Items where Subject is "32 BIOMEDICAL AND CLINICAL SCIENCES > 3202 Clinical sciences > 320214 Nephrology and urology"
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- 32 BIOMEDICAL AND CLINICAL SCIENCES (3304)
- 3202 Clinical sciences (1098)
- 320214 Nephrology and urology (122)
- 3202 Clinical sciences (1098)
- 32 BIOMEDICAL AND CLINICAL SCIENCES (3304)
A
Al Maraee, Gheed, Vangaveti, Venkat, and Mallett, Andrew (2023) Characterising patients and clinician experiences in comprehensive conservative care for kidney failure in Northern Queensland. Internal Medicine Journal, 53 (10). pp. 1819-1825.
Arora, Bharti, Khan, Munad, and Pridgeon, Simon (2023) Does histological prostatic inflammation during transurethral resection of the prostate for bladder outlet obstruction affect post-operative urinary outcomes? LUTS: Lower Urinary Tract Symptoms, 15 (2). pp. 57-62.
Anton Sagayanathan, Prasanth, Loganathan, Ajanthan, and Pridgeon, Simon (2022) Recurrent renal stone in thoracic ectopic kidney due to diaphragmatic hernia. ANZ Journal of Surgery, 92 (3). pp. 611-613.
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.
Aldridge, Melanie, Patel, Chirag, Mallett, Andrew J., and Trnka, Peter (2018) Antenatally diagnosed ADPKD. Kidney International Reports, 3 (5). pp. 1214-1217.
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Bakshi, Andrew, Jefferis, Julia, Wolfe, Rory, Wetmore, James B., McNeil, John J., Murray, Anne M., Polkinghorne, Kevan R., Mallett, Andrew J., and Lacaze, Paul (2023) Association of polygenic scores with chronic kidney disease phenotypes in a longitudinal study of older adults. Kidney International, 103 (6). pp. 1156-1166.
Brennan, Sonja, Watson, David L., Rudd, Donna M., and Kandasamy, Yogavijayan (2023) Kidney growth following preterm birth: evaluation with renal parenchyma ultrasonography. Pediatric Research, 93. pp. 1302-1306.
Brennan, Sonja, Watson, David, Schneider, Michal, Rudd, Donna, and Kandasamy, Yogavijayan (2021) Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number? Journal of Developmental Origins of Health and Disease, 12 (2). pp. 184-192.
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. 320.
Brennan, Sonja, Kandasamy, Yogavijayan, Rudd, Donna, Schneider, Michal, and Watson, David (2020) Fetal kidney charts of a novel measurement of the renal parenchymal thickness to evaluate fetal kidney growth and potential function. Prenatal Diagnosis, 40. pp. 860-869.
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). pp. 534-537.
Brennan, Sonja, Kandasamy, Yogavijayan, Rudd, Donna M., Schneider, Michal E., Jones, Rhondda E., and Watson, David L. (2020) The effect of diabetes during pregnancy on fetal renal parenchymal growth. Journal of Nephrology, 33. pp. 1079-1089.
Brennan, Sonja (2020) The renal parenchyma – evaluation of a novel ultrasound measurement to assess fetal renal development. PhD thesis, James Cook University.
C
Carroll, Daniel (2023) Paediatric Urology: A Simplified Approach to Dealing with Urinary Tract Dilatation. In: Carroll, Daniel, Stalewski, Harry, and Rathnamma, Bhanu Mariyappa, (eds.) Paediatric Surgery: Clinical Practice in Remote and Rural Settings, and in Tropical Regions. CRC Press, Boca Raton, FL, USA, pp. 127-138.
Chan, Samuel, Patel, Chirag, and Mallett, Andrew (2020) Pilot clinical and validation study of the PROPKD score in clinical practice amongst patients with Autosomal Dominant Polycystic Kidney Disease. Nephrology, 25 (2). pp. 274-275.
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. e1006620.
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 aCD46mutation in the setting ofSMARCAL1-mediated inherited kidney disease. Nephrology, 22 (S1). pp. 11-14.
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Diwan, Vishal, Hoy, Wendy E., Wang, Zaimin, Zhang, Jianzhen, Cameron, Anne, Venuthurupalli, Sree K., Fassett, Robert G., Chan, Samuel, Healy, Helen G., Tan, Ken-Soon, Baer, Richard, Mallett, Andrew, Gray, Nicholas, Mantha, Murty, Cherian, Roy, Mutatiri, Clyson, Madhan, Krishan, Kan, George, Mitchell, Geoffrey, Hossain, Shahadat, Wu, Danielle, Han, Thin, Kark, Adrian, Titus, Thomas, Ranganathan, Dwarakanatan, Bonner, Ann, Govindarajulu, Sridevi, and The NHMRC CKD.CRE and the CKD.QLD Collaborative, (2023) Hospitalizations Among Adults With CKD in Public Renal Specialty Practices: A Retrospective Study From Queensland, Australia. Kidney Medicine, 5 (9). 100700.
