Bernd Höppe

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

John A. Sayer, Edgar A. Otto, John F. O’Toole et al. · Nature Genetics · 2006 · 572 citations

Life Sciences, Genetics, Molecular Biology +6

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

Christoph Licht, Hans‐Joachim Anders, Bernd Höppe et al. · Kidney International · 2011 · 363 citations · Full text

Pharmacy, Nephrology, Pharmacotherapy +13

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Pierre Cochat, Sally A. Hulton, Cécile Acquaviva et al. · Nephrology Dialysis Transplantation · 2012 · 335 citations · Full text

Medicine, Biochemistry, Nephrology +17

Dent Disease with Mutations in OCRL1

R R Hoopes, Antony E. Shrimpton, Stephen J. Knohl et al. · The American Journal of Human Genetics · 2005 · 333 citations · Full text

Dentistry, Oral Biology, Oral Diagnosis +1

Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

Peter F. Zipfel, Matthew Edey, Stefan Heinen et al. · PLoS Genetics · 2007 · 324 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17