- Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene2009 | Second Faculty of Medicine
- Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results2009 | Second 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
- Influence of Endothelin-1 gene polymorphisms on the progression of autosomal dominant polycystic kidney disease2006 | First Faculty of Medicine
- The influence of the Genetic Background on the Interaction of Retioic Acid with Lx Mutation of the Rat2000 | First Faculty of Medicine
- Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia2011 | Second Faculty of Medicine
- Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients2015 | First Faculty of Medicine
- Genetic engineering questionsPublication without faculty affiliation
- Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q131999 | Second Faculty of Medicine
- Efficient CRISPR/Cas9-mediated gene disruption in the tetraploid protist Giardia intestinalis2022 | First Faculty of Medicine, Faculty of Science
- Superoxide Dismutase and Nicotinamide Adenine Dinucleotide Phosphate Quinone Oxidoreductase Polymorphisms and Pancreatic Cancer Risk2011 | First Faculty of Medicine
- Hirschsprung's disease and its genetic cause2013 | Faculty of Science, Second Faculty of Medicine
- Superoxide Dismutase and Nicotinamide Adenine Dinucleotide Phosphate Quinone Oxidoreductase Polymorphisms and Pancreatic Cancer Risk2011 | Second Faculty of Medicine
- Polymorphisms of dopamine-beta-hydroxylase in ADHD children2006 | Second Faculty of Medicine
- Polymorphisms and low plasma activity of Dopamine-beta-hydroxylase in ADHD children2006 | Second Faculty of Medicine
- Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity2023 | Second Faculty of Medicine, Faculty of Medicine in Hradec Králové, Faculty of Medicine in Pilsen
- Modulation of bilirubin neurotoxicity by the Abcb1 transporter in the Ugt1(-/-) lethal mouse model of neonatal hyperbilirubinemia2017 | First Faculty of Medicine
- Association of superoxide dismutases and NAD(P)H quinone oxidoreductases with prognosis of patients with breast carcinomas2012 | First Faculty of Medicine, Second Faculty of Medicine
- CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID2019 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové