Saltar al contenido principal

ETHNOS_APP

Inicio • Búsqueda • Revistas • Lista 0

Ditte Demontis

Datos Biográficos

ID10712349
NOMBREDitte Demontis
NOMBRESDitte
APELLIDODemontis
FIRMADEMONTIS D
AFILIACIONESAarhus University
ORCID0000-0001-9124-2766
VERIFICADONo
TOTAL DE OBRAS3
TOTAL DE CITAS0
TOTAL COMO AUTOR3
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2019
AÑO MÁS RECIENTE DE PUBLICACIÓN2022
ÍNDICE H0
  • Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Open Access•Vassily Trubetskoy, Antonio F Pardiñas et al.•ARTICLE•Nature•2022

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Open Access•Ditte Demontis, 23andMe Research Team et al.•ARTICLE•Nature Genetics•2019

    Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute substantially to ADHD susceptibility, but no variants have been robustly associated with ADHD. We report a genome-wide association meta-analysis of 20,183 individuals diagnosed with ADHD and 35,191 controls that identifies variants surpassing genome-wide significance in…

  • Identification of common genetic risk variants for autism spectrum disorder

    Open Access•John Grove, BUPGEN BUPGEN et al.•ARTICLE•Nature Genetics•2019

Sin obras prominentes en esta página.

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Open Access•Ditte Demontis, 23andMe Research Team et al.•ARTICLE•Nature Genetics•2019

    Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute substantially to ADHD susceptibility, but no variants have been robustly associated with ADHD. We report a genome-wide association meta-analysis of 20,183 individuals diagnosed with ADHD and 35,191 controls that identifies variants surpassing genome-wide significance in…

  • Identification of common genetic risk variants for autism spectrum disorder

    Open Access•John Grove, BUPGEN BUPGEN et al.•ARTICLE•Nature Genetics•2019

  • Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Open Access•Vassily Trubetskoy, Antonio F Pardiñas et al.•ARTICLE•Nature•2022

Biology (3 obras) · Gene (3 obras) · Genetic Associations and Epidemiology (3 obras) · Genetics (3 obras) · Computational biology (2 obras) · Genome (2 obras) · Genome-wide association study (2 obras) · Genomic variations and chromosomal abnormalities (2 obras) · Genotype (2 obras) · Psychology (2 obras)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae