- Functionally Significant Features in the 5' Untranslated Region of the ABCA1 Gene and Their Comparison in Vertebrates2019 | Faculty of Medicine in Pilsen
- 5' Untranslated Region Elements Show High Abundance and Great Variability in Homologous ABCA Subfamily Genes2020 | Faculty of Medicine in Pilsen
- Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5'-untranslated region of UNC45A2023 | Faculty of Medicine in Hradec Králové
- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | First Faculty of Medicine
- Single-Strand Sequencing of PCR Products of the MBL2 Gene with a Polyadenylated Sequencing Primer2012 | Faculty of Medicine in Hradec Králové
- Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency2009 | Third Faculty of Medicine
- Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma2023 | Faculty of Medicine in Pilsen
- Human beta-mannosidase cDNA characterization and first identification of a mutation associated with human beta-mannosidosis1998 | Second Faculty of Medicine
- Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer2021 | Faculty of Medicine in Pilsen
- HCVIVdb: The hepatitis-C IRES variation database2016 | Faculty of Science
- Hereditary hyperferritinemia-cataract syndrome in three Czech families: molecular genetic testing and clinical implications2020 | First Faculty of Medicine, Second Faculty of Medicine
- Germline CDKN1B loss-of-function variants cause pediatric cushing's disease with or without an MEN4 phenotype2020 | Second Faculty of Medicine