The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.

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Published in Nat Genet on March 17, 2013

Authors

Niels Weinhold1, David C Johnson2, Daniel Chubb3, Bowang Chen4, Asta Försti4,5, Fay J Hosking3, Peter Broderick3, Yussanne P Ma3, Sara E Dobbins3, Dirk Hose1,6, Brian A Walker2, Faith E Davies2, Martin F Kaiser2, Ni L Li2, Walter A Gregory7, Graham H Jackson8, Mathias Witzens-Harig1, Kai Neben1, Per Hoffmann9, Markus M Nöthen9,10, Thomas W Mühleisen9, Lewin Eisele11, Fiona M Ross12, Anna Jauch13, Hartmut Goldschmidt1,6, Richard S Houlston3, Gareth J Morgan2, Kari Hemminki4,5

Author Affiliations

1: Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
2: Haemato-Oncology Research Unit, Division of Molecular Pathology, Institute of Cancer Research, Surrey, UK.
3: Division of Genetics and Epidemiology, Institute of Cancer Research, Surrey, UK.
4: German Cancer Research Center, Heidelberg, Germany.
5: Center for Primary Health Care Research, Lund University, Malmo, Sweden.
6: National Centre for Tumour Diseases, Heidelberg, Germany.
7: University of Leeds, Leeds, UK.
8: Royal Victoria Infirmary, Newcastle-on-Tyne, UK.
9: Institute of Human Genetics, University of Bonn, Germany.
10: German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
11: Institute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
12: Cytogenetics Group, Wessex Regional Cytogenetic Laboratory, Salisbury, UK.
13: Institute of Human Genetics, University of Heidelberg, Germany.

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