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Genes|October 27, 2022
Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics StudyRosie O'Shea, Alasdair Wood, Chirag Patel, et al.
BMC Nephrology|August 24, 2019
Isolated proteinuria due to CUBN homozygous mutation - challenging the investigative paradigmKushani Jayasinghe, Susan M White, Peter G Kerr, et al.
Nephrology (Carlton, Vic.)|September 22, 2018
Renal genetics in Australia: Kidney medicine in the genomic ageKushani Jayasinghe, Catherine Quinlan, Zornitza Stark, et al.
Journal of Hypertension|September 9, 2024
Defining childhood hypertension: is it too complicated? An evaluation of the potential impact of different approaches in an Australian paediatric populationNicholas G Larkins, Catherine Choong, Markus Schlaich, et al.
Kidney International Reports|November 22, 2021
Cost-Effectiveness of Targeted Exome Analysis as a Diagnostic Test in Glomerular DiseasesKushani Jayasinghe, You Wu, Zornitza Stark, et al.
Archives of Disease in Childhood|January 15, 2025
Feasibility of home blood pressure screening in the paediatric outpatient clinic settingJessie R Mackay, Jonathan P Glenning, Brittany M Grantham, et al.
Pediatric Nephrology (Berlin, Germany)|November 22, 2011
Growth in PHEX-associated X-linked hypophosphatemic rickets: the importance of early treatmentCatherine Quinlan, Katie Guegan, Amaka Offiah, et al.
Kidney Medicine|August 1, 2020
Precision Medicine Diagnostics for Rare Kidney Disease: Twitter as a Tool in Clinical Genomic TranslationAndrew J Mallett, Catherine Quinlan, Chirag Patel, et al.
Frontiers in Medicine|June 20, 2022
The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown AetiologyJacqueline Soraru, Sadia Jahan, Catherine Quinlan, et al.
Kidney International Reports|February 22, 2021
Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical GenomicsKushani Jayasinghe, Catherine Quinlan, Andrew J Mallett, et al.
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