| Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management A Bierzynska, HJ McCarthy, K Soderquest, ES Sen, E Colby, WY Ding, ... Kidney international 91 (4), 937-947, 2017 | 280 | 2017 |
| Clinical practice: Diagnosis and management of Henoch–Schönlein purpura HJ McCarthy, EJ Tizard European journal of pediatrics 169, 643-650, 2010 | 269 | 2010 |
| Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome HJ McCarthy, A Bierzynska, M Wherlock, M Ognjanovic, L Kerecuk, ... Clinical Journal of the American Society of Nephrology 8 (4), 637-648, 2013 | 214 | 2013 |
| Defects of CRB2 cause steroid-resistant nephrotic syndrome L Ebarasi, S Ashraf, A Bierzynska, HY Gee, HJ McCarthy, S Lovric, ... The American Journal of Human Genetics 96 (1), 153-161, 2015 | 129 | 2015 |
| Initial steroid sensitivity in children with steroid-resistant nephrotic syndrome predicts post-transplant recurrence WY Ding, A Koziell, HJ McCarthy, A Bierzynska, MK Bhagavatula, ... Journal of the American Society of Nephrology 25 (6), 1342-1348, 2014 | 120 | 2014 |
| Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders AJ Mallett, HJ McCarthy, G Ho, K Holman, E Farnsworth, C Patel, ... Kidney international 92 (6), 1493-1506, 2017 | 89 | 2017 |
| Active proteases in nephrotic plasma lead to a podocin‐dependent phosphorylation of VASP in podocytes via protease activated receptor‐1 JJ Harris, HJ McCarthy, L Ni, M Wherlock, HG Kang, JF Wetzels, GI Welsh, ... The Journal of pathology 229 (5), 660-671, 2013 | 87 | 2013 |
| MAGI2 mutations cause congenital nephrotic syndrome A Bierzynska, K Soderquest, P Dean, E Colby, R Rollason, C Jones, ... Journal of the American Society of Nephrology 28 (5), 1614-1621, 2017 | 70 | 2017 |
| Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants AM Bournazos, LG Riley, S Bommireddipalli, L Ades, LS Akesson, ... Genetics in Medicine 24 (1), 130-145, 2022 | 54 | 2022 |
| Genetics in clinical practice: nephrotic and proteinuric syndromes HJ McCarthy, MA Saleem Nephron Experimental Nephrology 118 (1), e1-e8, 2010 | 40 | 2010 |
| Steroid sensitive nephrotic syndrome EM Hodson, D Hahn, SI Alexander, N Graf, H McCarthy Pediatric Kidney Disease, 405-442, 2023 | 34 | 2023 |
| A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder LK Jones, R Lam, KK McKee, M Aleksandrova, J Dowling, SI Alexander, ... Development 147 (21), dev189183, 2020 | 32 | 2020 |
| ADPedKD: a global online platform on the management of children with ADPKD S De Rechter, D Bockenhauer, LM Guay-Woodford, I Liu, AJ Mallett, ... Kidney international reports 4 (9), 1271-1284, 2019 | 22 | 2019 |
| A clinical approach to tubulopathies in children and young adults R Kermond, A Mallett, H McCarthy Pediatric Nephrology 38 (3), 651-662, 2023 | 17 | 2023 |
| A working partnership: a review of shared decision‐making in nephrology N Amir, HJ McCarthy, A Tong Nephrology 26 (11), 851-857, 2021 | 17 | 2021 |
| Treatment of recurrent focal segmental glomerulosclerosis post‐kidney transplantation in Australian and New Zealand children: a retrospective cohort study A Francis, M Didsbury, H McCarthy, T Kara Pediatric transplantation 22 (5), e13185, 2018 | 17 | 2018 |
| NAV-KIDS2 trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease A Van Zwieten, P Caldwell, K Howard, A Tong, JC Craig, S Alexander, ... BMC nephrology 20, 1-9, 2019 | 16 | 2019 |
| Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant ET Hoorntje, C Burns, L Marsili, B Corden, VN Parikh, GJ Te Meerman, ... Circulation: Genomic and Precision Medicine 16 (1), e003672, 2023 | 15 | 2023 |
| Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families HA Tanudisastro, K Holman, G Ho, E Farnsworth, K Fisk, T Gayagay, ... NPJ genomic medicine 6 (1), 20, 2021 | 15 | 2021 |
| Genomics in the renal clinic-translating nephrogenetics for clinical practice A Mallett, C Corney, H McCarthy, SI Alexander, H Healy Human Genomics 9, 1-4, 2015 | 13 | 2015 |
