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Autor: Meziane, Iman

1 záznamů v Medvik Filtry

Článek

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

Chattopadhyay, Subhayan
Autor Chattopadhyay, Subhayan Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany. Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany
Thomsen, Hauke
Autor Thomsen, Hauke Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany
Weinhold, Niels
Autor Weinhold, Niels Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany
Meziane, Iman
Autor Meziane, Iman Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany
Huhn, Stefanie
Autor Huhn, Stefanie Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany
da Silva Filho, Miguel Inacio
Autor da Silva Filho, Miguel Inacio Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany
Vodicka, Pavel
Autor Vodicka, Pavel Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 142 00, Prague, Czech Republic. Institute of Biology and Medical Genetics, 1st Medical Faculty, Charles University, Albertov 4, 128 00, Prague, Czech Republic. Faculty of Medicine and Biomedical Center in Pilsen, Charles University in Prague, 30605, Pilsen, Czech Republic
Vodickova, Ludmila
Autor Vodickova, Ludmila Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, 142 00, Prague, Czech Republic. Institute of Biology and Medical Genetics, 1st Medical Faculty, Charles University, Albertov 4, 128 00, Prague, Czech Republic. Faculty of Medicine and Biomedical Center in Pilsen, Charles University in Prague, 30605, Pilsen, Czech Republic
Hoffmann, Per
Autor Hoffmann, Per Institute of Human Genetics, University of Bonn, Bonn, Germany. Department of Biomedicine, University of Basel, Basel, Switzerland
Nöthen, Markus M
Autor Nöthen, Markus M Institute of Human Genetics, University of Bonn, Bonn, Germany. Department of Genomics, Life & Brain Research Center, University of Bonn, Bonn, Germany

Leukemia. 2020 ; 34 (4) : 1187-1191. [pub] 20191106

ISSN 1476-5551
Medvik
Zdroj

MeSH
celogenomová asociační studie metody MeSH
genetické lokusy * MeSH
jednonukleotidový polymorfismus * MeSH
kohortové studie MeSH
lidé MeSH
mnohočetný myelom etiologie patologie MeSH
monoklonální gamapatie nejasného významu etiologie patologie MeSH
nádorové biomarkery genetika MeSH
primární amyloidóza etiologie patologie MeSH
prognóza MeSH
Check Tag
lidé MeSH
Publikační typ
dopisy MeSH
práce podpořená grantem MeSH