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Mgr. Viktor Stránecký Ph.D.
Academic staff at First Faculty of Medicine
88 publications
Publications
publication
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4
2018 |
First Faculty of Medicine, Third Faculty of Medicine
publication
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
2018 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report
2017 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Large Copy-Number Variations in Patients With Statin-Associated Myopathy Affecting Statin Myopathy-Related Loci
2016 |
First Faculty of Medicine, Central Library of Charles University
publication
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
2016 |
First Faculty of Medicine
publication
A patient showing features of both SBBYSS and GPS supports the concept of a KAT6B-related disease spectrum, with mutations in mid-exon 18 possibly leading to combined phenotypes
2015 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump
2007 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Spontaneous nonsense mutation in the tuftelin 1 gene is associated with abnormal hair appearance and amelioration of glucose and lipid metabolism in the rat
2024 |
First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
publication
Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy
2024 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease
2023 |
First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
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