- Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene2010 | First Faculty of Medicine
- A novel high-resolution chipCE assay for rapid detection of EGFR gene mutations and amplifications in lung cancer therapy by a combination of fragment analysis, denaturing CE and MLPA2010 | Faculty of Science
- Genetics of spinal muscular atrophy2020 | Second Faculty of Medicine
- Aberrant methylation of tumour suppressor genes WT1, GATA5 and PAX5 in hepatocellular carcinoma2016 | Faculty of Medicine in Hradec Králové
- A Multilocus Technique for Risk Evaluation of Patients with Neuroblastoma2011 | Publication without faculty affiliation
- Changes in MYCN expression in human neuroblastoma cell lines following cisplatin treatment may not be related to MYCN copy numbers2013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers2016 | First Faculty of Medicine, Central Library of Charles University
- Localized mosaic neurofibromatosis type 12022 | Second Faculty of Medicine
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | Central Library of Charles University
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | Faculty of Medicine in Pilsen
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Giant angiofibromas in tuberous sclerosis complex: A possible role for localized lymphedema in their pathogenesis2012 | Faculty of Medicine in Pilsen, Second Faculty of Medicine
- Oncogene amplification and expression in pediatric solid tumors1998 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia2009 | Second Faculty of Medicine
- SMARCB1/INI1-deficient sinonasal carcinoma shows methylation of RASSF1 gene: A clinicopathological, immunohistochemical and molecular genetic study of a recently described entity2017 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population2011 | First Faculty of Medicine
- Lack of large intragenic rearrangements in dihydropyrimidine dehydrogenase (DPYD) gene in fluoropyrimidine-treated patients with high-grade toxicity.2009 | First Faculty of Medicine
- Promoter Methylation of GATA4, WIF1, NTRK1 and Other Selected Tumour Suppressor Genes in Ovarian Cancer2013 | Faculty of Medicine in Hradec Králové
- Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the czech population2011 | Faculty of Science, First Faculty of Medicine
- Methylation analysis of tumour suppressor genes in ovarian cancer using MS-MLPA2012 | Faculty of Medicine in Hradec Králové
- Mutations in the LMNA gene do not cause axonal CMT in Czech patients2009 | Second Faculty of Medicine
- Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients2013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 12007 | Second Faculty of Medicine
- Utilization of MLPA to detection of genetic changes in neuroblastoma2008 | Second Faculty of Medicine
- Epidermal Growth Factor Receptor Gene Amplification in Patients with Advanced-stage NSCLC2016 | Faculty of Science, Faculty of Medicine in Pilsen
- Methylation analysis of tumor suppressor genes in endometroid carcinoma of endometrium using MS-MLPA2013 | Faculty of Medicine in Hradec Králové
- A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 172007 | Second Faculty of Medicine
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | Second Faculty of Medicine
- Application of denaturing capillary electrophoresis for the detection of prognostic mutations in isocitrate dehydrogenase 1 and isocitrate dehydrogenase 2 genes in brain tumors2018 | Faculty of Science, First Faculty of Medicine