Publications
- Solving patients with rare diseases through programmatic reanalysis of genome-phenome data2021 | Second Faculty of Medicine
- Quality of life in patients with autosomal dominant tubulointerstitial kidney disease2019 | First Faculty of Medicine
- Psychosocial factors associated with genetic testing for some of hereditary forms of cancer2003 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom2022 | First Faculty of Medicine, Second Faculty of Medicine
- Ethical principles for the usage and sharing of genomic data from research2022 | First Faculty of Medicine, Second Faculty of Medicine
- Surrogate Motherhood - Selected Ethical and Legal Aspects2022 | First Faculty of Medicine
- Circulating Cell-Free DNA Extraction from Liquid Biopsy for Cancer Research2022 | First Faculty of Medicine
- New methodology of TMB assessment from tissue and liquid biopsy in NSCLC2022 | First Faculty of Medicine
- Time and Temperature Stability of TGF-β1, EGF and IGF-1 in 20% and 100% Human Serum2022 | First Faculty of Medicine
- Informing Parents about Newborn Screening: A European Comparison Study2021 | First Faculty of Medicine
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