| The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification AWG of the International, IAN Network, DC Cattran, R Coppo, HT Cook, ... Kidney international 76 (5), 534-545, 2009 | 1239 | 2009 |
| The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility AWG of the International, IAN Network, ISD Roberts, HT Cook, S Troyanov, ... Kidney international 76 (5), 546-556, 2009 | 1009 | 2009 |
| An international consensus approach to the management of atypical hemolytic uremic syndrome in children C Loirat, F Fakhouri, G Ariceta, N Besbas, M Bitzan, A Bjerre, R Coppo, ... Pediatric nephrology 31, 15-39, 2016 | 711 | 2016 |
| Minimal change disease M Vivarelli, L Massella, B Ruggiero, F Emma Clinical Journal of the American Society of Nephrology 12 (2), 332-345, 2017 | 584 | 2017 |
| Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia D Haffner, F Emma, L Seefried, W Högler, KM Javaid, D Bockenhauer, ... Nature Reviews Nephrology, 1-25, 2025 | 491 | 2025 |
| Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments R Coppo, S Troyanov, S Bellur, D Cattran, HT Cook, J Feehally, ... Kidney international 86 (4), 828-836, 2014 | 468 | 2014 |
| 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 | 379 | 2007 |
| Mitochondrial dysfunction in inherited renal disease and acute kidney injury F Emma, G Montini, SM Parikh, L Salviati Nature Reviews Nephrology 12 (5), 267-280, 2016 | 365 | 2016 |
| Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort A Trautmann, M Bodria, F Ozaltin, A Gheisari, A Melk, M Azocar, A Anarat, ... Clinical Journal of the American Society of Nephrology 10 (4), 592-600, 2015 | 345 | 2015 |
| Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney … RT Gansevoort, M Arici, T Benzing, H Birn, G Capasso, A Covic, ... Nephrology Dialysis Transplantation 31 (3), 337-348, 2016 | 344 | 2016 |
| The MEST score provides earlier risk prediction in lgA nephropathy SJ Barbour, G Espino-Hernandez, HN Reich, R Coppo, ISD Roberts, ... Kidney international 89 (1), 167-175, 2016 | 291 | 2016 |
| 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 | 282 | 2014 |
| Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome P Ruggenenti, B Ruggiero, P Cravedi, M Vivarelli, L Massella, M Marasà, ... Journal of the American Society of Nephrology 25 (4), 850-863, 2014 | 253 | 2014 |
| 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 | 249 | 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 |
| Nephropathic cystinosis: an international consensus document F Emma, G Nesterova, C Langman, A Labbé, S Cherqui, P Goodyer, ... Nephrology Dialysis Transplantation 29 (suppl_4), iv87-iv94, 2014 | 233 | 2014 |
| Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene J Walczak-Sztulpa, J Eggenschwiler, D Osborn, DA Brown, F Emma, ... The American Journal of Human Genetics 86 (6), 949-956, 2010 | 226 | 2010 |
| B cell reconstitution after rituximab treatment in idiopathic nephrotic syndrome M Colucci, R Carsetti, S Cascioli, F Casiraghi, A Perna, L Ravà, ... Journal of the American Society of Nephrology 27 (6), 1811-1822, 2016 | 217 | 2016 |
| The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults R Coppo, S Troyanov, R Camilla, RJ Hogg, DC Cattran, HT Cook, ... Kidney international 77 (10), 921-927, 2010 | 206 | 2010 |
| Semaphorin 3B–associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients S Sethi, H Debiec, B Madden, M Vivarelli, MC Charlesworth, A Ravindran, ... Kidney international 98 (5), 1253-1264, 2020 | 205 | 2020 |
