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Article

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

The American journal of psychiatry - 1 Feb 2012

Stergiakouli Evangelia, Hamshere Marian, Holmans Peter, Langley Kate, Zaharieva Irina, Hawi Ziarah, Kent Lindsey, Gill Michael, Williams Nigel, Owen Michael J, O'Donovan Michael, Thapar Anita

Abstract excerpt

OBJECTIVE: A major motivation for seeking disease-associated genetic variation is to identify novel risk processes. Although rare copy number variants (CNVs) appear to contribute to attention deficit hyperactivity disorder (ADHD), common risk variants (single-nucleotide polymorphisms [SNPs]) have not yet been detected using genome-wide association studies (GWAS). This raises the concern as to whether future...

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Identifiers

PMID: 22420046
DOI: 10.1176/appi.ajp.2011.11040551
PMCID: PMC3601404

Genes

CHRNA7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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