Davis, Justin, Tjipto, Alwie, Hegerty, Katharine, and Mallett, Andrew (2019) An audit of electron microscopy in the diagnosis of focal segmental glomerulosclerosis: are current pathological techniques missing important abnormalities in the glomerular basement membrane? F1000Research, 8. 1204.
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El-damanawi, Ragada, Viecelli, Andrea K., Pascoe, Elaine M., Craig, Jonathan C., Johnson, David W., Mallett, Andrew J., Hawley, Carmel M., and Hiemstra, Thomas F. (2019) Metformin for preventing the progression of chronic kidney disease. Cochrane Database of Systematic Reviews, 9. CD013414.
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Forbes, Thomas A., Howden, Sara E., Lawlor, Kynan, Phipson, Belinda, Maksimovic, Jovana, Hale, Lorna, Wilson, Sean, Quinlan, Catherine, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Trnka, Peter, Oshlack, Alicia, Patel, Chirag, Mallett, Andrew, Simons, Cas, and Little, Melissa H. (2018) Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms. American Journal of Human Genetics, 102 (5). pp. 816-831.
Furyk, Jeremy S., Chu, Kevin, Banks, Colin, Greenslade, Jaimi, Keijzers, Gerben, Thom, Ogilvie, Torpie, Tom, Dux, Carl, and Narula, Rajan (2016) Distal ureteric stones and tamsulosin: a double-blind, placebo-controlled, randomized, multicenter trial. Annals of Emergency Medicine, 67 (1). pp. 86-95.
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. The Open Urology & Nephrology Journal, 9. pp. 88-93.
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Gamage, Chandika D., Nanayakkara, Shanika, Sarathkumara, Yomani D., Muthusinghe, Devinda S., Shimizu, Kenta, Arikawa, Jiro, Lokupathirage, Sithumini M.W., Nanayakkara, Nishantha, Gunarathne, Lishanthe, Chandrajith, Rohana, Harada, Kouji H., Koizumi, Akio, and Yoshimatsu, Kumiko (2022) Hantavirus infection as a risk factor for chronic kidney disease of unknown aetiology (CKDu) and its prevalence in endemic areas of Sri Lanka since 2010 according to a retrospective serological analysis. Journal of Medical Microbiology, 71 (12). 001630.
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). pp. 219-223.
Gois, Pedro Henrique Franca, Healy, Helen G., Ranganathan, Dwarakanathan, Mallett, Andrew John, Webster, Angela C., Kanellis, John, Barraclough, Katherine, Wainstein, Marina, Johnson, David W., and Kerr, Peter G. (2021) Nephrology in Australia. In: Moura-Neto, José A., Ronco, Claudio, and Divino-Filho, José Carolino, (eds.) Nephrology Worldwide. Springer, Cham, pp. 701-721.
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. pp. 616-618.
Greenwood, Alice M., Gunnarsson, Ronny, Neuen, Brendon L., Oliver, Kimberley, Green, Stella J., and Baer, Richard A. (2017) Clinical presentation, treatment and outcome of focal segmental glomerulosclerosis in Far North Queensland Australian adults. Nephrology, 22 (7). pp. 520-530.
Gilhotra, Rajit A., Rodrigues, Beverly T., Vangaveti, Venkat N., Kan, George, Porter, David, Sangla, Kunwarjit S., and Malabu, Usman H. (2016) Non-traumatic lower limb amputation in patients with end-stage renal failure on dialysis: an Australian perspective. Renal Failure, 38. pp. 1-8.
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Hudson, Rebecca, Abeysekera, Natasha, Wolski, Penny, Simons, Cas, Francis, Leo, Farnsworth, Elizabeth, Bennetts, Bruce, Patel, Chirag, Spijker, Siebe, and Mallett, Andrew (2024) De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome. Journal of Nephrology, 37. pp. 191-197.
Hort, Yvonne, Sullivan, Patricia, Wedd, Laura, Fowles, Lindsay, Stevanovski, Igor, Deveson, Ira, Simons, Cas, Mallett, Andrew, Patel, Chirag, Furlong, Timothy, Cowley, Mark J., Shine, John, and Mallawaarachchi, Amali (2023) Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD. npj Genomic Medicine, 8. 16.
