Dr Andrew Mallett
Dr

Andrew Mallett

Email: 

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

212 works between 2012 and 2025
All (212) Journal Article (156) Book Chapter (1) Conference Publication (54) Other Outputs (1)

181 - 200 of 212 works

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

2015

Conference Publication

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

The T616C Trna(Phe) mutation causes mitochondrially inherited tubulointerstitial kidney disease

2015

Journal Article

End-Stage kidney disease due to fibrillary glomerulonephritis and immunotactoid glomerulopathy - outcomes in 66 consecutive ANZDATA registry cases

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

End-Stage kidney disease due to fibrillary glomerulonephritis and immunotactoid glomerulopathy - outcomes in 66 consecutive ANZDATA registry cases

2015

Conference Publication

Identifying and Integrating Consumer Perspectives in Clinical Practice Guidelines On Autosomal Dominant Polycystic Kidney Disease

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.

Identifying and Integrating Consumer Perspectives in Clinical Practice Guidelines On Autosomal Dominant Polycystic Kidney Disease

2015

Conference Publication

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

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

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

2015

Conference Publication

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

Heterogeneity of chronic kidney disease (CKD) by age in an Australian metropolitan renal service

2015

Conference Publication

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

Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy

2015

Conference Publication

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

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

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

2014

Journal Article

End-stage kidney disease due to Alport syndrome: Outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry cases

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

End-stage kidney disease due to Alport syndrome: Outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry cases

2014

Journal Article

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

NOS3 as a potential modifier of ADPKD phenotypic variability: progress towards an answer

2014

Journal Article

The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia

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

The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia

2014

Journal Article

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

Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant

2014

Conference Publication

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

Renal Oncocytosis in the Setting of a Rare Invalidated Flcn Gene Variant

2014

Conference Publication

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

Exomic Approaches to Diagnosis Amongst Australians with Genetic Renal Diseases

2014

Conference Publication

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

The Initial Six Months of An Australian Renal Genetics Clinic Service

2014

Conference Publication

Utilising Exome Sequencing to Identify Nephronophthisis Mutations Within An Australian Clinical Cohort

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

Utilising Exome Sequencing to Identify Nephronophthisis Mutations Within An Australian Clinical Cohort

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

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

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

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au