| Whole exome sequencing of patients with steroid-resistant nephrotic syndrome JK Warejko, W Tan, A Daga, D Schapiro, JA Lawson, S Shril, S Lovric, ... Clinical Journal of the American Society of Nephrology 13 (1), 53-62, 2018 | 228 | 2018 |
| Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ... Nature genetics 49 (10), 1529-1538, 2017 | 196 | 2017 |
| 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 | 185 | 2018 |
| Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis A Daga, AJ Majmundar, DA Braun, HY Gee, JA Lawson, S Shril, ... Kidney international 93 (1), 204-213, 2018 | 178 | 2018 |
| Whole-exome sequencing enables a precision medicine approach for kidney transplant recipients N Mann, DA Braun, K Amann, W Tan, S Shril, DM Connaughton, ... Journal of the American Society of Nephrology 30 (2), 201-215, 2019 | 134 | 2019 |
| Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment S Ashraf, H Kudo, J Rao, A Kikuchi, E Widmeier, JA Lawson, W Tan, ... Nature communications 9 (1), 1960, 2018 | 119 | 2018 |
| Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome DA Braun, S Lovric, D Schapiro, R Schneider, J Marquez, M Asif, ... The Journal of clinical investigation 128 (10), 4313-4328, 2018 | 113 | 2018 |
| Prevalence of arrhythmias late after the Fontan operation JJ Lasa, AC Glatz, A Daga, M Shah The American journal of cardiology 113 (7), 1184-1188, 2014 | 84 | 2014 |
| An international multicenter study comparing arrhythmia prevalence between the intracardiac lateral tunnel and the extracardiac conduit type of Fontan operations S Balaji, A Daga, DJ Bradley, SP Etheridge, IH Law, AS Batra, S Sanatani, ... The Journal of thoracic and cardiovascular surgery 148 (2), 576-581, 2014 | 82 | 2014 |
| Mutations in WDR4 as a new cause of Galloway–Mowat syndrome DA Braun, S Shril, A Sinha, R Schneider, W Tan, S Ashraf, T Hermle, ... American journal of medical genetics Part A 176 (11), 2460-2465, 2018 | 73 | 2018 |
| GAPVD1 and ANKFY1 mutations implicate RAB5 regulation in nephrotic syndrome T Hermle, R Schneider, D Schapiro, DA Braun, AT Van Der Ven, ... Journal of the American Society of Nephrology 29 (8), 2123-2138, 2018 | 55 | 2018 |
| Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome J Rao, S Ashraf, W Tan, AT Van Der Ven, HY Gee, DA Braun, K Fehér, ... The Journal of Clinical Investigation 127 (12), 4257-4269, 2017 | 48 | 2017 |
| Diagnosis and risk factors of acute kidney injury in very low birth weight infants A Daga, F Dapaah-Siakwan, S Rajbhandari, C Arevalo, A Salvador Pediatrics & Neonatology 58 (3), 258-263, 2017 | 46 | 2017 |
| Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis A Amar, AJ Majmundar, I Ullah, A Afzal, DA Braun, S Shril, A Daga, ... Human genetics 138, 211-219, 2019 | 41 | 2019 |
| Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort KM Vazzana, A Daga, B Goilav, EA Ogbu, DM Okamura, C Park, ... Lupus 30 (10), 1660-1670, 2021 | 30 | 2021 |
| Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome AK Solanki, E Widmeier, E Arif, S Sharma, A Daga, P Srivastava, ... Kidney international 96 (4), 883-889, 2019 | 30 | 2019 |
| Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome DA Braun, JK Warejko, S Ashraf, W Tan, A Daga, R Schneider, T Hermle, ... Nephrology Dialysis Transplantation 34 (3), 485-493, 2019 | 30 | 2019 |
| Mutations of the transcriptional corepressor ZMYM2 cause syndromic urinary tract malformations DM Connaughton, R Dai, DJ Owen, J Marquez, N Mann, ... The American Journal of Human Genetics 107 (4), 727-742, 2020 | 27 | 2020 |
| Whole exome sequencing reveals a monogenic cause of disease in≈ 43% of 35 families with midaortic syndrome JK Warejko, M Schueler, A Vivante, W Tan, A Daga, JA Lawson, ... Hypertension 71 (4), 691-699, 2018 | 26 | 2018 |
| Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children D Schapiro, A Daga, JA Lawson, AJ Majmundar, S Lovric, W Tan, ... Nephrology Dialysis Transplantation 34 (3), 474-485, 2019 | 20 | 2019 |
