Professor Andrew Mallett is a Nephrologist with a special interest in inherited kidney disease and nephrogenetics. After graduating from James Cook University (MBBS, 2006) he completed physician training at Mackay Base Hospital, Royal Brisbane and Women's Hospital and Princess Alexandra Hospital (MMed USyd, 2009; AFRACMA 2011; FRACP 2013; FASN 2016). Professor Mallett has undertaken a Churchill Fellowship and been a recurrent Visiting Fellow at Addenbrooke's Hospital (Cambridge, UK) and the Cambridge Institute for Medical Research (University of Cambridge). He has completed a PhD in nephrogenetics collaborating nationally and internationally, and is a Consultant Nephrologist at RBWH, co-leading the statewide Queensland Conjoint Renal Genetics Service. Professor Mallett is National Director of KidGen, the AGHA Renal Genetics Rare Disease Flagship.
Journal Article: Beyond DNA sequencing: genetic kidney disorders related to altered splicing
McCarthy, Hugh J, Mallett, Andrew J, Sullivan, Patricia, Cowley, Mark J and Mallawaarachchi, Amali C (2024). Beyond DNA sequencing: genetic kidney disorders related to altered splicing. Nephrology Dialysis Transplantation. doi: 10.1093/ndt/gfae022
Journal Article: Attitudes and barriers towards deprescribing in older patients experiencing polypharmacy: a narrative review
Robinson, Michael, Mokrzecki, Sophie and Mallett, Andrew J. (2024). Attitudes and barriers towards deprescribing in older patients experiencing polypharmacy: a narrative review. npj Aging, 10 (1) 6, 6. doi: 10.1038/s41514-023-00132-2
Journal Article: Describing and Explaining ADPKD Variability Within Families
Achi, Sai Santhoshini and Mallett, Andrew J. (2024). Describing and Explaining ADPKD Variability Within Families. Kidney International Reports. doi: 10.1016/j.ekir.2024.01.046
Genomic Approaches to Kidney Health and Disease
(2022–2025) Queensland Advancing Clinical Research Fellowship
Rab GTPase regulation in Ciliogenesis and Polycystic Kidney Disease
(2021–2022) PKD Foundation of Australia Limited
Implementation of Metformin theraPy to Ease DEcline of kidney function in PKD - the IMPEDE-PKD trial
(2020–2027) NHMRC MRFF - Rare Cancers, Rare Diseases and Unmet Need
Defining the cellular milieu within the clear cell renal cell carcinoma microenvironment
(2023) Doctor Philosophy
The IMPEDE-PKD Clinical Trial - Investigating the repurposing of metformin in ADPKD
Doctor Philosophy
Improving patient centred outcomes in kidney transplant recipients
Doctor Philosophy
Spatial transcriptomics in kidney tissue
Raghubar, Arti M., Crawford, Joanna, Jones, Kahli, Lam, Pui Y., Andersen, Stacey B., Matigian, Nicholas A., Ng, Monica S Y, Healy, Helen, Kassianos, Andrew J. and Mallett, Andrew J. (2023). Spatial transcriptomics in kidney tissue. Kidney research: experimental protocols. (pp. 233-282) edited by Tim D. Hewitson, Nigel D. Toussaint and Edward R. Smith. New York, NY USA: Humana New York. doi: 10.1007/978-1-0716-3179-9_17
Beyond DNA sequencing: genetic kidney disorders related to altered splicing
McCarthy, Hugh J, Mallett, Andrew J, Sullivan, Patricia, Cowley, Mark J and Mallawaarachchi, Amali C (2024). Beyond DNA sequencing: genetic kidney disorders related to altered splicing. Nephrology Dialysis Transplantation. doi: 10.1093/ndt/gfae022
Robinson, Michael, Mokrzecki, Sophie and Mallett, Andrew J. (2024). Attitudes and barriers towards deprescribing in older patients experiencing polypharmacy: a narrative review. npj Aging, 10 (1) 6, 6. doi: 10.1038/s41514-023-00132-2
Describing and Explaining ADPKD Variability Within Families
Achi, Sai Santhoshini and Mallett, Andrew J. (2024). Describing and Explaining ADPKD Variability Within Families. Kidney International Reports. doi: 10.1016/j.ekir.2024.01.046
Robinson, Michael, Vangaveti, Venkat, Mokrzecki, Sophie and Mallett, Andrew J. (2023). Polypharmacy in older patients presenting to a tertiary regional health service: identifying correlations between demographics, presentations and length of stay. Internal Medicine Journal, 53 (12), 2336-2340. doi: 10.1111/imj.16291
Monogenic and polygenic concepts in chronic kidney disease (CKD)
Jefferis, Julia, Hudson, Rebecca, Lacaze, Paul, Bakshi, Andrew, Hawley, Carmel, Patel, Chirag and Mallett, Andrew (2023). Monogenic and polygenic concepts in chronic kidney disease (CKD). Journal of Nephrology, 1-15. doi: 10.1007/s40620-023-01804-8
Yu, Dong, Malacova, Eva, Hurst, Cameron, Ng, Monica Suet Ying and Mallett, Andrew John (2023). Association of primary kidney disease type and donor relatedness with live donor kidney transplant outcomes: an analysis of ANZDATA. American Journal of Kidney Diseases, 82 (5), 569-580.e1. doi: 10.1053/j.ajkd.2023.04.004
Raghubar, Arti M., Matigian, Nicholas A., Crawford, Joanna, Francis, Leo, Ellis, Robert, Healy, Helen G., Kassianos, Andrew J., Ng, Monica S. Y., Roberts, Matthew J., Wood, Simon and Mallett, Andrew J. (2023). High risk clear cell renal cell carcinoma microenvironments contain protumour immunophenotypes lacking specific immune checkpoints. npj Precision Oncology, 7 (1) 88, 1-9. doi: 10.1038/s41698-023-00441-5
