Publications
- A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus2021 | First Faculty of Medicine
- Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders2021 | First Faculty of Medicine
- Hereditary hyperferritinemia-cataract syndrome in three Czech families: molecular genetic testing and clinical implications2020 | First Faculty of Medicine, Second Faculty of Medicine
- Congenital fibrosis of the extraocular muscles in a Czech family and its molecular genetic cause2019 | First Faculty of Medicine, Second Faculty of Medicine
- Replication of SNP associations with keratoconus in a Czech cohort2017 | First Faculty of Medicine, Second Faculty of Medicine
- Early Detection of Bilateral Cataracts In Utero May Represent a Manifestation of Severe Congenital Disease2016 | First Faculty of Medicine, Second Faculty of Medicine
- Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to indentifying the disease-causing variants2016 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants2016 | First Faculty of Medicine
- Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy2024 | First Faculty of Medicine, Second Faculty of Medicine
- Axenfeld-Rieger syndrome: more than meets the eye2023 | First Faculty of Medicine, Second Faculty of Medicine
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