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Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.
Niazi, Yasmeen; Paramasivam, Nagarajan; Blocka, Joanna; Kumar, Abhishek; Huhn, Stefanie; Schlesner, Matthias; Weinhold, Niels; Sijmons, Rolf; De Jong, Mirjam; Durie, Brian; Goldschmidt, Hartmut; Hemminki, Kari; Försti, Asta.
Afiliação
  • Niazi Y; Hopp Children's Cancer Center (KiTZ), 69120 Heidelberg, Germany.
  • Paramasivam N; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), 69120 Heidelberg, Germany.
  • Blocka J; Computational Oncology, Molecular Precision Oncology Program, National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.
  • Kumar A; Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
  • Huhn S; Department of Medical Oncology, Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
  • Schlesner M; Harvard Medical School, Boston, MA 02115, USA.
  • Weinhold N; Institute of Bioinformatics, International Technology Park, Bangalore 560066, India.
  • Sijmons R; Manipal Academy of Higher Education (MAHE), Manipal 576104, India.
  • De Jong M; Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
  • Durie B; National Center for Tumor Diseases Heidelberg (NCT), 69120 Heidelberg, Germany.
  • Goldschmidt H; Bioinformatics and Omics Data Analytics, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
  • Hemminki K; Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany.
  • Försti A; University Medical Center Groningen, University of Groningen, 9712 Groningen, The Netherlands.
Cells ; 12(1)2022 12 26.
Article em En | MEDLINE | ID: mdl-36611892
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Mieloma Múltiplo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Mieloma Múltiplo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article