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

Author

Listed:
  • Ram Ajore

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Abhishek Niroula

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine
    Broad Institute of Massachusetts Institute of Technology and Harvard University)

  • Maroulio Pertesi

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Caterina Cafaro

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Malte Thodberg

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Molly Went

    (Division of Genetics and Epidemiology, The Institute of Cancer Research)

  • Erik L. Bao

    (Broad Institute of Massachusetts Institute of Technology and Harvard University
    Division of Hematology/Oncology, Boston Children’s Hospital, Harvard Medical School
    Dana-Farber Cancer Institute, Harvard Medical School)

  • Laura Duran-Lozano

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Aitzkoa Lopez de Lapuente Portilla

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Thorunn Olafsdottir

    (deCODE Genetics/Amgen Inc.)

  • Nerea Ugidos-Damboriena

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine)

  • Olafur Magnusson

    (deCODE Genetics/Amgen Inc.)

  • Mehmet Samur

    (Dana-Farber Cancer Institute, Harvard Medical School)

  • Caleb A. Lareau

    (Broad Institute of Massachusetts Institute of Technology and Harvard University
    Division of Hematology/Oncology, Boston Children’s Hospital, Harvard Medical School
    Dana-Farber Cancer Institute, Harvard Medical School)

  • Gisli H. Halldorsson

    (deCODE Genetics/Amgen Inc.)

  • Gudmar Thorleifsson

    (deCODE Genetics/Amgen Inc.)

  • Gudmundur L. Norddahl

    (deCODE Genetics/Amgen Inc.)

  • Kristbjorg Gunnarsdottir

    (deCODE Genetics/Amgen Inc.)

  • Asta Försti

    (German Cancer Research Center (DKFZ)
    Hopp Children’s Cancer Center)

  • Hartmut Goldschmidt

    (University Hospital of Heidelberg)

  • Kari Hemminki

    (German Cancer Research Center (DKFZ)
    Charles University in Prague)

  • Frits van Rhee

    (Hopp Children’s Cancer Center)

  • Scott Kimber

    (Division of Genetics and Epidemiology, The Institute of Cancer Research)

  • Adam S. Sperling

    (Dana-Farber Cancer Institute, Harvard Medical School)

  • Martin Kaiser

    (Division of Genetics and Epidemiology, The Institute of Cancer Research)

  • Kenneth Anderson

    (Dana-Farber Cancer Institute, Harvard Medical School)

  • Ingileif Jonsdottir

    (deCODE Genetics/Amgen Inc.)

  • Nikhil Munshi

    (Dana-Farber Cancer Institute, Harvard Medical School)

  • Thorunn Rafnar

    (deCODE Genetics/Amgen Inc.)

  • Anders Waage

    (Norwegian University of Science and Technology)

  • Niels Weinhold

    (German Cancer Research Center (DKFZ)
    University Hospital of Heidelberg)

  • Unnur Thorsteinsdottir

    (deCODE Genetics/Amgen Inc.)

  • Vijay G. Sankaran

    (Broad Institute of Massachusetts Institute of Technology and Harvard University
    Division of Hematology/Oncology, Boston Children’s Hospital, Harvard Medical School
    Dana-Farber Cancer Institute, Harvard Medical School
    Harvard Stem Cell Institute)

  • Kari Stefansson

    (deCODE Genetics/Amgen Inc.)

  • Richard Houlston

    (Division of Genetics and Epidemiology, The Institute of Cancer Research)

  • Björn Nilsson

    (Hematology and Transfusion Medicine, Department of Laboratory Medicine
    Broad Institute of Massachusetts Institute of Technology and Harvard University)

Abstract

No abstract is available for this item.

Suggested Citation

  • Ram Ajore & Abhishek Niroula & Maroulio Pertesi & Caterina Cafaro & Malte Thodberg & Molly Went & Erik L. Bao & Laura Duran-Lozano & Aitzkoa Lopez de Lapuente Portilla & Thorunn Olafsdottir & Nerea Ug, 2022. "Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk," Nature Communications, Nature, vol. 13(1), pages 1-1, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-35411-1
    DOI: 10.1038/s41467-022-35411-1
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