RUNX1 germline variants in RUNX1-mutant AML: how frequent?
Author:
Affiliation:
1. Department of Hematology, Erasmus Medical Center Cancer Institute, Rotterdam, The Netherlands
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/137/10/1428/1802163/bloodbld2020008478.pdf
Reference16 articles.
1. High frequency of germline RUNX1 mutations in patients with RUNX1-mutated AML;Simon;Blood,2020
2. RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis;Schnittger;Blood,2011
3. RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures;Mendler;J Clin Oncol,2012
4. RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features [published correction appears in Leukemia. 2016;30(11):2282];Gaidzik;Leukemia,2016
5. Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies;Drazer;Blood Adv,2018
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2. Diagnosing familial platelet disorder with predisposition to myeloid malignancy: Lessons learned from a germline whole‐gene deletion of RUNX1;International Journal of Laboratory Hematology;2023-11-12
3. Germline and somatic drivers in inherited hematologic malignancies;Frontiers in Oncology;2023-10-13
4. Frequency and Functional Characterization of RUNX1 Germline Variants in Myeloid Neoplasms;Human Mutation;2023-06-02
5. RUNX1 mutation has no prognostic significance in paediatric AML: a retrospective study of the AML-BFM study group;Leukemia;2023-05-15
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