- Immunotherapy in the first line treatment of non-small cell lung cancer2020 | Faculty of Medicine in Pilsen
- A high TP53 mutation burden is a strong predictor of primary refractory mantle cell lymphoma2020 | First Faculty of Medicine
- Tumor mutation burden - a clinical oncologist's perspective2019 | First Faculty of Medicine
- High tumour mutational burden is associated with strong PD-L1 expression, HPV negativity, and worse survival in penile squamous cell carcinoma: an analysis of 165 cases2023 | First Faculty of Medicine, Third Faculty of Medicine
- Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden2022 | First Faculty of Medicine
- An autologous dendritic cell vaccine promotes anticancer immunity in patients with ovarian cancer with low mutational burden and cold tumors2022 | First Faculty of Medicine, Third Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Testicular Cancer in Monozygotic Twin Brothers with Urticaria Pigmentosa2018 | Second Faculty of Medicine
- EWSR1-PATZ1-rearranged sarcoma: a report of nine cases of spindle and round cell neoplasms with predilection for thoracoabdominal soft tissues and frequent expression of neural and skeletal muscle markers2021 | Faculty of Medicine in Pilsen
- Circulating Cell-Free DNA Extraction from Liquid Biopsy for Cancer Research2022 | First Faculty of Medicine
- Imunooncologic therapeutic options in small cell lung cancer (SCLC) therapy2020 | Faculty of Medicine in Pilsen
- The significance of the fusion partner gene genomic neighborhood analysis in translocation-defined tumors2022 | Faculty of Medicine in Pilsen
- TP53 mutation variant allele frequency is a potential predictor for clinical outcome of patients with lower-risk myelodysplastic syndromes2016 | First Faculty of Medicine
- Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency2022 | Second Faculty of Medicine
- Re: ERCC3, a new ovarian cancer susceptibility gene?2021 | First Faculty of Medicine
- Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders2020 | Second Faculty of Medicine
- Strategy of treatment of metastatic non-small-cell lung cancer - squamous cell carcinoma2016 | First Faculty of Medicine
- Rare Hereditary Burden associated with a Hypercalcemic Small-Cell Carcinoma of Cervix in a Young Female Patient2019 | Faculty of Medicine in Hradec Králové
- Circulating Cell-Free DNA and Colorectal Cancer: A Systematic Review2018 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Significance and benefit of testing for circulating tumour DNA in diagnosing and treating non-small cell lung cancer2021 | Faculty of Medicine in Pilsen
- Clear cell renal cell carcinoma with prominent microvascular hyperplasia: Morphologic, immunohistochemical and molecular-genetic analysis of 7 sporadic cases2022 | Faculty of Medicine in Pilsen
- Coexistence of gain-of-function JAK2 germ line mutations with JAK2(V617F) in polycythemia vera2016 | First Faculty of Medicine
- New methodology of TMB assessment from tissue and liquid biopsy in NSCLC2022 | First 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
- Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort2015 | First Faculty of Medicine, Third Faculty of Medicine
- Combined immunotherapy improves outcome for replication repair deficient (RRD) high-grade glioma failing anti-PD1 monotherapy: A report from the International RRD Consortium2024 | Second Faculty of Medicine
- Primary cutanous desmoplastic melanoma with collagen rosettes and pseudoglandular features2021 | Faculty of Medicine in Pilsen
- Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals2019 | Second Faculty of Medicine
- Differences in genome, transcriptome, miRNAome, and methylome in synchronous and metachronous liver metastasis of colorectal cancer2023 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
- Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma2023 | First Faculty of Medicine, Second Faculty of Medicine
- Prognostic potential of whole exome sequencing in the clinical management of metachronous colorectal cancer liver metastases2023 | Faculty of Medicine in Pilsen