Hoy, Wendy E., Wang, Zaimin, Zhang, Jianzhen, Diwan, Vishal, Cameron, Anne, Venuthurupalli, Sree K., Fassett, Robert G., Chan, Samuel, Healy, Helen G., Tan, Ken Soon, Baer, Richard, Mallett, Andrew J., Gray, Nicholas, Mantha, Murty, Cherian, Roy, Mutatiri, Clyson, Madhan, Krishan, Kan, George, Mitchell, Geoffrey, Hossain, Shahadat, Wu, Danielle, Han, Thin, Kark, Adrian, Titus, Thomas, Ranganathan, Dwarakanatan, Bonner, Ann, and Govindarajulu, Sridevi (2022) Chronic kidney disease in public renal practices in Queensland, Australia, 2011–2018. Nephrology, 27 (12). pp. 934-944.
Huppertz, Nina, Beetham, Kassia S., Howden, Erin J., Leicht, Anthony S., Isbel, Nicole M., and Coombes, Jeff S. (2020) A 12-month lifestyle intervention does not improve cardiac autonomic function in patients with chronic kidney disease. Autonomic Neuroscience: Basic and Clinical, 224. 102642.
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 (2020) Adult-Diagnosed Nonsyndromic Nephronophthisis in Australian Families Caused by Biallelic NPHP4 Variants. American Journal of Kidney Diseases, 76 (2). pp. 282-287.
Hill, Kathleen, Sharp, Rebecca, Childs, Jessie, Esterman, Adrian, Leu, Richard Le, Juneja, Rajiv, and Jesudason, Shilpa (2020) Cannulation practices at haemodialysis initiation via an arteriovenous fistula or arteriovenous graft. The Journal of Vascular Acces, 21 (5). pp. 573-581.
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, Goel, Himanshu, Mallawaarachchi, Amali C., Van Eerde, Albertien M., Ponlot, Eléonore, Kribs, Marc, 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). pp. 476-487.
Hoy, Wendy E., White, Andrew V., Tipiloura, Bernard, Singh, Gurmeet, Sharma, Suresh, Bloomfield, Hilary, Swanson, Cheryl E., Dowling, Alison, and McCredie, David A. (2016) The influence of birthweight, past poststreptococcal glomerulonephritis and current body mass index on levels of albuminuria in young adults: the multideterminant model of renal disease in a remote Australian Aboriginal population with high rates of renal disease and renal failure. Nephrology Dialysis Transplantation, 31 (6). pp. 971-977.
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Jefferis, Julia, Hudson, Rebecca, Lacaze, Paul, Bakshi, Andrew, Hawley, Carmel, Patel, Chirag, and Mallett, Andrew (2024) Monogenic and polygenic concepts in chronic kidney disease (CKD). Journal of Nephrology, 37. pp. 7-21.
Jahan, Sadia, Hale, Janine, Malacova, Eva, Hurst, Cameron, Kark, Adrian, and Mallett, Andrew (2024) Real world evaluation of kidney failure risk equations in predicting progression from chronic kidney disease to kidney failure in an Australian cohort. Journal of Nephrology, 37. pp. 231-237.
Jeyaruban, A., Hoy, W., Cameron, A., Healy, H., Wang, Z., Zhang, J., and Mallett, A. (2022) Determining the association between the type of intervention for ischaemic heart disease and mortality and morbidity in patients with chronic kidney disease. Internal Medicine Journal, 52 (7). pp. 1190-1195.
Jefferis, Julia, Pelecanos, Anita, Catts, Vibeke, and Mallett, Andrew (2022) The Heritability of Kidney Function Using an Older Australian Twin Population. Kidney International Reports, 7 (8). pp. 1819-1830.
Jayasinghe, Kushani, Quinlan, Catherine, Mallett, Andrew, 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). pp. 272-283.
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, and Quinlan, Catherine (2021) Clinical impact of genomic testing in patients with suspected monogenic kidney disease. Genetics in Medicine, 23 (1). pp. 183-191.
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). pp. 2850-2861.
Jacups, Susan P., Carter, Angus W., and Murray, Andrew (2020) Acute kidney injury in Indigenous intensive care patients. Australian Critical Care, 33 (5). pp. 452-457.
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). pp. 1086-1089.
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). pp. 839-844.
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. 10.
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, 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.
Jayasinghe, Kushani, White, Susan M., Kerr, Peter G., MacGregor, Duncan, Stark, Zornitza, Wilkins, Ella, Simons, Cas, Mallett, Andrew, and Quinlan, Catherine (2019) Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm. BMC Nephrology, 20. 330.