Diwan, Vishal, Hoy, Wendy E., Wang, Zaimin, Zhang, Jianzhen, 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 on behalf of the NHMRC CKD.CRE and the CKD.QLD Collaborative (2023). Hospitalizations among adults with CKD in public renal specialty practices: a retrospective study from Queensland, Australia. Kidney Medicine, 5 (9) 100700, 100700. doi: 10.1016/j.xkme.2023.100700
Watters, Tara K., Glass, Beverley D. and Mallett, Andrew J. (2023). Identifying the barriers to kidney transplantation for patients in rural and remote areas: a scoping review. Journal of Nephrology. doi: 10.1007/s40620-023-01755-0
Tolerogenic dendritic cells protect against acute kidney injury
Li, Jennifer S.Y., Robertson, Harry, Trinh, Katie, Raghubar, Arti M., Nguyen, Quan, Matigian, Nicholas, Patrick, Ellis, Thomson, Angus W., Mallett, Andrew J. and Rogers, Natasha M. (2023). Tolerogenic dendritic cells protect against acute kidney injury. Kidney International, 104 (3), 492-507. doi: 10.1016/j.kint.2023.05.008
Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD
Hort, Yvonne, Sullivan, Patricia, Wedd, Laura, Fowles, Lindsay, Stevanovski, Igor, Deveson, Ira, Simons, Cas, Mallett, Andrew, Patel, Chirag, Furlong, Timothy, Cowley, Mark J., Shine, John and Mallawaarachchi, Amali (2023). Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD. npj Genomic Medicine, 8 (1) 16, 1-9. doi: 10.1038/s41525-023-00362-z
The utility of spatial transcriptomics for solid organ transplantation
Li, Jennifer S.Y., Raghubar, Arti M., Matigian, Nicholas A., Ng, Monica S.Y., Rogers, Natasha M. and Mallett, Andrew J (2023). The utility of spatial transcriptomics for solid organ transplantation. Transplantation, 107 (7), 1463-1471. doi: 10.1097/tp.0000000000004466
De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome
Hudson, Rebecca, Abeysekera, Natasha, Wolski, Penny, Simons, Cas, Francis, Leo, Farnsworth, Elizabeth, Bennetts, Bruce, Patel, Chirag, Spijker, Siebe and Mallett, Andrew (2023). De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome. Journal of Nephrology. doi: 10.1007/s40620-023-01666-0
Jahan, Sadia, Hale, Janine, Malacova, Eva, Hurst, Cameron, Kark, Adrian and Mallett, Andrew (2023). Real world evaluation of kidney failure risk equations in predicting progression from chronic kidney disease to kidney failure in an Australian cohort. Journal of Nephrology, 1-7. doi: 10.1007/s40620-023-01680-2
Bakshi, Andrew, Jefferis, Julia, Wolfe, Rory, Wetmore, James B., McNeil, John J., Murray, Anne M., Polkinghorne, Kevan R., Mallett, Andrew J. and Lacaze, Paul (2023). Association of polygenic scores with chronic kidney disease phenotypes in a longitudinal study of older adults. Kidney International, 103 (6), 1156-1166. doi: 10.1016/j.kint.2023.03.017
Scuderi, Carla E., Parker, Suzanne L., Jacks, Margaret, John, George T., McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew J., Healy, Helen G., Roberts, Jason A. and Staatz, Christine E. (2023). Serum creatinine and tacrolimus assessment with VAMS finger-prick microsampling: a diagnostic test study. Kidney Medicine, 5 (4) 100610, 100610. doi: 10.1016/j.xkme.2023.100610
Stark, Zornitza, Boughtwood, Tiffany, Haas, Matilda, Braithwaite, Jeffrey, Gaff, Clara L., Goranitis, Ilias, Spurdle, Amanda B., Hansen, David P., Hofmann, Oliver, Laing, Nigel, Metcalfe, Sylvia, Newson, Ainsley J., Scott, Hamish S., Thorne, Natalie, Ward, Robyn L., Dinger, Marcel E., Best, Stephanie, Long, Janet C., Grimmond, Sean M., Pearson, John, Waddell, Nicola, Barnett, Christopher P., Cook, Matthew, Field, Michael, Fielding, David, Fox, Stephen B., Gecz, Jozef, Jaffe, Adam, Leventer, Richard J. ... North, Kathryn N. (2023). Australian genomics: outcomes of a 5-year national program to accelerate the integration of genomics in healthcare. American Journal of Human Genetics, 110 (3), 419-426. doi: 10.1016/j.ajhg.2023.01.018
Editorial: Genetics and epigenetics of chronic kidney disease
Hoefele, Julia, Rao, Jia and Mallett, Andrew J. (2023). Editorial: Genetics and epigenetics of chronic kidney disease. Frontiers in Medicine, 10 1078300, 1-2. doi: 10.3389/fmed.2023.1078300
Scuderi, Carla, Parker, Suzanne, Jacks, Margaret, John, George T., McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew, Healy, Helen, Roberts, Jason and Staatz, Christine (2023). Fingerprick microsampling methods can replace venepuncture for simultaneous therapeutic drug monitoring of tacrolimus, mycophenolic acid, and prednisolone concentrations in adult kidney transplant patients. Therapeutic Drug Monitoring, 45 (1), 69-78. doi: 10.1097/FTD.0000000000001024
Diagnostic utility and outcomes of inpatient investigations for syncope in a regional setting
Schembri, Laura, Vangaveti, Venkat and Mallett, Andrew (2023). Diagnostic utility and outcomes of inpatient investigations for syncope in a regional setting. Internal Medicine Journal, 53 (12), 2208-2215. doi: 10.1111/imj.16019
Mallett, 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
Al 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
Mallett, 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
