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BMC Medical Ethics|January 18, 2006
How international is bioethics? A quantitative retrospective studyPascal Borry, Paul Schotsmans, Kris DierickxExpert Review of Molecular Diagnostics|September 27, 2014
Attitudes of research participants and the general public towards genomic data sharing: a systematic literature reviewMahsa Shabani, Louise Bezuidenhout, Pascal BorryEMBO Reports|July 14, 2020
Data sharing platforms and the academic evaluation systemThijs Devriendt, Mahsa Shabani, Pascal BorryGenetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2017
A systematic analysis of online marketing materials used by providers of expanded carrier screeningDavit Chokoshvili, Pascal Borry, Danya F VearsXenotransplantation|July 6, 2017
Newspaper coverage of human-pig chimera research: A qualitative study on select media coverage of scientific breakthroughAbena Hagan-Brown, Maddalena Favaretto, Pascal BorryEMBO Molecular Medicine|March 12, 2015
From the principles of genomic data sharing to the practices of data access committeesMahsa Shabani, Bartha Maria Knoppers, Pascal BorryEuropean Journal of Human Genetics : EJHG|June 2, 2011
Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?Heidi Carmen Howard, Denise Avard, Pascal BorryJournal of Community Genetics|November 24, 2011
Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal storiesYeyang Su, Heidi C Howard, Pascal BorryJournal of Genetic Counseling|December 20, 2019
Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patientsDanya F Vears, Karine Sénécal, Pascal BorryFamilial Cancer|March 23, 2020
Genetic health professionals' experiences with initiating reanalysis of genomic sequence dataDanya F Vears, Karine Sénécal, Pascal BorryPageof 20