Correspondence: SEMA4A variation and risk of colorectal cancer.

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Title: Correspondence: SEMA4A variation and risk of colorectal cancer.
Authors: Kinnersley B; Division of Genetics and Epidemiology, The Institute of Cancer Research, Surrey, Sutton SM2 5NG, UK., Chubb D; Division of Genetics and Epidemiology, The Institute of Cancer Research, Surrey, Sutton SM2 5NG, UK., Dobbins SE; Division of Genetics and Epidemiology, The Institute of Cancer Research, Surrey, Sutton SM2 5NG, UK., Frampton M; Division of Genetics and Epidemiology, The Institute of Cancer Research, Surrey, Sutton SM2 5NG, UK., Buch S; Department of Medicine I, University Hospital Dresden, Dresden 23538, Germany., Timofeeva MN; Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh and Medical Research Council (MRC) Human Genetics Unit, Edinburgh EH4 2XU, UK., Castellví-Bel S; Department of Gastroenterology, Hospital Clínic, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Catalonia, Barcelona 8036, Spain., Farrington SM; Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh and Medical Research Council (MRC) Human Genetics Unit, Edinburgh EH4 2XU, UK., Forsti A; German Cancer Research Center, Heidelberg 69120, Germany., Hampe J; Department of Internal Medicine I, Hospital Schleswig-Holstein, Kiel 24105, Germany., Hemminki K; German Cancer Research Center, Heidelberg 69120, Germany., Hofstra RM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands.; University of Gronigen, University Medical Centre Gronigen, Department of Genetics, Gronigen 9700 RB, The Netherlands., Northwood E; Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds LS9 7TF, UK., Palles C; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK., Pinheiro M; Department of Genetics, Portugese Oncology Institute, Porto 4200-072, Portugal., Ruiz-Ponte C; Galician Public Foundation of Genomic Medicine, Centro de Investigación Biomédica en Red de Enfermedades Rares, Genomics Medicine Group, Hospital Clínico, Santiago de Compostela, University of Santiago de Compostela, Galicia 15782, Spain., Schafmayer C; Department of General and Thoracic Surgery, University Hospital Schleswig-Holstein, Kiel 24105, Germany., Teixeira MR; Department of Genetics, Portugese Oncology Institute, Porto 4200-072, Portugal., Westers H; University of Gronigen, University Medical Centre Gronigen, Department of Genetics, Gronigen 9700 RB, The Netherlands., van Wezel T; Leiden Department of Pathology, Leiden University Medical Center, Leiden, 2333 ZA, The Netherlands., Timothy Bishop D; Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds LS9 7TF, UK., Tomlinson I; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK., Dunlop MG; Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh and Medical Research Council (MRC) Human Genetics Unit, Edinburgh EH4 2XU, UK., Houlston RS; Division of Genetics and Epidemiology, The Institute of Cancer Research, Surrey, Sutton SM2 5NG, UK.
Source: Nature communications [Nat Commun] 2016 Mar 10; Vol. 7, pp. 10611. Date of Electronic Publication: 2016 Mar 10.
Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2041-1723
DOI:10.1038/ncomms10611