- Molecular screening of the stool for colorectal carcinoma2005 | Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Molecular screening in 45 patients with isolated cox deficiency for mutations in COX10, COX15 and SCO1 genesPublication without faculty affiliation
- Colorectal Adenomas-Genetics and Searching for New Molecular Screening Biomarkers2020 | Central Library of Charles University, First Faculty of Medicine, Faculty of Medicine in Pilsen
- Molecular screening and follow-up for BCR/ABL and MLL/AF4 rearrangements of children with acute lymphoblastic leukemia - a Czech Children Leukemia Working Group experience1995 | Central Library of Charles University, Second Faculty of Medicine
- Molecular Screening in ALK-Positive Anaplastic Large Cell Lymphoma: ALK Analysis, NGS Fusion Gene Detection, and T-cell Receptor Immunoprofiling2024 | Third Faculty of Medicine, Second Faculty of Medicine
- Entomological study in an anthroponotic cutaneous leishmaniasis focus in Morocco: Fauna survey, Leishmania infection screening, molecular characterization and MALDI-TOF MS protein profiling of relevant Phlebotomus species2022 | Faculty of Science
- Genetic testing of leiomyoma tissue in women younger than 30 years old might provide an effective screening approach for the hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC)2015 | Faculty of Medicine in Pilsen
- The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort2019 | First Faculty of Medicine
- Immunohistochemical and selected genetic reflex testing of all uterine leiomyosarcomas and STUMPs for ALK gene rearrangement may provide an efeective screening tool in identifying uterine ALK-rearranged mesenchymal tumors2018 | Faculty of Medicine in Pilsen
- Duplex methylation-specific semi-quantitative real-time PCR for cost-effective & time-efficient diagnostic screening of chromosome 15 and 14 imprinted regions2015 | Publication without faculty affiliation
- IDH1 and IDH2 mutations in patients with acute myeloid leukemia: Suitable targets for minimal residual disease monitoring?2018 | Faculty of Medicine in Hradec Králové
- Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series2021 | First Faculty of Medicine
- The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics2015 | First Faculty of Medicine
- Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants2016 | First Faculty of Medicine
- NR4A3 fusions characterize a distinctive peritoneal mesothelial neoplasm of uncertain biological potential with pure adenomatoid/microcystic morphology2023 | Faculty of Medicine in Pilsen
- The evolving landscape of biomarker testing for non-small cell lung cancer in Europe2021 | Faculty of Medicine in Hradec Králové