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2022 Journal Article Determining the association between the type of intervention for ischaemic heart disease and mortality and morbidity in patients with chronic kidney diseaseJeyaruban, Andrew, Hoy, Wendy, Cameron, Anne L., Healy, Helen G., Wang, Zaimin, Zhang, Jenny and Mallett, Andrew (2022). Determining the association between the type of intervention for ischaemic heart disease and mortality and morbidity in patients with chronic kidney disease. Internal Medicine Journal, 52 (7), 1190-1195. doi: 10.1111/imj.15297 |
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2022 Journal Article Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceKöttgen, Anna, Cornec-Le Gall, Emilie, Halbritter, Jan, Kiryluk, Krzysztof, Mallett, Andrew J., Parekh, Rulan S., Rasouly, Hila Milo, Sampson, Matthew G., Tin, Adrienne, Antignac, Corinne, Ars, Elisabet, Bergmann, Carsten, Bleyer, Anthony J., Bockenhauer, Detlef, Devuyst, Olivier, Florez, Jose C., Fowler, Kevin J., Franceschini, Nora, Fukagawa, Masafumi, Gale, Daniel P., Gbadegesin, Rasheed A., Goldstein, David B., Grams, Morgan E., Greka, Anna, Gross, Oliver, Guay-Woodford, Lisa M., Harris, Peter C., Hoefele, Julia, Hung, Adriana M. ... KDIGO Conference Participants (2022). Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International, 101 (6), 1126-1141. doi: 10.1016/j.kint.2022.03.019 |
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2022 Journal Article The HIDDEN Protocol: An Australian prospective cohort study to determine the utility of whole genome sequencing in kidney failure of unknown aetiologySoraru, Jacqueline, Jahan, Sadia, Quinlan, Catherine, Simons, Cas, Wardrop, Louise, O’Shea, Rosie, Wood, Alasdair, Mallawaarachchi, Amali, Patel, Chirag, Stark, Zornitza and Mallett, Andrew John (2022). The HIDDEN Protocol: An Australian prospective cohort study to determine the utility of whole genome sequencing in kidney failure of unknown aetiology. Frontiers in Medicine, 9 891223, 1-6. doi: 10.3389/fmed.2022.891223 |
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2022 Journal Article The evolving role of diagnostic genomics in kidney transplantationSoraru, Jacqueline, Chakera, Aron, Isbel, Nikky, Mallawaarachichi, Amali, Rogers, Natasha, Trnka, Peter, Patel, Chirag and Mallett, Andrew J. (2022). The evolving role of diagnostic genomics in kidney transplantation. Kidney International Reports, 7 (8), 1758-1771. doi: 10.1016/j.ekir.2022.05.019 |
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2022 Journal Article A clinical approach to tubulopathies in children and young adultsKermond, Rachael, Mallett, Andrew and McCarthy, Hugh (2022). A clinical approach to tubulopathies in children and young adults. Pediatric Nephrology, 38 (3), 1-12. doi: 10.1007/s00467-022-05606-1 |
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2022 Journal Article The heritability of kidney function using an older Australian twin populationJefferis, Julia, Pelecanos, Anita, Catts, Vibeke and Mallett, Andrew (2022). The heritability of kidney function using an older Australian twin population. Kidney International Reports, 7 (8), 1819-1830. doi: 10.1016/j.ekir.2022.05.012 |
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2022 Journal Article Corrigendum: “Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study.” (Kidney International Reports (2021) 6(9) (2481–2485), (S2468024921012390), (10.1016/j.ekir.2021.06.013))Ng, Monica S., Malacova, Eva, Hurst, Cameron, David, Michael C., Johnson, David W. and Mallett, Andrew J. (2022). Corrigendum: “Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study.” (Kidney International Reports (2021) 6(9) (2481–2485), (S2468024921012390), (10.1016/j.ekir.2021.06.013)). Kidney International Reports, 7 (3), 664-664. doi: 10.1016/j.ekir.2022.02.006 |
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2022 Journal Article Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNAViering, Daan, Schlingmann, Karl P., Hureaux, Marguerite, Nijenhuis, Tom, Mallett, Andrew, Chan, Melanie M. Y., van Beek, André, van Eerde, Albertien M., Coulibaly, Jean-Marie, Vallet, Marion, Decramer, Stéphane, Pelletier, Solenne, Klaus, Günter, Kömhoff, Martin, Beetz, Rolf, Patel, Chirag, Shenoy, Mohan, Steenbergen, Eric J., Anderson, Glenn, Bongers, Ernie M. H. F., Bergmann, Carsten, Panneman, Daan, Rodenburg, Richard J., Kleta, Robert, Houillier, Pascal, Konrad, Martin, Vargas-Poussou, Rosa, Knoers, Nine V. A. M., Bockenhauer, Detlef ... Genomics England Research Consortium (2022). Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA. Journal of the American Society of Nephrology : JASN, 33 (2), 305-325. doi: 10.1681/ASN.2021050596 |
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2022 Journal Article National and international kidney failure registries: characteristics, commonalities, and contrastsNg, Monica S.Y., Charu, Vivek, Johnson, David W., O'Shaughnessy, Michelle M. and Mallett, Andrew J. (2022). National and international kidney failure registries: characteristics, commonalities, and contrasts. Kidney International, 101 (1), 23-35. doi: 10.1016/j.kint.2021.09.024 |
