Professor Andrew Mallett
Professor

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

Professor Andrew Mallett is:
Available for supervision
Media expert

Search Professor Andrew Mallett’s works on UQ eSpace

267 works between 2012 and 2026
All (267) Book (1) Journal Article (209) Other Outputs (1) Conference Publication (55) Book Chapter (1)

221 - 240 of 267 works

2017

Journal Article

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

Mutations in mitochondrial DNA causing tubulointerstitial kidney disease

2017

Journal Article

Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome : MGRS triggering aHUS

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

Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome : MGRS triggering aHUS

2017

Journal Article

Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney disease

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

Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney disease

2017

Conference Publication

Paraneoplastic immunoglobulin a nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma

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.

Paraneoplastic immunoglobulin a nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma

2016

Other Outputs

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

Genetic diagnostics in genetic renal disease: Methods, applications and therapeutics

2016

Journal Article

Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: a case report

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

Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: a case report

2016

Journal Article

KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease

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

KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease

2016

Journal Article

Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease

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

Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease

2016

Journal Article

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

A multidisciplinary renal genetics clinic improves patient diagnosis

2015

Journal Article

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: Genetic Testing for Diagnosis

2015

Journal Article

KHA-CARI autosomal dominant polycystic kidney disease guideline: management of polycystic liver disease

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

KHA-CARI autosomal dominant polycystic kidney disease guideline: management of polycystic liver disease

2015

Journal Article

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: Pharmacological Management

2015

Journal Article

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: Management of Renal Stone Disease

2015

Journal Article

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

KHA-CARI autosomal dominant polycystic kidney disease guideline: genetics and genetic counseling

2015

Journal Article

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: Psychosocial Care

2015

Journal Article

Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohort

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

Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohort

2015

Journal Article

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

A protocol for the identification and validation of novel genetic causes of kidney disease

2015

Journal Article

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

Genomics in the renal clinic - translating nephrogenetics for clinical practice

2015

Conference Publication

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

Fibrillary glomerulonephritis: an apparent familial form?

2015

Conference Publication

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

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 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

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
  • 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

  • 2022 - 2025
    Genomic Approaches to Kidney Health and Disease
    Queensland Advancing Clinical Research Fellowship
    Open grant
  • 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

Professor 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 Professor 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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