- The most frequent methods used for DNA methylation analysis2011 | Faculty of Medicine in Hradec Králové
- MLPA analysis in children with mental retardationPublication without faculty affiliation
- Ověření nálezu změn metylace z analýzy MS-MLPA metodou přímé Sangerovy sekvenace po bisulfitové konverzi – optimalizace pro diagnostiku2023 | Second Faculty of Medicine
- Ověření nálezu změn metylace z analýzy MS-MLPA metodou přímé Sangerovy sekvenace po bisulfitové konverzi - využití v klinické laboratoři, výhody a limitace metody2022 | Second Faculty of Medicine
- Molecular pathological profiling of selected tumors of the central nervous system using the MLPA method2022 | Second Faculty of Medicine
- Methylation analysis of tumour suppressor genes in ovarian cancer using MS-MLPA2012 | Faculty of Medicine in Hradec Králové
- Low frequency of MLL-partial tandem duplications in paediatric acute myeloid leukaemia using MLPA as a novel DNA screenings technique2010 | Second Faculty of Medicine
- Methylation analysis of tumor suppressor genes in endometroid carcinoma of endometrium using MS-MLPA2013 | Faculty of Medicine in Hradec Králové
- Utilization of MLPA to detection of genetic changes in neuroblastoma2008 | Second Faculty of Medicine
- The MLPA Metod in diagnostic of SHOX gene and PAR1 deletionsPublication without faculty affiliation
- Alterations of CHEK2 gene in non-Hodgkin lymphoma patientsPublication without faculty affiliation
- 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
- Characterisation of ATM mutations in Slavic Ataxia telangiectasia patients2011 | First Faculty of Medicine, Second Faculty of Medicine
- Characterisation of ATM Mutations in Slavic Ataxia Telangiectasia Patients2011 | Second Faculty of Medicine
- Molecular cytogenetic characterization of pheochromocytoma2010 | Faculty of Science, Faculty of Mathematics and Physics, Faculty of Physical Education and Sport, First Faculty of Medicine, Second Faculty of Medicine
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Lack of large intragenic rearrangements in dihydropyrimidine dehydrogenase (DPYD) gene in fluoropyrimidine-treated patients with high-grade toxicity.2009 | First Faculty of Medicine
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | Second Faculty of Medicine
- Spectrum and Frequency of SLC26A4 Mutations Among Czech Patients with Early Hearing Loss with and without Enlarged Vestibular Aqueduct (EVA)2010 | Second Faculty of Medicine, Central Library of Charles University
- Importance of Tumour Suppressor Genes Methylation in Sinonasal Carcinomas2016 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- A rational approach to the CNS tumors diagnostics2022 | Second Faculty of Medicine
- Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 12007 | Second 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 Medicine in Pilsen
- 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 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease2014 | 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
- Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring2016 | Faculty of Physical Education and Sport, First Faculty of Medicine, Second Faculty of Medicine, 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
- Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population2011 | First Faculty of Medicine