| Endostatin induces endothelial cell apoptosis M Dhanabal, R Ramchandran, MJF Waterman, H Lu, B Knebelmann, ... Journal of Biological Chemistry 274 (17), 11721-11726, 1999 | 997 | 1999 |
| X-linked Alport syndrome: natural history in 195 families and genotype-phenotype correlations in males JP Jais, B Knebelmann, I Giatras, M De Marchi, G Rizzoni, A Renieri, ... Journal of the American Society of Nephrology 11 (4), 649-657, 2000 | 710 | 2000 |
| X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a “European Community Alport Syndrome Concerted … JP Jais, B Knebelmann, I Giatras, M De Marchi, G Rizzoni, A Renieri, ... Journal of the American Society of Nephrology 14 (10), 2603-2610, 2003 | 583 | 2003 |
| Targeted therapy in patients with PIK3CA-related overgrowth syndrome Q Venot, T Blanc, SH Rabia, L Berteloot, S Ladraa, JP Duong, E Blanc, ... Nature 558 (7711), 540-546, 2018 | 529 | 2018 |
| Lipocalin 2 is essential for chronic kidney disease progression in mice and humans A Viau, K El Karoui, D Laouari, M Burtin, C Nguyen, K Mori, E Pillebout, ... The Journal of clinical investigation 120 (11), 4065-4076, 2010 | 457 | 2010 |
| The von Hippel-Lindau tumor suppressor gene product interacts with Sp1 to repress vascular endothelial growth factor promoter activity D Mukhopadhyay, B Knebelmann, HT Cohen, S Ananth, VP Sukhatme Molecular and cellular biology 17 (9), 5629-5639, 1997 | 429 | 1997 |
| Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy O Gross, C Licht, HJ Anders, B Hoppe, B Beck, B Tönshoff, B Höcker, ... Kidney international 81 (5), 494-501, 2012 | 403 | 2012 |
| Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome A Servais, V Frémeaux-Bacchi, M Lequintrec, R Salomon, J Blouin, ... Journal of medical genetics 44 (3), 193-199, 2007 | 385 | 2007 |
| Antiangiogenic activity of restin, NC10 domain of human collagen XV: comparison to endostatin R Ramchandran, M Dhanabal, R Volk, MJF Waterman, M Segal, H Lu, ... Biochemical and biophysical research communications 255 (3), 735-739, 1999 | 381 | 1999 |
| Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney … RT Gansevoort, M Arici, T Benzing, H Birn, G Capasso, A Covic, ... Nephrology Dialysis Transplantation 31 (3), 337-348, 2016 | 348 | 2016 |
| Anti-CTLA4 antibody–induced lupus nephritis F Fadel, KE Karoui, B Knebelmann New England Journal of Medicine 361 (2), 211-212, 2009 | 338 | 2009 |
| Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases L Heidet, S Decramer, A Pawtowski, V Moriniere, F Bandin, ... Clinical Journal of the American Society of Nephrology 5 (6), 1079-1090, 2010 | 329 | 2010 |
| Cyst infections in patients with autosomal dominant polycystic kidney disease M Salle, JR Zahar, JP Gru, B Knebelmann, F Fakhouri Clinical Journal of the American Society of Nephrology 4 (7), 1183-1189, 2009 | 292 | 2009 |
| Autosomal dominant polycystic kidney disease: the changing face of clinical management ACM Ong, O Devuyst, B Knebelmann, G Walz The Lancet 385 (9981), 1993-2002, 2015 | 291 | 2015 |
| Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ... The American Journal of Human Genetics 93 (5), 915-925, 2013 | 250 | 2013 |
| Steroid-sensitive nephrotic syndrome: from childhood to adulthood F Fakhouri, N Bocquet, P Taupin, C Presne, MF Gagnadoux, P Landais, ... American journal of kidney diseases 41 (3), 550-557, 2003 | 247 | 2003 |
| Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes C Arrondel, N Vodovar, B Knebelmann, JP Gru, MC Gubler, C Antignac, ... Journal of the American Society of Nephrology 13 (1), 65-74, 2002 | 246 | 2002 |
| Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution MC Gubler, B Knebelmann, A Beziau, M Broyer, Y Pirson, F Haddoum, ... Kidney international 47 (4), 1142-1147, 1995 | 221 | 1995 |
| Thrombotic microangiopathy secondary to VEGF pathway inhibition by sunitinib G Bollée, N Patey, G Cazajous, C Robert, JM Goujon, F Fakhouri, ... Nephrology Dialysis Transplantation 24 (2), 682-685, 2009 | 220 | 2009 |
| Rituximab in severe lupus nephritis: early B-cell depletion affects long-term renal outcome C Melander, M Salle, P Trolliet, S Candon, X Belenfant, E Daugas, P Re, ... Clinical Journal of the American Society of Nephrology 4 (3), 579-587, 2009 | 215 | 2009 |
Laurence HeidetAPHPVerified email at aphp.fr
