Jean‐Pierre Grünfeld

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Sandrine Barbaux, Patrick Niaudet, Marie-Claire Gübler et al. · Nature Genetics · 1997 · 748 citations

Life Sciences, Genetics, Molecular Genetics +6

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Aude Servais, Laure‐Hélène Noël, Lubka T. Roumenina et al. · Kidney International · 2012 · 567 citations

Medicine, Immunology, Nephrology +17

The risk of developing end-stage renal disease in patients with type 2 diabetes and nephropathy: The RENAAL Study

William F. Keane, Barry M. Brenner, Dick de Zeeuw et al. · Kidney International · 2003 · 546 citations

Medicine, Endocrinology, Nephrology +11

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

Octogenarians Reaching End-Stage Renal Disease

Dominique Joly, Dany Anglicheau, Corinne Alberti et al. · Journal of the American Society of Nephrology · 2003 · 309 citations

Medicine, Internal Medicine, Nephrology +16