- CNVs in patients with epilepsy - Czech experiencePublication without faculty affiliation
- Genetická diagnostika epilepsií ve FN Motol aneb význam detekce CNVs pomocí metody array CGH2019 | Second 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
- Prognostic Factors of Early Morphological Response to Treatment with Ranibizumab in Patients with Wet Age-Related Macular Degeneration2015 | Faculty of Medicine in Hradec Králové
- Base of mechanism of action in anticonvulsant? Variant analysis of CNV gen GSK3-beta in bipolar patients2008 | First Faculty of Medicine
- Ranibizumab for the treatment of choroidal neovascularization due to cause other than age related macular degeneration2019 | Faculty of Medicine in Hradec Králové
- Stereotactic radiotherapy for neovascular age-related macular degeneration: year 2 results of the INTREPID study2015 | Publication without faculty affiliation
- STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population2018 | Second Faculty of Medicine
- Asymmetric response to ranibizumab in mixed choroidal neovascularization in a neovascular age-related macular degeneration diagnosed on OCT angiography - case report2021 | Third Faculty of Medicine
- RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data2022 | Second Faculty of Medicine
- Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders2014 | First Faculty of Medicine
- Natural history of KBG syndrome in a large European cohort2022 | Second Faculty of Medicine
- Stereotactic radiotherapy for wet age-related macular degeneration (INTREPID): influence of baseline characteristics on clinical response2015 | Publication without faculty affiliation
- Two-year results of a combined regimen of aflibercept treatment in three types of choroidal neovascular membrane in the wet form of age-related macular degeneration: Real-life evidence in the Czech Republic2021 | Faculty of Medicine in Hradec Králové, Third Faculty of Medicine
- Aflibercept for Vascularised Serous Pigment Epithelial Detachment: One-Year Anatomical and Functional Results2020 | First Faculty of Medicine
- Application of SNP array method in pranatal diagnosis2011 | First Faculty of Medicine
- Monozygotic Twins with 17q21.31 Microdeletion Syndrome2014 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Brolucizumab - A New Player In The Field Of Anti-VEGF Therapy Of Neovascular Age-Related Macular Degeneration. A Review2022 | First Faculty of Medicine
- Interferon signaling restrains renal cell carcinoma heterogeneity2023 | Second Faculty of Medicine
- Single-cell analysis of circulating tumor cells2019 | Faculty of Medicine in Pilsen
- Expanding the morphologic spectrum of chromophobe renal cell carcinoma: A study of 8 cases with papillary architecture2020 | Faculty of Medicine in Pilsen
- Complete Ascertainment of Intragenic Copy Number Mutations (CNMs) in the CFTR Gene and its Implications for CNM Formation at Other Autosomal Loci2010 | Second Faculty of Medicine
- Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?2012 | Faculty of Medicine in Hradec Králové
- Diagnostic implications of genetic copy number variation in epilepsy plus2019 | Second Faculty of Medicine
- Results of transpupillary thermotherapy in pacients with ARMD 6 months after treatment (pilot study)2006 | First Faculty of Medicine
- Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects2020 | Second Faculty of Medicine
- Large Copy-Number Variations in Patients With Statin-Associated Myopathy Affecting Statin Myopathy-Related Loci2016 | First Faculty of Medicine, Central Library of Charles University
- Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene2019 | Second Faculty of Medicine, Central Library of Charles University
- Clinically relevant copy-number variants in exome sequencing data of patients with dystonia2021 | First Faculty of Medicine
- Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals2023 | Second Faculty of Medicine