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2021 Journal Article Australia and New Zealand renal gene panel testing in routine clinical practice of 542 familiesTanudisastro, Hope A., Holman, Katherine, Ho, Gladys, Farnsworth, Elizabeth, Fisk, Katrina, Gayagay, Thet, Hackett, Emma, Jenkins, Gemma, Krishnaraj, Rahul, Lai, Tiffany, Wong, Karen, Patel, Chirag, Mallawaarachchi, Amali, Mallett, Andrew J., Bennetts, Bruce, Alexander, Stephen I. and McCarthy, Hugh J. (2021). Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine, 6 (1) 20, 20. doi: 10.1038/s41525-021-00184-x |
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2021 Journal Article Cost-effectiveness of targeted exome analysis as a diagnostic test in glomerular diseasesJayasinghe, Kushani, Wu, You, Stark, Zornitza, Kerr, Peter G., Mallett, Andrew J., Gaff, Clara, Martyn, Melissa, Goranitis, Ilias and Quinlan, Catherine (2021). Cost-effectiveness of targeted exome analysis as a diagnostic test in glomerular diseases. Kidney International Reports, 6 (11), 2850-2861. doi: 10.1016/j.ekir.2021.08.028 |
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2021 Journal Article Monogenic nephrolithiasis—collision of phenotypes, genotypes, and phenocopiesMallett, Andrew (2021). Monogenic nephrolithiasis—collision of phenotypes, genotypes, and phenocopies. Kidney International Reports, 6 (11), 2737-2739. doi: 10.1016/j.ekir.2021.09.012 |
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2021 Journal Article Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney diseaseTran, Ngan K., Lea, Rodney A., Holland, Samuel, Nguyen, Quan, Raghubar, Arti M., Sutherland, Heidi G., Benton, Miles C., Haupt, Larisa M., Blackburn, Nicholas B., Curran, Joanne E., Blangero, John, Mallett, Andrew J. and Griffiths, Lyn R. (2021). Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific reports, 11 (1) 19425, 19425. doi: 10.1038/s41598-021-98935-4 |
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2021 Journal Article Pharmacist-led education for final year medical students: a pilot studyMokrzecki, Sophie, Pain, Tilley, Mallett, Andrew and Perks, Stephen (2021). Pharmacist-led education for final year medical students: a pilot study. Frontiers in Medicine, 8 732054, 1-8. doi: 10.3389/fmed.2021.732054 |
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2021 Journal Article Birt-Hogg-Dubé syndrome and hereditary leiomyomatosis and renal cell carcinoma syndrome: An effective multidisciplinary approach to hereditary renal cancer predisposing syndromesAl-Shinnag, Mohammad, Marfan, Helen, Susman, Rachel, Wakeling, Jan, Gustafson, Sonja, Wood, Simon and Mallett, Andrew John (2021). Birt-Hogg-Dubé syndrome and hereditary leiomyomatosis and renal cell carcinoma syndrome: An effective multidisciplinary approach to hereditary renal cancer predisposing syndromes. Frontiers in Oncology, 11 738822, 738822. doi: 10.3389/fonc.2021.738822 |
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2021 Journal Article Bleeding complications of percutaneous kidney biopsy: Does gender matter?Anpalahan, Aksharaa, Malacova, Eva, Hegerty, Katharine, Mallett, Andrew, Ranganathan, Dwarakanathan, Healy, Helen G. and Gois, Pedro Henrique Franca (2021). Bleeding complications of percutaneous kidney biopsy: Does gender matter?. Kidney360, 2 (8), 1308-1312. doi: 10.34067/kid.0002432021 |
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2021 Journal Article Hyperuricaemia, gout and allopurinol in the CKD Queensland registryJeyaruban, A., Hoy, W., Cameron, A., Healy, H., Wang, Z., Zhang, J. and Mallett, A. (2021). Hyperuricaemia, gout and allopurinol in the CKD Queensland registry. Journal of Nephrology, 34 (3), 753-762. doi: 10.1007/s40620-020-00937-4 |
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2021 Journal Article Clinical versus research genomics in kidney diseaseMallett, Andrew J., Knoers, Nine, Sayer, John and Stark, Zornitza (2021). Clinical versus research genomics in kidney disease. Nature Reviews Nephrology, 17 (9), 570-571. doi: 10.1038/s41581-021-00436-0 |
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2021 Journal Article Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencingMallawaarachchi, Amali C., Lundie, Ben, Hort, Yvonne, Schonrock, Nicole, Senum, Sarah R., Gayevskiy, Velimir, Minoche, Andre E., Hollway, Georgina, Ohnesorg, Thomas, Hinchcliffe, Marcus, Patel, Chirag, Tchan, Michel, Mallett, Andrew, Dinger, Marcel E., Rangan, Gopala, Cowley, Mark J., Harris, Peter C., Burnett, Leslie, Shine, John and Furlong, Timothy J. (2021). Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics, 29 (5), 760-770. doi: 10.1038/s41431-020-00796-4 |
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2021 Journal Article Attitudes and practices of Australian nephrologists toward implementation of clinical genomicsJayasinghe, Kushani, Quinlan, Catherine, Mallett, Andrew J., Kerr, Peter G., McClaren, Belinda, Nisselle, Amy, Mallawaarachchi, Amali, Polkinghorne, Kevan R., Patel, Chirag, Best, Stephanie and Stark, Zornitza (2021). Attitudes and practices of Australian nephrologists toward implementation of clinical genomics. Kidney International Reports, 6 (2), 272-283. doi: 10.1016/j.ekir.2020.10.030 |
