Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

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Veröffentlicht in:	Leukemia 2020-04, Vol.34 (4), p.1187-1191
Hauptverfasser:	Chattopadhyay, Subhayan, Thomsen, Hauke, Weinhold, Niels, Meziane, Iman, Huhn, Stefanie, da Silva Filho, Miguel Inacio, Vodicka, Pavel, Vodickova, Ludmila, Hoffmann, Per, Nöthen, Markus M., Jöckel, Karl-Heinz, Schmidt, Börge, Landi, Stefano, Hajek, Roman, Hallmans, Göran, Pettersson-Kymmer, Ulrika, Ohlsson, Claes, Milani, Paolo, Merlini, Giampaolo, Rowcieno, Dorota, Hawkins, Philip, Hegenbart, Ute, Palladini, Giovanni, Wechalekar, Ashutosh, Schönland, Stefan O., Houlston, Richard, Goldschmidt, Hartmut, Hemminki, Kari, Försti, Asta
Format:	Artikel
Sprache:	eng
Schlagworte:	38 45 45/43 631/67/1990/804 631/67/68 692/308/174 692/499 Amyloidosis Benign monoclonal gammopathy Biomarkers, Tumor - genetics cancer genetics Cancer Research Care and treatment Cohort Studies Critical Care Medicine Development and progression Endocrinology and Diabetes Endokrinologi och diabetes epidemiology Etiology Genetic aspects Genetic Loci Genome-wide association studies Genome-Wide Association Study - methods Health aspects Hematology Humans Immunoglobulin Light-chain Amyloidosis - etiology Immunoglobulin Light-chain Amyloidosis - pathology Intensive Internal Medicine Letter Medicine Medicine & Public Health Methods Monoclonal gammopathy Monoclonal Gammopathy of Undetermined Significance - etiology Monoclonal Gammopathy of Undetermined Significance - pathology Multiple myeloma Multiple Myeloma - etiology Multiple Myeloma - pathology myeloma Oncology Polymorphism, Single Nucleotide Prognosis risk factors Single nucleotide polymorphisms
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ISSN:	0887-6924 1476-5551 1476-5551
DOI:	10.1038/s41375-019-0619-1