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2020 Journal Article Toward transparency in nephrology researchFrancis, Anna and Mallett, Andrew (2020). Toward transparency in nephrology research. Kidney International Reports, 5 (2), 118-120. doi: 10.1016/j.ekir.2019.11.019 |
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2020 Journal Article Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD studyJahan, Sadia, Sarathchandran, Subashini, Akhter, Shamina, Goldblatt, Jack, Stark, Samantha, Crawford, Douglas, Mallett, Andrew and Thomas, Mark (2020). Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study. Orphanet Journal of Rare Diseases, 15 (1) 10, 10. doi: 10.1186/s13023-019-1290-3 |
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2020 Journal Article Genetic Kidney Disease in Southern TasmaniaBrailsford, Gabrielle, Cash, Ellie, Burke, Jo, Kirkland, Geoff, Wallis, Mathew, Mallett, Andrew and Jose, Matthew D. (2020). Genetic Kidney Disease in Southern Tasmania. Kidney International Reports, 5 (4), 534-537. doi: 10.1016/j.ekir.2020.01.015 |
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2019 Journal Article Adult-diagnosed nonsyndromic nephronophthisis in Australian families caused by biallelic NPHP4 variantsHudson, Rebecca, Patel, Chirag, Hawley, Carmel M., O'Shea, Stacey, Snelling, Paul, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Francis, Leo, Simons, Cas and Mallett, Andrew (2019). Adult-diagnosed nonsyndromic nephronophthisis in Australian families caused by biallelic NPHP4 variants. American Journal of Kidney Diseases, 76 (2), 282-287. doi: 10.1053/j.ajkd.2019.08.031 |
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2019 Journal Article Proposed minimum information guideline for kidney disease - Research and clinical data reporting: A cross-sectional studyKumuthini, Judit, Van Woerden, Christiaan, Mallett, Andrew, Zass, Lyndon, Chaouch, Melek, Thompson, Michael, Johnston, Katherine, Mbiyavanga, Mamana, Baichoo, Shakuntala, Mungloo-DIlmohamud, Zahra, Patel, Chirag and Mulder, Nicola (2019). Proposed minimum information guideline for kidney disease - Research and clinical data reporting: A cross-sectional study. BMJ Open, 9 (11) e029539, e029539. doi: 10.1136/bmjopen-2019-029539 |
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2019 Journal Article ADPedKD: A Global Online Platform on the Management of Children With ADPKDDe Rechter, Stéphanie, Bockenhauer, Detlef, Guay-Woodford, Lisa M., Liu, Isaac, Mallett, Andrew J., Soliman, Neveen A., Sylvestre, Lucimary C., Schaefer, Franz, Liebau, Max C., Mekahli, Djalila, ADPedKD Consortium, Adamczyk, P., Akinci, N., Alpay, H., Ardelean, C., Ayasreh, N., Aydin, Z., Bael, A., Baudouin, V., Bayrakci, U. S., Bensman, A., Bialkevich, H., Biebuyck, A., Boyer, O., Bjanid, O., Bryłka, A., Çalışkan, S., Cambier, A., Camelio, A. ... Zachwieja, K. (2019). ADPedKD: A Global Online Platform on the Management of Children With ADPKD. Kidney International Reports, 4 (9), 1271-1284. doi: 10.1016/j.ekir.2019.05.015 |
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2019 Journal Article Isolated proteinuria due to CUBN homozygous mutation - challenging the investigative paradigmJayasinghe, Kushani, White, Susan M., Kerr, Peter G., MacGregor, Duncan, Stark, Zornitza, Wilkins, Ella, Simons, Cas, Mallett, Andrew and Quinlan, Catherine (2019). Isolated proteinuria due to CUBN homozygous mutation - challenging the investigative paradigm. BMC Nephrology, 20 (1) 330, 330. doi: 10.1186/s12882-019-1474-z |
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2019 Journal Article Pilot clinical and validation study of the PROPKD score in clinical practice amongst patients with Autosomal Dominant Polycystic Kidney DiseaseChan, Samuel, Patel, Chirag and Mallett, Andrew J. (2019). Pilot clinical and validation study of the PROPKD score in clinical practice amongst patients with Autosomal Dominant Polycystic Kidney Disease. Nephrology, 25 (3), 274-275. doi: 10.1111/nep.13640 |
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2019 Journal Article Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocolJayasinghe, Kushani, Stark, Zornitza, Patel, Chirag, Mallawaarachchi, Amali, McCarthy, Hugh, Faull, Randall, Chakera, Aron, Sundaram, Madhivanan, Jose, Matthew, Kerr, Peter, Wu, You, Wardrop, Louise, Goranitis, Ilias, Best, Stephanie, Martyn, Melissa, Quinlan, Catherine and Mallett, Andrew J. (2019). Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol. BMJ Open, 9 (8) e029541, e029541. doi: 10.1136/bmjopen-2019-029541 |
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2019 Journal Article An audit of electron microscopy in the diagnosis of focal segmental glomerulosclerosis: are current pathological techniques missing important abnormalities in the glomerular basement membrane?Davis, Justin, Tjipto, Alwie, Hegerty, Katharine and Mallett, Andrew (2019). An audit of electron microscopy in the diagnosis of focal segmental glomerulosclerosis: are current pathological techniques missing important abnormalities in the glomerular basement membrane?. F1000Research, 8 1204, 1-13. doi: 10.12688/f1000research.19997.1 |
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2019 Journal Article SAT-193 CLINICAL AUDIT OF THE VALIDATION OF A MODEL TO PREDICT PROGRESSION OF CHRONIC KIDNEY DISEASE TO END STAGE KIDNEY DISEASEJAHAN, S., Hegerty, K., Kark, A., Hale, J. and Mallett, A. (2019). SAT-193 CLINICAL AUDIT OF THE VALIDATION OF A MODEL TO PREDICT PROGRESSION OF CHRONIC KIDNEY DISEASE TO END STAGE KIDNEY DISEASE. Kidney International Reports, 4 (7). doi: 10.1016/j.ekir.2019.05.227 |
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2019 Journal Article Genome-wide association study of medication-use and associated disease in the UK BiobankWu, Yeda, Byrne, Enda M., Zheng, Zhili, Kemper, Kathryn E., Yengo, Loic, Mallett, Andrew J., Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2019). Genome-wide association study of medication-use and associated disease in the UK Biobank. Nature Communications, 10 (1) 1891, 1891. doi: 10.1038/s41467-019-09572-5 |
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2019 Journal Article Precision medicine diagnostics for rare kidney disease: Twitter as a tool in clinical genomic translationMallett, Andrew J., Quinlan, Catherine, Patel, Chirag, Fowles, Lindsay, Crawford, Joanna, Gattas, Michael, Baer, Richard, Bennetts, Bruce, Ho, Gladys, Holman, Katherine and Simons, Cas (2019). Precision medicine diagnostics for rare kidney disease: Twitter as a tool in clinical genomic translation. Kidney Medicine, 1 (5), 315-318. doi: 10.1016/j.xkme.2019.06.006 |
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2019 Journal Article Metformin for preventing the progression of chronic kidney disease (Protocol)El‐Damanawi, Ragada, Viecelli, Andrea K., Pascoe, Elaine M., Craig, Jonathan C., Johnson, David W., Mallett, Andrew J., Hawley, Carmel M. and Hiemstra, Thomas F. (2019). Metformin for preventing the progression of chronic kidney disease (Protocol). Cochrane Database of Systematic Reviews, 2019 (9) CD013414. doi: 10.1002/14651858.CD013414 |
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2018 Other Outputs Genetic analyses of medication-use and implications for precision medicineWu, Yeda, Byrne, Enda M., Zheng, Zhili, Kemper, Kathryn E., Yengo, Loic, Mallett, Andrew J., Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2018). Genetic analyses of medication-use and implications for precision medicine. doi: 10.1101/501049 |
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2018 Journal Article Renal genetics in Australia: kidney medicine in the genomic ageJayasinghe, Kushani, Quinlan, Cathy, Stark, Zornitza, Patel, Chirag, Mallawaarachchi, Amali, Wardrop, Louise, Kerr, Peter G., Trnka, Peter, Mallett, Andrew J. and KidGen Collaborative (2018). Renal genetics in Australia: kidney medicine in the genomic age. Nephrology, 24 (3), 279-286. doi: 10.1111/nep.13494 |
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2018 Journal Article Paraneoplastic immunoglobulin A nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma - a case reportNg, Monica Suet Ying, Francis, Leo, Pillai, Elango and Mallett, Andrew John (2018). Paraneoplastic immunoglobulin A nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma - a case report. BMC Nephrology, 19 (1) 224, 224. doi: 10.1186/s12882-018-1034-y |
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2018 Journal Article CFHR5 nephropathy in a Greek-Cypriot Australian family: ancestry-informed precision medicineNg, Monica S. Y., McClymont, Kelly, McCallum, Naomi, Dua, Rahul, Holman, Katherine, Bennetts, Bruce, Ho, Gladys, Patel, Chirag and Mallett, Andrew J. (2018). CFHR5 nephropathy in a Greek-Cypriot Australian family: ancestry-informed precision medicine. Kidney International Reports, 3 (5), 1222-1228. doi: 10.1016/j.ekir.2018.04.007 |
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2018 Conference Publication Validation of a web-based clinical decision support system to predict end-stage kidney disease in an Australian immunoglobin a nephropathy cohortNg, M. S., Harfield, M., Francis, L. and Mallett, A. J. (2018). Validation of a web-based clinical decision support system to predict end-stage kidney disease in an Australian immunoglobin a nephropathy cohort. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, NSW, Australia, 8–12 September 2018. Richmond, VIC, Australia: John Wiley & Sons. |
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2018 Journal Article Antenatally diagnosed ADPKDAldridge, Melanie, Patel, Chirag, Mallett, Andrew and Trnka, Peter (2018). Antenatally diagnosed ADPKD. Kidney International Reports, 3 (5), 1214-1217. doi: 10.1016/j.ekir.2018.05.002 |
