Dr Andrew Mallett
Dr

Andrew Mallett

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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

Search Professor Andrew Mallett’s works on UQ eSpace

233 works between 2012 and 2025
All (233) Journal Article (176) Other Outputs (1) Conference Publication (55) Book Chapter (1)

121 - 140 of 233 works

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

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))

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.

Trimethoprim and sulphathiazole pharmacokinetic evaluation in adult kidney transplant recipients.

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

Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA

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

National and international kidney failure registries: characteristics, commonalities, and contrasts

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

Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families

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

Cost-effectiveness of targeted exome analysis as a diagnostic test in glomerular diseases

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

Monogenic nephrolithiasis—collision of phenotypes, genotypes, and phenocopies

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

The Emerging Role of Whole-Genome Investigation to Identify Undetected Nephropathies: The HIDDEN Study

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

Rab GTPase Regulation in Ciliogenesis and Polycystic Kidney Disease

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

Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease

2021

Journal Article

Pharmacist-led education for final year medical students: a pilot study

Mokrzecki, 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

Pharmacist-led education for final year medical students: a pilot study

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

Birt-Hogg-Dubé syndrome and hereditary leiomyomatosis and renal cell carcinoma syndrome: An effective multidisciplinary approach to hereditary renal cancer predisposing syndromes

2021

Conference Publication

Trimethoprim-sulfamethoxazole pharmacokinetic evaluation in adult kidney transplant patients

Scuderi, C.E., Jahan, S., Parker, S. L., Jacks, M., John, G., McWhinney, B., Ungerer, J., Mallett, A., Healy, H., Roberts, J.A. and Staatz, C. E. (2021). Trimethoprim-sulfamethoxazole pharmacokinetic evaluation in adult kidney transplant patients. Australian and New Zealand Society of Nephrology conference, Online, September 2021.

Trimethoprim-sulfamethoxazole pharmacokinetic evaluation in adult kidney transplant patients

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

Bleeding complications of percutaneous kidney biopsy: Does gender matter?

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

Hyperuricaemia, gout and allopurinol in the CKD Queensland registry

2021

Journal Article

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

Clinical versus research genomics in kidney disease

2021

Journal Article

Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing

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

Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing

2021

Journal Article

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

Per-treatment post hoc analysis of clinical trial outcomes with tolvaptan in ADPKD

2021

Journal Article

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

Attitudes and practices of Australian nephrologists toward implementation of clinical genomics

2021

Journal Article

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

Clinical impact of genomic testing in patients with suspected monogenic kidney disease

Current funding

  • 2025 - 2026
    KidGen Collaborative: Effective, efficient and equitable care of patients with genetic kidney disease through a national network of multidisciplinary clinics and education programs
    Commonwealth Department of Health
    Open grant
  • 2023 - 2028
    IMPEDE-PKD: Metformin to protect kidney function in polycystic kidney disease
    University of Otago
    Open grant
  • 2022 - 2025
    Genomic Approaches to Kidney Health and Disease
    Queensland Advancing Clinical Research Fellowship
    Open grant
  • 2020 - 2027
    Implementation of Metformin theraPy to Ease DEcline of kidney function in PKD - the IMPEDE-PKD trial
    NHMRC MRFF - Rare Cancers, Rare Diseases and Unmet Need
    Open grant

Past funding

  • 2021 - 2022
    Rab GTPase regulation in Ciliogenesis and Polycystic Kidney Disease
    PKD Foundation of Australia Limited
    Open grant
  • 2020 - 2023
    KidGen Clinics, Education, Data and Research (KidGen CEDAR): Improving Care and Outcomes of Australians with Genetic Kidney Disease
    Commonwealth Department of Health
    Open grant
  • 2020 - 2021
    Applying Spatial Transcriptomics to Discover Kidney Disease Pathways and Optimize Clinical Kidney Biopsy Assessment
    Metro North Hospital and Health Service
    Open grant
  • 2018 - 2020
    IMPEDE-PKD (Implementation of Metformin therapy to Ease Decline of kidney function in PKD). A Clinical Trial Investigating Metformin to slow the progression of renal dysfunction in ADPKD
    PKD Foundation of Australia Limited
    Open grant
  • 2018
    The HIDDEN Study (wHole genome Investigation to iDentify unDEtected Nephropathies) - Applying Genomics to Understand Unexplained End Stage Kidney Disease
    Royal Brisbane and Women's Hospital
    Open grant
  • 2016 - 2019
    Applying functional genomics to kidney disease (NHMRC Project Grant Administered by Murdoch Children's Research Institute)
    Murdoch Childrens Research Institute
    Open grant

Availability

Dr Andrew Mallett is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Supervision history

Current supervision

Completed supervision

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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