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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F20%3A00078396" target="_blank" >RIV/00209805:_____/20:00078396 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.nature.com/articles/s41588-020-0610-9#article-info" target="_blank" >https://www.nature.com/articles/s41588-020-0610-9#article-info</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41588-020-0610-9" target="_blank" >10.1038/s41588-020-0610-9</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

  • Original language description

    Genome-wide association studies have discovered hundreds of loci associated with complex brain disorders, but it remains unclear in which cell types these loci are active. Here we integrate genome-wide association study results with single-cell transcriptomic data from the entire mouse nervous system to systematically identify cell types underlying brain complex traits. We show that psychiatric disorders are predominantly associated with projecting excitatory and inhibitory neurons. Neurological diseases were associated with different cell types, which is consistent with other lines of evidence. Notably, Parkinson&apos;s disease was genetically associated not only with cholinergic and monoaminergic neurons (which include dopaminergic neurons) but also with enteric neurons and oligodendrocytes. Using post-mortem brain transcriptomic data, we confirmed alterations in these cells, even at the earliest stages of disease progression. Our study provides an important framework for understanding the cellular basis of complex brain maladies, and reveals an unexpected role of oligodendrocytes in Parkinson&apos;s disease.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10603 - Genetics and heredity (medical genetics to be 3)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Nature genetics

  • ISSN

    1061-4036

  • e-ISSN

  • Volume of the periodical

    52

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    482-493

  • UT code for WoS article

    000529000400002

  • EID of the result in the Scopus database

    2-s2.0-85084195663