| Blue silver: a very sensitive colloidal Coomassie G‐250 staining for proteome analysis G Candiano, M Bruschi, L Musante, L Santucci, GM Ghiggeri, ... Electrophoresis 25 (9), 1327-1333, 2004 | 2523 | 2004 |
| Genome-wide association study identifies susceptibility loci for IgA nephropathy AG Gharavi, K Kiryluk, M Choi, Y Li, P Hou, J Xie, S Sanna-Cherchi, ... Nature genetics 43 (4), 321-327, 2011 | 700 | 2011 |
| Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens K Kiryluk, Y Li, F Scolari, S Sanna-Cherchi, M Choi, M Verbitsky, D Fasel, ... Nature genetics 46 (11), 1187-1196, 2014 | 670 | 2014 |
| Renal outcome in patients with congenital anomalies of the kidney and urinary tract S Sanna-Cherchi, P Ravani, V Corbani, S Parodi, R Haupt, G Piaggio, ... Kidney international 76 (5), 528-533, 2009 | 469 | 2009 |
| IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 AG Gharavi, Y Yan, F Scolari, FP Schena, GM Frasca, GM Ghiggeri, ... Nature genetics 26 (3), 354-357, 2000 | 452 | 2000 |
| Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study S Weber, V Moriniere, T Knüppel, M Charbit, J Dusek, GM Ghiggeri, ... Journal of the American Society of Nephrology 17 (10), 2864-2870, 2006 | 426 | 2006 |
| MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single … M Seri, A Pecci, F Di Bari, R Cusano, M Savino, E Panza, A Nigro, P Noris, ... Medicine 82 (3), 203-215, 2003 | 415 | 2003 |
| Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, L Nigro, ... Nature genetics 26 (1), 103-105, 2000 | 404 | 2000 |
| COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement F Diomedi-Camassei, S Di Giandomenico, FM Santorelli, G Caridi, ... Journal of the American Society of Nephrology 18 (10), 2773-2780, 2007 | 377 | 2007 |
| 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 | 338 | 2011 |
| Autoimmunity in membranous nephropathy targets aldose reductase and SOD2 M Prunotto, ML Carnevali, G Candiano, C Murtas, M Bruschi, E Corradini, ... Journal of the American Society of Nephrology 21 (3), 507-519, 2010 | 313 | 2010 |
| Circulating suPAR in two cohorts of primary FSGS C Wei, H Trachtman, J Li, C Dong, AL Friedman, JJ Gassman, ... Journal of the American Society of Nephrology 23 (12), 2051-2059, 2012 | 289 | 2012 |
| Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics L Rampoldi, G Caridi, D Santon, F Boaretto, I Bernascone, G Lamorte, ... Human molecular genetics 12 (24), 3369-3384, 2003 | 277 | 2003 |
| Copy-number disorders are a common cause of congenital kidney malformations S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ... The American Journal of Human Genetics 91 (6), 987-997, 2012 | 256 | 2012 |
| Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis G Caridi, R Bertelli, A Carrea, M Di Duca, P Catarsi, M Artero, M Carraro, ... Journal of the American Society of Nephrology 12 (12), 2742-2746, 2001 | 254 | 2001 |
| Short-term effects of rituximab in children with steroid-and calcineurin-dependent nephrotic syndrome: a randomized controlled trial P Ravani, A Magnasco, A Edefonti, L Murer, R Rossi, L Ghio, E Benetti, ... Clinical Journal of the American Society of Nephrology 6 (6), 1308-1315, 2011 | 245 | 2011 |
| Long-term outcome of steroid-resistant nephrotic syndrome in children A Trautmann, S Schnaidt, BS Lipska-Ziętkiewicz, M Bodria, F Ozaltin, ... Journal of the American Society of Nephrology 28 (10), 3055-3065, 2017 | 240 | 2017 |
| Broadening the spectrum of diseases related to podocin mutations G Caridi, R Bertelli, M Di Duca, M Dagnino, F Emma, AO Muda, F Scolari, ... Journal of the American Society of Nephrology 14 (5), 1278-1286, 2003 | 234 | 2003 |
| SIX2 and BMP4 mutations associate with anomalous kidney development S Weber, JC Taylor, P Winyard, KF Baker, J Sullivan-Brown, R Schild, ... Journal of the American Society of Nephrology 19 (5), 891-903, 2008 | 231 | 2008 |
| Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children R Dall'Amico, GM Ghiggeri, M Carraro, M Artero, L Ghio, E Zamorani, ... American Journal of Kidney Diseases 34 (6), 1048-1055, 1999 | 224 | 1999 |
