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Nature|January 8, 2025
Heritable polygenic editing: the next frontier in genomic medicine?Peter M Visscher, Christopher Gyngell, Loic Yengo, et al.Journal of Human Genetics|August 2, 2020
Genetics experience impacts attitudes towards germline gene editing: a survey of over 1500 members of the publicAbbie Jedwab, Danya F Vears, Cheryl Tse, et al.The Medical Journal of Australia|January 14, 2026
Genomic Newborn Screening: Commodity or Public Good?Christopher Gyngell, Sebastian Lunke, Danya Vears, et al.Children (Basel, Switzerland)|May 27, 2023
Rapid Genomic Testing in Intensive Care: Health Professionals' Perspectives on Ethical ChallengesKatie Arkell, Christopher Gyngell, Zornitza Stark, et al.Bioethics|April 7, 2022
Moving from 'fully' to 'appropriately' informed consent in genomics: The PROMICE frameworkJulian J Koplin, Christopher Gyngell, Julian Savulescu, et al.Pediatrics|November 28, 2022
Rapid Genome Sequencing: Consent for New Technologies in the Neonatal Intensive Care ContextFiona Lynch, Trisha Prentice, Lynn Gillam, et al.Journal of Bioethical Inquiry|August 2, 2023
The Parliamentary Inquiry into Mitochondrial Donation Law Reform (Maeve's Law) Bill 2021 in Australia: A Qualitative AnalysisJemima W Allen, Christopher Gyngell, Julian J Koplin, et al.Pediatrics|January 3, 2019
Rapid Challenges: Ethics and Genomic Neonatal Intensive CareChristopher Gyngell, Ainsley J Newson, Dominic Wilkinson, et al.Prenatal Diagnosis|September 10, 2019
Sex selection and non-invasive prenatal testing: A review of current practices, evidence, and ethical issuesHilary Bowman-Smart, Julian Savulescu, Christopher Gyngell, et al.Journal of Medical Ethics|June 1, 2023
Storing paediatric genomic data for sequential interrogation across the lifespanChristopher Gyngell, Fiona Lynch, Danya Vears, et al.Pageof 6