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.

B

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.

D

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.

E

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.

F

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.

G

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.

H

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.

J

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.

K

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.

L

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.

M

Mesfine, Belete Biadgo, Vojisavljevic, Danica, Kapoor, Ranjna, Watson, David, Kandasamy, Yogavijayan, and Rudd, Donna (2024) Urinary Nephrin: A Potential Biomarker of Early Glomerular Injury in a Cohort of Pregnant Women Attending Routine Antenatal Care Services. International Journal of Nephrology, 2024. 9089557.

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, 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. pp. 1054-1065.

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, Corney, Christopher, Mccarthy, Hugh, Alexander, Stephen I., and Healy, Helen (2015) Genomics in the renal clinic - translating nephrogenetics for clinical practice. Human Genomics, 9.

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, Wendy E., Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy, Helen, and Little, Melissa (2015) A protocol for the identification and validation of novel genetic causes of kidney disease. BMC Nephrology, 16. 152.

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.

N

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.

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.

Nesbitt, Alexander L., Kapoor, Jada, Piesse, Charlotte, Evans, Garrath, Antoniou, Stefan, Smith, Philip, and Pridgeon, Simon W. (2019) Prediction of pathological stage at radical prostatectomy: do commonly used prostate cancer nomograms apply to men from Far North Queensland? Australian and New Zealand Journal of Surgery, 89 (1-2). pp. 111-114.

Ng, Monica S.Y., McClymont, Kelly, McCallum, Naomi, Dua, Rahul, Holman, Katherine, Bennetts, Bruce, Ho, Gladys, Patel, Chirag, and Mallett, Andrew (2018) CFHR5 nephropathy in a Greek-Cypriot Australian family: ancestry-informed precision medicine. Kidney International Reports, 3 (5). pp. 1222-1228.

Ng, Monica Suet Ying, Francis, Leo, Pillai, Elango, and Mallett, Andrew John (2018) Paraneoplastic immunoglobulin A nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma – a case report. BMC Nephrology, 19 (1). 224.

Neuen, Brendon L., Leather, Nicole, Greenwood, Alice M., Gunnarsson, Ronny, Cho, Yeoungjee, and Mantha, Murty L. (2016) Neutrophil–lymphocyte ratio predicts cardiovascular and all-cause mortality in hemodialysis patients. Renal Failure, 38 (1). pp. 70-76.

O

O’Shea, Rosie, Wood, Alasdair, Patel, Chirag, Mccarthy, Hugh J., Mallawaarachchi, Amali, Quinlan, Catherine, Simons, Cas, Stark, Zornitza, and Mallett, Andrew J. (2022) Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study. Genes, 13 (10). 1804.

P

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). pp. 550-556.

R

Raghubar, Arti M., Matigian, Nicholas A., Crawford, Joanna, Francis, Leo, Ellis, Robert, Healy, Helen G., Kassianos, Andrew J., Ng, Monica S.Y., Roberts, Matthew J., Wood, Simon, and Mallett, Andrew J. (2023) High risk clear cell renal cell carcinoma microenvironments contain protumour immunophenotypes lacking specific immune checkpoints. npj Precision Oncology, 7. 88.

Raghubar, Arti M., Crawford, Joanna, Jones, Kahli, Lam, Pui Y., Andersen, Stacey B., Matigian, Nicholas A., Ng, Monica S.Y., Healy, Helen, Kassianos, Andrew J., and Mallett, Andrew J. (2023) Spatial Transcriptomics in Kidney Tissue. In: Hewitson, Tim D., Toussaint, Nigel D., and Smith, Edward R., (eds.) Kidney Research: Experimental protocols. Methods in Molecular Biology . Springer, New York, NY, USA, pp. 233-282.

