Publications
- Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease2023 | First Faculty of Medicine, Second Faculty of Medicine
- Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres2022 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Improvement of Diagnostic Yield by an Additional Amplicon Module to Hybridization-Based Next-Generation Sequencing Panels2022 | First Faculty of Medicine
- Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis2020 | First Faculty of Medicine, Second Faculty of Medicine
- Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene2019 | First Faculty of Medicine
- Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report2018 | First Faculty of Medicine
- Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease2015 | First Faculty of Medicine, Second Faculty of Medicine
- Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease2014 | First Faculty of Medicine
- Mutational Analysis of ACTN4, Encoding alpha-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method2013 | First Faculty of Medicine
- Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome2012 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
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