Theory designed strategies to support implementation of genomics in nephrology
Kansal, 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
Cellular milieu in clear cell renal cell carcinoma
Raghubar, 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
O’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
Chronic kidney disease in public renal practices in Queensland, Australia, 2011‐2018
Hoy, 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
Gird your kidneys? A novel approach to ADPKD therapeutics
Mallett, Andrew (2022). Gird your kidneys? A novel approach to ADPKD therapeutics. Journal of Nephrology, 36 (3), 1-2. doi: 10.1007/s40620-022-01425-7
Raghubar, 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
Jeyaruban, 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
Köttgen, 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
Soraru, 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
The evolving role of diagnostic genomics in kidney transplantation
Soraru, 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
A clinical approach to tubulopathies in children and young adults
Kermond, 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
The heritability of kidney function using an older Australian twin population
Jefferis, 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
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
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA
Viering, 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
National and international kidney failure registries: characteristics, commonalities, and contrasts
Ng, 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
Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families
Tanudisastro, 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
Cost-effectiveness of targeted exome analysis as a diagnostic test in glomerular diseases
Jayasinghe, 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
Monogenic nephrolithiasis—collision of phenotypes, genotypes, and phenocopies
Mallett, 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
Tran, 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
Al-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
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
Hyperuricaemia, gout and allopurinol in the CKD Queensland registry
Jeyaruban, 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
Clinical versus research genomics in kidney disease
Mallett, 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
Mallawaarachchi, 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
Attitudes and practices of Australian nephrologists toward implementation of clinical genomics
Jayasinghe, 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
Per-treatment post hoc analysis of clinical trial outcomes with tolvaptan in ADPKD
Mallett, Andrew J., Perrone, Ronald D., Rangan, Gopala, Hawley, Carmel, El-Damanawi, Ragada, Hiemstra, Thomas F., Arellano, Carolina Townsend, Lee, Jennifer and Torres, Vicente E. (2021). Per-treatment post hoc analysis of clinical trial outcomes with tolvaptan in ADPKD. Kidney International Reports, 6 (4), 1032-1040. doi: 10.1016/j.ekir.2021.01.014
Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study
Ng, Monica S., Malacova, Eva, Hurst, Cameron, Johnson, David W. and Mallett, Andrew J. (2021). Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study. Kidney International Reports, 6 (9), 2481-2485. doi: 10.1016/j.ekir.2021.06.013
Clinical impact of genomic testing in patients with suspected monogenic kidney disease
Jayasinghe, Kushani, Stark, Zornitza, Kerr, Peter G., Gaff, Clara, Martyn, Melissa, Whitlam, John, Creighton, Belinda, Donaldson, Elizabeth, Hunter, Matthew, Jarmolowicz, Anna, Johnstone, Lilian, Krzesinski, Emma, Lunke, Sebastian, Lynch, Elly, Nicholls, Kathleen, Patel, Chirag, Prawer, Yael, Ryan, Jessica, See, Emily J., Talbot, Andrew, Trainer, Alison, Tytherleigh, Rigan, Valente, Giulia, Wallis, Mathew, Wardrop, Louise, West, Kirsty H., White, Susan M., Wilkins, Ella, Mallett, Andrew J. and Quinlan, Catherine (2021). Clinical impact of genomic testing in patients with suspected monogenic kidney disease. Genetics in Medicine, 23 (1), 183-191. doi: 10.1038/s41436-020-00963-4
Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease
Gately, Ryan, Lock, Gregory, Patel, Chirag, Clouston, John, Hawley, Carmel and Mallett, Andrew (2021). Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease. Kidney International Reports, 6 (1), 219-223. doi: 10.1016/j.ekir.2020.10.001
Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
Huynh, Vinh T., Audrézet, Marie-Pierre, Sayer, John A., Ong, Albert C., Lefevre, Siriane, Le Brun, Valoris, Després, Aurore, Senum, Sarah R., Chebib, Fouad T., Barroso-Gil, Miguel, Patel, Chirag, Mallett, Andrew J., Goel, Himanshu, Mallawaarachchi, Amali C., Van Eerde, Albertien M, Ponlot, Eléonore, Kribs, Marc, Genkyst Study Group, Genomics England Research Consortium, Le Meur, Yannick, Harris, Peter C. and Cornec-Le Gall, Emilie (2020). Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease. Kidney international, 98 (2), 476-487. doi: 10.1016/j.kint.2020.02.022