Raghubar, Arti M., Pham, Duy T., Tan, Xiao, Grice, Laura F., Crawford, Joanna, Lam, Pui Yeng, Andersen, Stacey B., Yoon, Sohye, Teoh, Siok Min, Matigian, Nicholas A., Stewart, Anne, Francis, Leo, Ng, Monica S.Y., Healy, Helen G., Combes, Alexander N., Kassianos, Andrew J., Nguyen, Quan, and Mallett, Andrew J. (2022) Spatially Resolved Transcriptomes of Mammalian Kidneys Illustrate the Molecular Complexity and Interactions of Functional Nephron Segments. Frontiers in Medicine, 9. 873923.

Ritte, Rebecca E., Lawton, Paul, Hughes, Jaquelyne T., Barzi, Federica, Brown, Alex, Mills, Phillip, Hoy, Wendy, O'dea, Kerin, Cass, Alan, and Maple-Brown, Louise (2020) Chronic kidney disease and socio-economic status: a cross sectional study. Ethnicity and Health, 25 (1). pp. 93-109.

S

Scuderi, Carla, Parker, Suzanne, Jacks, Margaret, John, George T., McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew, Healy, Helen, Roberts, Jason, and Staatz, Christine (2023) Fingerprick Microsampling Methods Can Replace Venepuncture for Simultaneous Therapeutic Drug Monitoring of Tacrolimus, Mycophenolic Acid, and Prednisolone Concentrations in Adult Kidney Transplant Patients. Therapeutic Drug Monitoring, 45 (1). pp. 69-78.

Scuderi, Carla E., Parker, Suzanne L., Jacks, Margaret, John, George T., McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew J., Healy, Helen G., Roberts, Jason A., and Staatz, Christine E. (2023) Serum Creatinine and Tacrolimus Assessment With VAMS Finger-Prick Microsampling: A Diagnostic Test Study. Kidney Medicine, 5 (4). 100610.

Soraru, Jacqueline, Chakera, Aron, Isbel, Nikky, Mallawaarachichi, Amali, Rogers, Natasha, Trnka, Peter, Patel, Chirag, and Mallett, Andrew J. (2022) The Evolving Role of Diagnostic Genomics in Kidney Transplantation. Kidney International Reports, 7 (8). pp. 1758-1771.

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). pp. 873-881.

Sutherland, Megan R., Vojisavljevic, Danica, and Black, Mary Jane (2020) A practical guide to the stereological assessment of glomerular number, size, and cellular composition. The Anatomical Record, 303 (10). pp. 2679-2692.

Sutherland, Megan R., Chatfield, Mark D., Davison, Belinda, Vojisavljevic, Danica, Alison, Kent L., Hoy, Wendy E., Singh, Gurmeet R., and Black, Mary Jane (2019) Renal dysfunction is already evident within the first month of life in Australian Indigenous infants born preterm. Kidney International, 96 (5). pp. 1205-1216.

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). pp. 618-622.

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). pp. 22-26.

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Tanudisastro, Hope A., Holman, Katherine, Ho, Gladys, Farnsworth, Elizabeth, Fisk, Katrina, Gayagay, Thet, Hackett, Emma, Jenkins, Gemma, Krishnaraj, Rahul, Lai, Tiffany, Wong, Karen, Patel, Chirag, Mallawaarachchi, Amali, Mallett, Andrew, Bennetts, Bruce, Alexander, Stephen I., and McCarthy, Hugh J. (2021) Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine, 6. 20.

Tran, Ngan K., Lea, Rodney A., Holland, Samuel, Nguyen, Quan, Raghubar, Arti M., Sutherland, Heidi G., Benton, Miles C., Haupt, Larisa M., Blackburn, Nicholas B., Curran, Joanne E., Blangero, John, Mallett, Andrew, and Griffiths, Lyn R. (2021) Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific Reports, 11. 19425.

