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Nordic OCD & Related Disorders Consortium: Rationale, design, and methods.
Mataix-Cols, David; Hansen, Bjarne; Mattheisen, Manuel; Karlsson, Elinor K; Addington, Anjené M; Boberg, Julia; Djurfeldt, Diana R; Halvorsen, Matthew; Lichtenstein, Paul; Solem, Stian; Lindblad-Toh, Kerstin; Haavik, Jan; Kvale, Gerd; Rück, Christian; Crowley, James J.
Afiliação
  • Mataix-Cols D; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Hansen B; Stockholm Health Care Services, Stockholm, Sweden.
  • Mattheisen M; Haukeland University Hospital, OCD-Team, Bergen, Norway.
  • Karlsson EK; Department of Clinical Psychology, University of Bergen, Bergen, Norway.
  • Addington AM; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
  • Boberg J; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Djurfeldt DR; Center for Integrative Sequencing, iSEQ, Department of Biomedicine, Aarhus University, Denmark.
  • Halvorsen M; Department of Psychiatry, Psychosomatics, and Psychotherapy, University of Würzburg, Germany.
  • Lichtenstein P; Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Solem S; Program in Bioinformatics & Integrative Biology and Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts.
  • Lindblad-Toh K; Genomics Research Branch, National Institute of Mental Health in Bethesda, Bethesda, Maryland.
  • Haavik J; Stockholm Health Care Services, Stockholm, Sweden.
  • Kvale G; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Rück C; Stockholm Health Care Services, Stockholm, Sweden.
  • Crowley JJ; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina.
Am J Med Genet B Neuropsychiatr Genet ; 183(1): 38-50, 2020 01.
Article em En | MEDLINE | ID: mdl-31424634
ABSTRACT
Obsessive-compulsive disorder (OCD) is a debilitating psychiatric disorder, yet its etiology is unknown and treatment outcomes could be improved if biological targets could be identified. Unfortunately, genetic findings for OCD are lagging behind other psychiatric disorders. Thus, there is a pressing need to understand the causal mechanisms implicated in OCD in order to improve clinical outcomes and to reduce morbidity and societal costs. Specifically, there is a need for a large-scale, etiologically informative genetic study integrating genetic and environmental factors that presumably interact to cause the condition. The Nordic countries provide fertile ground for such a study, given their detailed population registers, national healthcare systems and active specialist clinics for OCD. We thus formed the Nordic OCD and Related Disorders Consortium (NORDiC, www.crowleylab.org/nordic), and with the support of NIMH and the Swedish Research Council, have begun to collect a large, richly phenotyped and genotyped sample of OCD cases. Our specific aims are geared toward answering a number of key questions regarding the biology, etiology, and treatment of OCD. This article describes and discusses the rationale, design, and methodology of NORDiC, including details on clinical measures and planned genomic analyses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Obsessivo-Compulsivo Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Obsessivo-Compulsivo Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Ano de publicação: 2020 Tipo de documento: Article