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Dr Andrew Mallett
Dr

Andrew Mallett

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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

199 works between 2012 and 2025

101 - 120 of 199 works

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

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

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

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 Outcomes of People With Fabry Disease — ANZDATA Registry Study

2021

Journal Article

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

Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease

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

2020

Conference Publication

Spatial Transcriptomics (ST): Integrating Molecular Profiles with Histomorphology in Kidney Tissue Sections

Raghubar, Arti M., Pham, Duy T., Tan, Xiao, Grice, Laura F., Lam, Pui Yeng, Crawford, Joanna, Andersen, Stacey, Yoon, Sohye, Holland, Samuel E., Francis, Leo, Combes, Alexander N., Kassianos, Andrew J., Healy, Helen G., Nguyen, Quan and Mallett, Andrew J. (2020). Spatial Transcriptomics (ST): Integrating Molecular Profiles with Histomorphology in Kidney Tissue Sections. Kidney Week, Online, 19-25 October 2020. Washington, DC United States: American Society of Nephrology. doi: 10.1681/asn.20203110s112b

Spatial Transcriptomics (ST): Integrating Molecular Profiles with Histomorphology in Kidney Tissue Sections

2020

Conference Publication

Multidisciplinary Renal Genetics Clinics: Family Perspectives and Preferences

Wilkins, Ella J., Quinlan, Catherine, Mallett, Andrew J. and Stark, Zornitza (2020). Multidisciplinary Renal Genetics Clinics: Family Perspectives and Preferences. Kidney Week, Online, 19-25 October 2020. Washington, DC United States: American Society of Nephrology. doi: 10.1681/asn.20203110s1511a

Multidisciplinary Renal Genetics Clinics: Family Perspectives and Preferences

2020

Journal Article

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

Protocol and establishment of a Queensland renal biopsy registry in Australia

2020

Journal Article

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

DNAJB11-Related Atypical ADPKD in a Kidney Transplant Donor

2020

Journal Article

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

Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease

2020

Journal Article

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

ABO blood group relationships to kidney transplant recipient and graft outcomes

2020

Journal Article

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

Kidney transplant recipient’s perceptions of blood testing through microsampling and venepuncture

2020

Journal Article

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

A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder

2020

Journal Article

Impact of cardiovascular events on mortality and progression of renal dysfunction in a Queensland CKD cohort

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

Impact of cardiovascular events on mortality and progression of renal dysfunction in a Queensland CKD cohort

2020

Journal Article

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

Clinical and healthcare utilization outcomes of parathyroidectomy in CKD and dialysis patients

2020

Journal Article

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

Diagnoses of uncertain significance: kidney genetics in the 21st century

2020

Journal Article

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

Parental health spillover effects of paediatric rare genetic conditions

2020

Journal Article

The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia

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

The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia

Funding

Current funding

  • 2025
    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

Supervision

Availability

Dr Andrew Mallett is:
Available for supervision

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Supervision history

Current supervision

Completed supervision

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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