- Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours2014 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Application of SNP array method in pranatal diagnosis2011 | First Faculty of Medicine
- Molecular cytogenetic analysis of chromosomal aberrations in cells of low grade gliomas and its contribution for tumour classification2014 | First Faculty of Medicine
- A rational approach to the CNS tumors diagnostics2022 | Second Faculty of Medicine
- Methylation pattern in the diagnosis and prognosis of brain cancer2021 | Second Faculty of Medicine
- SNP Array and Phenotype Correlation Shows That FLI1 Deletion Per se is Not Responsible for Thrombocytopenia Development in Jacobsen Syndrome2012 | Publication without faculty affiliation
- From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype2012 | First Faculty of Medicine
- A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications2014 | Second Faculty of Medicine
- An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement2014 | First Faculty of Medicine, Second Faculty of Medicine
- Diagnostic implications of genetic copy number variation in epilepsy plus2019 | Second Faculty of Medicine
- Unusual case of inflammatory rhabdomyoblastic tumor in a pediatric patient2023 | Second Faculty of Medicine, Central Library of Charles University
- A patient with de novo 0.45Mb deletion of 2p16.1: The role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome2013 | Second Faculty of Medicine
- Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p152013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Rare case of patient with DiGeorge syndrome and limbs anomalies: the benefit of SNP microarray analysis?2015 | Second Faculty of Medicine
- DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family2012 | Second Faculty of Medicine, Central Library of Charles University
- Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 32016 | First Faculty of Medicine, Second Faculty of Medicine
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | First Faculty of Medicine
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | Second Faculty of Medicine
- Early Diagnosis of the Chromosomal Deletion 5q14.2-q21.3 in a Preterm Newborn: Case Report2013 | First Faculty of Medicine
- Phenotypic Variability in a Large Czech Family with a Dynamin 2-Associated Charcot-Marie-Tooth Neuropathy2011 | Second Faculty of Medicine
- Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC22016 | First Faculty of Medicine
- The use of museum skins for genomic analyses of temporal genetic diversity in wild species2019 | Faculty of Science
- Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis2016 | First Faculty of Medicine, Central Library of Charles University
- Genomic analysis of spermatocytic tumors demonstrates recurrent molecular alterations in cases with malignant clinical behavior2024 | Faculty of Medicine in Pilsen