidur, Stefansson Hreinn, Stefansson Kari, Magnusson Pall, Gudmundsson Olafur O, Gustafsson Omar, Holmans Peter, Owen Michael J, O'Donovan Michael, Thapar Anita

Abstract excerpt

BACKGROUND: Large, rare chromosomal deletions and duplications known as copy number variants (CNVs) have been implicated in neurodevelopmental disorders similar to attention-deficit hyperactivity disorder (ADHD). We aimed to establish whether burden of CNVs was increased in ADHD, and to investigate whether identified CNVs were enriched for loci previously identified in autism and schizophrenia. METHODS: We...

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Identifiers

PMID: 20888040
DOI: 10.1016/S0140-6736(10)61109-9
PMCID: PMC2965350

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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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