| 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 | 698 | 2011 |
| Diagnostic utility of exome sequencing for kidney disease EE Groopman, M Marasa, S Cameron-Christie, S Petrovski, VS Aggarwal, ... New England Journal of Medicine 380 (2), 142-151, 2019 | 677 | 2019 |
| 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 | 670 | 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 | 469 | 2009 |
| 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 | 415 | 2012 |
| Scara5 is a ferritin receptor mediating non-transferrin iron delivery JY Li, N Paragas, RM Ned, A Qiu, M Viltard, T Leete, IR Drexler, X Chen, ... Developmental cell 16 (1), 35-46, 2009 | 388 | 2009 |
| 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 | 256 | 2012 |
| Isolated polycystic liver disease genes define effectors of polycystin-1 function W Besse, K Dong, J Choi, S Punia, SV Fedeles, M Choi, AR Gallagher, ... The Journal of clinical investigation 127 (5), 1772-1785, 2017 | 226 | 2017 |
| 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 | 217 | 2019 |
| 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 | 207 | 2018 |
| Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract AT Van Der Ven, DM Connaughton, H Ityel, N Mann, M Nakayama, ... Journal of the American Society of Nephrology 29 (9), 2348-2361, 2018 | 196 | 2018 |
| 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 | 195 | 2003 |
| 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 | 186 | 2007 |
| The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis J Xie, L Liu, N Mladkova, Y Li, H Ren, W Wang, Z Cui, L Lin, X Hu, X Yu, ... Nature communications 11 (1), 1600, 2020 | 168 | 2020 |
| α–Intercalated cells defend the urinary system from bacterial infection N Paragas, R Kulkarni, M Werth, KM Schmidt-Ott, C Forster, R Deng, ... The Journal of clinical investigation 124 (7), 2963-2976, 2014 | 164 | 2014 |
| 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 | 153 | 2013 |
| Genetic drivers of kidney defects in the DiGeorge syndrome E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ... New England Journal of Medicine 376 (8), 742-754, 2017 | 151 | 2017 |
| HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort R Thomas, S Sanna-Cherchi, BA Warady, SL Furth, FJ Kaskel, ... Pediatric Nephrology 26, 897-903, 2011 | 147 | 2011 |
| Genetic basis of human congenital anomalies of the kidney and urinary tract S Sanna-Cherchi, R Westland, GM Ghiggeri, AG Gharavi The Journal of clinical investigation 128 (1), 4-15, 2018 | 138 | 2018 |
| Clinical implications of the solitary functioning kidney R Westland, MF Schreuder, JB Van Goudoever, S Sanna-Cherchi, ... Clinical Journal of the American Society of Nephrology 9 (5), 978-986, 2014 | 130 | 2014 |
