| 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 | 233 | 2011 |
| Rituximab in children with resistant idiopathic nephrotic syndrome A Magnasco, P Ravani, A Edefonti, L Murer, L Ghio, M Belingheri, ... Journal of the American Society of Nephrology 23 (6), 1117-1124, 2012 | 200 | 2012 |
| Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus‐specific database M Bower, R Salomon, J Allanson, C Antignac, F Benedicenti, E Benetti, ... Human mutation 33 (3), 457-466, 2012 | 147 | 2012 |
| The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis V Palazzo, A Provenzano, F Becherucci, G Sansavini, B Mazzinghi, ... Kidney international 91 (5), 1243-1255, 2017 | 110 | 2017 |
| Genetic screening in adolescents with steroid-resistant nephrotic syndrome BS Lipska, P Iatropoulos, R Maranta, G Caridi, F Ozaltin, A Anarat, A Balat, ... Kidney international 84 (1), 206-213, 2013 | 108 | 2013 |
| The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I-Diagnosis and treatment of the first … A Pasini, E Benetti, G Conti, L Ghio, M Lepore, L Massella, D Molino, ... Italian journal of pediatrics 43, 1-15, 2017 | 102 | 2017 |
| Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract S Gimelli, G Caridi, S Beri, K McCracken, R Bocciardi, P Zordan, ... Human mutation 31 (12), 1352-1359, 2010 | 88 | 2010 |
| Molecular and clinical characterization of patients with overlapping 10p deletions A Lindstrand, H Malmgren, A Verri, E Benetti, M Eriksson, A Nordgren, ... American journal of medical genetics Part A 152 (5), 1233-1243, 2010 | 69 | 2010 |
| Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia L Murer, E Benetti, L Artifoni Pediatric Nephrology 22, 788-797, 2007 | 66 | 2007 |
| Lupus nephritis in children and adolescents: results of the Italian Collaborative Study B Ruggiero, M Vivarelli, A Gianviti, E Benetti, L Peruzzi, G Barbano, ... Nephrology Dialysis Transplantation 28 (6), 1487-1496, 2013 | 65 | 2013 |
| C5 convertase blockade in membranoproliferative glomerulonephritis: a single-arm clinical trial P Ruggenenti, E Daina, A Gennarini, C Carrara, S Gamba, M Noris, ... American Journal of Kidney Diseases 74 (2), 224-238, 2019 | 53 | 2019 |
| A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis E Benetti, G Caridi, C Malaventura, M Dagnino, E Leonardi, L Artifoni, ... Clinical Journal of the American Society of Nephrology 5 (4), 698-702, 2010 | 48 | 2010 |
| Pediatric transplantation in Europe during the COVID‐19 pandemic: early impact on activity and healthcare D Doná, J Torres Canizales, E Benetti, M Cananzi, F De Corti, E Calore, ... Clinical transplantation 34 (10), e14063, 2020 | 47 | 2020 |
| PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies S Negrisolo, E Benetti, S Centi, M Della Vella, G Ghirardo, GF Zanon, ... Clinical genetics 80 (6), 581-585, 2011 | 47 | 2011 |
| Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury L Barzon, L Murer, M Pacenti, MA Biasol, M Della Vella, E Benetti, ... The Journal of infectious diseases 199 (3), 372-380, 2009 | 46 | 2009 |
| Deciphering variability of PKD1 and PKD2 in an Italian cohort of 643 patients with autosomal dominant polycystic kidney disease (ADPKD) P Carrera, S Calzavara, R Magistroni, JT Den Dunnen, F Rigo, S Stenirri, ... Scientific reports 6 (1), 30850, 2016 | 39 | 2016 |
| Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy G Caridi, F Lugani, M Dagnino, M Gigante, A Iolascon, M Falco, ... Nephrology Dialysis Transplantation 29 (suppl_4), iv80-iv86, 2014 | 39 | 2014 |
| Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis S Melchionda, T Palladino, S Castellana, M Giordano, E Benetti, ... Journal of human genetics 61 (9), 811-821, 2016 | 37 | 2016 |
| Clinical and molecular characterization of COVID-19 hospitalized patients E Benetti, A Giliberti, A Emiliozzi, F Valentino, L Bergantini, C Fallerini, ... Plos one 15 (11), e0242534, 2020 | 36 | 2020 |
| Transplant renal artery stenosis in children: risk factors and outcome after endovascular treatment G Ghirardo, M De Franceschi, E Vidal, A Vidoni, G Ramondo, E Benetti, ... Pediatric Nephrology 29, 461-467, 2014 | 36 | 2014 |
