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Publications by T Haferlach

Mutation Analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 Patients With MDS or Secondary AML

Leukemia

English

Landscape of TET2 Mutations in Acute Myeloid Leukemia

English

Landscape of Genetic Lesions in 944 Patients With Myelodysplastic Syndromes

English

An Accumulation of Cytogenetic and Molecular Genetic Events Characterizes the Progression From MDS to Secondary AML: An Analysis of 38 Paired Samples Analyzed by Cytogenetics, Molecular Mutation Analysis and SNP Microarray Profiling

English

SOX11 Overexpression Is a Specific Marker for Mantle Cell Lymphoma and Correlates With T(11;14) Translocation, CCND1 Expression and an Adverse Prognosis

English

The New Provisional WHO Entity ‘RUNX1 Mutated AML’ Shows Specific Genetics but No Prognostic Influence of Dysplasia

English

BAALC Expression: A Suitable Marker for Prognostic Risk Stratification and Detection of Residual Disease in Cytogenetically Normal Acute Myeloid Leukemia

English

MATE1 Regulates Cellular Uptake and Sensitivity to Imatinib in CML Patients

English

Karyotype Instability Between Diagnosis and Relapse in 117 Patients With Acute Myeloid Leukemia: Implications for Resistance Against Therapy

English

Comparison of Chromosome Banding Analysis, Interphase- And Hypermetaphase-Fish, Qualitative and Quantitative PCR for Diagnosis and for Follow-Up in Chronic Myeloid Leukemia: A Study on 350 Cases

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by T Haferlach

Mutation Analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 Patients With MDS or Secondary AML

Landscape of TET2 Mutations in Acute Myeloid Leukemia

Landscape of Genetic Lesions in 944 Patients With Myelodysplastic Syndromes

An Accumulation of Cytogenetic and Molecular Genetic Events Characterizes the Progression From MDS to Secondary AML: An Analysis of 38 Paired Samples Analyzed by Cytogenetics, Molecular Mutation Analysis and SNP Microarray Profiling

SOX11 Overexpression Is a Specific Marker for Mantle Cell Lymphoma and Correlates With T(11;14) Translocation, CCND1 Expression and an Adverse Prognosis

The New Provisional WHO Entity ‘RUNX1 Mutated AML’ Shows Specific Genetics but No Prognostic Influence of Dysplasia

BAALC Expression: A Suitable Marker for Prognostic Risk Stratification and Detection of Residual Disease in Cytogenetically Normal Acute Myeloid Leukemia

MATE1 Regulates Cellular Uptake and Sensitivity to Imatinib in CML Patients

Karyotype Instability Between Diagnosis and Relapse in 117 Patients With Acute Myeloid Leukemia: Implications for Resistance Against Therapy

Comparison of Chromosome Banding Analysis, Interphase- And Hypermetaphase-Fish, Qualitative and Quantitative PCR for Diagnosis and for Follow-Up in Chronic Myeloid Leukemia: A Study on 350 Cases