30 results on '"Borry, Pascal"'
Search Results
2. Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking community
3. “Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals
4. Disclosure of genetic risk in the family: A survey of the Flemish general population
5. Policies to regulate data sharing of cohorts via data infrastructures: An interview study with funding agencies
6. Exploring informed choice in preconception reproductive genetic carrier screening by using a modified Multidimensional Measure of Informed Choice
7. A review of normative documents on preimplantation genetic testing: Recommendations for PGT-P
8. The patient with 41 reports: Analysis of laboratory exome sequencing reporting of a “virtual patient”
9. Policies to Regulate Data Sharing of Cohorts Via Data Infrastructures: An Interview Study with Funding Agencies
10. Disclosure of genetic information to family members: a systematic review of normative documents
11. Analysis of laboratory reporting practices using a quality assessment of a virtual patient
12. Clinical management, ethics and informed consent related to multi‐gene panel‐based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH
13. Digital tools for sharing genetic information with family members
14. Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing
15. Variant data sharing by clinical laboratories through public databases: consent, privacy and further contact for research policies
16. Forensic Epigenetic Age Estimation and Beyond: Ethical and Legal Considerations
17. Raw Genomic Data: Storage, Access, and Sharing
18. Reporting practices for variants of uncertain significance from next generation sequencing technologies
19. Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers
20. Ethical considerations for genetic testing in the context of mandated cardiac screening before athletic participation
21. Attitudes of European Geneticists Regarding Expanded Carrier Screening
22. “You want the right amount of oversight”: interviews with data access committee members and experts on genomic data access
23. Biohistorical materials and contemporary privacy concerns-the forensic case of King Albert I
24. Anonymity 2.0: direct-to-consumer genetic testing and donor conception
25. “I prefer a child with …”: designer babies, another controversial patent in the arena of direct-to-consumer genomics
26. “Trust is not something you can reclaim easily”: patenting in the field of direct-to-consumer genetic testing
27. Why eight EU Member States signed, but not yet ratified the Convention for Human Rights and Biomedicine
28. A proposal for a model of informed consent for the collection, storage and use of biological materials for research purposes
29. Attitudes towards predictive genetic testing in minors for familial breast cancer: A systematic review
30. Patient rights in EU Member States after the ratification of the Convention on Human Rights and Biomedicine
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