Wilson BJ - Search Results

1

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. Among authors: wilson bj. Community Genet. 2008;11(1):43-51. doi: 10.1159/000111639. Epub 2008 Jan 15. Community Genet. 2008. PMID: 18196917

2

Identifying mental health services in clinical genetic settings.

Cappelli M, Esplen MJ, Wilson BJ, Dorval M, Bottorff JL, Ly M, Carroll JC, Allanson J, Humphreys E, Rayson D. Cappelli M, et al. Among authors: wilson bj. Clin Genet. 2009 Oct;76(4):326-31. doi: 10.1111/j.1399-0004.2009.01250.x. Clin Genet. 2009. PMID: 19917019

3

Attitude and knowledge about genetics and genetic testing.

Etchegary H, Cappelli M, Potter B, Vloet M, Graham I, Walker M, Wilson B. Etchegary H, et al. Public Health Genomics. 2010;13(2):80-8. doi: 10.1159/000220034. Epub 2009 May 19. Public Health Genomics. 2010. PMID: 19451701

4

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

5

Canada: public health genomics.

Little J, Potter B, Allanson J, Caulfield T, Carroll JC, Wilson B. Little J, et al. Public Health Genomics. 2009;12(2):112-20. doi: 10.1159/000156113. Epub 2008 Sep 14. Public Health Genomics. 2009. PMID: 19039255

6

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

7

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

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

The current state of cancer family history collection tools in primary care: a systematic review.

Qureshi N, Carroll JC, Wilson B, Santaguida P, Allanson J, Brouwers M, Raina P. Qureshi N, et al. Genet Med. 2009 Jul;11(7):495-506. doi: 10.1097/GIM.0b013e3181a7e8e0. Genet Med. 2009. PMID: 19521245 Free article. Review.

10

Family history: impact on coronary heart disease risk assessment beyond guideline-defined factors.

Hasanaj Q, Wilson BJ, Little J, Montazeri Z, Carroll JC; CIHR Emerging Team in Genomics in Screening. Hasanaj Q, et al. Among authors: wilson bj. Public Health Genomics. 2013;16(5):208-14. doi: 10.1159/000353460. Epub 2013 Jul 25. Public Health Genomics. 2013. PMID: 23886802 Free article.

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