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Annual Review of Medicine|September 6, 2011
Direct-to-consumer genetic testing: perceptions, problems, and policy responsesTimothy Caulfield, Amy L McGuireCanadian Journal of Public Health = Revue Canadienne De Sante Publique|April 22, 2006
Legal foundations for a national public health agency in CanadaNola M Ries, Timothy CaulfieldCanadian Journal of Surgery. Journal Canadien De Chirurgie|October 12, 2022
Donation and transplantation coverage in the Canadian media: a content analysis of story focus over 2 decadesAlessandro R Marcon, Timothy CaulfieldTrends in Biotechnology|April 20, 2006
Gene patents, health care policy and licensing schemesTimothy Caulfield, Barbara von TigerstromTrends in Biotechnology|July 6, 2010
Role and reality: technology transfer at Canadian universitiesTania M Bubela, Timothy CaulfieldBMC Medical Ethics|December 15, 2004
Variations and voids: the regulation of human cloning around the worldShaun D Pattinson, Timothy CaulfieldGenetics in Medicine : Official Journal of the American College of Medical Genetics|November 24, 2012
"Trust is not something you can reclaim easily": patenting in the field of direct-to-consumer genetic testingSigrid Sterckx, Julian Cockbain, Heidi Howard, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Variant data sharing by clinical laboratories through public databases: consent, privacy and further contact for research policiesMahsa Shabani, Stephanie O M Dyke, Luca Marelli, et al.European Journal of Human Genetics : EJHG|August 26, 2018
Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent formsDanya F Vears, Emilia Niemiec, Heidi Carmen Howard, et al.European Journal of Health Law|June 15, 2007
Minors and informed consent: a comparative approachLoes Stultiëns, Tom Goffin, Pascal Borry, et al.Pageof 35