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Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F11%3A00002944" target="_blank" >RIV/00216208:11120/11:00002944 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023001:_____/11:00002739 RIV/00023752:_____/11:00001162

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.neulet.2011.02.024" target="_blank" >http://dx.doi.org/10.1016/j.neulet.2011.02.024</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.neulet.2011.02.024" target="_blank" >10.1016/j.neulet.2011.02.024</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients

  • Original language description

    FOXP2, the first gene known to be involved in the development of speech and language, can be considered to be, a priori, a candidate gene in schizophrenia, given the mounting evidence that the underlying core deficit in this disease could be a failure ofstructures relevant to normal language processing. To investigate the potential link between grey matter concentration (GMC) changes in patients with schizophrenia and the FOXP2 rs2396753 polymorphism previously reported to be associated with hallucinations in schizophrenia, we analysed high-resolution anatomical magnetic resonance images of 40 genotyped patients with schizophrenia and 36 healthy controls, using optimised voxel-based morphometry (VBM). Here we show that the common SNP rs2396753 (C > A)gene variant of the FOXP2 gene has significant effects on GMC in patients with schizophrenia, within regions of the brain known to be affected by this disease. Our data suggest that GMC reductions in schizophrenia may be driven by C alle

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FL - Psychiatry, sexology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/1M0517" target="_blank" >1M0517: Center of Neuropsychiatric Studies 2005-2009 (Neurobiology in Clinical Application)</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Neuroscience Letters

  • ISSN

    0304-3940

  • e-ISSN

  • Volume of the periodical

    493

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    IE - IRELAND

  • Number of pages

    5

  • Pages from-to

    131-135

  • UT code for WoS article

    000289582100016

  • EID of the result in the Scopus database