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18 results on '"Avard, Denise"'

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1. Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities.

2. To disclose, or not to disclose? Context matters.

3. Public views on participating in newborn screening using genome sequencing.

4. Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk.

5. Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider.

6. Personalized medicine and access to health care: potential for inequitable access?

7. Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

8. Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

9. Health-related direct-to-consumer genetic testing: a review of companies’ policies with regard to genetic testing in minors.

10. Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information.

11. Improved Understanding of Genetic and Genomic Influences on Drug Disposition and Action: Implications for Children.

13. SCIENCE AND SOCIETY: Children and incompetent adults in genetic research: consent and safeguards.

14. Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform.

15. The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

16. Direct-to-consumer genome scanning services. Also for children?

18. Newborn screening by tandem mass spectrometry: ethical and social issues.

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