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2023 Journal Article From the internet to the COVID-19 pandemic: how technological advances and a tumultuous world have changed scientific publishing and meetingsTorreggiani, Massimo, Piccoli, Giorgina Barbara and Mallett, Andrew (2023). From the internet to the COVID-19 pandemic: how technological advances and a tumultuous world have changed scientific publishing and meetings. Journal of Nephrology, 36 (8), 2165-2167. doi: 10.1007/s40620-023-01740-7 |
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2022 Journal Article The prevalence of Fabry disease in a statewide chronic kidney disease cohort – Outcomes of the aCQuiRE (Ckd.Qld fabRy Epidemiology) studyMallett, Andrew, Kearey, Phoebe Jane, Cameron, Anne, Healy, Helen G., Denaro, Charles, Thomas, Mark, Lee, Vincent W., Stark, Samantha Louise, Fuller, Maria, Wang, Zaimin and Hoy, Wendy E. (2022). The prevalence of Fabry disease in a statewide chronic kidney disease cohort – Outcomes of the aCQuiRE (Ckd.Qld fabRy Epidemiology) study. BMC Nephrology, 23 (1) 169, 169. doi: 10.1186/s12882-022-02805-8 |
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2022 Journal Article Characterising patients and clinician experiences in comprehensive conservative care for kidney failure in northern QueenslandAl Maraee, Gheed, Vangaveti, Venkat and Mallett, Andrew (2022). Characterising patients and clinician experiences in comprehensive conservative care for kidney failure in northern Queensland. Internal Medicine Journal, 53 (10), 1819-1825. doi: 10.1111/imj.15977 |
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2022 Journal Article Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the futureMallett, Andrew J. (2022). Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the future. Current Opinion in Nephrology and Hypertension, 31 (6), 541-547. doi: 10.1097/MNH.0000000000000836 |
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2022 Journal Article Theory designed strategies to support implementation of genomics in nephrologyKansal, Arushi, Quinlan, Catherine, Stark, Zornitza, Kerr, Peter G., Mallett, Andrew J., Lakshmanan, Chandni, Best, Stephanie and Jayasinghe, Kushani (2022). Theory designed strategies to support implementation of genomics in nephrology. Genes, 13 (10) 1919, 1-14. doi: 10.3390/genes13101919 |
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2022 Journal Article Cellular milieu in clear cell renal cell carcinomaRaghubar, Arti M., Roberts, Matthew J., Wood, Simon, Healy, Helen G., Kassianos, Andrew J. and Mallett, Andrew J. (2022). Cellular milieu in clear cell renal cell carcinoma. Frontiers in Oncology, 12 943583, 1-10. doi: 10.3389/fonc.2022.943583 |
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2022 Journal Article Participant choice towards receiving potential additional findings in an Australian nephrology research genomics studyO’Shea, Rosie, Wood, Alasdair, Patel, Chirag, McCarthy, Hugh J., Mallawaarachchi, Amali, Quinlan, Catherine, Simons, Cas, Stark, Zornitza and Mallett, Andrew J. (2022). Participant choice towards receiving potential additional findings in an Australian nephrology research genomics study. Genes, 13 (10) 1804, 1-7. doi: 10.3390/genes13101804 |
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2022 Journal Article Chronic kidney disease in public renal practices in Queensland, Australia, 2011‐2018Hoy, Wendy E., Wang, Zaimin, Zhang, Jianzhen, Diwan, Vishal, Cameron, Anne, Venuthurupalli, Sree K., Fassett, Robert G., Chan, Samuel, Healy, Helen G., Tan, Ken‐Soon, Baer, Richard, Mallett, Andrew J., Gray, Nicholas, Mantha, Murty, Cherian, Roy, Mutatiri, Clyson, Madhan, Krishan, Kan, George, Mitchell, Geoffrey, Hossain, Shahadat, Wu, Danielle, Han, Thin, Kark, Adrian, Titus, Thomas, Ranganathan, Dwarakanatan, Bonner, Ann, Govindarajulu, Sridevi and the NHMRC CKD. CRE and the CKD.QLD Collaborative. (2022). Chronic kidney disease in public renal practices in Queensland, Australia, 2011‐2018. Nephrology, 27 (12), 934-944. doi: 10.1111/nep.14111 |
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2022 Journal Article Spatially resolved transcriptomes of mammalian kidneys illustrate the molecular complexity and interactions of functional nephron segmentsRaghubar, Arti M., Pham, Duy T., Tan, Xiao, Grice, Laura F., Crawford, Joanna, Lam, Pui Yeng, Andersen, Stacey B., Yoon, Sohye, Teoh, Siok Min, Matigian, Nicholas A., Stewart, Anne, Francis, Leo, Ng, Monica S. Y., Healy, Helen G., Combes, Alexander N., Kassianos, Andrew J., Nguyen, Quan and Mallett, Andrew J. (2022). Spatially resolved transcriptomes of mammalian kidneys illustrate the molecular complexity and interactions of functional nephron segments. Frontiers in Medicine, 9 873923, 873923. doi: 10.3389/fmed.2022.873923 |
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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 |
