Wilson BJ - Search Results

1

Stakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocol.

Nicholls SG, Tessier L, Etchegary H, Brehaut JC, Potter BK, Hayeems RZ, Chakraborty P, Marcadier J, Milburn J, Pullman D, Turner L, Wilson BJ. Nicholls SG, et al. Among authors: wilson bj. BMJ Open. 2014 Nov 24;4(11):e006782. doi: 10.1136/bmjopen-2014-006782. BMJ Open. 2014. PMID: 25421341 Free PMC article.

2

Consent for newborn screening: parents' and health-care professionals' experiences of consent in practice.

Etchegary H, Nicholls SG, Tessier L, Simmonds C, Potter BK, Brehaut JC, Pullman D, Hayeems R, Zelenietz S, Lamoureux M, Milburn J, Turner L, Chakraborty P, Wilson B. Etchegary H, et al. Eur J Hum Genet. 2016 Nov;24(11):1530-1534. doi: 10.1038/ejhg.2016.55. Epub 2016 Jun 15. Eur J Hum Genet. 2016. PMID: 27302842 Free PMC article.

3

Public attitudes towards genomic risk profiling as a component of routine population screening.

Nicholls SG, Wilson BJ, Craigie SM, Etchegary H, Castle D, Carroll JC, Potter BK, Lemyre L, Little J. Nicholls SG, et al. Among authors: wilson bj. Genome. 2013 Oct;56(10):626-33. doi: 10.1139/gen-2013-0070. Epub 2013 Aug 31. Genome. 2013. PMID: 24237344 Free PMC article.

4

Consent for newborn screening: the attitudes of health care providers.

Miller FA, Hayeems RZ, Carroll JC, Wilson B, Little J, Allanson J, Bytautas JP, Paynter M, Christensen R, Chaktraborty P. Miller FA, et al. Public Health Genomics. 2010;13(3):181-90. doi: 10.1159/000240966. Epub 2009 Sep 22. Public Health Genomics. 2010. PMID: 19776551

5

Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening.

Miller FA, Hayeems RZ, Bombard Y, Little J, Carroll JC, Wilson B, Allanson J, Paynter M, Bytautas JP, Christensen R, Chakraborty P. Miller FA, et al. J Med Ethics. 2009 Oct;35(10):626-34. doi: 10.1136/jme.2009.030346. J Med Ethics. 2009. PMID: 19793944

6

Expectations and values about expanded newborn screening: a public engagement study.

Hayeems RZ, Miller FA, Bombard Y, Avard D, Carroll J, Wilson B, Little J, Chakraborty P, Bytautas J, Giguere Y, Allanson J, Axler R. Hayeems RZ, et al. Health Expect. 2015 Jun;18(3):419-29. doi: 10.1111/hex.12047. Epub 2013 Feb 1. Health Expect. 2015. PMID: 23369110 Free PMC article.

7

Using Newborn Screening Bloodspots for Research: Public Preferences for Policy Options.

Hayeems RZ, Miller FA, Barg CJ, Bombard Y, Cressman C, Painter-Main M, Wilson B, Little J, Allanson J, Avard D, Giguere Y, Chakraborty P, Carroll JC. Hayeems RZ, et al. Pediatrics. 2016 Jun;137(6):e20154143. doi: 10.1542/peds.2015-4143. Epub 2016 May 17. Pediatrics. 2016. PMID: 27244855

8

Ethical, legal, and social issues in health technology assessment for prenatal/preconceptional and newborn screening: a workshop report.

Potter BK, Avard D, Entwistle V, Kennedy C, Chakraborty P, McGuire M, Wilson BJ. Potter BK, et al. Among authors: wilson bj. Public Health Genomics. 2009;12(1):4-10. doi: 10.1159/000153430. Epub 2008 Sep 3. Public Health Genomics. 2009. PMID: 19023190 Free PMC article.

9

Bringing personalized medicine to the community through public engagement.

Etchegary H, Wilson B. Etchegary H, et al. Per Med. 2013 Sep;10(7):647-659. doi: 10.2217/pme.13.65. Per Med. 2013. PMID: 29768762

10

Psychosocial aspects of venous thromboembolic disease: an exploratory study.

Etchegary H, Wilson B, Brehaut J, Lott A, Langlois N, Wells PS. Etchegary H, et al. Thromb Res. 2008;122(4):491-500. doi: 10.1016/j.thromres.2007.12.001. Epub 2008 Jan 29. Thromb Res. 2008. PMID: 18234291

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