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Pascal Borry

Showing results (111-120 of 236) with videos related to

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Familial Cancer|June 3, 2009
Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minorsPascal Borry, Heidi C Howard, Karine Sénécal, et al.
European Journal of Health Law|June 15, 2007
Minors and informed consent: a comparative approachLoes Stultiëns, Tom Goffin, Pascal Borry, et al.
Plos Biology|January 1, 2016
Controlled Access under Review: Improving the Governance of Genomic Data AccessMahsa Shabani, Stephanie O M Dyke, Yann Joly, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|May 15, 2023
Informed Consent and Debriefing When Deceiving Participants: A Systematic Review of Research Ethics GuidelinesKamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Medicine, Health Care, and Philosophy|June 26, 2025
REC review of deceptive studies: diversifying guidance for diverse review needsKamiel Verbeke, Dieter Baeyens, Tomasz Krawczyk, et al.
Ethics & Human Research|May 7, 2025
What's in a Lie? How Researchers Judge the Justifiability of DeceptionKamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Genetics 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.
Health Policy (Amsterdam, Netherlands)|March 24, 2007
Patient rights in EU Member States after the ratification of the Convention on Human Rights and BiomedicineHerman Nys, Loes Stultiëns, Pascal Borry, et al.
Pageof 24

Showing results (111-120 of 236) with videos related to

Sort By:
Pageof 24
Familial Cancer|June 3, 2009
Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minorsPascal Borry, Heidi C Howard, Karine Sénécal, et al.
European Journal of Health Law|June 15, 2007
Minors and informed consent: a comparative approachLoes Stultiëns, Tom Goffin, Pascal Borry, et al.
Plos Biology|January 1, 2016
Controlled Access under Review: Improving the Governance of Genomic Data AccessMahsa Shabani, Stephanie O M Dyke, Yann Joly, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|May 15, 2023
Informed Consent and Debriefing When Deceiving Participants: A Systematic Review of Research Ethics GuidelinesKamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Medicine, Health Care, and Philosophy|June 26, 2025
REC review of deceptive studies: diversifying guidance for diverse review needsKamiel Verbeke, Dieter Baeyens, Tomasz Krawczyk, et al.
Ethics & Human Research|May 7, 2025
What's in a Lie? How Researchers Judge the Justifiability of DeceptionKamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Genetics 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.
Health Policy (Amsterdam, Netherlands)|March 24, 2007
Patient rights in EU Member States after the ratification of the Convention on Human Rights and BiomedicineHerman Nys, Loes Stultiëns, Pascal Borry, et al.
Pageof 24