- Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability2023 | First Faculty of Medicine
- Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability2010 | Second Faculty of Medicine
- Bioinformatic analysis of miRNAs targeting the key nuclear receptors regulating CYP3A4 gene expression: The challenge of the CYP3A4 "missing heritability" enigma2015 | Faculty of Pharmacy in Hradec Králové
- Effect of Occupational Exposures on Lung Cancer Susceptibility: A Study of Gene-Environment Interaction Analysis2015 | First Faculty of Medicine
- Central European Group on Genetics of Movement Disorders2023 | Second Faculty of Medicine, First Faculty of Medicine
- Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-62022 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics2020 | First Faculty of Medicine