Tan, Wei Shen, Teo, Chin Hai, Chan, Delcos, Heinrich, Malgorzata, Feber, Andrew, Sarpong, Rachael, Allan, Jennifer, Williams, Norman, Brew-Graves, Chris, Ng, Chirk Jenn, Kelly, John D., and DETECT II Trail Collaborators (2019) Mixed-methods approach to exploring patients’ perspectives on the acceptability of a urinary biomarker test in replacing cystoscopy for bladder cancer surveillance. BJU International, 124 (3). pp. 408-417.

Tong, A., 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). pp. 122-32.

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.

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.

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Viering, Daan, Schlingmann, Karl-Peter, Hureaux, Marguerite, Nijhenhuis, Tom, Mallett, Andrew, Chan, Melanie MY, van Beek, André, van Eerde, Albertien M, Coulibaly, Jean-Marie, Vallet, Marion, Decramer, Stéphane, Pelletier, Solenne, Klaus, Günter, Komhoff, Martin, Beetz, Rolf, Patel, Chirag, Shenoy, Mohan, Steenbergen, Eric J., Anderson, Glenn, Bongers, Ernie M.H.F., Bermann, Carsten, Penneman, Daan, Rodenburg, Richard J., Kleta, Robert, Houillier, Pascal, Konrad, Martin, Vargas-Poussou, Rosa, Knoers, Nine, Bockenhauer, Detlef, de Baaij, Jeroen, and Genomics England Research Consortium (2022) Gitelman-like syndrome caused by pathogenic variants in mtDNA. Journal of the American Society of Nephrology, 33 (2). pp. 305-325.

W

Watters, Tara K., Glass, Beverley D., and Mallett, Andrew J. (2024) Identifying the barriers to kidney transplantation for patients in rural and remote areas: a scoping review. Journal of Nephrology. (In Press)

Wu, You, Jayasinghe, Kushani, Stark, Zornitza, Quinlan, Catherine, Patel, Chirag, Mccarthy, Hugh, Mallawaarachchi, Amali C., Kerr, Peter G., Alexander, Stephen I., Mallett, Andrew J., and Goranitis, Ilias (2024) Response to Lombardi and Mesnard. Genetics in Medicine, 26 (1). 100989.

Wu, You, Jayasinghe, Kushani, Stark, Zornitza, Quinlan, Catherine, Patel, Chirag, McCarthy, Hugh, Mallawaarachchi, Amali C., Kerr, Peter G., Alexander, Stephen, Mallett, Andrew J., Goranitis, Ilias, and The KidGen Collaborative investigators (2023) Genomic testing for suspected monogenic kidney disease in children and adults: A health economic evaluation. Genetics in Medicine, 25 (11). 100942.

White, Kyle C., Serpa-Neto, Ary, Hurford, Rod, Clement, Pierre, Laupland, Kevin B., See, Emily, McCullough, James, White, Hayden, Shekar, Kiran, Tabah, Alexis, Ramanan, Mahesh, Garrett, Peter, Attokaran, Antony G., Luke, Stephen, Senthuran, Siva, McIlroy, Philippa, Bellomo, Rinaldo, and Queensland Critical Care Research Network (QCCRN) (2023) Sepsis-associated acute kidney injury in the intensive care unit: incidence, patient characteristics, timing, trajectory, treatment, and associated outcomes. A multicenter, observational study. Intensive Care Medicine, 49 (9). pp. 1079-1089.

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). pp. 1363-1366.

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. pp. 2445-2454.

Wu, Yeda, Byrne, Enda M., Zheng, Zhili, Kemper, Kathryn E., Yengo, Loic, Mallett, Andrew J., Yang, Jian, Visscher, Peter M., and Wray, Naomi R. (2019) Genome-wide association study of medication-use and associated disease in the UK Biobank. Nature Communications, 10. 1891.

Wilson, Gregory J., Kark, Adrian L., Francis, Leo P., Hoy, Wendy, Healy, Helen G., and Mallett, Andrew (2017) The increasing rates of acute interstitial nephritis in Australia: a single centre case series. BMC Nephrology, 18. 329.

