Comprehensive study on ERG gene expression in normal karyotype acute myeloid leukemia: ERG expression is of limited prognostic value, whereas the accumulation of adverse prognostic...

od Weber, S, Haferlach, T, Haferlach, C, Kern, W
izdano v Blood Cancer J (2016)

Molecular analysis of myelodysplastic syndrome with isolated deletion of the long arm of chromosome 5 reveals a specific spectrum of molecular mutations with prognostic impact: a s...

od Meggendorfer, Manja, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten
izdano v Haematologica (2017)

Advancing leukemia diagnostics: Role of Next Generation Sequencing (NGS) in acute myeloid leukemia

od Haferlach, Torsten
izdano v Hematol Rep (2020)

The time has come for next-generation sequencing in routine diagnostic workup in hematology

od Haferlach, Torsten
izdano v Haematologica (2021)

The diagnosis of BCR/ABL-negative chronic myeloproliferative diseases (CMPD): a comprehensive approach based on morphology, cytogenetics, and molecular markers

od Haferlach, Torsten, Bacher, Ulrike, Kern, Wolfgang, Schnittger, Susanne, Haferlach, Claudia
Izdano 2007

Gene expression profiling for the diagnosis of acute leukaemia

od Haferlach, T, Kohlmann, A, Bacher, U, Schnittger, S, Haferlach, C, Kern, W
Izdano 2007

Serial assessment of suspected myelodysplastic syndromes: significance of flow cytometric findings validated by cytomorphology, cytogenetics, and molecular genetics

od Kern, Wolfgang, Haferlach, Claudia, Schnittger, Susanne, Alpermann, Tamara, Haferlach, Torsten
Izdano 2013

Molecular landscape of acute promyelocytic leukemia at diagnosis and relapse

od Fasan, Annette, Haferlach, Claudia, Perglerovà, Karolina, Kern, Wolfgang, Haferlach, Torsten
izdano v Haematologica (2017)

The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms

od Meggendorfer, Manja, Jeromin, Sabine, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten
izdano v Haematologica (2018)

Molecular genetic characterization of myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or PCM1-JAK2

od Baer, Constance, Muehlbacher, Verena, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten
izdano v Haematologica (2018)

Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis

od Flach, Johanna, Dicker, Frank, Schnittger, Susanne, Kohlmann, Alexander, Haferlach, Torsten, Haferlach, Claudia
Izdano 2010

Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells

od Bacher, Ulrike, Haferlach, Claudia, Alpermann, Tamara, Kern, Wolfgang, Schnittger, Susanne, Haferlach, Torsten
Izdano 2011

Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA

od Schnittger, Susanne, Bacher, Ulrike, Haferlach, Claudia, Kern, Wolfgang, Alpermann, Tamara, Haferlach, Torsten
Izdano 2011

Detection and characterization of homozygosity of mutated CALR by copy neutral loss of heterozygosity in myeloproliferative neoplasms among cases with high CALR mutation loads or w...

od Stengel, Anna, Jeromin, Sabine, Haferlach, Torsten, Meggendorfer, Manja, Kern, Wolfgang, Haferlach, Claudia
izdano v Haematologica (2019)

The benefit of population-based studies for older patients with acute myeloid leukemia

od Bacher, Ulrike, Haferlach, Torsten
Izdano 2012

The power and potential of integrated diagnostics in acute myeloid leukaemia

od Haferlach, Torsten, Schmidts, Ines
izdano v Br J Haematol (2019)

The new provisional WHO entity ‘RUNX1 mutated AML' shows specific genetics but no prognostic influence of dysplasia

od Haferlach, T, Stengel, A, Eckstein, S, Perglerová, K, Alpermann, T, Kern, W, Haferlach, C, Meggendorfer, M
izdano v Leukemia (2016)

Acute myeloid leukemias with ring sideroblasts show a unique molecular signature straddling secondary acute myeloid leukemia and de novo acute myeloid leukemia

od Martin-Cabrera, Pedro, Jeromin, Sabine, Perglerovà, Karolína, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten
izdano v Haematologica (2017)

Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations

od Alexander Höllein, Niroshan Nadarajah, Manja Meggendorfer, Sabine Jeromin, Wolfgang Kern, Claudia Haferlach, Torsten Haferlach
Izdano 2019-02-01

Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia

od Meggendorfer, Manja, Haferlach, Torsten, Alpermann, Tamara, Jeromin, Sabine, Haferlach, Claudia, Kern, Wolfgang, Schnittger, Susanne
izdano v Haematologica (2014)