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Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
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.
Afiliación
  • Yousaf A; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany. afsheen.yousaf@kgu.de.
  • Waltes R; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
  • Haslinger D; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
  • Klauck SM; Division of Molecular Genome Analysis and Division of Cancer Genome Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Duketis E; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
  • Sachse M; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
  • Voran A; Department of Child and Adolescent Psychiatry, Saarland University, Homburg, Germany.
  • Biscaldi M; Department of Child and Adolescent Psychiatry, University Hospital Freiburg, Freiburg, Germany.
  • Schulte-Rüther M; Translational Brain Medicine, Department of Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, RWTH Aachen University, Aachen, Germany.
  • Cichon S; JARA-BRAIN, Aachen, Germany.
  • Nöthen M; Institute of Neuroscience and Medicine (INM-1), Research Center Juelich, Juelich, Germany.
  • Ackermann J; Human Genomics Research Group and Division of Medical Genetics, Department of Biomedicine, University of Basel, Basel, Switzerland.
  • Koch I; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Freitag CM; Department of Genomics, University of Bonn, Bonn, Germany.
  • Chiocchetti AG; Department of Genomics, University of Bonn, Bonn, Germany.
Transl Psychiatry ; 10(1): 215, 2020 07 05.
Article en En | MEDLINE | ID: mdl-32624584
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Transl Psychiatry Año: 2020 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Transl Psychiatry Año: 2020 Tipo del documento: Article País de afiliación: Alemania