Overview
Background
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.
Availability
- Dr Andrew Mallett is:
- Available for supervision
- Media expert
Works
Search Professor Andrew Mallett’s works on UQ eSpace
2022
Journal Article
Determining the association between the type of intervention for ischaemic heart disease and mortality and morbidity in patients with chronic kidney disease
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
2022
Journal Article
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
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
2022
Journal Article
The HIDDEN Protocol: An Australian prospective cohort study to determine the utility of whole genome sequencing in kidney failure of unknown aetiology
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
2022
Journal Article
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
2022
Journal Article
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
2022
Journal Article
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
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
2022
Conference Publication
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, NJ, United States: Wiley.
2022
Journal Article
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
2022
Journal Article
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
2021
Journal Article
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
2021
Journal Article
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
2021
Journal Article
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
2021
Conference Publication
The Emerging Role of Whole-Genome Investigation to Identify Undetected Nephropathies: The HIDDEN Study
Mallett, Andrew J., Mallawaarachchi, Amali, Stark, Zornitza, Simons, Cas, Quinlan, Catherine, Patel, Chirag and The KidGen Collaborative (2021). The Emerging Role of Whole-Genome Investigation to Identify Undetected Nephropathies: The HIDDEN Study. Kidney Week, Online, 4-7 November 2021. Washington, DC United States: American Society of Nephrology. doi: 10.1681/asn.20213210s1415c
2021
Conference Publication
Rab GTPase Regulation in Ciliogenesis and Polycystic Kidney Disease
Mcconnachie, Dominique J., Mallett, Andrew J., Stow, Jennifer L. and Protein trafficking and inflammation group (2021). Rab GTPase Regulation in Ciliogenesis and Polycystic Kidney Disease. Kidney Week, Online, 4-7 November 2021. Washington, DC United States: American Society of Nephrology. doi: 10.1681/asn.20213210s1397e
2021
Journal Article
Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease
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
2021
Journal Article
Birt-Hogg-Dubé syndrome and hereditary leiomyomatosis and renal cell carcinoma syndrome: An effective multidisciplinary approach to hereditary renal cancer predisposing syndromes
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
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
2021
Journal Article
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
2021
Journal Article
MO1005ADPEDKD: A GLOBAL ONLINE PLATFORM TO EXPLORE THE CHILDHOOD PHENOTYPE OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE*
Dachy, Angélique, De Rechter, Stéphanie, Guay-Woodford, Lisa, Mallett, Andrew John, Harris, Tess, Bockenhauer, Detlef, Schaefer, Franz, Liebau, Max and Mekahli, Djalila (2021). MO1005ADPEDKD: A GLOBAL ONLINE PLATFORM TO EXPLORE THE CHILDHOOD PHENOTYPE OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE*. Nephrology Dialysis Transplantation, 36 (Supplement_1). doi: 10.1093/ndt/gfab108.002
Funding
Current funding
Past funding
Supervision
Availability
- Dr Andrew Mallett is:
- Available for supervision
Before you email them, read our advice on how to contact a supervisor.
Supervision history
Current supervision
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Doctor Philosophy
The IMPEDE-PKD Clinical Trial - Investigating the repurposing of metformin in ADPKD
Principal Advisor
Other advisors: Professor David Johnson, Dr Christine Staatz, Professor Carmel Hawley, Associate Professor Andrea Viecelli
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Doctor Philosophy
Establishing the Role of Metformin for Autosomal Dominant Polycystic Kidney Disease Management
Principal Advisor
Other advisors: Professor David Johnson, Dr Christine Staatz, Professor Carmel Hawley, Associate Professor Andrea Viecelli
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Doctor Philosophy
Sample sub-group algorithm bias analysis for machine learning evaluation in the clinical domain
Associate Advisor
Other advisors: Professor Clair Sullivan, Professor Guido Zuccon, Mr Anton Van Der Vegt, Professor Emma McBryde
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Doctor Philosophy
Improving patient centred outcomes in kidney transplant recipients
Associate Advisor
Other advisors: Dr Christine Staatz
Completed supervision
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2023
Doctor Philosophy
Defining the cellular milieu within the clear cell renal cell carcinoma microenvironment
Principal Advisor
Other advisors: Dr Andrew Kassianos, Dr Quan Nguyen
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2024
Doctor Philosophy
Improving patient centred outcomes in kidney transplant recipients
Associate Advisor
Other advisors: Dr Christine Staatz
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2022
Doctor Philosophy
Rab GTPase Regulation of Primary Cilia in Renal Epithelium
Associate Advisor
Other advisors: Professor Jennifer Stow
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2022
Master Philosophy
Rab GTPase Regulation of Cell Surface Protrusions
Associate Advisor
Other advisors: Professor Jennifer Stow
Media
Enquiries
Contact Dr Andrew Mallett directly for media enquiries about:
- Alport Syndrome
- clinical genomic
- genetic kidney disease
- genetics
- genomics
- inherited kidney disease
- kidney
- kidney disease
- kidney genetics
- nephrology
- polycystic kidney disease
- renal genetics
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