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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Last data update: Apr 25, 2024
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Molecular profile of patients with myelofibrosis: a 10-year experience.
Dias Lara Faria Souza et al. Einstein (Sao Paulo, Brazil) 2023 21eAO0100
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The Genetic Basis of Primary Myelofibrosis and Its Clinical Relevance.
Rumi Elisa et al. International journal of molecular sciences 2020 Nov 21(23)
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Australasian Trends in Allogeneic Stem Cell Transplantation for Myelofibrosis in the Molecular Era: A retrospective analysis from The Australasian Bone Marrow Transplant Recipient Registry.
Lwin Y et al. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2020 Aug
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[Analysis of gene mutations and clinic features in 108 patients with myeloproliferative neoplasm].
Tan Y X et al. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2020 Jul 41(7) 576-582
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Genomic characterization and prognostication applied to a Brazilian cohort of patients with myelofibrosis.
Nonino Alexandre et al. International journal of hematology 2020 Jun
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Mutational profiling in myelofibrosis: implications for management.
Bose Prithviraj et al. International journal of hematology 2019 Oct
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Screening for ASXL1 and SRSF2 mutations is imperative for treatment decision-making in otherwise low or intermediate-1 risk patients with myelofibrosis.
Tefferi Ayalew et al. British journal of haematology 2018 183(4) 678-681
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Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Genomic Sequence Analysis Panels in the Treatment of Hematolymphoid Diseases (L37606)
The U.S. Centers for Medicare & Medicaid Services
Philadelphia chromosome-negative classical myeloproliferative neoplasms: revised management recommendations from European LeukemiaNet.
Barbui Tiziano et al. Leukemia 2018 32(5) 1057-1069
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Next-Generation Sequencing in Myeloproliferative Neoplasms: Is This Indicated in All Patients?
Mina Alain Antoine et al. Current hematologic malignancy reports 2019 Apr
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Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis.
Gill Harinder et al. Annals of hematology 2018 Dec
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Classification and Personalized Prognosis in Myeloproliferative Neoplasms.
Grinfeld Jacob et al. The New England journal of medicine 2018 379(15) 1416-1430
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GIPSS: genetically inspired prognostic scoring system for primary myelofibrosis.
Tefferi Ayalew et al. Leukemia 2018 Mar
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Incidence, Survival, and Risk Factors for Adults with Acute Myeloid Leukemia Not Otherwise Specified and Acute Myeloid Leukemia with Recurrent Genetic Abnormalities: Analysis of the Surveillance, Epidemiology, and End Results (SEER) Database, 2001-2013.
Song Xiaolu et al. Acta haematologica 2018 Feb 139(2) 115-127
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Telomeres and Telomerase in Hematopoietic Dysfunction: Prognostic Implications and Pharmacological Interventions.
Vasko Theresa et al. International journal of molecular sciences 2017 Oct 18(11)
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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