- The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease2005 | Second Faculty of Medicine
- Mutations in CBL occur frequently in juvenile myelomonocytic leukemia2009 | Second Faculty of Medicine
- Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia2015 | Second Faculty of Medicine
- Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases2019 | Third Faculty of Medicine
- Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia2010 | Second Faculty of Medicine
- Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome2014 | Second Faculty of Medicine
- Delece 18p v mozaice u pacienta s fenotypem připomínajícím syndrom Noonanové2016 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Mathematics and Physics
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | First Faculty of Medicine
- Somatické mutace u myelodysplastického syndromu a jejich klinické využití2016 | First Faculty of Medicine
- Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia2008 | Second Faculty of Medicine
- High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH2019 | Second Faculty of Medicine
- Second allogeneic stem cell transplantation can rescue a significant proportion of patients with JMML relapsing after first allograft2023 | Second Faculty of Medicine
- RASA4 undergoes DNA hypermethylation in resistant juvenile myelomonocytic leukemia2014 | Second Faculty of Medicine
- RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia2017 | Second Faculty of Medicine
- Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup2024 | Second Faculty of Medicine
- Evaluation of gene expression signatures predictive of cytogenetic and molecular subtypes of pediatric acute myeloid leukemia2011 | Second Faculty of Medicine
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | Second Faculty of Medicine
- Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?2023 | Second Faculty of Medicine
