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Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Cai, Na; Revez, Joana A; Adams, Mark J; Andlauer, Till F M; Breen, Gerome; Byrne, Enda M; Clarke, Toni-Kim; Forstner, Andreas J; Grabe, Hans J; Hamilton, Steven P; Levinson, Douglas F; Lewis, Cathryn M; Lewis, Glyn; Martin, Nicholas G; Milaneschi, Yuri; Mors, Ole; Müller-Myhsok, Bertram; Penninx, Brenda W J H; Perlis, Roy H; Pistis, Giorgio; Potash, James B; Preisig, Martin; Shi, Jianxin; Smoller, Jordan W; Streit, Fabien; Tiemeier, Henning; Uher, Rudolf; Van der Auwera, Sandra; Viktorin, Alexander; Weissman, Myrna M; Kendler, Kenneth S; Flint, Jonathan.
Afiliação
  • Cai N; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. na.cai@helmholtz-muenchen.de.
  • Revez JA; European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, UK. na.cai@helmholtz-muenchen.de.
  • Adams MJ; Helmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany. na.cai@helmholtz-muenchen.de.
  • Andlauer TFM; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Breen G; Division of Psychiatry, University of Edinburgh, Edinburgh, UK.
  • Byrne EM; Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, Germany.
  • Clarke TK; Department of Neurology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
  • Forstner AJ; NIHR Maudsley Biomedical Research Centre, King's College London, London, UK.
  • Grabe HJ; Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
  • Hamilton SP; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Levinson DF; Division of Psychiatry, University of Edinburgh, Edinburgh, UK.
  • Lewis CM; Department of Biomedicine, University of Basel, Basel, Switzerland.
  • Lewis G; Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.
  • Martin NG; Centre for Human Genetics, University of Marburg, Marburg, Germany.
  • Milaneschi Y; Department of Psychiatry and Psychotherapy, University Medicine Greifswald, Greifswald, Germany.
  • Mors O; Department of Psychiatry, Kaiser Permanente Northern California, San Francisco, CA, USA.
  • Müller-Myhsok B; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, CA, USA.
  • Penninx BWJH; Social, Genetic and Developmental Psychiatry Centre, King's College London, London, UK.
  • Perlis RH; Department of Medical & Molecular Genetics, King's College London, London, UK.
  • Pistis G; Division of Psychiatry, University College London, London, UK.
  • Potash JB; Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Preisig M; Department of Psychiatry, Amsterdam UMC, Vrije Universiteit and GGZinGeest, Amsterdam, the Netherlands.
  • Shi J; Psychosis Research Unit, Aarhus University Hospital, Risskov, Denmark.
  • Smoller JW; iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Copenhagen, Denmark.
  • Streit F; Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, Germany.
  • Tiemeier H; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Uher R; Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
  • Van der Auwera S; Department of Psychiatry, Amsterdam UMC, Vrije Universiteit and GGZinGeest, Amsterdam, the Netherlands.
  • Viktorin A; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
  • Weissman MM; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
  • Kendler KS; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Flint J; Department of Psychiatry, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Nat Genet ; 52(4): 437-447, 2020 04.
Article em En | MEDLINE | ID: mdl-32231276
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Transtorno Depressivo Maior Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Transtorno Depressivo Maior Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article