| C3 glomerulopathy: consensus report MC Pickering, VD D'agati, CM Nester, RJ Smith, M Haas, GB Appel, ... Kidney international 84 (6), 1079-1089, 2013 | 735 | 2013 |
| Atrasentan and renal events in patients with type 2 diabetes and chronic kidney disease (SONAR): a double-blind, randomised, placebo-controlled trial. ZD Heerspink HJL, Parving HH, Andress DL, Bakris G, Correa-Rotter R, Hou FF ... Lancet 393 (10184), 1937-1947, 2019 | 544 | 2019 |
| 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 | 300 | 2011 |
| Monogenic causes of chronic kidney disease in adults DM Connaughton, C Kennedy, S Shril, N Mann, SL Murray, PA Williams, ... Kidney international 95 (4), 914-928, 2019 | 248 | 2019 |
| 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 | 167 | 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 | 158 | 2011 |
| A hybrid CFHR3-1 gene causes familial C3 glomerulopathy TH Malik, PJ Lavin, EG de Jorge, KA Vernon, KL Rose, MP Patel, ... Journal of the American Society of Nephrology 23 (7), 1155-1160, 2012 | 156 | 2012 |
| Pathogenesis and therapy of focal segmental glomerulosclerosis: an update R Gbadegesin, P Lavin, J Foreman, M Winn Pediatric nephrology 26, 1001-1015, 2011 | 133 | 2011 |
| 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, 2011 | 91 | 2011 |
| 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 | 90 | 2013 |
| The irish kidney gene project-prevalence of family history in patients with kidney disease in Ireland DM Connaughton, S Bukhari, P Conlon, E Cassidy, M O'Toole, ... Nephron 130 (4), 293-301, 2015 | 72 | 2015 |
| Noninvasive immunohistochemical diagnosis and novel MUC1 mutations causing autosomal dominant tubulointerstitial kidney disease M Živná, K Kidd, A Přistoupilová, V Barešová, M DeFelice, B Blumenstiel, ... Journal of the American Society of Nephrology 29 (9), 2418-2431, 2018 | 61 | 2018 |
| A novel missense mutation of Wilms’ Tumor 1 causes autosomal dominant FSGS G Hall, RA Gbadegesin, P Lavin, G Wu, Y Liu, EC Oh, L Wang, ... Journal of the American Society of Nephrology 26 (4), 831-843, 2015 | 59 | 2015 |
| Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector X Luo, G Hall, S Li, A Bird, PJ Lavin, MP Winn, AR Kemper, TT Brown, ... Molecular therapy 19 (11), 1961-1970, 2011 | 39 | 2011 |
| Higher tacrolimus trough levels on days 2–5 post‐renal transplant are associated with reduced rates of acute rejection CM O’Seaghdha, R McQuillan, AM Moran, P Lavin, A Dorman, P O’Kelly, ... Clinical transplantation 23 (4), 462-468, 2009 | 37 | 2009 |
| Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity G Hall, J Rowell, F Farinelli, RA Gbadegesin, P Lavin, G Wu, A Homstad, ... American Journal of Physiology-Renal Physiology 306 (12), F1442-F1450, 2014 | 35 | 2014 |
| Therapeutic targets in focal and segmental glomerulosclerosis PJ Lavin, R Gbadegesin, TV Damodaran, MP Winn Current opinion in nephrology and hypertension 17 (4), 386-392, 2008 | 33 | 2008 |
| Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS R Gbadegesin, B Bartkowiak, PJ Lavin, N Mukerji, G Wu, B Bowling, ... Pediatric Nephrology 24, 281-285, 2009 | 32 | 2009 |
| Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland S Cormican, DM Connaughton, C Kennedy, S Murray, M Živná, S Kmoch, ... Renal failure 41 (1), 832-841, 2019 | 30 | 2019 |
| Utility of genomic testing after renal biopsy SL Murray, A Dorman, KA Benson, DM Connaughton, CP Stapleton, ... American journal of nephrology 51 (1), 43-53, 2020 | 29 | 2020 |
