Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Christopher, Gyngell"'
Autor:
Brett J. Kagan, Michael Mahlis, Anjali Bhat, Josh Bongard, Victor M. Cole, Phillip Corlett, Christopher Gyngell, Thomas Hartung, Bianca Jupp, Michael Levin, Tamra Lysaght, Nicholas Opie, Adeel Razi, Lena Smirnova, Ian Tennant, Peter Thestrup Wade, Ge Wang
Publikováno v:
The Innovation, Vol 5, Iss 5, Pp 100658- (2024)
Summary: Disagreements about language use are common both between and within fields. Where interests require multidisciplinary collaboration or the field of research has the potential to impact society at large, it becomes critical to minimize these
Externí odkaz:
https://doaj.org/article/2c33612d627242ab9945fafc6f861c74
Autor:
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison D. Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F. Vears
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-9 (2024)
Abstract Background Implementing genomic sequencing into newborn screening programs allows for significant expansion in the number and scope of conditions detected. We sought to explore public preferences and perspectives on which conditions to inclu
Externí odkaz:
https://doaj.org/article/b3d5879a00c745cba889677a3608c841
Autor:
John Christodoulou, Christopher Gyngell, Stephanie Best, Clara Gaff, Zornitza Stark, Ilias Goranitis, Marc Clausen, Yvonne Bombard, Lilian Downie, Sebastian Lunke, David J Amor, Alison Yeung, Simon Sadedin, Fiona Lynch, Sophie E Bouffler, Danya F Vears, Jade Caruana, Alison Archibald, Paul De Fazio, Ronda F Greaves, Sebastian Hollizeck, Anaita Kanga-Parabia, Nitzan Lang, Riccarda Peters, Erin Tutty, Stefanie Eggers, Crystle Lee, Meaghan Wall
Publikováno v:
BMJ Open, Vol 14, Iss 4 (2024)
Introduction Newborn bloodspot screening (NBS) is a highly successful public health programme that uses biochemical and other assays to screen for severe but treatable childhood-onset conditions. Introducing genomic sequencing into NBS programmes inc
Externí odkaz:
https://doaj.org/article/1ec6b926ff6c4aefb989eebe1d307a84
Autor:
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison D. Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F. Vears
Publikováno v:
International Journal of Neonatal Screening, Vol 10, Iss 1, p 6 (2024)
Recent dramatic reductions in the timeframe in which genomic sequencing can deliver results means its application in time-sensitive screening programs such as newborn screening (NBS) is becoming a reality. As genomic NBS (gNBS) programs are developed
Externí odkaz:
https://doaj.org/article/95edab3abc984cfc9564ef9b524d3b50
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-4 (2021)
Genetic variants that influence susceptibility to COVID-19 have recently been identified. In this manuscript, we identify and discuss some of the ethical and practical issues raised by these studies. We first outline the ethical case for providing CO
Externí odkaz:
https://doaj.org/article/4c2dd9f8c8d34dc29acd7e38c8bb3615
Autor:
Sachini Poogoda, Fiona Lynch, Zornitza Stark, Dominic Wilkinson, Julian Savulescu, Danya Vears, Christopher Gyngell
Publikováno v:
Children, Vol 10, Iss 6, p 970 (2023)
Rapid genomic testing (rGT) enables genomic information to be available in a matter of hours, allowing it to be used in time-critical settings, such as intensive care units. Although rGT has been shown to improve diagnostic rates in a cost-effective
Externí odkaz:
https://doaj.org/article/c85c325607be49cfb11d95f13c487b3c
Publikováno v:
Children, Vol 10, Iss 5, p 824 (2023)
Ultra-rapid genomic sequencing (urGS) is increasingly used in neonatal and pediatric intensive care settings (NICU/PICU), demonstrating high diagnostic and clinical utility. This study aimed to explore the perspectives of healthcare professionals (HP
Externí odkaz:
https://doaj.org/article/81f86040a7884abea91015bc5150c2cf
Publikováno v:
Trends in Biotechnology. 41(8):985-987
Representations of brain organoids in the media are often negatively or positively exaggerated without appropriate discussion. Here, we examine two topics (the possibility of consciousness and medical applications) and call on scientists, ethicists,
Publikováno v:
Journal of Bioethical Inquiry. 19:395-406
DNA databases have significant commercial value. Direct-to-consumer genetic testing companies have built databanks using samples and information voluntarily provided by customers. As the price of genetic analysis falls, there is growing interest in b
Autor:
Hilary Bowman-Smart, Danya F. Vears, Gemma R. Brett, Melissa Martyn, Zornitza Stark, Christopher Gyngell
Publikováno v:
European Journal of Human Genetics. 30:1036-1043
Rapid genomic sequencing (rGS) is being increasingly used in neonatal and paediatric intensive care units. While there is emerging evidence of clinical utility and cost-effectiveness, concerns have been raised regarding the impact of delivering genom