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Publications by A Tefferi

DNMT3A and IDH Mutations in Acute Myeloid Leukemia and Other Myeloid Malignancies: Associations With Prognosis and Potential Treatment Strategies

Leukemia

English

SF3B1 Mutations in Primary Myelofibrosis: Clinical, Histopathology and Genetic Correlates Among 155 Patients

English

Monosomal Karyotype in Myelodysplastic Syndromes, With or Without Monosomy 7 or 5, Is Prognostically Worse Than an Otherwise Complex Karyotype

English

Differential Distribution of CCDC26 Glioma-Risk Alleles in Myeloid Malignancies With Mutant IDH1 Compared With Their IDH2R140-mutated or IDH-unmutated Counterparts

English

Incidence and Risk Factors for Bleeding in 1104 Patients With Essential Thrombocythemia or Prefibrotic Myelofibrosis Diagnosed According to the 2008 WHO Criteria

English

Trisomy 11: Prevalence Among 22 403 Unique Patient Cytogenetic Studies and Clinical Correlates

English

An Overview on CALR and CSF3R Mutations and a Proposal for Revision of WHO Diagnostic Criteria for Myeloproliferative Neoplasms

English

WHO-defined ‘Myelodysplastic Syndrome With Isolated Del(5q)’ in 88 Consecutive Patients: Survival Data, Leukemic Transformation Rates and Prevalence of JAK2, MPL and IDH Mutations

English

Prognostic Impact of Bone Marrow Fibrosis in Polycythemia Vera: Validation of the IWG-MRT Study and Additional Observations

English

Definition and Management of Ruxolitinib Treatment Failure in Myelofibrosis

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by A Tefferi

DNMT3A and IDH Mutations in Acute Myeloid Leukemia and Other Myeloid Malignancies: Associations With Prognosis and Potential Treatment Strategies

SF3B1 Mutations in Primary Myelofibrosis: Clinical, Histopathology and Genetic Correlates Among 155 Patients

Monosomal Karyotype in Myelodysplastic Syndromes, With or Without Monosomy 7 or 5, Is Prognostically Worse Than an Otherwise Complex Karyotype

Differential Distribution of CCDC26 Glioma-Risk Alleles in Myeloid Malignancies With Mutant IDH1 Compared With Their IDH2R140-mutated or IDH-unmutated Counterparts

Incidence and Risk Factors for Bleeding in 1104 Patients With Essential Thrombocythemia or Prefibrotic Myelofibrosis Diagnosed According to the 2008 WHO Criteria

Trisomy 11: Prevalence Among 22 403 Unique Patient Cytogenetic Studies and Clinical Correlates

An Overview on CALR and CSF3R Mutations and a Proposal for Revision of WHO Diagnostic Criteria for Myeloproliferative Neoplasms

WHO-defined ‘Myelodysplastic Syndrome With Isolated Del(5q)’ in 88 Consecutive Patients: Survival Data, Leukemic Transformation Rates and Prevalence of JAK2, MPL and IDH Mutations

Prognostic Impact of Bone Marrow Fibrosis in Polycythemia Vera: Validation of the IWG-MRT Study and Additional Observations

Definition and Management of Ruxolitinib Treatment Failure in Myelofibrosis