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Accountability in Research|November 9, 2023
Governance of research and product improvement studies in consumer mental health apps. Interviews with researchers and app developersKamiel Verbeke, Charu Jain, Ambra Shpendi, et al.Plos One|March 24, 2018
The author who wasn't there? Fairness and attribution in publications following access to population biobanksErika Kleiderman, Amy Pack, Pascal Borry, et al.Human Genetics|June 28, 2011
Closure of population biobanks and direct-to-consumer genetic testing companiesMa'n H Zawati, Pascal Borry, Heidi Carmen HowardMedicine, Health Care, and Philosophy|August 18, 2015
"You hoped we would sleep walk into accepting the collection of our data": controversies surrounding the UK care.data scheme and their wider relevance for biomedical researchSigrid Sterckx, Vojin Rakic, Julian Cockbain, et al.Plos One|July 1, 2025
Vulnerability in research ethics: A systematic review of policy guidelines and documentsAsia Grigis, Giorgia Beretta, Pascal Borry, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 18, 2008
Attitudes regarding predictive genetic testing in minors: a survey of European clinical geneticistsPascal Borry, Tom Goffin, Herman Nys, et al.Heliyon|May 9, 2024
Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking communitySofie Claerhout, Hanna Noppe, Betty Cohn, et al.Personalized Medicine|May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticistsDavit Chokoshvili, Sandra Janssens, Danya Vears, et al.Xenotransplantation|December 1, 2021
Should you need an organ… Flemish secondary school students' attitudes toward xenotransplantation and transgenetic organ donationMaryn Reyneke, Nel Kerckhof, Rachna Dherwani, et al.The Mount Sinai Journal of Medicine, New York|August 16, 2008
Predictive genetic testing in minors for adult-onset genetic diseasesPascal Borry, Tom Goffin, Herman Nys, et al.Pageof 22