| Tolvaptan in patients with autosomal dominant polycystic kidney disease VE Torres, AB Chapman, O Devuyst, RT Gansevoort, JJ Grantham, ... New England Journal of Medicine 367 (25), 2407-2418, 2012 | 1809 | 2012 |
| Evolving importance of kidney disease: from subspecialty to global health burden KU Eckardt, J Coresh, O Devuyst, RJ Johnson, A Köttgen, AS Levey, ... The Lancet 382 (9887), 158-169, 2013 | 1426 | 2013 |
| Genome-wide association analyses identify 18 new loci associated with serum urate concentrations A Köttgen, E Albrecht, A Teumer, V Vitart, J Krumsiek, C Hundertmark, ... Nature genetics 45 (2), 145-154, 2013 | 929 | 2013 |
| Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression M Trudu, S Janas, C Lanzani, H Debaix, C Schaeffer, M Ikehata, L Citterio, ... Nature medicine 19 (12), 1655-1660, 2013 | 382 | 2013 |
| NHE2 and NHE3 are human and rabbit intestinal brush-border proteins WA Hoogerwerf, SC Tsao, O Devuyst, SA Levine, CH Yun, JW Yip, ... American Journal of Physiology-Gastrointestinal and Liver Physiology 270 (1 …, 1996 | 358 | 1996 |
| The pathophysiology of the peritoneal membrane O Devuyst, PJ Margetts, N Topley Journal of the American Society of Nephrology 21 (7), 1077-1085, 2010 | 348 | 2010 |
| Cubilin is essential for albumin reabsorption in the renal proximal tubule S Amsellem, J Gburek, G Hamard, R Nielsen, TE Willnow, O Devuyst, ... Journal of the American Society of Nephrology 21 (11), 1859-1867, 2010 | 347 | 2010 |
| Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules EI Christensen, O Devuyst, G Dom, R Nielsen, P Van Der Smissen, ... Proceedings of the National Academy of Sciences 100 (14), 8472-8477, 2003 | 347 | 2003 |
| The rediscovery of uromodulin (Tamm–Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease L Rampoldi, F Scolari, A Amoroso, GM Ghiggeri, O Devuyst Kidney international 80 (4), 338-347, 2011 | 344 | 2011 |
| Mice lacking renal chloride channel, CLC-5, are a model for Dent’s disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis SS Wang, O Devuyst, PJ Courtoy, XT Wang, H Wang, Y Wang, ... Human Molecular Genetics 9 (20), 2937-2945, 2000 | 344 | 2000 |
| Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease O Devuyst, PT Christie, PJ Courtoy, R Beauwens, RV Thakker Human molecular genetics 8 (2), 247-257, 1999 | 344 | 1999 |
| Mutations in SEC63 cause autosomal dominant polycystic liver disease S Davila, L Furu, AG Gharavi, X Tian, T Onoe, Q Qian, A Li, Y Cai, ... Nature genetics 36 (6), 575-577, 2004 | 343 | 2004 |
| Genetic loci influencing kidney function and chronic kidney disease JC Chambers, W Zhang, GM Lord, P van der Harst, DA Lawlor, JS Sehmi, ... Nature genetics 42 (5), 373-375, 2010 | 337 | 2010 |
| Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival—an analysis of data from the ERA-EDTA Registry EM Spithoven, A Kramer, E Meijer, B Orskov, C Wanner, JM Abad, ... Nephrology Dialysis Transplantation 29 (suppl 4), iv15-iv25, 2014 | 286 | 2014 |
| CUBN is a gene locus for albuminuria CA Böger, MH Chen, A Tin, M Olden, A Köttgen, IH De Boer, ... Journal of the American Society of Nephrology 22 (3), 555-570, 2011 | 285 | 2011 |
| DentLs disease O Devuyst, RV Thakker | 278 | 2010 |
| Spectrum of mutations in Gitelman syndrome R Vargas-Poussou, K Dahan, D Kahila, A Venisse, E Riveira-Munoz, ... Journal of the American Society of Nephrology 22 (4), 693-703, 2011 | 271 | 2011 |
| Vascular proliferation and enhanced expression of endothelial nitric oxide synthase in human peritoneum exposed to long-term peritoneal dialysis S Combet, T Miyata, P Moulin, D Pouthier, E Goffin, O Devuyst Journal of the American Society of Nephrology 11 (4), 717-728, 2000 | 271 | 2000 |
| A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin K Dahan, O Devuyst, M Smaers, D Vertommen, G Loute, JM Poux, B Viron, ... Journal of the American Society of Nephrology 14 (11), 2883-2893, 2003 | 259 | 2003 |
| Rare inherited kidney diseases: challenges, opportunities, and perspectives O Devuyst, NVAM Knoers, G Remuzzi, F Schaefer The Lancet 383 (9931), 1844-1859, 2014 | 246 | 2014 |
