928 results on '"Borry, Pascal"'
Search Results
2. Polygenic embryo screening: quo vadis?
3. Clinician perspectives on policy approaches to genetic risk disclosure in families
4. Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review
5. 23 X and Y
6. Table of Contents
7. Title Page, Copyright
8. Cover
9. Recommended Literature
10. About the Authors
11. 19 Personalizing Medicine to Fit Your Genetic Profile
12. 16 Mudbloods
13. 21 Consumer Genomics
14. 18 The Godfather
15. 22 Genes and Patents
16. 14 Genome Hackers
17. 20 Gene Therapy, a Medicine?
18. 15 A Neanderthal in All of Us?
19. 17 My Olympic DNA
20. 13 HELP! The Government Has My DNA!
21. 11 Everyone’s Genome Investigated
22. 12 Finding out More Than You Would Want to Know
23. 10 As Long as it Stays in the Family
24. 3 A Gene, a Genome, and Then What?
25. 9 Designer Babies
26. 8 New Test Tracks for Fetus DNA
27. 7 We Are All Carriers
28. 6 Give Me Back My DNA!
29. 5 Angelina Jolie’s Choice
30. 1 The Genome: The Cookbook of Life
31. 4 Genetic Disorders
32. 2 Reading Genomes
33. Introduction
34. Contact investigation in multidrug-resistant tuberculosis: ethical challenges
35. Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study
36. Reconciling the biomedical data commons and the GDPR: three lessons from the EUCAN ELSI collaboratory
37. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
38. Safeguarding Users of Consumer Mental Health Apps in Research and Product Improvement Studies: an Interview Study
39. Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
40. Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores
41. Informing a European guidance framework on electronic informed consent in clinical research: a qualitative study
42. Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening
43. Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking community
44. Can I use the placebo effect to treat injured or Ill athletes?
45. Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review
46. Expanded Non-invasive Prenatal Testing (NIPT): Can the Child’s Right to an Open Future Help Set the Scope?
47. “Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals
48. Ethical concerns in integrating sport-related concussion (SRC) genetic testing into return-to-play (RTP) protocols
49. Toward better governance of human genomic data
50. Disclosure of genetic risk in the family: A survey of the Flemish general population
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