Inherited predisposition to acute myeloid leukemia.
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Summary
Testing for familial predisposition to myeloid malignancies is becoming more common with the recognition of multiple familial syndromes, and new predisposition alleles are likely to be identified.
- Type
- article
- Published
- 2014-10-01
- Cited by
- 91
- References
- 116
- OpenAlex
- https://openalex.org/W2013273720
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:21896694
Keywords
Myeloid leukemia, Medicine, Dyskeratosis congenita, Myeloid, Bone marrow failure
References
- Familial myelodysplasia and acute myeloid leukaemia – a review
- Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
- Familial myelodysplastic syndrome/acute leukemia syndromes: a review and utility for translational investigations
- Dyskeratosis congenita: Advances in the understanding of the telomerase defect and the role of stem cell transplantation
- Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
- Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure.
- Profiles in leukemia.
- GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia
- Haploinsufficiency of GATA-2 perturbs adult hematopoietic stem-cell homeostasis.
- Telomerase and Idiopathic Pulmonary Fibrosis
- A Spectrum of Severe Familial Liver Disorders Associate with Telomerase Mutations
- ANKRD26-related thrombocytopenia and myeloid malignancies.
- Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
- Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
- Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure.
- Development of hairy cell leukemia in familial platelet disorder with predisposition to acute myeloid leukemia
- A missense mutation in ANKRD26 segregates with thrombocytopenia.
- RUNX1/core binding factor A2 regulates platelet 12-lipoxygenase gene (ALOX12): studies in human RUNX1 haplodeficiency.
- Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.
- Identification of amino acid residues in protein SRP72 required for binding to a kinked 5e motif of the human signal recognition particle RNA
Cited by
- Correspondence Regarding the Consensus Statement from the Worldwide Network for Blood and Marrow Transplantation Standing Committee on Donor Issues.
- Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults
- Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia
- Myeloid Neoplasms with Germline Predisposition: A New Provisional Entity Within the World Health Organization Classification.
- Selecting Sample Preparation Workflows for Mass Spectrometry-Based Proteomic and Phosphoproteomic Analysis of Patient Samples with Acute Myeloid Leukemia
- Genetic predisposition to leukemia and other hematologic malignancies.
- Discussing and managing hematologic germ line variants.
- Introduction to cancer genetic susceptibility syndromes.
- Somatic mutations in murine models of leukemia and lymphoma: disease specificity and clinical relevance
- Initial Diagnostic Workup of Acute Leukemia: Guideline From the College of American Pathologists and the American Society of Hematology.
- Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary
- Familial CEBPA-mutated acute myeloid leukemia.
- Recognition of familial myeloid neoplasia in adults.
- Predispositions to Leukemia in Down Syndrome and Other Hereditary Disorders
- Familial Myelodysplastic/Acute Leukemia Syndromes—Myeloid Neoplasms with Germline Predisposition
- Understanding the molecular basis of acute myeloid leukemias: where are we now?
- RUNX1 Mutations in Inherited and Sporadic Leukemia
- Germ line predisposition to myeloid malignancies appearing in adulthood
- The histopathology of bone marrow failure in children.
- Hereditary Myelodysplastic Syndrome and Acute Myeloid Leukemia: Diagnosis, Questions, and Controversies
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