Publications
- A comprehensive molecular analysis of 113 primary ovarian clear cell carcinomas reveals common therapeutically significant aberrations2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen, Second Faculty of Medicine
- HER2 status as a potential predictive biomarker for ovarian clear cell carcinoma2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen, Second Faculty of Medicine
- Microsatellite Instability in Non-Endometrioid Ovarian Epithelial Tumors: A study of 400 cases Comparing Immunohistochemistry, PCR, and NGS Based Testing with Mutation Status of MMR Genes2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- A comprehensive analysis of the expression, epigenetic and genetic changes of HNF1B and ECI2 in 122 cases of high-grade serous ovarian carcinoma2021 | First Faculty of Medicine
- Expression, Epigenetic, and Genetic Changes of HNF1B in Colorectal Lesions: an Analysis of 145 Cases2020 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Identification of novel HNF1B mRNA splicing variants and their qualitative and semi-quantitative profile in selected healthy and tumour tissues2020 | First Faculty of Medicine
- Analysis of expression, epigenetic, and genetic changes of HNF1B in 130 kidney tumours2020 | First Faculty of Medicine
- Somatic genomic and transcriptomic characterization of primary ovarian serous borderline tumors and low-grade serous carcinomas2024 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Second Faculty of Medicine
- 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
- Uterine cellular leiomyomas are characterized by common HMGA2 aberrations, followed by chromosome 1p deletion and MED12 mutation: morphological, molecular, and immunohistochemical study of 52 cases2022 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
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