Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jane Kaye

Showing results (61-70 of 99) with videos related to

Pageof 10
Sort By:
Genome Biology|September 16, 2014
Building a data sharing model for global genomic researchPatricia Kosseim, Edward S Dove, Carman Baggaley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2018
Sharing data for future research-engaging participants' views about data governance beyond the original project: a DIRECT StudyNisha Shah, Victoria Coathup, Harriet Teare, et al.
European Journal of Human Genetics : EJHG|February 1, 2019
Motivations for data sharing-views of research participants from four European countries: A DIRECT studyNisha Shah, Victoria Coathup, Harriet Teare, et al.
Journal of Medical Ethics|May 28, 2011
From genomic databases to translation: a call to actionBartha Maria Knoppers, Jennifer R Harris, Paul R Burton, et al.
Orphanet Journal of Rare Diseases|November 30, 2016
Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasiaLydia Forestier-Zhang, Laura Watts, Alison Turner, et al.
BMC Medical Ethics|June 5, 2016
Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiativesJ Patrick Woolley, Michelle L McGowan, Harriet J A Teare, et al.
European Journal of Human Genetics : EJHG|January 26, 2012
Legislation on direct-to-consumer genetic testing in seven European countriesPascal Borry, Rachel E van Hellemondt, Dominique Sprumont, et al.
Medical Law International|September 26, 2017
Exploring the potential duty of care in clinical genomics under UK lawColin Mitchell, Corrette Ploem, Victoria Chico, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|November 16, 2019
Dynamic Consent: An Evaluation and Reporting FrameworkMegan Prictor, Megan A Lewis, Ainsley J Newson, et al.
Biopreservation and Biobanking|April 16, 2016
Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
Genome Biology|September 16, 2014
Building a data sharing model for global genomic researchPatricia Kosseim, Edward S Dove, Carman Baggaley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2018
Sharing data for future research-engaging participants' views about data governance beyond the original project: a DIRECT StudyNisha Shah, Victoria Coathup, Harriet Teare, et al.
European Journal of Human Genetics : EJHG|February 1, 2019
Motivations for data sharing-views of research participants from four European countries: A DIRECT studyNisha Shah, Victoria Coathup, Harriet Teare, et al.
Journal of Medical Ethics|May 28, 2011
From genomic databases to translation: a call to actionBartha Maria Knoppers, Jennifer R Harris, Paul R Burton, et al.
Orphanet Journal of Rare Diseases|November 30, 2016
Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasiaLydia Forestier-Zhang, Laura Watts, Alison Turner, et al.
BMC Medical Ethics|June 5, 2016
Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiativesJ Patrick Woolley, Michelle L McGowan, Harriet J A Teare, et al.
European Journal of Human Genetics : EJHG|January 26, 2012
Legislation on direct-to-consumer genetic testing in seven European countriesPascal Borry, Rachel E van Hellemondt, Dominique Sprumont, et al.
Medical Law International|September 26, 2017
Exploring the potential duty of care in clinical genomics under UK lawColin Mitchell, Corrette Ploem, Victoria Chico, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|November 16, 2019
Dynamic Consent: An Evaluation and Reporting FrameworkMegan Prictor, Megan A Lewis, Ainsley J Newson, et al.
Biopreservation and Biobanking|April 16, 2016
Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, et al.
Pageof 10