Publications
- The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood2023 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine
- Cluster analysis of facial phenotypes in autism spectrum disorders based on 3D facial models2023 | Faculty of Science, Second Faculty of Medicine
- High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic2022 | Second Faculty of Medicine, First Faculty of Medicine
- Improving structural variant clustering to reduce the negative effect of the breakpoint uncertainty problem2021 | Second Faculty of Medicine, First Faculty of Medicine
- The key role of purine metabolism in the folate-dependent phenotype of autism spectrum disorders: An in silico analysis2020 | Second Faculty of Medicine
- Body coloration and mechanisms of colour production in Archelosauria: The case of deirocheline turtles2019 | Faculty of Science, Second Faculty of Medicine
- Modules in the metabolic network of E.coli with regulatory interactions2013 | Faculty of Science
- Complex cytogenetic and molecular genetic diagnostics of congenital heart defectsPublication without faculty affiliation
- Algorithm for relatedness prediction on the basis of structural variantsPublication without faculty affiliation
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