Wang, Feng, Zhang, Guangyuan, Xing, Tao, Lu, Zeyuan, Li, Junhui, Peng, Cheng, Liu, Guohua, and Wang, Niansong (2015) Renalase contributes to the renal protection of delayed ischaemic preconditioning via the regulation of hypoxia-inducible factor-1a. Journal of Cellular and Molecular Medicine, 19 (6). pp. 1400-1409.

Wang, Feng, Cai, Hongyan, Zhao, Qing, Xing, Tao, Li, Junhui, and Wang, Niansong (2014) Epinephrine evokes renalase secretion via α-adrenoceptor/NF-κB pathways in renal proximal tubular epithelial cells. Kidney and Blood Pressure Research, 39. pp. 252-259.

Wang, Feng, Zhang, Guangyuan, Zhou, Yang, Gui, Dingkun, Li, Junhui, Xing, Tao, and Wang, Niansong (2014) Magnolin protects against contrast induced nephropathy in rats via anti-oxidation and anti-apoptosis. Oxidative Medicine and Cellular Longevity, 2014. 203458.

Wang, Feng, Li, Junhui, Xing, Tao, Xie, Yuting, and Wang, Niansong (2014) Serum renalase is related to catecholamine levels and renal function. Clinical and Experimental Nephrology, 19. pp. 92-98.

Wang, Feng, Xing, Tao, Wang, Niansong, and Liu, Limei (2012) Clinical significance of plasma CD146 and P-selectin in patients with type 2 diabetic nephropathy. Cytokine, 57 (1). pp. 127-129.

Wang, Feng, Xing, Tao, Li, Junhui, Bai, Mei, Hu, Ruimin, Zhao, Zhonghua, Tian, Shoufu, Zhang, Zhigang, and wang, Niansong (2012) Renalase’s expression and distribution in renal tissue and cells. PLoS ONE, 7. e46442.

Wang, Feng, Xing, Tao, Li, Junhui, He, Yingzi, Bai, Mei, and Wang, Niansong (2012) Survey on hospital-acquired urinary tract infection in neurological intensive care unit. Journal of Pathology, Microbiology and Immunology - the APMIS journal, 121 (3). pp. 197-201.

Wang, Feng, Xing, Daniel, Wang, Niansong, and Huang, Yajuan (2011) A Clinical Study of Pregnancy-Associated Renal Insufficiency. Kidney and Blood Pressure Research, 34 (1). pp. 34-40.

Wang, Feng, Xing, Tao, and Wang, Niansong (2011) Construction and DNA immunization of human renalase eukaryotic expression vector. Clinical Kidney Journal, 4 (3). p. 221.

Y

Yaxley, Julian, Wilkinson, Catherine, Davidson-West, Shaun, and Mantha, Murty (2024) Clavicular hook: Cuffed haemodialysis catheter insertion using a paramedian tunnel in patients with recurrent tip migration. The Journal of Vascular Acces, 25 (2). pp. 669-672.

Yu, Dong, Malacova, Eva, Hurst, Cameron, Ng, Monica Suet Ying, and Mallett, Andrew John (2023) Association of Primary Kidney Disease Type and Donor Relatedness With Live Donor Kidney Transplant Outcomes: An Analysis of ANZDATA. American Journal of Kidney Diseases, 82 (5). pp. 569-580.

Ying, Tracey, Hill, Prue, Desmond, Michael, Agar, John, and Mallett, Andrew (2015) Fibrillary glomerulonephritis: An apparent familial form? Nephrology, 20 (7). pp. 506-509.

Z

Zhao, Binghui, Zhao, Qing, Li, Junhui, Xing, Tao, Wang, Feng, and Wang, Niansong (2015) Renalase protects against contrast-induced nephropathy in Sprague-Dawley rats. PLoS ONE, 10 (1). e0116583.