Niels Weinhold1, Tobias Meissner2, David C Johnson3, Anja Seckinger1, Jérôme Moreaux4, Asta Försti5, Bowang Chen6, Jolanta Nickel1, Daniel Chubb7, Andrew C Rawstron8, Chi Doughty8, Nasrin B Dahir3, Dil B Begum3, Kwee Young9, Brian A Walker3, Per Hoffmann10, Marcus M Nöthen11, Faith E Davies3, Bernard Klein4, Hartmut Goldschmidt12, Gareth J Morgan3, Richard S Houlston7, Dirk Hose13, Kari Hemminki5. 1. Department of Internal Medicine V, University of Heidelberg, Germany. 2. Department of Internal Medicine V, University of Heidelberg, Germany Department of Molecular & Experimental Medicine, The Scripps Research Institute, La Jolla, CA, USA. 3. Centre for Myeloma Research, Division of Molecular Pathology, Institute of Cancer Research, Sutton, Surrey, SM2 5NG, UK. 4. INSERM, Unité 1040, Institut de Recherche en Biothérapie, Centre Hospitalier Universitaire de Montpellier, Hôpital Saint Eloi, Avenue Augustin Fliche, 34295 Montpellier, France. 5. German Cancer Research Center, Heidelberg, Germany Center for Primary Health Care Research, Lund University, Malmo, Sweden. 6. German Cancer Research Center, Heidelberg, Germany. 7. Molecular and Population Genetics, Division of Genetics and Epidemiology, Institute of Cancer Research, Sutton, Surrey, UK. 8. Haematological Malignancy Diagnostic Service Laboratory, St James University Hospital, Leeds, UK. 9. Department of Haematology, University College London Hospital, UK. 10. Institute of Human Genetics, University of Bonn, Germany Division of Medical Genetics, Department of Biomedicine, University of Basel, Switzerland. 11. Institute of Human Genetics, University of Bonn, Germany Department of Genomics, Life & Brain Center, University of Bonn, Germany. 12. Department of Internal Medicine V, University of Heidelberg, Germany National Centre for Tumor Diseases, Heidelberg, Germany. 13. Department of Internal Medicine V, University of Heidelberg, Germany National Centre for Tumor Diseases, Heidelberg, Germany dirk.hose@med.uni-heidelberg.de.
Abstract
Entities:
Keywords:
eQTL; multiple myeloma; risk; single nucleotide polymorphism
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