- Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability2023 | 1. lékařská fakulta
- Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability2010 | 2. lékařská fakulta
- Bioinformatic analysis of miRNAs targeting the key nuclear receptors regulating CYP3A4 gene expression: The challenge of the CYP3A4 "missing heritability" enigma2015 | Farmaceutická fakulta v Hradci Králové
- Effect of Occupational Exposures on Lung Cancer Susceptibility: A Study of Gene-Environment Interaction Analysis2015 | 1. lékařská fakulta
- Central European Group on Genetics of Movement Disorders2023 | 2. lékařská fakulta, 1. lékařská fakulta
- Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-62022 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics2020 | 1. lékařská fakulta