- Transient myeloproliferative syndrome in newborn without Down syndrome phenotype: a unique case report2019 | First Faculty of Medicine
- Molecular Analysis of Chromosome 21 in a Patient With a Phenotype of Down Syndrome and Apparently Normal Karyotype1996 | Second Faculty of Medicine
- Analysis of FOXL2 detects three novel mutations and an atypical phenotype of blepharophimosis-ptosis-epicanthus inversus syndrome2016 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay2018 | Second Faculty of Medicine, First Faculty of Medicine
- "Dry mouth" and "Flammer" syndromes-neglected risks in adolescents and new concepts by predictive, preventive and personalised approach2018 | Faculty of Medicine in Pilsen
- Risks associated with the stroke predisposition at young age: facts and hypotheses in light of individualized predictive and preventive approach2019 | Faculty of Medicine in Pilsen
- Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature2017 | Second Faculty of Medicine
- Prostate cancer management: long-term beliefs, epidemic developments in the early twenty-first century and 3PM dimensional solutions2020 | Faculty of Medicine in Pilsen