- Differences in cyto- and molecular genetic aberrations between children < 2 years and older children with acute myeloid leukaemiaPublication without faculty affiliation
- Differences in cyto- and molecular genetic aberrations between young (<2YR) and older children with acute myeloid leukemiaPublication without faculty affiliation
- Salivary Gland Mucinous Adenocarcinoma With Minor (Mammary Analogue) Secretory and Low-Grade In Situ Carcinoma Components Sharing the Same ETV6-RET Translocation and With No Other Molecular Genetic Aberrations Detected on NGS Analysis2020 | Faculty of Medicine in Pilsen
- Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours2014 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Immunotherapy in the first line treatment of non-small cell lung cancer2021 | Publication without faculty affiliation
- The clinical and biological characteristics of NUP98-KDM5A in pediatric acute myeloid leukemia2021 | Second Faculty of Medicine
- Entrectinib in the treatment of patients with ROS1‑positive advanced non‑small cell lung cancer2021 | Publication without faculty affiliation
- Nonsmall cell lung cancer with RET gene fusion2021 | Publication without faculty affiliation
- Lung cancer on virtual ASCO 20212021 | Publication without faculty affiliation
- Sequencing-based analysis of clonal evolution of 25 mantle cell lymphoma patients at diagnosis and after failure of standard immunochemotherapy2023 | First Faculty of Medicine, Second Faculty of Medicine
- PHF6 mutations in paediatric acute myeloid leukaemia2016 | Second Faculty of Medicine
- New developments in molecular diagnostics of carcinomas of the salivary glands: "translocation carcinomas"2016 | Faculty of Medicine in Pilsen
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | 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
- Genomic landscape of pediatric B-other acute lymphoblastic leukemia in a consecutive European cohort2019 | Second Faculty of Medicine
- Homeobox gene expression in acute myeloid leukemia is linked to typical underlying molecular aberrations2014 | Second Faculty of Medicine
- Implication of cytogenetic and molecular cytogenetic analysis in diagnosis of hematological malignancies in the era of the new sequencing techniques2019 | First Faculty of Medicine
- Lorlatinib in the treatment of non‑small cell lung cancer2020 | Publication without faculty affiliation
- ZAP-70 in B-cell chronic lymphocytic leukemia: clinical significance and methods of detection2006 | Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | First Faculty of Medicine
- The role of TEL and AML1 genes in the pathogenesis of hematologic malignancies2001 | Second Faculty of Medicine
- Aetiology of childhood ALL and AML, molecular genetics and minimal residual disease2015 | Second Faculty of Medicine
- Localization of AML-related nucleophosmin mutant depends on its subtype and is highly affected by its interaction with wild-type NPM2017 | Central Library of Charles University
- Vulvar pigmented epithelioid melanocytoma with a novel HTT-PKN1 fusion: a case report2020 | Faculty of Medicine in Pilsen
- Next generation sequencing and the molecular tumor board from the point of view of oncologists2021 | First Faculty of Medicine
- CD30+clonal T-cell lymphoid proliferation of the skin in a patient with hypereosinophilic syndrome2015 | Faculty of Medicine in Pilsen
- Renal Cell Carcinoma With Leiomyomatous Stroma: A Group of Tumors With Indistinguishable Histopathologic Features, But 2 Distinct Genetic Profiles: Next-Generation Sequencing Analysis of 6 Cases Negative for Aberrations Related to the VHL gene2018 | Faculty of Medicine in Pilsen
- AML-associated mutation of nucleophosmin compromises its interaction with nucleolin2018 | Central Library of Charles University
- Distinctive role of K(V)1.1 subunit in the biology and functions of low threshold K+ channels with implications for neurological disease2016 | Central Library of Charles University
- The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered2021 | Second Faculty of Medicine