DNAJB11-Related Atypical ADPKD in a Kidney Transplant Donor
Wilson, Gregory J., Wood, Simon, Patel, Chirag, Oliver, Kimberley, John, George, Ranganathan, Dwarakanathan, Mallett, Andrew and Isbel, Nicole (2020). DNAJB11-Related Atypical ADPKD in a Kidney Transplant Donor. Kidney International Reports, 5 (8), 1363-1366. doi: 10.1016/j.ekir.2020.05.022
Protocol and establishment of a Queensland renal biopsy registry in Australia
Burke, Joseph Patrick, Aljishi, Manaf, Francis, Leo, Hoy, Wendy, Divi, Dakshinamurthy, Cherian, Roy, Frazier, Jeremy, Gobe, Glenda, Gois, Pedro, Govindarajulu, Sridevi, Huynh, Sonny, Jesudason, Shilpanjali, John, George, Madhan, Krishan, Mallett, Andrew, Manickam, Valli, Mutatiri, Clyson, Ng, Shu-Kay, Thet, Zaw, Trnka, Peter, Venuthurupalli, Sree Krishna and Ranganathan, Dwarakanathan (2020). Protocol and establishment of a Queensland renal biopsy registry in Australia. BMC Nephrology, 21 (1) 320, 320. doi: 10.1186/s12882-020-01983-7
ABO blood group relationships to kidney transplant recipient and graft outcomes
Ng, Monica S. Y., Ullah, Shahid, Wilson, Gregory, McDonald, Stephen, Sypek, Matthew and Mallett, Andrew J. (2020). ABO blood group relationships to kidney transplant recipient and graft outcomes. PLoS One, 15 (7) e0236396, e0236396. doi: 10.1371/journal.pone.0236396
Kidney transplant recipient’s perceptions of blood testing through microsampling and venepuncture
Scuderi, Carla E., Parker, Suzanne L., Jacks, Margaret, John, George, McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew, Roberts, Jason A., Healy, Helen and Staatz, Christine E. (2020). Kidney transplant recipient’s perceptions of blood testing through microsampling and venepuncture. Bioanalysis, 12 (13) bio-2020-0057, 873-881. doi: 10.4155/bio-2020-0057
A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder
Jones, Lynelle K., Lam, Rachel, McKee, Karen K., Aleksandrova, Maya, Dowling, John, Alexander, Stephen I., Mallawaarachchi, Amali, Cottle, Denny L., Short, Kieran M., Pais, Lynn, Miner, Jeffery H., Mallett, Andrew J., Simons, Cas, McCarthy, Hugh, Yurchenco, Peter D. and Smyth, Ian M. (2020). A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder. Development, 147 (21) dev189183, dev.189183. doi: 10.1242/dev.189183
Jeyaruban, Andrew, Hoy, Wendy, Cameron, Anne, Healy, Helen, Wang, Zaimin, Zhang, Jianzhen and Mallett, Andrew (2020). Impact of cardiovascular events on mortality and progression of renal dysfunction in a Queensland CKD cohort. Nephrology, 25 (11), e13745-844. doi: 10.1111/nep.13745
Clinical and healthcare utilization outcomes of parathyroidectomy in CKD and dialysis patients
Jones, Scott A., Hegerty, Katharine, Scuderi, Carla, Eglington, Jessica, Green, Ben and Mallett, Andrew (2020). Clinical and healthcare utilization outcomes of parathyroidectomy in CKD and dialysis patients. Kidney International Reports, 5 (7), 1086-1089. doi: 10.1016/j.ekir.2020.04.026
Diagnoses of uncertain significance: kidney genetics in the 21st century
Gale, Daniel P., Mallett, Andrew, Patel, Chirag, Sneddon, Tam P., Rehm, Heidi L., Sampson, Matthew G. and Bockenhauer, Detlef (2020). Diagnoses of uncertain significance: kidney genetics in the 21st century. Nature Reviews Nephrology, 16 (11), 616-618. doi: 10.1038/s41581-020-0277-6
Parental health spillover effects of paediatric rare genetic conditions
Wu, You, Al-Janabi, Hareth, Mallett, Andrew, Quinlan, Catherine, Scheffer, Ingrid E., Howell, Katherine B., Christodoulou, John, Leventer, Richard J., Lockhart, Paul J., Stark, Zornitza, Boughtwood, Tiffany and Goranitis, Ilias (2020). Parental health spillover effects of paediatric rare genetic conditions. Quality of Life Research, 29 (9), 2445-2454. doi: 10.1007/s11136-020-02497-3
Mallett, Andrew, Kearey, Phoebe, Cameron, Anne, Healy, Helen, Denaro, Charles, Thomas, Mark, Lee, Vincent W., Stark, Samantha, Fuller, Maria and Hoy, Wendy E. (2020). The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia. BMC Nephrology, 21 (1) 58, 58. doi: 10.1186/s12882-020-01717-9
Toward transparency in nephrology research
Francis, 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
Jahan, 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
Genetic Kidney Disease in Southern Tasmania
Brailsford, 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
Hudson, 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
Kumuthini, 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
ADPedKD: A Global Online Platform on the Management of Children With ADPKD
De 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
Isolated proteinuria due to CUBN homozygous mutation - challenging the investigative paradigm
Jayasinghe, 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
Chan, 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
Jayasinghe, 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
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
Genome-wide association study of medication-use and associated disease in the UK Biobank
Wu, 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
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
