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Roadmap for a precision-medicine initiative in the Nordic region.
Njølstad, Pål Rasmus; Andreassen, Ole Andreas; Brunak, Søren; Børglum, Anders D; Dillner, Joakim; Esko, Tõnu; Franks, Paul W; Freimer, Nelson; Groop, Leif; Heimer, Hakon; Hougaard, David M; Hovig, Eivind; Hveem, Kristian; Jalanko, Anu; Kaprio, Jaakko; Knudsen, Gun Peggy; Melbye, Mads; Metspalu, Andres; Mortensen, Preben Bo; Palmgren, Juni; Palotie, Aarno; Reed, Wenche; Stefánsson, Hreinn; Stitziel, Nathan O; Sullivan, Patrick F; Thorsteinsdóttir, Unnur; Vaudel, Marc; Vuorio, Eero; Werge, Thomas; Stoltenberg, Camilla; Stefánsson, Kári.
Afiliación
  • Njølstad PR; Center for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway. pal.njolstad@uib.no.
  • Andreassen OA; Department of Pediatrics, Haukeland University Hospital, Bergen, Norway. pal.njolstad@uib.no.
  • Brunak S; Medical and Population Genetics Program, Broad Institute of Harvard and MIT, Cambridge, MA, USA. pal.njolstad@uib.no.
  • Børglum AD; NORMENT Centre, Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.
  • Dillner J; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Esko T; Disease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Franks PW; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Freimer N; iSEQ, Centre for Integrative Sequencing, Aarhus University, Aarhus, Denmark.
  • Groop L; iPSYCH, Lundbeck Foundation Initiative for Integrative Psychiatric Research, Aarhus, Denmark.
  • Heimer H; Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Hougaard DM; Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.
  • Hovig E; The Estonian Genome Center, University of Tartu, Tartu, Estonia.
  • Hveem K; Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jalanko A; Genetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.
  • Kaprio J; Department of Public Health and Clinical Medicine, Section for Medicine, Umeå University, Umeå, Sweden.
  • Knudsen GP; Department of Nutrition, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
  • Melbye M; Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Metspalu A; Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA.
  • Mortensen PB; UCLA Center for Neurobehavioral Genetics, Los Angeles, CA, USA.
  • Palmgren J; Genetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.
  • Palotie A; FIMM Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
  • Reed W; School of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Stefánsson H; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Stitziel NO; iPSYCH-The Lundbeck Foundation Initiative for Psychiatric Research, Copenhagen, Denmark.
  • Sullivan PF; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
  • Thorsteinsdóttir U; Institute of Cancer Genetics and Informatics, Oslo University Hospital, Oslo, Norway.
  • Vaudel M; Department of Informatics, University of Oslo, Oslo, Norway.
  • Vuorio E; K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health, Norwegian University of Science and Technology, Trondheim, Norway.
  • Werge T; HUNT Research Center, Department of Public Health, Norwegian University of Science and Technology, Levanger, Norway.
  • Stoltenberg C; Department of Medicine, Levanger Hospital, Levanger, Norway.
  • Stefánsson K; Genomics and Biomarkers Unit, National Institute for Health and Welfare, Helsinki, Finland.
Nat Genet ; 51(6): 924-930, 2019 06.
Article en En | MEDLINE | ID: mdl-30988515
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_cobertura_universal Asunto principal: Medicina de Precisión Tipo de estudio: Sysrev_observational_studies Aspecto: Implementation_research Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Noruega
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_cobertura_universal Asunto principal: Medicina de Precisión Tipo de estudio: Sysrev_observational_studies Aspecto: Implementation_research Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Noruega