| 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 | 624 | 2014 |
| Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis K Kiryluk, Y Li, S Sanna-Cherchi, M Rohanizadegan, H Suzuki, F Eitner, ... PLoS genetics 8 (6), e1002765, 2012 | 392 | 2012 |
| 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 |
| The molecular basis of lecithin: cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families L Calabresi, L Pisciotta, A Costantin, I Frigerio, I Eberini, P Alessandrini, ... Arteriosclerosis, thrombosis, and vascular biology 25 (9), 1972-1978, 2005 | 206 | 2005 |
| The copy number variation landscape of congenital anomalies of the kidney and urinary tract M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ... Nature genetics 51 (1), 117-127, 2019 | 193 | 2019 |
| 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 | 147 | 2013 |
| TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype M Gigante, G Caridi, E Montemurno, M Soccio, M d'Apolito, G Cerullo, ... Clinical Journal of the American Society of Nephrology 6 (7), 1626-1634, 2011 | 122 | 2011 |
| NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum K Bouchireb, O Boyer, O Gribouval, F Nevo, E Huynh‐Cong, V Morinière, ... Human mutation 35 (2), 178-186, 2014 | 102 | 2014 |
| Complement modulation of anti-aging factor klotho in ischemia/reperfusion injury and delayed graft function G Castellano, A Intini, A Stasi, C Divella, M Gigante, P Pontrelli, R Franzin, ... American Journal of Transplantation 16 (1), 325-333, 2016 | 100 | 2016 |
| Exome-wide association study identifies GREB1L mutations in congenital kidney malformations S Sanna-Cherchi, K Khan, R Westland, P Krithivasan, L Fievet, ... The American Journal of Human Genetics 101 (5), 789-802, 2017 | 97 | 2017 |
| Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome S Sanna-Cherchi, KE Burgess, SN Nees, G Caridi, PL Weng, M Dagnino, ... Kidney international 80 (4), 389-396, 2011 | 95 | 2011 |
| WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes F Aucella, L Bisceglia, P De Bonis, M Gigante, G Caridi, G Barbano, ... Pediatric Nephrology 21, 1393-1398, 2006 | 73 | 2006 |
| Sirolimus and proteinuria in renal transplant patients: evidence for a dose-dependent effect on slit diaphragm-associated proteins G Stallone, B Infante, P Pontrelli, M Gigante, E Montemurno, A Loverre, ... Transplantation 91 (9), 997-1004, 2011 | 70 | 2011 |
| Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations G Caridi, M Gigante, P Ravani, A Trivelli, G Barbano, F Scolari, ... Clinical Journal of the American Society of Nephrology 4 (6), 1065-1072, 2009 | 67 | 2009 |
| Natural history of congenital dyserythropoietic anemia type II A Iolascon, J Delaunay, SN Wickramasinghe, S Perrotta, M Gigante, ... Blood, The Journal of the American Society of Hematology 98 (4), 1258-1260, 2001 | 65 | 2001 |
| Effects of daily hemodialysis on heart rate variability: results from the Frequent Hemodialysis Network (FHN) Daily Trial CT Chan, GM Chertow, JT Daugirdas, TH Greene, P Kotanko, B Larive, ... Nephrology Dialysis Transplantation 29 (1), 168-178, 2014 | 60 | 2014 |
| Dysfunctional DC subsets in RCC patients: ex vivo correction to yield an effective anti-cancer vaccine M Gigante, A Blasi, A Loverre, V Mancini, M Battaglia, FP Selvaggi, ... Molecular immunology 46 (5), 893-901, 2009 | 57 | 2009 |
| Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach M Gigante, F Monno, R Roberto, N Laforgia, MB Assael, S Livolti, ... Journal of nephrology 15 (6), 696-702, 2002 | 57 | 2002 |
| miR-29b and miR-198 overexpression in CD8+ T cells of renal cell carcinoma patients down-modulates JAK3 and MCL-1 leading to immune dysfunction M Gigante, P Pontrelli, W Herr, M Gigante, M D’Avenia, G Zaza, ... Journal of translational medicine 14, 1-13, 2016 | 52 | 2016 |
