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 | 2425 | 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 | 637 | 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 | 572 | 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 | 428 | 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 | 425 | 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 | 399 | 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 | 385 | 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 | 379 | 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 | 361 | 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 | 319 | 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: JASN 21 (3), 507, 2010 | 302 | 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: JASN 23 (12), 2051, 2012 | 274 | 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 | 268 | 2003 |
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 | 247 | 2001 |
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 | 241 | 2012 |
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: CJASN 6 (6), 1308, 2011 | 228 | 2011 |
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 | 220 | 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 | 214 | 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 | 207 | 1999 |
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis CM Louie, G Caridi, VS Lopes, F Brancati, A Kispert, MA Lancaster, ... Nature genetics 42 (2), 175-180, 2010 | 200 | 2010 |