| Literature DB >> 24529980 |
Angela Heck1, Matthias Fastenrath2, Sandra Ackermann3, Bianca Auschra3, Horst Bickel4, David Coynel2, Leo Gschwind2, Frank Jessen5, Hanna Kaduszkiewicz6, Wolfgang Maier5, Annette Milnik7, Michael Pentzek8, Steffi G Riedel-Heller9, Stephan Ripke10, Klara Spalek11, Patrick Sullivan12, Christian Vogler7, Michael Wagner5, Siegfried Weyerer13, Steffen Wolfsgruber5, Dominique J-F de Quervain14, Andreas Papassotiropoulos15.
Abstract
Working memory, the capacity of actively maintaining task-relevant information during a cognitive task, is a heritable trait. Working memory deficits are characteristic for many psychiatric disorders. We performed genome-wide gene set enrichment analyses in multiple independent data sets of young and aged cognitively healthy subjects (n = 2,824) and in a large schizophrenia case-control sample (n = 32,143). The voltage-gated cation channel activity gene set, consisting of genes related to neuronal excitability, was robustly linked to performance in working memory-related tasks across ages and to schizophrenia. Functional brain imaging in 707 healthy participants linked this gene set also to working memory-related activity in the parietal cortex and the cerebellum. Gene set analyses may help to dissect the molecular underpinnings of cognitive dimensions, brain activity, and psychopathology.Entities:
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Year: 2014 PMID: 24529980 PMCID: PMC4205276 DOI: 10.1016/j.neuron.2014.01.010
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173