Mallett, 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
Renal genetics in Australia: kidney medicine in the genomic age
Jayasinghe, 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
Ng, 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
Aldridge, 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
CFHR5 nephropathy in a Greek-Cypriot Australian family: ancestry-informed precision medicine
Ng, 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
Forbes, Thomas A., Howden, Sara E., Lawlor, Kynan, Phipson, Belinda, Maksimovic, Jovana, Hale, Lorna, Wilson, Sean, Quinlan, Catherine, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Trnka, Peter, Oshlack, Alicia, Patel, Chirag, Mallett, Andrew, Simons, Cas and Little, Melissa H. (2018). Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms. American Journal of Human Genetics, 102 (5), 816-831. doi: 10.1016/j.ajhg.2018.03.014
Meeting report of the 2017 KidGen Renal Genetics Symposium
Jayasinghe, Kushani, Quinlan, Cathy, Stark, Zornitza, Patel, Chirag, Sampson, Matthew G., Saleem, Moin and Mallett, Andrew J. (2018). Meeting report of the 2017 KidGen Renal Genetics Symposium. Human Genomics, 12 (1) 5, 1-6. doi: 10.1186/s40246-018-0137-7
The increasing rates of acute interstitial nephritis in Australia: a single centre case series
Wilson, 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
Mallett, 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
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease
Connor, 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
Mahmood, 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
Chan, 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
Rangan, 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
Francis, 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
A multidisciplinary renal genetics clinic improves patient diagnosis
Mallett, 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
Tong, 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
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis
Tchan, 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
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone Disease
Mallett, 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
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Pharmacological Management
Mallett, 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
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care
Tong, 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
KHA-CARI autosomal dominant polycystic kidney disease guideline: genetics and genetic counseling
Patel, 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
Savige, 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
Mallett, 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
A protocol for the identification and validation of novel genetic causes of kidney disease
Mallett, 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
Genomics in the renal clinic - translating nephrogenetics for clinical practice
Mallett, 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
Mallett, Andrew, Tang, Wen, Hart, Gareth, McDonald, Stephen P., Hawley, Carmel M., Badve, Sunil V., Boudville, Neil, Brown, Fiona G., Campbell, Scott B., Clayton, Philip A. and Johnson, David W. (2015). End-Stage kidney disease due to fibrillary glomerulonephritis and immunotactoid glomerulopathy - outcomes in 66 consecutive ANZDATA registry cases. American Journal of Nephrology, 42 (3), 177-184. doi: 10.1159/000440815
Mallett, Andrew, Tang, Wen, Clayton, Philip A., Stevenson, Sarah, McDonald, Stephen P., Hawley, Carmel M., Badve, Sunil V., Boudville, Neil, Brown, Fiona G., Campbell, Scott B. and Johnson, David W. (2014). End-stage kidney disease due to Alport syndrome: Outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry cases. Nephrology Dialysis Transplantation, 29 (12), 2277-2286. doi: 10.1093/ndt/gfu254
NOS3 as a potential modifier of ADPKD phenotypic variability: progress towards an answer
Mallett, Andrew and Sandford, Richard (2014). NOS3 as a potential modifier of ADPKD phenotypic variability: progress towards an answer. Nephrology, 19 (12), 733-734. doi: 10.1111/nep.12331
Mallett, Andrew, Patel, Chirag, Salisbury, Anne, Wang, Zaimin, Healy, Helen and Hoy, Wendy (2014). The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia. Orphanet Journal of Rare Diseases, 9 (1) 98. doi: 10.1186/1750-1172-9-98
Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant
Stevenson, Sarah, Mallett, Andrew, Oliver, Kimberley, Hyland, Valentine, Hawley, Carmel, de Malmanche, Theo and Isbel, Nicole (2014). Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant. Nephrology, 19 (S1), 22-26. doi: 10.1111/nep.12195
Sustained remission of systemic lupus erythematosus related calciphylaxis
Mallett, A., John, G. T., Ranganathan, D., Kark, A., Berquier, I., Casey, J., Healy, H. and Francis, L. (2012). Sustained remission of systemic lupus erythematosus related calciphylaxis. Lupus, 21 (4), 441-444. doi: 10.1177/0961203311425526
Trimethoprim-sulfamethoxazole pharmacokinetic evaluation in adult kidney transplant recipients.
