- Familial gastrointestinal stromal tumor with germ line mutation of the juxtamembrane domain of the KIT gene observed in relatively young women2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Detection of germ line mutations in the BRCA1 gene by the protein truncation test.1999 | Faculty of Physical Education and Sport
- Detection of germ-line mutation in the BRCA 1 gene by the protein truncation test.1999 | Faculty of Physical Education and Sport
- Coexistence of gain-of-function JAK2 germ line mutations with JAK2V617F in polycythemia vera2016 | Faculty of Science
- Coexistence of gain-of-function JAK2 germ line mutations with JAK2(V617F) in polycythemia vera2016 | First Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Central Library of Charles University
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | Second Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | Faculty of Medicine in Hradec Králové
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg2005 | First Faculty of Medicine
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Exon 5 of the RET proto-oncogene: A newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321 Arg2005 | First Faculty of Medicine
- A method for detection of germinal mutations in the p53 tumor suppressor gene1996 | Second Faculty of Medicine
- Bilateral renal tumors; conventional clear cell carcinoma and contralateral t(6;11)/t(X;17)-like tumor Histomorphologic, immunohistochemical, ultrastructural and molecular genetic studies including the report of a novel mutation in the VHL gene2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Polymorphic variants involved in methylation regulation: a strategy to discover risk loci for pancreatic ductal adenocarcinoma2023 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
- Alterations of CHEK2 forkhead-associated domain increase the risk of Hodgkin lymphoma2011 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- The CHEK2 gene I157T mutation and other alterations in its proximity increase the risk of sporadic colorectal cancer in the Czech population2009 | First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- Novel germline mutations in Czech FAP familiesPublication without faculty affiliation
- Tumor suppressor genes1997 | Second Faculty of Medicine
- Screening of six risk exons of the RET proto-oncogene in families with medullary thyroid carcinoma in the Czech Republic2004 | Second Faculty of Medicine
- Insight into the pathogenesis of sporadic basal cell carcinoma2004 | Second Faculty of Medicine
- Birt-Hogg-Dubé syndrome2012 | Second Faculty of Medicine
- Testing of mutations in BRCA1 and BECA2 genes in tumor tissues - possibilities and limitations2016 | Faculty of Medicine in Hradec Králové
- Whole-body magnetic resonance imaging in pediatric oncology - recommendations by the Oncology Task Force of the ESPR2020 | Second Faculty of Medicine
- Clinical findings with implications for genetic testing in families with clustering of colorectal cancer1998 | Second Faculty of Medicine
- Hereditary thyroid carcinoma and its molecular diagnostics2014 | Central Library of Charles University
- Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer2015 | First Faculty of Medicine
- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation2016 | Second Faculty of Medicine
- Genetic testing of leiomyoma tissue in women younger than 30 years old might provide an effective screening approach for the hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC)2015 | Faculty of Medicine in Pilsen