Kateřina Hodaňová
Charles University(CZ)General University Hospital in Prague(CZ)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Lysosomal Storage Disorders Research, Ion Transport and Channel Regulation, Kidney Stones and Urolithiasis Treatments, Glycosylation and Glycoproteins Research
Most-Cited Works
- → 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
- → Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1(2020)137 cited
- → Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome(2006)125 cited
- → Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness(2015)94 cited