Publications
- Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL-USP2 fusions2019 | First Faculty of Medicine, Second Faculty of Medicine
- An activating mutation of GNB1 is associated with resistance to tyrosine kinase inhibitors in ETV6-ABL1-positive leukemia2017 | First Faculty of Medicine, Second Faculty of Medicine
- Monitoring of childhood ALL using BCR-ABL1 genomic breakpoints identifies a subgroup with CML-like biology2017 | Second Faculty of Medicine
- Aetiology of childhood ALL and AML, molecular genetics and minimal residual disease2015 | Second Faculty of Medicine
- Acute Leukemias with ETV6/ABL1 (TEL/ABL) Fusion: Poor Prognosis and Prenatal Origin2010 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Quantification of fusion transcript reveals a subgroup with distinct biological properties and predicts relapse in BCR/ABL-positive ALL: implications for residual disease monitoring2009 | 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
- Genomic DNA-based measurable residual disease monitoring in pediatric acute myeloid leukemia: unselected consecutive cohort study2024 | Second Faculty of Medicine
- CD371+ pediatric B-cell acute lymphoblastic leukemia: propensity to lineage switch and slow early response to treatment2024 | Second Faculty of Medicine
- Restored biosynthetic pathways induced by MSCs serve as rescue mechanism in leukemia cells after L-asparaginase therapy2023 | Second Faculty of Medicine, Faculty of Science
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