- Congenital muscular dystrophies2012 | Second Faculty of Medicine
- The contribution to the understanding of the immunogenetic background of the embryo implantation: The detection of naturally appearing cytokine gene mutations2005 | Central Library of Charles University, Faculty of Medicine in Pilsen
- Leukemia inhibitory factor gene mutations in the population of infertile women are not restricted to nulligravid patients2006 | Central Library of Charles University
- Etiology of Osteogenesis Imperfecta: COL1A1 Gene Mutations in Czech PatientsPublication without faculty affiliation
- Congenital myopathies +12012 | Second Faculty of Medicine
- Up-to-date insight into significance of gene mutation for androgenic receptor in the pathogenesis of prostate cancer2004 | Third Faculty of Medicine
- Prevalence of heterozygous HFE gene mutation in chronic liver disease2007 | First Faculty of Medicine, Third Faculty of Medicine
- Plasmapheresis-induced Clinical Improvement in a Patient with Steroid-Resitant Nephrotic Syndrome Due to Podocin (NPHS2) Gene Mutation2010 | Second Faculty of Medicine
- Collagen type I gene mutations of alpha 1 chain (Col1A1) in Czech patients with Osteogenesis Imperfecta Syndrome2003 | Faculty of Science
- New fibrillin gene mutation - possible cause of ascending aortic dilation in patients with aortic valve disease: Preliminary results2009 | First Faculty of Medicine, Third Faculty of Medicine
- Comparative study of TERT gene mutation analysis on voided liquid-based urine cytology and paraffin-embedded tumorous tissue2016 | Central Library of Charles University, Faculty of Medicine in Pilsen
- Clinical characteristics of three Czech families with catecholaminergic polymorphic ventricular tachycardia and pilot results of RyR2 gene mutation analysis2010 | First Faculty of Medicine, Faculty of Physical Education and Sport
- HFE gene mutations in patients with rheumatic diseases2005 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Physical Education and Sport
- TP53 gene mutations are rare in nondysplastic Barrett's esophagus2006 | Second Faculty of Medicine
- Gene mutation causing asthma2013 | First Faculty of Medicine
- Seven Novel Acid Sphingomyelinase Gene Mutations in Niemann-Pick Type A and B Patients2003 | First Faculty of Medicine
- Seven Novel Acid Sphingomyelinase Gene Mutations in Niemann-Pick Type A and B Patients2003 | Faculty of Physical Education and Sport
- Arginin519 -cystein COL2A1 gene mutation in czech osteoarthritis population.2005 | Faculty of Science
- The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy1991 | Second Faculty of Medicine
- Etiology of Osteogenesis Imperfecta: COL1A1 Gene Mutations in Czech Patients2003 | First Faculty of Medicine, Faculty of Mathematics and Physics
- Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias2015 | Second Faculty of Medicine
- Leigh Disease: Biochemical and Molecular Studies in Seven Children with SURF1 Gene MutationsPublication without faculty affiliation
- TP53 gene mutation in Barrett´s exophagusPublication without faculty affiliation
- The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome2006 | Publication without faculty affiliation
- Gastrointestinal stromal tumor of the pancreas: case report with documentation of KIT gene mutation2005 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Incidence of mitochondrial cytochrome c-oxidase gene mutations in patients with acquired idiopathic sideroblastic anemiaPublication without faculty affiliation
- Iron overload and HFE gene mutations in Czech patients with chronic liver diseases2012 | Third Faculty of Medicine
- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency +12009 | Faculty of Medicine in Hradec Králové