| 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 | 636 | 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 | 454 | 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 | 443 | 2000 |
| 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 | 400 | 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 | 373 | 2007 |
| 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 | 276 | 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 | 252 | 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 | 251 | 2001 |
| 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 | 233 | 2003 |
| 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 | 206 | 2010 |
| Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin R Bertelli, F Ginevri, G Caridi, M Dagnino, S Sandrini, M Di Duca, F Emma, ... American Journal of Kidney Diseases 41 (6), 1314-1321, 2003 | 194 | 2003 |
| Whole-exome sequencing in adults with chronic kidney disease: a pilot study S Lata, M Marasa, Y Li, DA Fasel, E Groopman, V Jobanputra, H Rasouly, ... Annals of internal medicine 168 (2), 100-109, 2018 | 193 | 2018 |
| Genetic approaches to human renal agenesis/hypoplasia and dysplasia S Sanna-Cherchi, G Caridi, PL Weng, F Scolari, F Perfumo, AG Gharavi, ... Pediatric nephrology 22, 1675-1684, 2007 | 174 | 2007 |
| Uromodulin storage diseases: clinical aspects and mechanisms F Scolari, G Caridi, L Rampoldi, R Tardanico, C Izzi, D Pirulli, A Amoroso, ... American journal of kidney diseases 44 (6), 987-999, 2004 | 164 | 2004 |
| Genotype–phenotype associations in WT1 glomerulopathy BS Lipska, B Ranchin, P Iatropoulos, J Gellermann, A Melk, F Ozaltin, ... Kidney international 85 (5), 1169-1178, 2014 | 160 | 2014 |
| NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms G Caridi, F Perfumo, GM Ghiggeri Pediatric research 57 (7), 54-61, 2005 | 155 | 2005 |
| CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS) M Gigante, P Pontrelli, E Montemurno, L Roca, F Aucella, R Penza, ... Nephrology Dialysis Transplantation 24 (6), 1858-1864, 2009 | 153 | 2009 |
| Mutations in DSTYK and Dominant Urinary Tract Malformations S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ... New England Journal of Medicine 369 (7), 621-629, 2013 | 149 | 2013 |
| Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor–dependent idiopathic nephrotic syndrome P Ravani, A Ponticelli, C Siciliano, A Fornoni, A Magnasco, F Sica, ... Kidney international 84 (5), 1025-1033, 2013 | 142 | 2013 |
| Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome) GM Ghiggeri, G Caridi, U Magrini, A Sessa, A Savoia, M Seri, A Pecci, ... American Journal of Kidney Diseases 41 (1), 95-104, 2003 | 129 | 2003 |
Gian Marco GhiggeriU.O.C. Nefrologia, Dialisi e Trapianto, Istituto Giannina Gaslini在 ospedale-gaslini.ge.it 的电子邮件经过验证
