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    Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns? by Vears DF, Savulescu J, Christodoulou J, Wall M, Newson AJ

    Published 2023-07-01
    “…Danya F Vears,1,2 Julian Savulescu,3– 6 John Christodoulou,1,2 Meaghan Wall,7 Ainsley J Newson8 1Murdoch Children’s Research Institute, The Royal Children’s Hospital, Parkville, Victoria, Australia; 2University of Melbourne, Melbourne, Victoria, 3052, Australia; 3Chen Su Lan Centennial Professor in Medical Ethics, Centre for Biomedical Ethics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; 4Visiting Professorial Fellow in Biomedical Ethics, Murdoch Children’s Research Institute, Parkville, Victoria, Australia; 5Distinguished Visiting Professor in Law, Melbourne University, Carlton, Victoria, Australia; 6Oxford Uehiro Centre for Practical Ethics, University of Oxford, Oxford, UK; 7Victorian Clinical Genetics Service, Murdoch Children’s Research Institute, Parkville, Victoria, Australia; 8Faculty of Medicine & Health, Sydney School of Public Health, Sydney Health Ethics, The University of Sydney, Sydney, New South Wales, AustraliaCorrespondence: Danya F Vears, Biomedical Ethics Research Group, Murdoch Children’s Research Institute, Parkville, Victoria, 3052, Australia, Email danya.vears@mcri.edu.auAbstract: The introduction of genomic sequencing technologies into routine newborn screening programs in some form is not only inevitable but also already occurring in some settings. …”
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