Skip to contents

  1. Bracher, Susanne; Fuhrmann, Irene; Jeromin, Sabine; Nadarajah, Niroshan; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia; Stengel, Anna

    Clonal evolution in chronic lymphocytic leukemia is associated with an unmutated IGHV status and frequently leads to a combination of loss of TP53 and TP53 mutation

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    Springer Science and Business Media LLC, 2022

    Published in: Molecular Biology Reports, 49 (2022) 12, Seite 12247-12252

  2. Stengel, Anna; Jeromin, Sabine; Haferlach, Torsten; Meggendorfer, Manja; Kern, Wolfgang; Haferlach, Claudia

    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 with progressive disease

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    Ferrata Storti Foundation (Haematologica), 2019

    Published in: Haematologica, 104 (2019) 5, Seite e187-e190

  3. Höllein, Alexander; Jeromin, Sabine; Meggendorfer, Manja; Fasan, Annette; Nadarajah, Niroshan; Kern, Wolfgang; Haferlach, Claudia; Haferlach, Torsten

    Minimal residual disease (MRD) monitoring and mutational landscape in AML with RUNX1-RUNX1T1: a study on 134 patients

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    Springer Science and Business Media LLC, 2018

    Published in: Leukemia, 32 (2018) 10, Seite 2270-2274

  4. Martin-Cabrera, Pedro; Jeromin, Sabine; Perglerovà, Karolína; Haferlach, Claudia; Kern, Wolfgang; Haferlach, Torsten

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

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    Ferrata Storti Foundation (Haematologica), 2017

    Published in: Haematologica, 102 (2017) 4, Seite e125-e128

  5. Haferlach, Claudia; Jeromin, Sabine; Nadarajah, Niroshan; Zenger, Melanie; Kern, Wolfgang; Haferlach, Torsten

    Cytogenetic and Molecular Genetic Clonal Evolution in CLL Is Associated with an Unmutated IGHV Status and Frequently Leads to a Combination of Loss of 17p and TP53 mutation

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    American Society of Hematology, 2016

    Published in: Blood, 128 (2016) 22, Seite 3213-3213

  6. Stengel, Anna; Meggendorfer, Manja; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia; Jeromin, Sabine

    Homozygosity of Mutated Calreticulin in Myeloproliferative Neoplasms By an Acquired Chromosome 19p UPD Is Associated with Deletions in the Long Arm of Chromosome 5 and SF3B1 Mutations

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    American Society of Hematology, 2016

    Published in: Blood, 128 (2016) 22, Seite 3145-3145

  7. Haferlach, Claudia; Jeromin, Sabine; Stengel, Anna; Meggendorfer, Manja; Zenger, Melanie; Kern, Wolfgang; Haferlach, Torsten

    In Chronic Lymphocytic Leukemia the Gain of the Short Arm of Chromosome 2 Is Highly Associated with an Unmutated IGHV status, 11q/ATM Deletion, SF3B1 Mutation and a Complex Karyotype

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    American Society of Hematology, 2016

    Published in: Blood, 128 (2016) 22, Seite 4379-4379

  8. Martin-Cabrera, Pedro; Jeromin, Sabine; Alpermann, Tamara; Perglerová, Karolína; Haferlach, Claudia; Kern, Wolfgang; Haferlach, Torsten

    Higher Percentages of Ring Sideroblasts and SF3B1 Mutations in Patients with AML Correlate with Mutations in TP53 and Adverse Cytogenetics, but Have No Independent Impact on Outcome

    Articles
    View online
    Close

    Bookmarks

    You can manage bookmarks using lists, please log in to your user account for this.

    American Society of Hematology, 2015

    Published in: Blood, 126 (2015) 23, Seite 3847-3847