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Kandasamy, Yogavijayan, and Baker, Stephanie (2023) An Exploratory Review on the Potential of Artificial Intelligence for Early Detection of Acute Kidney Injury in Preterm Neonates. Diagnostics, 13 (18). 2865.
Kermond, Rachael, Mallett, Andrew, and McCarthy, Hugh (2023) A clinical approach to tubulopathies in children and young adults. Pediatric Nephrology, 38. pp. 651-662.
KDIGO Conference Participants, (2022) Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International, 101 (6). pp. 1126-1141.
Kansal, Arushi, Quinlan, Catherine, Stark, Zornitza, Kerr, Peter G., Mallett, Andrew J., Lakshmanan, Chandni, Best, Stephanie, and Jayasinghe, Kushani (2022) Theory Designed Strategies to Support Implementation of Genomics in Nephrology. Genes, 13. 1919.
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.
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Li, Jennifer S.Y., Robertson, Harry, Trinh, Katie, Raghubar, Arti M., Nguyen, Quan, Matigian, Nicholas, Patrick, Ellis, Thomson, Angus W., Mallett, Andrew J., and Rogers, Natasha M. (2023) Tolerogenic dendritic cells protect against acute kidney injury. Kidney International, 104 (3). pp. 492-507.
Lopez-Garcia, Sergio Camilo, Emma, Francesco, Walsh, Stephen B., Fila, Marc, Hooman, Nakysa, Zaniew, Marcin, Bertholet-Thomas, Aurélia, Colussi, Giacomo, Burgmaier, Kathrin, Levtchenko, Elena, Sharma, Jyoti, Singhal, Jyoti, Soliman, Neveen A., Ariceta, Gema, Basu, Biswanath, Murer, Luisa, Tasic, Velibor, Tsygin, Alexey, Decramer, Stéphane, Gil-Peña, Helena, Koster-Kamphuis, Linda, La Scola, Claudio, Gellermann, Jutta, Konrad, Martin, Lilien, Marc, Francisco, Telma, Tramma, Despoina, Trnka, Peter, Yüksel, Selçuk, Caruso, Maria Rosa, Chromek, Milan, Ekinci, Zelal, Gambaro, Giovanni, Kari, Jameela A., König, Jens, Taroni, Francesca, Thumfart, Julia, Trepiccione, Francesco, Winding, Louise, Wühl, Elke, Ağbaş, Ayşe, Belkevich, Anna, Vargas-Poussou, Rosa, Blanchard, Anne, Conti, Giovanni, Boyer, Olivia, Dursun, Ismail, Pınarbaşı, Ayşe Seda, Melek, Engin, Miglinas, Marius, Novo, Robert, Mallett, Andrew, Milosevic, Danko, Szczepanska, Maria, Wente, Sarah, Cheong, Hae Il, Sinha, Rajiv, Gucev, Zoran, Dufek, Stephanie, Iancu, Daniela, European dRTA Consortium, , Kleta, Robert, Schaefer, Franz, and Bockenhauer, Detlef (2019) Treatment and long-term outcome in primary distal renal tubular acidosis. Nephrology Dialysis Transplantation, 34 (6). pp. 981-991.
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Mallett, Andrew (2023) Gird your kidneys? A novel approach to ADPKD therapeutics. Journal of Nephrology, 36. pp. 933-934.
Miller, Kate M., Van Beneden, Chris, McDonald, Malcolm, Hla, Thel K., Wong, William, Pedgrift, Helen, Kaslow, David C., Cherian, Thomas, Carapetis, Jonathan R., Scheel, Amy, Seale, Anna, Bowen, Asha C., Moore, Hannah C., Lamagni, Theresa, and Rodriguez-Iturbe, Bernardo (2022) Standardization of Epidemiological Surveillance of Acute Poststreptococcal Glomerulonephritis. Open Forum Infectious Diseases, 9 (Supplement 1). S57-S64.
Mallett, Andrew J. (2022) Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the future. Current Opinion in Nephrology and Hypertension, 31 (6). pp. 541-547.
Mallett, Andrew, Kearey, Phoebe Jane, Cameron, Anne, Healy, Helen G., Denaro, Charles, Thomas, Mark, Lee, Vincent W., Stark, Samantha Louise, Fuller, Maria, Wang, Zaimin, and Hoy, Wendy E. (2022) The prevalence of Fabry disease in a statewide chronic kidney disease cohort – Outcomes of the aCQuiRE (Ckd.Qld fabRy Epidemiology) study. BMC Nephrology, 23 (1). 169.
