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Prof Andrew J Mallett, MBBS MMed PhD CF AFRACMA FASN FRCP FRACP
Prof Andrew J Mallett, MBBS MMed PhD CF AFRACMA FASN FRCP FRACP
Professor of Medicine, James Cook University (CMD); Clinical Fellow, The University of Queensland
Verified email at health.qld.gov.au - Homepage
Title
Cited by
Cited by
Year
Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms
TA Forbes, SE Howden, K Lawlor, B Phipson, J Maksimovic, L Hale, ...
The American Journal of Human Genetics 102 (5), 816-831, 2018
1762018
Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms
TA Forbes, SE Howden, K Lawlor, B Phipson, J Maksimovic, L Hale, ...
The American Journal of Human Genetics 102 (5), 816-831, 2018
1762018
Genome-wide association study of medication-use and associated disease in the UK Biobank
Y Wu, EM Byrne, Z Zheng, KE Kemper, L Yengo, AJ Mallett, J Yang, ...
Nature communications 10 (1), 1891, 2019
1642019
Ciliopathies and the kidney: A review
DJ McConnachie, JL Stow, AJ Mallett
American Journal of Kidney Diseases 77 (3), 410-419, 2021
1492021
Treatment and long-term outcome in primary distal renal tubular acidosis
SC Lopez-Garcia, F Emma, SB Walsh, M Fila, N Hooman, M Zaniew, ...
Nephrology Dialysis Transplantation 34 (6), 981-991, 2019
962019
Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders
AJ Mallett, HJ McCarthy, G Ho, K Holman, E Farnsworth, C Patel, ...
Kidney international 92 (6), 1493-1506, 2017
862017
Clinical impact of genomic testing in patients with suspected monogenic kidney disease
K Jayasinghe, Z Stark, PG Kerr, C Gaff, M Martyn, J Whitlam, B Creighton, ...
Genetics in Medicine 23 (1), 183-191, 2021
772021
The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia
A Mallett, C Patel, A Salisbury, Z Wang, H Healy, W Hoy
Orphanet Journal of Rare Diseases 9, 1-9, 2014
762014
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.
TM Connor, S Hoer, A Mallett, DP Gale, A Gomez-Duran, V Posse, ...
PLoS genetics 13 (3), e1006620, 2017
652017
End-stage kidney disease due to Alport syndrome: outcomes in 296 consecutive Australia and New Zealand Dialysis and Transplant Registry cases
A Mallett, W Tang, PA Clayton, S Stevenson, SP McDonald, CM Hawley, ...
Nephrology Dialysis Transplantation 29 (12), 2277-2286, 2014
592014
Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
VT Huynh, MP Audrézet, JA Sayer, AC Ong, S Lefevre, V Le Brun, ...
Kidney international 98 (2), 476-487, 2020
472020
Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal‐dominant polycystic kidney disease
A Tong, DJ Tunnicliffe, P Lopez‐Vargas, A Mallett, C Patel, J Savige, ...
Nephrology 21 (2), 122-132, 2016
452016
Identifying And Integrating Consumer Perspectives In Clinical Practice Guidelines On Autosomal Dominant Polycystic Kidney Disease
DJ Tunnicliffe, A Tong, P Lopez-Vargas, A Mallett, C Patel, J Savige, ...
Nephrology 20, 51-52, 2015
45*2015
Identifying and Integrating Consumer Perspectives in clinical practice guidelines on Autosomal Dominant Polycystic Kidney Disease
D.J. Tunnicliffe, A. Tong, P. Lopez-Vargas, A. Mallett, C. Patel, J. Savige ...
Nephrology 20 (S3), 51, 2015
45*2015
KHA‐CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease
GK Rangan, SI Alexander, KL Campbell, MAJ Dexter, VW Lee, ...
Nephrology 21 (8), 705-716, 2016
442016
Parental health spillover effects of paediatric rare genetic conditions
Y Wu, H Al-Janabi, A Mallett, C Quinlan, IE Scheffer, KB Howell, ...
Quality of Life Research 29, 2445-2454, 2020
402020
Genetics in chronic kidney disease: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
A Köttgen, E Cornec-Le Gall, J Halbritter, K Kiryluk, AJ Mallett, RS Parekh, ...
Kidney International 101 (6), 1126-1141, 2022
392022
A multidisciplinary renal genetics clinic improves patient diagnosis
A Mallett, LF Fowles, J McGaughran, H Healy, C Patel
The Medical journal of Australia 204 (2), 58-59, 2016
352016
A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder
LK Jones, R Lam, KK McKee, M Aleksandrova, J Dowling, SI Alexander, ...
Development 147 (21), dev189183, 2020
322020
Gitelman-like syndrome caused by pathogenic variants in mtDNA
D Viering, KP Schlingmann, M Hureaux, T Nijenhuis, A Mallett, ...
Journal of the American Society of Nephrology 33 (2), 305-325, 2022
312022
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Articles 1–20