Scuderi, C.E., Parker, S.L., Jacks, M., John, G.T., McWhinney, B., Ungerer, J., Mallett, A.J., Healy, H.G., Roberts, J.A. and Staatz, C.E. (2023). Trimethoprim-sulfamethoxazole pharmacokinetic evaluation in adult kidney transplant recipients.. World Congress on Pharmacy and Pharmaceutical Sciences., Brisbane, QLD Australia, 24-28 September 2023.
A Secondary Analysis of Concurrent use of Metformin and Tolvaptan in ADPKD Tolvaptan Trials
Stanley, I., Palma, A., Viecelli, A., Johnson. D., Hawley, C., Staatz, C. and Mallett, A. (2023). A Secondary Analysis of Concurrent use of Metformin and Tolvaptan in ADPKD Tolvaptan Trials. Asian Pacific Society of Dialysis Access (APSDA) Conference, Cairns, QLD Australia, 22-24th October 2023. HOBOKEN: WILEY.
Scuderi, Carla, Parker, Suzanne, Jacks, Margaret, John, George, McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew, Healy, Helen, Roberts, Jason and Staatz, Christine (2022). Can microsampling methods replace venepuncture for simultaneous therapeutic drug monitoring of tacrolimus, mycophenolic acid and prednisolone concentrations in adult kidney transplant patients?. 57th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, NSW Australia, 17-19 October 2022. Richmond, VIC Australia: John Wiley & Sons.
Trimethoprim and sulphathiazole pharmacokinetic evaluation in adult kidney transplant recipients.
Scuderi, C., Jahan, S., Parker, S., Wallis, S., Jacks, M., John, G., McWhinney, B., Ungerer, J., Mallett. A., Healy, H., Roberts, J. and Staatz, C. (2022). Trimethoprim and sulphathiazole pharmacokinetic evaluation in adult kidney transplant recipients. . Society of Hospital Pharmacists of Australia conference, Adelaide, SA Australia, 24-26 February 2022. HOBOKEN: WILEY.
Ng, 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.
Hudson, R., Patel, C., Hawley, C., O'Shea, S., Snelling, P., Crawford, J., Simons, C. and Mallett, A. J. (2018). Adult-diagnosed non-syndromic nephronophthesis in Australian families caused by biallelic NPHP4 variants. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, Australia, 8-12 September 2018. Richmond, VIC 3121 Australia: Wiley-Blackwell Publishing Asia.
Jeyaruban, A., Hoy, W. E., Cameron, A., Healy, H. G., Zhang, J. and Mallett, A. J. (2018). Assessing the impact of hyperuricaemia, gout and allopurinol treatment on progression of renal function in patients with chronic kidney disease. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, Australia, 8-12 September 2018. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia.
Clinical outcomes of parathyroidectomy in chronic kidney disease patients
Jones, S., Hegerty, K., Scuderi, C., Eglington, J., Green, B. and Mallett, A. J. (2018). Clinical outcomes of parathyroidectomy in chronic kidney disease patients. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, NSW Australia, 8-12 September 2018. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia.
Cost-effectiveness in kidney medicine: is cinacalcet superior to parathyroidectomy?
Hegerty, K., Jones, S., Scuderi, C., Eglington, J., Broadbent, T., Zhang, H. and Mallett, A. J. (2018). Cost-effectiveness in kidney medicine: is cinacalcet superior to parathyroidectomy?. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, NSW Australia, 8-12 September 2018. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia.
Jeyaruban, A., Hoy, W. E., Cameron, A., Healy, H. G., Zhang, J. and Mallett, A. J. (2018). Does the type of intervention for ischaemic heart disease impact on mortality and morbidity in patients with chronic kidney disease?. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, Australia, 8-12 September 2018. Richmond, VIC, Australia: Wiley-Blackwell.
Long-term outcome and treatment practices in distal renal tubular acidosis
Lopez Garcia, Sergio Camilo , Emma, Francesco , Walsh, Stephen , Fila, Marc , Hooman, Nakysa , Marcin, Zaniew , Bertholet‐Thomas, Aurélia , Colussi, Giacomo , Ebner, Kathrin , Levtchenko, Elena , Sharma, Jyoti , Singhal, Jyoti , Soliman, Neveen A. , Ariceta, Gema , Basu, Biswanath, Murer, Luisa , Tasic, Velibor , Tsygin, Alexey , Decramer, Stéphane , Gil-peña, Helena , Koster‐kamphuis, Linda , La Scola, Claudio , Gellermann, Jutta , Konrad, Martin , Lilien, Marc , Francisco, Telma , Tramma, Despoina , Trnka, Peter , Yuksel, Selcuk ... Bockenhauer, Detlef (2018). Long-term outcome and treatment practices in distal renal tubular acidosis. 51st Annual ESPN Meeting, Antalya, Turkey, October 2018. Heidelberg, Germany: Springer. doi: 10.1007/s00467-018-4028-x
Micro proteomic profiling in the diagnosis of kidney disease
Raghubar, A., Wang, X., Kassianos, A. J., Ng, M. S., Dave, K. A., Norris, E., Headlam, M. J., Healy, H. G. and Mallett, A. J. (2018). Micro proteomic profiling in the diagnosis of kidney disease. 54th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), Sydney, Australia, 8–12 September 2018. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.13441
Chan, S., Patel, C. and Mallett, A. J. (2018). PROPKD score predicts kidney decline in clinical practice amongst Australian patients with autosomal dominant polycystic kidney disease. Australian and New Zealand Society of Nephrology (ANZSN) Annual Scientific Meeting, Sydney, NSW, Australia, 8-12 September 2018. Hoboken, NJ, United States: Wiley.
