Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma-Reference-Cited by-同舟云学术

Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma

Published:2018-07-26 Issue:8 Volume:143 Page:2076-2078
ISSN:0020-7136
Container-title:International Journal of Cancer
language:en
Short-container-title:Int. J. Cancer

Author:

Bandapalli Obul Reddy¹^ORCID,Paramasivam Nagarajan²³,Giangiobbe Sara¹⁴,Kumar Abhishek¹,Benisch Wolfgang⁵,Engert Andreas⁶,Witzens‐Harig Mathias⁷,Schlesner Mathias²⁸,Hemminki Kari¹⁹,Försti Asta¹⁹

Affiliation:

1. Division of Molecular Genetic EpidemiologyGerman Cancer Research Center (DKFZ), Im Neuenheimer Feld 580HeidelbergD‐69120 Germany

2. Division of Theoretical BioinformaticsGerman Cancer Research Center (DKFZ)Heidelberg Germany

3. Medical faculty HeidelbergHeidelberg UniversityHeidelberg Germany

4. Department of Pathophysiology and TransplantationUniversità degli Studi di MilanoMilan Italy

5. Department of Pediatric Oncology, Hematology and ImmunologyUniversity of HeidelbergHeidelberg Germany

6. German Hodgkin Study Group, Department of Internal MedicineUniversity HospitalCologne50931 Germany

7. Department of Medicine VUniversity Hospital of HeidelbergHeidelberg Germany

8. Bioinformatics and Omics Data AnalyticsGerman Cancer Research Center (DKFZ)HeidelbergD69120 Germany

9. Center for Primary Health Care Research, Lund UniversityMalmö Sweden

Funder

University of Milan & Italian Ministry of Instruction

Publisher

Wiley

Subject

Cancer Research,Oncology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ijc.31576

Reference10 articles.

1. Part II: Hodgkin's lymphoma—diagnosis and treatment

2. Risk of familial classical Hodgkin lymphoma by relationship, histology, age, and sex: a joint study from five Nordic countries

3. Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cells

4. Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma

5. Identification of homozygous deletion inACANand other candidate variants in familial classical Hodgkin lymphoma by exome sequencing

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