- Genome-wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma2017 | Central Library of Charles University
- Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL2019 | Second Faculty of Medicine
- Spitz tumors with ROS1 fusions: a clinicopathological study of 6 cases, including FISH for chromosomal copy number alterations and mutation analysis using next-generation sequencing2020 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Central Library of Charles University
- Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathways2018 | First Faculty of Medicine
- The clinical utility of optical genome mapping for the assessment of genomic aberrations in acute lymphoblastic leukemia2021 | Second Faculty of Medicine
- Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome2017 | Second Faculty of Medicine
- Genomic analysis of head and neck cancer cases from two high incidence regions2018 | First Faculty of Medicine, Second Faculty of Medicine
- Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia2011 | Second Faculty of Medicine
- The PD-L1-Associated Carcinogenesis May Encompass Oncogenes UHRF2 and PTPRDPublication without faculty affiliation
- Intertumoral Heterogeneity within Medulloblastoma Subgroups2017 | Central Library of Charles University
- PPM1D activity promotes the replication stress caused by cyclin E1 overexpression2023 | Central Library of Charles University
- From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype2012 | First Faculty of Medicine
- RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data2022 | Second Faculty of Medicine
- Intragenic NF1 deletions in sinonasal mucosal malignant melanoma2022 | Faculty of Medicine in Hradec Králové
- Large Germline Deletions of the CYLD Gene in Patients With Brooke-Spiegler Syndrome and Multiple Familial Trichoepithelioma2014 | Faculty of Medicine in Pilsen
- Risk factors and outcomes in children with high-risk B-cell precursor and T-cell relapsed acute lymphoblastic leukaemia: combined analysis of ALLR3 and ALL-REZ BFM 2002 clinical trials2021 | Second Faculty of Medicine
- The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples2022 | Second Faculty of Medicine
- Comparison of the biomarkers for targeted therapies in primary extra-mammary and mammary Paget's disease2020 | Faculty of Medicine in Pilsen
- Heterogeneity within the PF-EPN-B ependymoma subgroup2018 | Central Library of Charles University
- IKZF1(plus) Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia2018 | Second Faculty of Medicine