Steffen Neuber
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, Renal and related cancers, Biomedical Research and Pathophysiology, Renal cell carcinoma treatment, Parathyroid Disorders and Treatments
Most-Cited Works
- → Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease(2017)199 cited
- → An Efficient and Comprehensive Strategy for Genetic Diagnostics of Polycystic Kidney Disease(2015)73 cited
- → Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes(2020)45 cited
- → Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting(2019)22 cited
- → Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assembly(2021)20 cited
- → Mutations and variants identified in other genes for cystic and polycystic kidney disease.(2015)
- → FP049AN EFFICIENT AND COMPREHENSIVE STRATEGY FOR GENETIC DIAGNOSTICS OF POLYCYSTIC KIDNEY DISEASE(2015)
- → Posttranslationale Modifikation und subzelluläre Verteilung von Plakophilin 3 in normalen und Tumorzellen(2013)