Publications
- Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?2017 | Second Faculty of Medicine
- Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme2016 | Second Faculty of Medicine
- Frameshift mutations in the insulin gene leading to prolonged molecule of insulin in two families with Maturity-Onset Diabetes of the Young2015 | Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Two Independent Genetic Factors Responsible for the Associations of the IBD5 Locus with Crohn's Disease in the Czech Population2011 | Second Faculty of Medicine
- The CTLA4 variants may interact with the IL23R-and NOD2-conferred risk in development of Crohn's disease2010 | Second Faculty of Medicine
- Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs2008 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | Second Faculty of Medicine
- SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary2024 | Second Faculty of Medicine
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine
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