| Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible B Hinkes, RC Wiggins, R Gbadegesin, CN Vlangos, D Seelow, ... Nature genetics 38 (12), 1397-1405, 2006 | 658 | 2006 |
| Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2) BG Hinkes, B Mucha, CN Vlangos, R Gbadegesin, J Liu, K Hasselbacher, ... Pediatrics 119 (4), e907-e919, 2007 | 576 | 2007 |
| COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ... The Journal of clinical investigation 121 (5), 2013-2024, 2011 | 435 | 2011 |
| Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis S Akilesh, H Suleiman, H Yu, MC Stander, P Lavin, R Gbadegesin, ... The Journal of clinical investigation 121 (10), 4127-4137, 2011 | 294 | 2011 |
| Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis AF Malone, PJ Phelan, G Hall, U Cetincelik, A Homstad, AS Alonso, ... Kidney international 86 (6), 1253-1259, 2014 | 239 | 2014 |
| Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) R Gbadegesin, BG Hinkes, BE Hoskins, CN Vlangos, SF Heeringa, J Liu, ... Nephrology dialysis transplantation 23 (4), 1291-1297, 2008 | 183 | 2008 |
| Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome B Hinkes, C Vlangos, S Heeringa, B Mucha, R Gbadegesin, J Liu, ... Journal of the American Society of Nephrology 19 (2), 365-371, 2008 | 182 | 2008 |
| Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS RA Gbadegesin, G Hall, A Adeyemo, N Hanke, I Tossidou, J Burchette, ... Journal of the American Society of Nephrology 25 (9), 1991-2002, 2014 | 166 | 2014 |
| TRPC6 enhances angiotensin II-induced albuminuria J Eckel, PJ Lavin, EA Finch, N Mukerji, J Burch, R Gbadegesin, G Wu, ... Journal of the American Society of Nephrology 22 (3), 526-535, 2011 | 153 | 2011 |
| HLA-DQA1 and PLCG2 are candidate risk loci for childhood-onset steroid-sensitive nephrotic syndrome RA Gbadegesin, A Adeyemo, NJA Webb, LA Greenbaum, ... Journal of the American Society of Nephrology 26 (7), 1701-1710, 2015 | 137 | 2015 |
| Pathogenesis and therapy of focal segmental glomerulosclerosis: an update R Gbadegesin, P Lavin, J Foreman, M Winn Pediatric nephrology 26, 1001-1015, 2011 | 131 | 2011 |
| Intraleucocytic malaria pigment and clinical severity of malaria in children OK Amodu, AA Adeyemo, PE Olumese, RA Gbadegesin Transactions of the Royal Society of Tropical Medicine and Hygiene 92 (1), 54-56, 1998 | 131 | 1998 |
| Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis HHS Wang, RA Gbadegesin, JW Foreman, SK Nagaraj, DR Wigfall, ... The Journal of urology 193 (3), 963-969, 2015 | 119 | 2015 |
| AKI in children hospitalized with nephrotic syndrome MN Rheault, L Zhang, DT Selewski, M Kallash, CL Tran, M Seamon, ... Clinical Journal of the American Society of Nephrology 10 (12), 2110-2118, 2015 | 116 | 2015 |
| Role of TGF-β1 in renal parenchymal scarring following childhood urinary tract infection SA Cotton, RA Gbadegesin, S Williams, PEC Brenchley, NJA Webb Kidney international 61 (1), 61-67, 2002 | 111 | 2002 |
| Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome SF Heeringa, CN Vlangos, G Chernin, B Hinkes, R Gbadegesin, J Liu, ... Nephrology Dialysis Transplantation 23 (11), 3527-3533, 2008 | 110 | 2008 |
| Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis RA Gbadegesin, PJ Lavin, G Hall, B Bartkowiak, A Homstad, R Jiang, ... Kidney international 81 (1), 94-99, 2012 | 89 | 2012 |
| Significance of hemolysis on extracorporeal life support after cardiac surgery in children R Gbadegesin, S Zhao, J Charpie, PD Brophy, WE Smoyer, JJ Lin Pediatric nephrology 24, 589-595, 2009 | 86 | 2009 |
| TNXB mutations can cause vesicoureteral reflux RA Gbadegesin, PD Brophy, A Adeyemo, G Hall, IR Gupta, D Hains, ... Journal of the American Society of Nephrology 24 (8), 1313-1322, 2013 | 84 | 2013 |
| Nephrotic syndrome R Gbadegesin, WE Smoyer Comprehensive Pediatric Nephrology: Text with CD-ROM, 205-218, 2008 | 78 | 2008 |
