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Article

Brain function in carriers of a genome-wide supported bipolar disorder variant.

Archives of general psychiatry - 1 Aug 2010

Erk Susanne, Meyer-Lindenberg Andreas, Schnell Knut, Opitz von Boberfeld Carola, Esslinger Christine, Kirsch Peter, Grimm Oliver, Arnold Claudia, Haddad Leila, Witt Stephanie H, Cichon Sven, Nöthen Markus M, Rietschel Marcella, Walter Henrik

Abstract excerpt

CONTEXT: The neural abnormalities underlying genetic risk for bipolar disorder, a severe, common, and highly heritable psychiatric condition, are largely unknown. An opportunity to define these mechanisms is provided by the recent discovery, through genome-wide association, of a single-nucleotide...

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PMID: 20679588
DOI: 10.1001/archgenpsychiatry.2010.94

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20679588-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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