291 results on '"Avard, Denise"'
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2. Pharmacogenomics: Ethical, Social, and Public Policy Issues
3. Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases
4. Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process
5. Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities
6. Regulatory Approval for New Pharmacogenomic Tests: A Comparative Overview
7. Newborn Blood Spot Screening in Four Countries: Stakeholder Involvement
8. Newborn Screening by Tandem Mass Spectrometry: Ethical and Social Issues
9. Genetics and Society Project
10. Expectations and values about expanded newborn screening: a public engagement study
11. Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
12. From stakeholders to shareholders: engaging consumers in health research
13. A guide to the perplexed: how to navigate conflicting research ethics policies
14. Health-related direct-to-consumer genetic testing: a review of companies’ policies with regard to genetic testing in minors
15. Defining the scope of public engagement: examining the 'right not to know' in public health genomics
16. Research ethics boards and challenges for public participation.
17. Improved Understanding of Genetic and Genomic Influences on Drug Disposition and Action: Implications for Children
18. A new twist on an old problem: primary care physicians and results from direct-to-consumer genetic testing
19. Variability in the storage and use of newborn dried bloodspots in Canada: is it time for national standards?
20. Partnering in Oncogenetic Research – The INHERIT BRCAs Experience: Opportunities and Challenges
21. List of Contributors
22. Beyond ELSIs
23. Clinical Management Recommendations for Surveillance and Risk-Reduction Strategies for Hereditary Breast and Ovarian Cancer Among Individuals Carrying a Deleterious BRCA1 or BRCA2 Mutation
24. La protection de l'information genetique dans le domaine medical au Quebec: principe general de confidentialite et questions soulevees par les dispositions d'exception.
25. Cohort Profile: The Maternal-Infant Research on Environmental Chemicals Research Platform
26. Paediatric biobanks: What makes them so unique?
27. Forward Look: Tenth Anniversary of the Human Genome Sequence and 21st Century Postgenomics Global Health — A Close Up on Africa and Womenʼs Health
28. Pediatric research and the return of individual research results
29. ‘Principled’ personalized medicine?
30. Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer
31. Storing newborn blood spots: modern controversies.
32. Emerging issues in paediatric health research consent forms in Canada: working towards best practices
33. Recruiting Terminally Ill Patients into Non-Therapeutic Oncology Studies: views of Health Professionals
34. Childhood deaths from toy balloons
35. 10. Intégrer l’éthique dans la recherche
36. La malréglementation
37. A National Survey of Use of Obstetric Procedures and Technologies in Canadian Hospitals: Routine or Based on Existing Evidence?
38. Ethical dimensions of genetics in pediatric neurology: A look into the future
39. Breast-feeding policies and practices in Canadian hospitals providing maternity care
40. Canada's Poorest Citizens: Looking for Solutions for Children
41. Low-Birth-Weight Symposium: Summary of Proceedings
42. Ethics, industry and 'animal farm'
43. Chapter 11 - Beyond ELSIs: Where to from Here? From “Regulating” to Anticipating and Shaping the Innovation Trajectory in Personalized Medicine
44. Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options
45. FMT Happens: Regulating Fecal Microbiota Therapy in Canada; What You Need to Know
46. Beyond dissemination: A knowledge translation model to drive change in pediatric genetics
47. Ethics education for clinician–researchers in genetics: The combined approach
48. SOCIO-ETHICAL ISSUES IN PERSONALIZED MEDICINE: A SYSTEMATIC REVIEW OF ENGLISH LANGUAGE HEALTH TECHNOLOGY ASSESSMENTS OF GENE EXPRESSION PROFILING TESTS FOR BREAST CANCER PROGNOSIS
49. Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities
50. Ethics watch DIRECT-TO-CONSUMER GENOME SCANNING SERVICES. ALSO FOR CHILDREN?
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