Ng, 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.
Fibrillary glomerulonephritis: an apparent familial form?
Ying, Tracey, Hill, Prue, Desmond, Michael, Agar, John and Mallett, Andrew (2015). Fibrillary glomerulonephritis: an apparent familial form?. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12447
Wilson, G, J., Kark, A., Mallett, A., Cameron, A., Wang, Z., Kirby, J., Healy, H.G. and Hoy, W. E. (2015). Acute kidney injury (AKI) associated with chronic kidney disease (CKD) in the renal practices of the Royal Brisbane and Women's Hospital (RBWH)through the CKD.QLD registry. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 Septemebr 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12544
Heterogeneity of chronic kidney disease (CKD) by age in an Australian metropolitan renal service
Mahmood, U., Hoy, W. E., Kark, A., Healy, H. G., Mallett, A, Rawlings, C., Wang, Z., Kirby, J. and Cameron, A. (2015). Heterogeneity of chronic kidney disease (CKD) by age in an Australian metropolitan renal service. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12544
Tunnicliffe, D. J., Tong, A., Lopez-Vargas, P., Mallett, A., Patel, C., Savige, J., Campbell, K., Patel, M., Tchan, M., Alexander, S. I., Lee, V., Craig, J. C. and Rangan, G. (2015). Identifying and Integrating Consumer Perspectives in Clinical Practice Guidelines On Autosomal Dominant Polycystic Kidney Disease. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia.
Mahmood, U., Hoy, W. E., Kark, A., Healy, H. G., Mallett, A., Rawlings, C., Wang, Z., Kirby, J., Coleman, S. and Cameron, A. (2015). Profiles of very elderly patients with chronic kidney disease (CKD) in the public renal specialty practices of the Royal Brisbane and Women's Hospital (RBWH) in Queensland. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12544
Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy
Mallett, A., Mordaunt, D., Sonawane, R., Walker, A., Kausman, J., Peters, H., White, S., Stark, Z., Trnka, P., Patel, C., Crawford, J., Holman, K., Farnsworth, E., Ho, G., Alexander, S., Bennetts, B., Healy, H., Little, M., Simons, C. and Yaplito-Lee, J. (2015). Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12543
Mallett, A., Mordaunt, D., Crafter, S., Mctaggart, S., Kark, A., Patel, C., Crawford, J., Holman, K., Farnsworth, E., Ho, G., Healy, H., Alexander, S., Bennetts, B., Little, M. and Simons, C. (2015). The Heterozygous P.R76W Hnf4A Variant Is Associated with Atypical Autosomal Dominant De Toni-Fanconi-Debre Syndrome and Can Be Diagnosed Utilising Diagnostic Clinical Exomic Analysis. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12543
The T616C Trna(Phe) mutation causes mitochondrially inherited tubulointerstitial kidney disease
Mallett, A., Hoer, S., John, G., Burke, J., Patel, C., Crawford, J., Hyland, V., Healy, H., Little, M., Simons, C., Connor, T. and Maxwell, P. (2015). The T616C Trna(Phe) mutation causes mitochondrially inherited tubulointerstitial kidney disease. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, Australia, 7-9 September 2015. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12543
Coincident Iga Nephropathy in An Australian Patient with Fabry'S Disease
Rawlings, C., Francis, L., Mallett, A., John, G. and Denaro, C. (2014). Coincident Iga Nephropathy in An Australian Patient with Fabry'S Disease. 50th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Melbourne, VIC Australia, 25-27 August 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12303
Exomic Approaches to Diagnosis Amongst Australians with Genetic Renal Diseases
Mallett, A., Ho, G., Mccarthy, H., Fletcher, J., Mallawaarachchi, A., Little, M., Jueppner, H., Sawyer, A., Bennetts, B. and Alexander, S. (2014). Exomic Approaches to Diagnosis Amongst Australians with Genetic Renal Diseases. 50th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Melbourne, VIC Australia, 25-27 August 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12302
Renal Oncocytosis in the Setting of a Rare Invalidated Flcn Gene Variant
Rawlings, C., Susman, R., Mallett, A., Francis, L. and Kark, A. (2014). Renal Oncocytosis in the Setting of a Rare Invalidated Flcn Gene Variant. 50th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Melbourme, VIC Australia, 25-27 August 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12303
The Initial Six Months of An Australian Renal Genetics Clinic Service
Mallett, A., Patel, C., Mcgaughran, J. and Healy, H. (2014). The Initial Six Months of An Australian Renal Genetics Clinic Service. 50th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Melbourne, VIC Australia, 25-27 August 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12302
Mallawaarachchi, A., Mallett, A., Sawyer, A., Mccarthy, H., Fletcher, J., Chapman, J., Bennetts, B., Ho, G., Jueppner, H., Hahn, D. and Alexander, S. (2014). Utilising Exome Sequencing to Identify Nephronophthisis Mutations Within An Australian Clinical Cohort. 50th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Melbourne, VIC Australia, 25-27 August 2014. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12302
