Publications
- Chromosome 21 gain is dispensable for transient myeloproliferative disorder driven by a novel GATA1 mutation2020 | Second Faculty of Medicine
- Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement2019 | First Faculty of Medicine, Second Faculty of Medicine
- Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort2019 | Second Faculty of Medicine
- International cooperative study identifies treatment strategy in childhood ambiguous lineage leukemia2018 | First Faculty of Medicine, Second Faculty of Medicine
- ETV6/RUNX1-like acute lymphoblastic leukemia: A novel B-cell precursor leukemia subtype associated with the CD27/CD44 immunophenotype2017 | Second Faculty of Medicine
- Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome2016 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
- Distinct bilineal leukemia immunophenotypes are not genetically determined2016 | Second Faculty of Medicine
- TEL/AML1-Positive Patients Lacking TEL Exon 5 Resemble Canonical TEL/AML1 Cases2011 | Second Faculty of Medicine
- The identification of (ETV6)/RUNX1-regulated genes in lymphopoiesis using histone deacetylase inhibitors in ETV6/RUNX1-positive lymphoid leukemic cells2007 | Second Faculty of Medicine
- Immunophenotyping of leukemias in bone marrow, peripheral blood, effusion, and cerebrospinal fluid samples using flow cytometry [Gate: atypical cells]Publication without faculty affiliation
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