| 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 | 225 | 2018 |
| Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency S Lovric, S Goncalves, HY Gee, B Oskouian, H Srinivas, WI Choi, S Shril, ... The Journal of clinical investigation 127 (3), 912-928, 2017 | 196 | 2017 |
| 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 | 185 | 2008 |
| 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 | 175 | 2018 |
| Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior–Løken syndrome J Helou, EA Otto, M Attanasio, SJ Allen, MA Parisi, I Glass, B Utsch, ... Journal of medical genetics 44 (10), 657-663, 2007 | 135 | 2007 |
| 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 | 111 | 2018 |
| Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity DA Braun, M Schueler, J Halbritter, HY Gee, JD Porath, JA Lawson, ... Kidney international 89 (2), 468-475, 2016 | 99 | 2016 |
| A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan A Abid, S Khaliq, S Shahid, A Lanewala, M Mubarak, S Hashmi, J Kazi, ... Gene 502 (2), 133-137, 2012 | 59 | 2012 |
| Clinicopathologic characteristics and steroid response of IgM nephropathy in children presenting with idiopathic nephrotic syndrome M Mubarak, JI Kazi, S Shakeel, A Lanewala, S Hashmi, F Akhter Apmis 119 (3), 180-186, 2011 | 54 | 2011 |
| Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis T Jobst-Schwan, V Klämbt, M Tarsio, JF Heneghan, AJ Majmundar, ... Kidney international 97 (3), 567-579, 2020 | 53 | 2020 |
| The Spectrum of Histopathological Lesions in Children Presenting with Steroid‐Resistant Nephrotic Syndrome at a Single Center in Pakistan M Mubarak, JI Kazi, S Shakeel, A Lanewala, S Hashmi The Scientific World Journal 2012 (1), 681802, 2012 | 50 | 2012 |
| Etiology, clinical profile and short-term outcome of acute kidney injury in children at a tertiary care pediatric nephrology center in Pakistan V Tresa, A Yaseen, AA Lanewala, S Hashmi, S Khatri, I Ali, M Mubarak Renal failure 39 (1), 26-31, 2017 | 46 | 2017 |
| Pediatric kidney transplantation in the developing world: challenges and solutions SAH Rizvi, S Sultan, MN Zafar, SAA Naqvi, AA Lanewala, S Hashmi, ... American Journal of Transplantation 13 (9), 2441-2449, 2013 | 40 | 2013 |
| Acute kidney injury in idiopathic nephrotic syndrome of childhood is a major risk factor for the development of chronic kidney disease A Yaseen, V Tresa, AA Lanewala, S Hashmi, I Ali, S Khatri, M Mubarak Renal failure 39 (1), 323-327, 2017 | 39 | 2017 |
| Pain prevalence in patients with chronic kidney disease. PC Pham, K Dewar, S Hashmi, E Toscano, PM Pham, PA Pham, PT Pham Clinical nephrology 73 (4), 294-299, 2010 | 33 | 2010 |
| Analysis of genes encoding laminin β2 and related proteins in patients with Galloway–Mowat syndrome A Dietrich, V Matejas, M Bitzan, S Hashmi, C Kiraly-Borri, SP Lin, ... Pediatric Nephrology 23, 1779-1786, 2008 | 31 | 2008 |
| Pathology of idiopathic nephrotic syndrome in children: are the adolescents different from young children? M Mubarak, JI Kazi, A Lanewala, S Hashmi, F Akhter Nephrology Dialysis Transplantation 27 (2), 722-726, 2012 | 27 | 2012 |
| Histopathological Spectrum and short-term outcome of treatment with cyclophosphamide in relapsing steroid-sensitive nephrotic Syndrome IA Bajeer, S Khatri, V Tresa, S Hashmi, M Mubarak, AA Lanewala J Coll Physicians Surg Pak 28 (6), 436-439, 2018 | 13 | 2018 |
| Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome A Abid, S Shahid, M Shakoor, AA Lanewala, S Hashmi, S Khaliq Frontiers in Genetics 9, 214, 2018 | 9 | 2018 |
| Short-term outcome of clinical and histopathologic variants of mesangiocapillary glomerulonephritis in children: A retrospective analysis from a tertiary care center S Khatri, IA Bajeer, V Tresa, S Hashmi, M Mubarak, AA Lanewala JPMA 68 (1199), 2018 | 8 | 2018 |