Mallett, A., Salisbury, A., Wang, Z., Healy, H. G. and Hoy, W. E. (2013). Acute kidney injury, analgesic nephropathy and toxin-mediated kidney injury in an Australian chronic kidney disease (CKD) cohort. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Mallett, A., Salisbury, A., Wang, Z., Healy, H.G. and Hoy, W.E. (2013). Acute kidney injury, analgestic nephropathy and toxin-mediated kidney injury in an Australian chronic kidney disease (CKD) cohort.. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Mallett, A., Salisbury, A., Wang, Z., Healy, H. G. and Hoy, W. E. (2013). Alport syndrome and thin basement membrane nephropathy in the Queensland chronic kidney disease (CKD) registry. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Mallett, A., Salisbury, A., Wang, Z., Healy, H. G. and Hoy, W. E. (2013). Autosomal dominant polycystic kidney disease in an Australian chronic kidney disease (CKD) population. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Chronic kidney disease (CKD) is not renal replacement therapy (RRT): the CKD.QLD registry dataset
Healy, H., Salisbury, A., Wang, Z., Mallett, A., Huynh, S., Mohandas, T., Sanghi, P., Heffernan, D., Fassett, R. and Hoy, W. (2013). Chronic kidney disease (CKD) is not renal replacement therapy (RRT): the CKD.QLD registry dataset. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Chronic kidney disease (CKD) patient outcomes: a longitudinal report from the CKD.QLD registry
Salisbury, A., Mallett, A., Wang, Z., Healy, H. G., Huynh, S., Smith, S., Heffernan, D. and Hoy, W. E. (2013). Chronic kidney disease (CKD) patient outcomes: a longitudinal report from the CKD.QLD registry. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD, Australia, 9-11 September 2013. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121
Chronic kidney disease is a different population: the CKD. Qld registry dataset
Healy, Helen, Wang, Zaimin, Mallett, Andrew, Huynh, Sonny, Coleman, Sonya, Kark, Adrian, Salisbury, Anne, Venuthurupalli, Sree Krishna, Fassett, Robert and Hoy, Wendy (2013). Chronic kidney disease is a different population: the CKD. Qld registry dataset. The Royal Australasian College of Physicians Future Directions in Health Congress 2013 (RACP), Perth WA, Australia, 26-29 May 2013. Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/imj.12150
Clinical PKD1 sequencing in Queensland
Kozlov, S., Mallett, A., Woods, R., Healy, H., Rowell, J., Mcgaughran, J. and Hyland, V. (2012). Clinical PKD1 sequencing in Queensland. 48th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Auckland, New Zealand, 27-29 August 2012. Richmond, VIC, Australia: Wiley-Blackwell. doi: 10.1111/j.1440-1797.2012.01632.x
The Ckd.Qld Registry provides an epidemiological platform for answering future clinical questions
Healy, H., Wang, Z., Mallett, A., Huynh, S., Coleman, S., Kark, A., Salsibury, A., Venuthurupalli, S. K., Fassett, R. G. and Hoy, W. E. (2012). The Ckd.Qld Registry provides an epidemiological platform for answering future clinical questions. 48th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Auckland, New Zealand, 27-29 August 2012. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1797.2012.01633.x
The characteristics of uninephric chronic kidney disease patients
Mallett, A., Wang, Z., Healy, H., John, J., Fassett, R. G., Salisbury, A. and Hoy, W. E. (2012). The characteristics of uninephric chronic kidney disease patients. 48th Annual Scientific Meeting of the Australia and New Zealand Society of Nephrology, Auckland, New Zealand, 27-29 August 2012. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1797.2012.01633.x
Genetic diagnostics in genetic renal disease: Methods, applications and therapeutics
Mallett, 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
Genomic Approaches to Kidney Health and Disease
(2022–2025) Queensland Advancing Clinical Research Fellowship
Rab GTPase regulation in Ciliogenesis and Polycystic Kidney Disease
(2021–2022) PKD Foundation of Australia Limited
Implementation of Metformin theraPy to Ease DEcline of kidney function in PKD - the IMPEDE-PKD trial
(2020–2027) NHMRC MRFF - Rare Cancers, Rare Diseases and Unmet Need
(2020–2023) Commonwealth Department of Health
(2020–2021) Metro North Hospital and Health Service
(2018–2020) PKD Foundation of Australia Limited
(2018) Royal Brisbane and Women's Hospital
(2016–2019) Murdoch Childrens Research Institute
The IMPEDE-PKD Clinical Trial - Investigating the repurposing of metformin in ADPKD
Doctor Philosophy — Principal Advisor
Improving patient centred outcomes in kidney transplant recipients
Doctor Philosophy — Associate Advisor
Other advisors:
Defining the cellular milieu within the clear cell renal cell carcinoma microenvironment
(2023) Doctor Philosophy — Principal Advisor
Other advisors:
Rab GTPase Regulation of Cell Surface Protrusions
(2022) Master Philosophy — Associate Advisor
Other advisors:
Rab GTPase Regulation of Primary Cilia in Renal Epithelium
(2022) Doctor Philosophy — Associate Advisor
Other advisors: