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SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder.
Merker, Sören; Reif, Andreas; Ziegler, Georg C; Weber, Heike; Mayer, Ute; Ehlis, Ann-Christine; Conzelmann, Annette; Johansson, Stefan; Müller-Reible, Clemens; Nanda, Indrajit; Haaf, Thomas; Ullmann, Reinhard; Romanos, Marcel; Fallgatter, Andreas J; Pauli, Paul; Strekalova, Tatyana; Jansch, Charline; Vasquez, Alejandro Arias; Haavik, Jan; Ribasés, Marta; Ramos-Quiroga, Josep Antoni; Buitelaar, Jan K; Franke, Barbara; Lesch, Klaus-Peter.
Afiliação
  • Merker S; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Reif A; Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt, Frankfurt, Germany.
  • Ziegler GC; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Weber H; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Mayer U; Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt, Frankfurt, Germany.
  • Ehlis AC; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Conzelmann A; Department of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany.
  • Johansson S; Department of Psychology I, University of Würzburg, Würzburg, Germany.
  • Müller-Reible C; Department of Child and Adolescent Psychiatry, University of Tübingen, Tübingen, Germany.
  • Nanda I; K.G. Jebsen Centre for Neuropsychiatric Disorders, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Haaf T; Department of Human Genetics, Biozentrum, University of Würzburg, Würzburg, Germany.
  • Ullmann R; Department of Human Genetics, Biozentrum, University of Würzburg, Würzburg, Germany.
  • Romanos M; Department of Human Genetics, Biozentrum, University of Würzburg, Würzburg, Germany.
  • Fallgatter AJ; Max-Planck Institute for Molecular Genetics, Berlin, Germany.
  • Pauli P; Bundeswehr Institute of Radiobiology, University of Ulm, Ulm, Germany.
  • Strekalova T; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Würzburg, Würzburg, Germany.
  • Jansch C; Department of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany.
  • Vasquez AA; Department of Psychology I, University of Würzburg, Würzburg, Germany.
  • Haavik J; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Ribasés M; Laboratory of Psychiatric Neurobiology, Institute of Molecular Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
  • Ramos-Quiroga JA; Department of Translational Neuroscience, School of Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.
  • Buitelaar JK; Division of Molecular Psychiatry, ADHD Clinical Research Unit, Laboratory of Translational Neuroscience, Center of Mental Health, University of Würzburg, Würzburg, Germany.
  • Franke B; Departments of Human Genetics and Psychiatry, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Lesch KP; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
J Child Psychol Psychiatry ; 58(7): 798-809, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28224622
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Encéfalo / Transportador de Glucose Tipo 3 / Função Executiva Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Adult / Child / Humans País/Região como assunto: Europa Idioma: En Revista: J Child Psychol Psychiatry Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Encéfalo / Transportador de Glucose Tipo 3 / Função Executiva Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Adult / Child / Humans País/Região como assunto: Europa Idioma: En Revista: J Child Psychol Psychiatry Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha