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2017 Journal Article The increasing rates of acute interstitial nephritis in Australia: a single centre case seriesWilson, Gregory J., Kark, Adrian L., Francis, Leo P., Hoy, Wendy, Healy, Helen G. and Mallett, Andrew J. (2017). The increasing rates of acute interstitial nephritis in Australia: a single centre case series. BMC Nephrology, 18 (1) 329, 1-8. doi: 10.1186/s12882-017-0747-7 |
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2017 Journal Article Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disordersMallett, Andrew J., McCarthy, Hugh J., Ho, Gladys, Holman, Katherine, Farnsworth, Elizabeth, Patel, Chirag, Fletcher, Jeffery T., Mallawaarachchi, Amali, Quinlan, Catherine, Bennetts, Bruce and Alexander, Stephen I. (2017). Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders. Kidney International, 92 (6), 1493-1506. doi: 10.1016/j.kint.2017.06.013 |
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2017 Journal Article Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseConnor, Thomas M., Hoer, Simon, Mallett, Andrew, Gale, Daniel P., Gomez-Duran, Aurora, Posse, Viktor, Antrobus, Robin, Moreno, Pablo, Sciacovelli, Marco, Frezza, Christian, Duff, Jennifer, Sheerin, Neil S., Sayer, John A., Ashcroft, Margaret, Wiesener, Michael S., Hudson, Gavin, Gustafsson, Claes M., Chinnery, Patrick F. and Maxwell, Patrick H. (2017). Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. PLoS Genetics, 13 (3) e1006620, e1006620. doi: 10.1371/journal.pgen.1006620 |
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2017 Journal Article Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney diseaseChan, Samuel, Mallett, Andrew J., Patel, Chirag, Francis, Ross S., Johnson, David W., Mudge, David W. and Isbel, Nicole M. (2017). Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney disease. Nephrology, 22 (S1), 11-14. doi: 10.1111/nep.12933 |
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2017 Journal Article Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome : MGRS triggering aHUSMahmood, Usman, Isbel, Nicole, Mollee, Peter, Mallett, Andrew, Govindarajulu, Sridevi and Francis, Ross (2017). Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome : MGRS triggering aHUS. Nephrology, 22 (S1), 15-17. doi: 10.1111/nep.12934 |
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2017 Conference Publication Paraneoplastic immunoglobulin a nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphomaNg, M. S. Y., Francis, L., Pillai, E. and Mallett, A. J. (2017). Paraneoplastic immunoglobulin a nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma. Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Darwin, NT, Australia, 4–6 September 2017. Richmond, VIC, Australia: Wiley. |
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2016 Other Outputs Genetic diagnostics in genetic renal disease: Methods, applications and therapeuticsMallett, Andrew (2016). Genetic diagnostics in genetic renal disease: Methods, applications and therapeutics. PhD Thesis, School of Medicine, The University of Queensland. doi: 10.14264/414964 |
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2016 Journal Article KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney diseaseRangan, Gopala K., Alexander, Stephen I., Campbell, Katrina L., Dexter, Mark A. J., Lee, Vincent W., Lopez-Vargas, Pamela, Mai, Jun, Mallett, Andrew, Patel, Chirag, Patel, Manish, Tchan, Michel C., Tong, Allison, Tunnicliffe, David J., Vladica, Philip and Savige, Judy (2016). KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease. Nephrology, 21 (8), 705-716. doi: 10.1111/nep.12658 |
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2016 Journal Article Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: a case reportFrancis, Anna, Burke, John, Francis, Leo, McTaggart, Steven and Mallett, Andrew (2016). Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: a case report. Open Urology & Nephrology Journal, 9 (1), 88-93. doi: 10.2174/1874303X01609010088 |
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2016 Journal Article A multidisciplinary renal genetics clinic improves patient diagnosisMallett, Andrew, Fowles, Lindsay F., McGaughran, Julie, Healy, Helen and Patel, Chirag (2016). A multidisciplinary renal genetics clinic improves patient diagnosis. Medical Journal of Australia, 204 (2), 58-59. doi: 10.5694/mja15.01157 |
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2016 Journal Article Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney diseaseTong, Allison, Tunnicliffe, David J., Lopez-Vargas, Pamela, Mallett, Andrew, Patel, Chirag, Savige, Judy, Campbell, Katrina, Patel, Manish, Tchan, Michel C., Alexander, Stephen I., Lee, Vincent, Craig, Jonathan C., Fassett, Robert and Rangan, Gopala K. (2016). Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease. Nephrology, 21 (2), 122-132. doi: 10.1111/nep.12579 |
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2015 Journal Article KHA-CARI autosomal dominant polycystic kidney disease guideline: genetics and genetic counselingPatel, Chirag, Tchan, Michel, Savige, Judy, Mallett, Andrew, Tong, Allison, Tunnicliffe, David J. and Rangan, Gopala K. (2015). KHA-CARI autosomal dominant polycystic kidney disease guideline: genetics and genetic counseling. Seminars in Nephrology, 35 (6), 550-556. doi: 10.1016/j.semnephrol.2015.10.003 |
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2015 Journal Article KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial CareTong, Allison, Mallett, Andrew, Lopez-Vargas, Pamela and Rangan, Gopala K. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care. Seminars in Nephrology, 35 (6), 590-594.e5. doi: 10.1016/j.semnephrol.2015.10.010 |
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2015 Journal Article KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for DiagnosisTchan, Michel, Savige, Judy, Patel, Chirag, Mallett, Andrew, Tong, Allison, Tunnicliffe, David J. and Rangan, Gopala K. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis. Seminars in Nephrology, 35 (6), 545-549.e2. doi: 10.1016/j.semnephrol.2015.10.007 |
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2015 Journal Article KHA-CARI autosomal dominant polycystic kidney disease guideline: management of polycystic liver diseaseSavige, Judy, Mallett, Andrew, Tunnicliffe, David J. and Rangan, Gopala K. (2015). KHA-CARI autosomal dominant polycystic kidney disease guideline: management of polycystic liver disease. Seminars in Nephrology, 35 (6), 618-622. doi: 10.1016/j.semnephrol.2015.10.015 |
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2015 Journal Article KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Pharmacological ManagementMallett, Andrew, Lee, Vincent W., Mai, Jun Mai, Lopez-Vargas, Pamela and Rangan, Gopala K. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Pharmacological Management. Seminars in Nephrology, 35 (6), 582-589.e17. doi: 10.1016/j.semnephrol.2015.10.009 |
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2015 Journal Article KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone DiseaseMallett, Andrew, Patel, Manish, Tunnicliffe, David J. and Rangan, Gopala K. (2015). KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone Disease. Seminars in Nephrology, 35 (6), 603-606.e3. doi: 10.1016/j.semnephrol.2015.10.012 |
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2015 Journal Article Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohortMallett, A., Hughes, P., Szer, J., Tuckfield, A., Van Eps, C., Cambell, S. B., Hawley, C., Burke, J., Kausman, J., Hewitt, I., Parnham, A., Ford, S. and Isbel, N. (2015). Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohort. Internal Medicine Journal, 45 (10), 1054-1065. doi: 10.1111/imj.12864 |
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2015 Journal Article A protocol for the identification and validation of novel genetic causes of kidney diseaseMallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, Alexander, Stephen I., Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, Hoy, Wedy E., Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy H. and Little, Melissa (2015). A protocol for the identification and validation of novel genetic causes of kidney disease. BMC Nephrology, 16 (152) 148, 152. doi: 10.1186/s12882-015-0148-8 |
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2015 Journal Article Genomics in the renal clinic - translating nephrogenetics for clinical practiceMallett, Andrew, Corney, Christopher, McCarthy, Hugh, Alexander, Stephen I. and Healy, Helen (2015). Genomics in the renal clinic - translating nephrogenetics for clinical practice. Human Genomics, 9 (13) 13, 13. doi: 10.1186/s40246-015-0035-1 |
