74 results on '"Avard, Denise"'
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2. Pharmacogenomics: Ethical, Social, and Public Policy Issues
3. List of Contributors
4. Beyond ELSIs
5. Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options
6. FMT Happens: Regulating Fecal Microbiota Therapy in Canada; What You Need to Know
7. Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process
8. Beyond dissemination: A knowledge translation model to drive change in pediatric genetics
9. Ethics education for clinician–researchers in genetics: The combined approach
10. SOCIO-ETHICAL ISSUES IN PERSONALIZED MEDICINE: A SYSTEMATIC REVIEW OF ENGLISH LANGUAGE HEALTH TECHNOLOGY ASSESSMENTS OF GENE EXPRESSION PROFILING TESTS FOR BREAST CANCER PROGNOSIS
11. Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities
12. 10. Intégrer l’éthique dans la recherche
13. Medical Research Involving Children: A Review of International Policy Statements
14. Attitudes of parents toward the return of targeted and incidental genomic research findings in children
15. To disclose, or not to disclose? Context matters
16. FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
17. Whole-Genome Sequencing in Newborn Screening Programs
18. Public views on participating in newborn screening using genome sequencing
19. Defining the Scope of Public Engagement: Examining the “Right Not to Know” in Public Health Genomics
20. Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases
21. A new twist on an old problem: primary care physicians and results from direct-to-consumer genetic testing
22. Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting
23. Cohort Profile: The Maternal‐Infant Research on Environmental Chemicals Research Platform
24. Attitudes to the return of incidental and targeted genomic findings obtained in a high-risk pediatric cancer versus an inherited genetic condition research setting.
25. Expectations and values about expanded newborn screening: a public engagement study
26. Emerging issues in paediatric health research consent forms in Canada: working towards best practices
27. Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk
28. Chapitre 11. Favoriser l'implication du public pour accroître la légitimité des prises de décision en matière de politiques de santé ?
29. RMGA Statement of Principles on the Return of Research Results and Incidental Findings
30. Physician Recruitment of Patients to Non-Therapeutic Oncology Clinical Trials: Ethics Revisited
31. noncc de principes du RMGA sur la communication des rrsultats de recherche et des ddcouvertes fortuites (RMGA Statement of Principles on the Return of Research Results and Incidental Findings)
32. Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
33. Recruiting Terminally Ill Patients into Non-Therapeutic Oncology Studies: views of Health Professionals
34. Attitudes of Researchers to the Return of Incidental and Targeted Genomic Findings Obtained in a Research Setting to Participants
35. Personalized medicine and access to health care: potential for inequitable access?
36. Pharmacogenetics of Opioids for the Treatment of Acute Maternal Pain During Pregnancy and Lactation
37. Informed Consent in Genetics
38. Citizens’ Values Regarding Research With Stored Samples From Newborn Screening in Canada
39. Are We Asking the Right Ethics Questions on Drug Shortages? Suggestions for a Global and Anticipatory Ethics Framework
40. Attitudes Towards Patient Involvement in Non-Therapeutic Research Interview
41. Vaccines of the 21st Century and Vaccinomics: Data-Enabled Science Meets Global Health to Spark Collective Action for Vaccine Innovation
42. Editorial (Forward Look: Tenth Anniversary of the Human Genome Sequence and 21st Century Postgenomics Global Health - A Close Up on Africa and Womens Health)
43. Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?
44. Paediatric biobanks: What makes them so unique?
45. Pediatric Research and the Return of Individual Research Results
46. Direct-to-consumer genetic testing: driving choice?
47. Public involvement in health genomics: the reality behind the policies
48. Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening
49. Informed Consent and Multiplex Genetic Screening
50. ‘Principled’ personalized medicine?
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