| Phenotype-genotype correlations and estimated carrier frequencies of primary hyperoxaluria K Hopp, AG Cogal, EJ Bergstralh, BM Seide, JB Olson, AM Meek, ... Journal of the American Society of Nephrology 26 (10), 2559-2570, 2015 | 246 | 2015 |
| Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis CG Monico, S Rossetti, R Belostotsky, AG Cogal, RM Herges, BM Seide, ... Clinical Journal of the American Society of Nephrology 6 (9), 2289-2295, 2011 | 148 | 2011 |
| Predictors of incident ESRD among patients with primary hyperoxaluria presenting prior to kidney failure F Zhao, EJ Bergstralh, RA Mehta, LE Vaughan, JB Olson, BM Seide, ... Clinical Journal of the American Society of Nephrology 11 (1), 119-126, 2016 | 92 | 2016 |
| Primary hyperoxaluria type 1 DS Milliner, PC Harris, DJ Sas, AG Cogal, JC Lieske | 70 | 2022 |
| Phenotypic and genetic analysis of epiphytic Pseudomonas syringae populations from sweet cherry in Michigan LJ Renick, AG Cogal, GW Sundin Plant disease 92 (3), 372-378, 2008 | 70 | 2008 |
| Glomerular pathology in Dent disease and its association with kidney function X Wang, F Anglani, L Beara-Lasic, AJ Mehta, LE Vaughan, LH Hernandez, ... Clinical Journal of the American Society of Nephrology 11 (12), 2168-2176, 2016 | 65 | 2016 |
| Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis CG Monico, A Weinstein, Z Jiang, AL Rohlinger, AG Cogal, BB Bjornson, ... American journal of kidney diseases 52 (6), 1096-1103, 2008 | 56 | 2008 |
| Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2 P Singh, JK Viehman, RA Mehta, AG Cogal, L Hasadsri, D Oglesbee, ... Nephrology Dialysis Transplantation 37 (5), 869-875, 2022 | 37 | 2022 |
| Dent disease JC Lieske, DS Milliner, L Beara-Lasic, P Harris, A Cogal, E Abrash | 29 | 2017 |
| Pyridoxine responsiveness in a type 1 primary hyperoxaluria patient with a rare (atypical) AGXT gene mutation P Singh, FT Chebib, AG Cogal, DK Gavrilov, PC Harris, JC Lieske Kidney international reports 5 (6), 955-958, 2020 | 27 | 2020 |
| GeneReviews DS Milliner, PC Harris, AG Cogal, MP Adam, HH Ardinger, RA Pagon University of Washington, Seattle University of Washington, Seattle …, 1993 | 20 | 1993 |
| Comprehensive genetic analysis reveals complexity of monogenic urinary stone disease AG Cogal, J Arroyo, RJ Shah, KJ Reese, BN Walton, LM Reynolds, ... Kidney international reports 6 (11), 2862-2884, 2021 | 19 | 2021 |
| Functional and transport analyses of CLCN5 genetic changes identified in Dent disease patients X Tang, MR Brown, AG Cogal, D Gauvin, PC Harris, JC Lieske, ... Physiological reports 4 (8), e12776, 2016 | 19 | 2016 |
| Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts L Beara-Lasic, A Cogal, K Mara, F Enders, RA Mehta, Z Haskic, SL Furth, ... Pediatric Nephrology 35, 633-640, 2020 | 18 | 2020 |
| Investigators of Rare Kidney Stone Consortium: Predictors of incident ESRD among patients with primary hyperoxaluria presenting prior to kidney failure F Zhao, EJ Bergstralh, RA Mehta, LE Vaughan, JB Olson, BM Seide, ... Clin J Am Soc Nephrol 11 (119-126), 26656319, 2016 | 16 | 2016 |
| High prevalence of kidney cysts in patients with CYP24A1 deficiency C Hanna, TA Potretzke, AG Cogal, YG Mkhaimer, PJ Tebben, VE Torres, ... Kidney International Reports 6 (7), 1895-1903, 2021 | 12 | 2021 |
| Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation D Duran, SC Jin, T Despenza, C Nelson-Williams, AG Cogal, EW Abrash, ... Human Genome Variation 3 (1), 1-6, 2016 | 9 | 2016 |
| Kidney cysts in hypophosphatemic rickets with hypercalciuria: a case series C Hanna, TA Potretzke, M Chedid, LJ Rangel, J Arroyo, D Zubidat, ... Kidney Medicine 4 (3), 100419, 2022 | 8 | 2022 |
| Clinical and molecular characterization of primary hyperoxaluria in Egypt NA Soliman, MA Elmonem, SM Abdelrahman, MM Nabhan, YA Fahmy, ... Scientific reports 12 (1), 15886, 2022 | 6 | 2022 |
| The site and type of CLCN5 genetic variation impact the resulting Dent disease-1 phenotype MG Arnous, J Arroyo, AG Cogal, F Anglani, HG Kang, D Sas, PC Harris, ... Kidney International Reports 8 (6), 1220-1230, 2023 | 3 | 2023 |
