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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2023
Genomic testing for suspected monogenic kidney disease in children and adults: A health economic evaluationYou Wu, Kushani Jayasinghe, Zornitza Stark, et al.
JAMA Pediatrics|December 1, 2025
Lifestyle Interventions Addressing Blood Pressure in Children: A Systematic ReviewCharlotte H Tiplady, Jonathan P Mynard, Moya Vandeleur, et al.
Kidney International|August 29, 2017
Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disordersAndrew J Mallett, Hugh J McCarthy, Gladys Ho, et al.
The Biological Bulletin|August 24, 2019
Venom Composition Does Not Vary Greatly Between Different Nematocyst Types Isolated from the Primary Tentacles of <i>Olindias sambaquiensis</i> (Cnidaria: Hydrozoa)Liam B Doonan, Steven Lynham, Catherine Quinlan, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 9, 2020
Parental health spillover effects of paediatric rare genetic conditionsYou Wu, Hareth Al-Janabi, Andrew Mallett, et al.
Journal of the American Society of Nephrology : JASN|September 27, 2022
Kidney Organoids Generated Using an Allelic Series of NPHS2 Point Variants Reveal Distinct Intracellular Podocin MistraffickingAude Dorison, Irene Ghobrial, Alison Graham, et al.
Nature Communications|December 6, 2018
3D organoid-derived human glomeruli for personalised podocyte disease modelling and drug screeningLorna J Hale, Sara E Howden, Belinda Phipson, et al.
BMJ Open|August 7, 2019
Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocolKushani Jayasinghe, Zornitza Stark, Chirag Patel, et al.
American Journal of Human Genetics|May 1, 2018
Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic MechanismsThomas A Forbes, Sara E Howden, Kynan Lawlor, et al.
European Journal of Human Genetics : EJHG|August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementationMichael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
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