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Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

Ajore, Ram
Autor Ajore, Ram Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Niroula, Abhishek
Autor Niroula, Abhishek ORCID Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden Broad Institute of Massachusetts Institute of Technology and Harvard University, 415 Main Street, Boston, MA, 02142, USA
Pertesi, Maroulio
Autor Pertesi, Maroulio ORCID Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Cafaro, Caterina
Autor Cafaro, Caterina Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Thodberg, Malte
Autor Thodberg, Malte ORCID Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Went, Molly
Autor Went, Molly Division of Genetics and Epidemiology, The Institute of Cancer Research, 123 Old Brompton Road, London, SW7 3RP, United Kingdom
Bao, Erik L
Autor Bao, Erik L ORCID Broad Institute of Massachusetts Institute of Technology and Harvard University, 415 Main Street, Boston, MA, 02142, USA Division of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Duran-Lozano, Laura
Autor Duran-Lozano, Laura Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Lopez de Lapuente Portilla, Aitzkoa
Autor Lopez de Lapuente Portilla, Aitzkoa Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Olafsdottir, Thorunn
Autor Olafsdottir, Thorunn ORCID deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Ugidos-Damboriena, Nerea
Autor Ugidos-Damboriena, Nerea Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden
Magnusson, Olafur
Autor Magnusson, Olafur deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Samur, Mehmet
Autor Samur, Mehmet ORCID Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Lareau, Caleb A
Autor Lareau, Caleb A ORCID Broad Institute of Massachusetts Institute of Technology and Harvard University, 415 Main Street, Boston, MA, 02142, USA Division of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Halldorsson, Gisli H
Autor Halldorsson, Gisli H ORCID deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Thorleifsson, Gudmar
Autor Thorleifsson, Gudmar deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Norddahl, Gudmundur L
Autor Norddahl, Gudmundur L deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Gunnarsdottir, Kristbjorg
Autor Gunnarsdottir, Kristbjorg deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Försti, Asta
Autor Försti, Asta ORCID German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany Hopp Children's Cancer Center, Heidelberg, Germany
Goldschmidt, Hartmut
Autor Goldschmidt, Hartmut ORCID Department of Internal Medicine V, University Hospital of Heidelberg, 69120, Heidelberg, Germany
Hemminki, Kari
Autor Hemminki, Kari German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany Faculty of Medicine and Biomedical Center in Pilsen, Charles University in Prague, Prague, 30605, Czech Republic
van Rhee, Frits
Autor van Rhee, Frits Hopp Children's Cancer Center, Heidelberg, Germany
Kimber, Scott
Autor Kimber, Scott Division of Genetics and Epidemiology, The Institute of Cancer Research, 123 Old Brompton Road, London, SW7 3RP, United Kingdom
Sperling, Adam S
Autor Sperling, Adam S ORCID Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Kaiser, Martin
Autor Kaiser, Martin ORCID Division of Genetics and Epidemiology, The Institute of Cancer Research, 123 Old Brompton Road, London, SW7 3RP, United Kingdom
Anderson, Kenneth
Autor Anderson, Kenneth ORCID Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Jonsdottir, Ingileif
Autor Jonsdottir, Ingileif ORCID deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Munshi, Nikhil
Autor Munshi, Nikhil ORCID Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Rafnar, Thorunn
Autor Rafnar, Thorunn ORCID deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Waage, Anders
Autor Waage, Anders Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Box 8905, N-7491, Trondheim, Norway
Weinhold, Niels
Autor Weinhold, Niels German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120, Heidelberg, Germany Department of Internal Medicine V, University Hospital of Heidelberg, 69120, Heidelberg, Germany
Thorsteinsdottir, Unnur
Autor Thorsteinsdottir, Unnur deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Sankaran, Vijay G
Autor Sankaran, Vijay G ORCID Broad Institute of Massachusetts Institute of Technology and Harvard University, 415 Main Street, Boston, MA, 02142, USA Division of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA Harvard Stem Cell Institute, Cambridge, MA, USA
Stefansson, Kari
Autor Stefansson, Kari ORCID deCODE Genetics/Amgen Inc., Sturlugata 8, 101, Reykjavik, Iceland
Houlston, Richard
Autor Houlston, Richard ORCID Division of Genetics and Epidemiology, The Institute of Cancer Research, 123 Old Brompton Road, London, SW7 3RP, United Kingdom
Nilsson, Björn
Autor Nilsson, Björn ORCID Hematology and Transfusion Medicine, Department of Laboratory Medicine, BMC B13, 221 84, Lund, Sweden. bjorn.nilsson@med.lu.se Broad Institute of Massachusetts Institute of Technology and Harvard University, 415 Main Street, Boston, MA, 02142, USA. bjorn.nilsson@med.lu.se

Nature communications. 2022 Dec 13 ; 13 (1) : 7725. [epub] 20221213

Nat Commun
ISSN 2041-1723
Zdroj

Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu tisková chyba

Perzistentní odkaz https://www.medvik.cz/link/pmid36513657

Online Plný text

PubMed 36513657
PubMed Central PMC9747780
DOI 10.1038/s41467-022-35411-1
PII: 10.1038/s41467-022-35411-1
Knihovny.cz E-zdroje

Publikační typ
tisková chyba MeSH

Broad Institute of Massachusetts Institute of Technology and Harvard University 415 Main Street Boston MA 02142 USA

Dana Farber Cancer Institute Harvard Medical School Boston MA USA

Department of Cancer Research and Molecular Medicine Norwegian University of Science and Technology Box 8905 N 7491 Trondheim Norway

Department of Internal Medicine 5 University Hospital of Heidelberg 69120 Heidelberg Germany

Division of Genetics and Epidemiology The Institute of Cancer Research 123 Old Brompton Road London SW7 3RP United Kingdom

Division of Hematology Oncology Boston Children's Hospital Harvard Medical School Boston MA USA

eCODE Genetics Amgen Inc Sturlugata 8 101 Reykjavik Iceland

Faculty of Medicine and Biomedical Center in Pilsen Charles University Prague Prague 30605 Czech Republic

German Cancer Research Center Im Neuenheimer Feld 580 D 69120 Heidelberg Germany

Harvard Stem Cell Institute Cambridge MA USA

Hematology and Transfusion Medicine Department of Laboratory Medicine BMC B13 221 84 Lund Sweden

Hopp Children's Cancer Center Heidelberg Germany

Erratum pro

Nat Commun. 2022 Jan 10;13(1):151. doi: 10.1038/s41467-021-27666-x. PubMed

Citace poskytuje Crossref.org

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Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

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