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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

Ckd. Qld fabRy epidemiology (aCQuiRE) study: Fabry Disease Prevalence Among Patients with CKD : PO1605

Mallett, Andrew J., Kearey, Phoebe J., (Salisbury), Anne Cameron, Healy, Helen G., Denaro, Charles P., Thomas, Mark A., Lee, Vincent W., Fuller, Maria, Hoy, Wendy E. and aCQuiRE Study Team (2020). Ckd. Qld fabRy epidemiology (aCQuiRE) study: Fabry Disease Prevalence Among Patients with CKD : PO1605. Kidney Week, Virtual Meeting, Virtual, 19 - 25 October 2020. Washington, DC, United States: American Society of Nephrology. doi: 10.1681/asn.20203110s1509d

Ckd. Qld fabRy epidemiology (aCQuiRE) study: Fabry Disease Prevalence Among Patients with CKD : PO1605

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

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

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

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

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

2020

Journal Article

Toward transparency in nephrology research

Francis, Anna and Mallett, Andrew (2020). Toward transparency in nephrology research. Kidney International Reports, 5 (2), 118-120. doi: 10.1016/j.ekir.2019.11.019

Toward transparency in nephrology research

2020

Journal Article

Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study

Jahan, Sadia, Sarathchandran, Subashini, Akhter, Shamina, Goldblatt, Jack, Stark, Samantha, Crawford, Douglas, Mallett, Andrew and Thomas, Mark (2020). Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study. Orphanet Journal of Rare Diseases, 15 (1) 10, 10. doi: 10.1186/s13023-019-1290-3

Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study

2020

Journal Article

Genetic Kidney Disease in Southern Tasmania

Brailsford, Gabrielle, Cash, Ellie, Burke, Jo, Kirkland, Geoff, Wallis, Mathew, Mallett, Andrew and Jose, Matthew D. (2020). Genetic Kidney Disease in Southern Tasmania. Kidney International Reports, 5 (4), 534-537. doi: 10.1016/j.ekir.2020.01.015

Genetic Kidney Disease in Southern Tasmania

2019

Journal Article

Adult-diagnosed nonsyndromic nephronophthisis in Australian families caused by biallelic NPHP4 variants

Hudson, Rebecca, Patel, Chirag, Hawley, Carmel M., O'Shea, Stacey, Snelling, Paul, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Francis, Leo, Simons, Cas and Mallett, Andrew (2019). Adult-diagnosed nonsyndromic nephronophthisis in Australian families caused by biallelic NPHP4 variants. American Journal of Kidney Diseases, 76 (2), 282-287. doi: 10.1053/j.ajkd.2019.08.031

Adult-diagnosed nonsyndromic nephronophthisis in Australian families caused by biallelic NPHP4 variants

2019

Journal Article

Proposed minimum information guideline for kidney disease - Research and clinical data reporting: A cross-sectional study

Kumuthini, Judit, Van Woerden, Christiaan, Mallett, Andrew, Zass, Lyndon, Chaouch, Melek, Thompson, Michael, Johnston, Katherine, Mbiyavanga, Mamana, Baichoo, Shakuntala, Mungloo-DIlmohamud, Zahra, Patel, Chirag and Mulder, Nicola (2019). Proposed minimum information guideline for kidney disease - Research and clinical data reporting: A cross-sectional study. BMJ Open, 9 (11) e029539, e029539. doi: 10.1136/bmjopen-2019-029539

Proposed minimum information guideline for kidney disease - Research and clinical data reporting: A cross-sectional study