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Modifiable pathways for colorectal cancer: a mendelian randomisation analysis.
Cornish, Alex J; Law, Philip J; Timofeeva, Maria; Palin, Kimmo; Farrington, Susan M; Palles, Claire; Jenkins, Mark A; Casey, Graham; Brenner, Hermann; Chang-Claude, Jenny; Hoffmeister, Michael; Kirac, Iva; Maughan, Tim; Brezina, Stefanie; Gsur, Andrea; Cheadle, Jeremy P; Aaltonen, Lauri A; Tomlinson, Ian; Dunlop, Malcolm G; Houlston, Richard S.
Afiliação
  • Cornish AJ; Division of Genetics and Epidemiology, Institute of Cancer Research, London, UK. Electronic address: alex.cornish@icr.ac.uk.
  • Law PJ; Division of Genetics and Epidemiology, Institute of Cancer Research, London, UK.
  • Timofeeva M; Cancer Research UK Edinburgh Centre and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Palin K; Medicum and Genome-Scale Biology Research Program, Research Programs Unit, Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Farrington SM; Cancer Research UK Edinburgh Centre and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Palles C; Gastrointestinal Cancer Genetics Laboratory, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Jenkins MA; Centre for Epidemiology and Biostatistics, University of Melbourne, Melbourne, VIC, Australia.
  • Casey G; Center for Public Health Genomics, University of Virginia, Virginia, VA, USA.
  • Brenner H; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany; German Cancer Consortium, German Cancer Research Center, Heidelberg, Germany; Division of Preventive Oncology, German Cancer Research Center, Heidelberg, Germany; Division of Preventive Oncology
  • Chang-Claude J; Unit of Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany; Cancer Epidemiology Group, University Medical Center Hamburg-Eppendorf, University Cancer Center Hamburg, Hamburg, Germany.
  • Hoffmeister M; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany.
  • Kirac I; Department of Surgical Oncology, University Hospital for Tumours, Sestre milosrdnice University Hospital Centre, Zagreb, Croatia.
  • Maughan T; Department of Oncology, University of Oxford, Oxford, UK.
  • Brezina S; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
  • Gsur A; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
  • Cheadle JP; Institute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Aaltonen LA; Medicum and Genome-Scale Biology Research Program, Research Programs Unit, Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Tomlinson I; Edinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Dunlop MG; Cancer Research UK Edinburgh Centre and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Houlston RS; Division of Genetics and Epidemiology, Institute of Cancer Research, London, UK.
Lancet Gastroenterol Hepatol ; 5(1): 55-62, 2020 01.
Article em En | MEDLINE | ID: mdl-31668584
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: DNA de Neoplasias / Neoplasias Colorretais / Biomarcadores Tumorais / Medição de Risco / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Análise da Randomização Mendeliana Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Lancet Gastroenterol Hepatol Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: DNA de Neoplasias / Neoplasias Colorretais / Biomarcadores Tumorais / Medição de Risco / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Análise da Randomização Mendeliana Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Lancet Gastroenterol Hepatol Ano de publicação: 2020 Tipo de documento: Article