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Fetal Diagnosis and Therapy|January 18, 2023
Oligohydramnios or Anhydramnios and Ultrasonically Normal Renal Echotexture Secondary to Autosomal Recessive Renal Tubular Dysgenesis: An Important Consideration in the Prenatal SettingRemi Banuelos, Amali Mallawaarachchi, Helen Doyle, et al.
Kidney360|January 2, 2026
Genetic Testing in Cystic Kidney DiseaseJacqueline Soraru, Andrew J Mallett, Hugh McCarthy, et al.
Seminars in Nephrology|July 13, 2025
Should Genetic Testing be Indicated and Implemented for Chronic Kidney Disease of Unknown Cause?Julia Jefferis, Amali Mallawaarachchi, Nine Knoers, et al.
Clinical Kidney Journal|July 27, 2017
Novel complement factor H gene mutation causing atypical haemolytic uraemic syndrome: early Eculizumab prevents acute dialysisJames Collett, Amali Mallawaarachchi, Eddy Fischer, et al.
Transplantation|January 23, 2026
Genetic Testing in Prospective Kidney Donors: Current Evidence and Clinical Practice in AustraliaSadia Jahan, Amali Mallawaarachchi, Julia Jefferis, et al.
Kidney Diseases (Basel, Switzerland)|April 13, 2026
Burden of Glomerular Diseases in Australia: A Data Linkage StudyNeeru Agarwal, Kristy P Robledo, Angus Ritchie, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 21, 2023
Mitochondrial DNA 13513G>A Mutation Causing Leber Hereditary Optic Neuropathy Associated With Adult-Onset Renal FailureGrace Swart, Clare L Fraser, Meena Shingde, 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.
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.
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.
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