Viktor Stránecký
Charles University(CZ)General University Hospital in Prague(CZ)
Publications by Year
Research Areas
BRCA gene mutations in cancer, Genomics and Rare Diseases, Mitochondrial Function and Pathology, RNA modifications and cancer, Cellular transport and secretion
Most-Cited Works
- → Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver(2012)381 cited
- → Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis(2011)261 cited
- → TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy(2008)197 cited
- → Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure(2009)163 cited
- → Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia(2016)155 cited
- → Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation(2014)139 cited