Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

Autism spectrum disorders (ASD) are highly heritable and are characterized by deficits in social communication and restricted and repetitive behaviors. Twin studies on phenotypic subdomains suggest a differing underlying genetic etiology. Studying genetic variation explaining phenotypic variance wil...

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Publicado no:Transl Psychiatry
Main Authors: Yousaf, Afsheen, Waltes, Regina, Haslinger, Denise, Klauck, Sabine M., Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M., Chiocchetti, Andreas G.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7335742/
https://ncbi.nlm.nih.gov/pubmed/32624584
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-020-00906-2
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