Mallett, Andrew J., Knoers, Nine, Sayer, John, and Stark, Zornitza (2021) Clinical versus research genomics in kidney disease. Nature Reviews Nephrology, 17 (9). pp. 570-571.
McConnachie, Dominique J., Stow, Jennifer, and Mallett, Andrew (2021) Ciliopathies and the kidney: a review. American Journal of Kidney Diseases, 77 (3). pp. 410-419.
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. pp. 760-770.
Mallett, Andrew (2021) Monogenic nephrolithiasis-collision of phenotypes, genotypes, and phenocopies. Kidney International Reports, 6 (11). pp. 2737-2739.
Mallett, Andrew J., Perrone, Ronald D., Rangan, Gopala, Hawley, Carmel, El-Damanawi, Ragada, Hiemstra, Thomas F., Townsend Arellano, Carolina, Lee, Jennifer, and Torres, Vicente E. (2021) Per-treatment post-hoc analysis of clinical trial outcomes with Tolvaptan in autosomal dominant polycystic kidney disease. Kidney International Reports, 6. pp. 1032-1040.
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. 58.
Mallett, Andrew J., Quinlan, Catherine, Patel, Chirag, Fowles, Lindsay, Crawford, Joanna, Gattas, Michael, Baer, Richard, Bennetts, Bruce, Ho, Gladys, Holman, Katherine, and Simons, Cas (2019) Precision medicine diagnostics for rare kidney disease: Twitter as a tool in clinical genomic translation. Kidney Medicine, 1 (5). pp. 315-318.
Mallett, Andrew J., McCarthy, Hugh J., Ho, Gladys, Holman, Katherine, Farnsworth, Elizabeth, Patel, Chirag, Fletcher, Jeffery T., Mallawaarachchi, Amali, Quinlan, Catherine, Bennetts, Bruce, and Alexander, Stephen I. (2017) Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders. Kidney International, 92. pp. 1493-1506.
Mahmood, Usman, Isbel, Nicole, Mollee, Peter, Mallett, Andrew, Govindarajulu, Sridevi, and Francis, Ross (2017) Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome. Nephrology, 22 (Suppl. 1). pp. 15-17.
Maple-Brown, Louise J., Hughes, Jaquelyne T., Ritte, Rebecca, Barzi, Federica, Hoy, Wendy E., Lawton, Paul D., Jones, Graham R.D., Death, Elizabeth, Simmonds, Alison, Sinha, Ashim K., Cherian, Sajiv, Thomas, Mark A.B., McDermott, Robyn, Brown, Alex D.H., O'dea, Kerin, Jerums, George, Cass, Alan, and MacIsaac, Richard J. (2016) Progression of kidney disease in Indigenous Australians: the eGFR follow-up study. Clinical Journal of the American Society of Nephrology, 11 (6). pp. 993-1004.
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). pp. 58-59.
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. pp. 177-184.
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. pp. 2277-2286.
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. 98.
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Ng, Monica S.Y., Charu, Vivek, Johnson, David W., O’Shaughnessy, Michelle M., and Mallett, Andrew (2022) National and international kidney failure registries: characteristics, commonalities, and contrasts. Kidney International, 101 (1). pp. 23-35.
Ng, Monica S., Malacova, Eva, Hurst, Cameron, Johnson, David W., and Mallett, Andrew (2021) Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study. Kidney International Reports, 6 (9). pp. 2481-2485.
Nisselle, Amy, Janinski, Monika, Martyn, Melissa, McClaren, Belinda, Kaunein, Nadia, Maguire, Jane, Riggs, Erin Rooney, Barlow-Stewart, Kristine, Belcher, Andrea, Bernat, John A., Best, Stephanie, Bishop, Michelle, Carroll, June C., Cornel, Martina, Dissanayake, Vajira H.W., Dodds, Agnes, Dunlop, Kate, Garg, Gunjan, Gear, Russell, Graves, Debra, Knight, Ken, Korf, Bruce, Kumar, Dhavendra, Laurino, Mercy, Ma, Alan, Mallett, Andrew, McCarthy, Maria, McEwen, Alison, Mulder, Nicola, Patel, Chirag, Quinlan, Catherine, Reed, Kate, Sinnerbrink, Ingrid, Slavotinek, Anne, Suppiah, Vijayaprakash, Terrill, Bronwyn, Tobias, Edward S., Tonkin, Emma, Trumble, Steve, Wessels, Tina-Marie, Metcalfe, Sylvia, Jordan, Helen, and Gaff, Clara (2021) Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics). Genetics in Medicine, 23 (7). pp. 1356-1365.
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