Miller FA - Search Results

1

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

2

Genetic services for hereditary breast/ovarian and colorectal cancers - physicians' awareness, use and satisfaction.

Carroll JC, Cappelli M, Miller F, Wilson BJ, Grunfeld E, Peeters C, Hunter AG, Gilpin C, Prakash P. Carroll JC, et al. Community Genet. 2008;11(1):43-51. doi: 10.1159/000111639. Epub 2008 Jan 15. Community Genet. 2008. PMID: 18196917

3

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results.

Miller FA, Giacomini M, Ahern C, Robert JS, de Laat S. Miller FA, et al. BMC Med Ethics. 2008 Feb 22;9:4. doi: 10.1186/1472-6939-9-4. BMC Med Ethics. 2008. PMID: 18294373 Free PMC article.

4

Duty to disclose what? Querying the putative obligation to return research results to participants.

Miller FA, Christensen R, Giacomini M, Robert JS. Miller FA, et al. J Med Ethics. 2008 Mar;34(3):210-3. doi: 10.1136/jme.2006.020289. J Med Ethics. 2008. PMID: 18316466

5

A systematic review of the effects of disclosing carrier results generated through newborn screening.

Hayeems RZ, Bytautas JP, Miller FA. Hayeems RZ, et al. Among authors: miller fa. J Genet Couns. 2008 Dec;17(6):538-49. doi: 10.1007/s10897-008-9180-1. Epub 2008 Oct 28. J Genet Couns. 2008. PMID: 18956236 Review.

6

Questioning the consensus: managing carrier status results generated by newborn screening.

Miller FA, Robert JS, Hayeems RZ. Miller FA, et al. Am J Public Health. 2009 Feb;99(2):210-5. doi: 10.2105/AJPH.2008.136614. Epub 2008 Dec 4. Am J Public Health. 2009. PMID: 19059852 Free PMC article.

7

Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility.

Etchegary H, Miller F, deLaat S, Wilson B, Carroll J, Cappelli M. Etchegary H, et al. J Genet Couns. 2009 Jun;18(3):252-64. doi: 10.1007/s10897-009-9218-z. Epub 2009 Mar 18. J Genet Couns. 2009. PMID: 19294336

8

The helix in the labyrinth: do we need genetic health services and policy research?

Miller FA, Wilson B, Grimshaw J, Battista R, Blancquaert I, Carroll JC, Rousseau F, Slater B. Miller FA, et al. Healthc Policy. 2008 Aug;4(1):30-8. Healthc Policy. 2008. PMID: 19377339 Free PMC article.

9

Carrier detection and clinical uncertainty: the case for public health ethics.

Miller FA, Hayeems RZ, Robert JS. Miller FA, et al. Am J Public Health. 2009 Aug;99(8):1349-50. doi: 10.2105/AJPH.2009.162008. Epub 2009 Jun 18. Am J Public Health. 2009. PMID: 19542029 Free PMC article. No abstract available.

10

Postal survey of physicians and laboratories: practices and perceptions of molecular oncology testing.

Miller FA, Krueger P, Christensen RJ, Ahern C, Carter RF, Kamel-Reid S. Miller FA, et al. BMC Health Serv Res. 2009 Jul 30;9:131. doi: 10.1186/1472-6963-9-131. BMC Health Serv Res. 2009. PMID: 19643018 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

344 results

Search Page

Filters