Parfrey PS - Search Results

1

The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome.

Stuckless S, Parfrey PS, Woods MO, Cox J, Fitzgerald GW, Green JS, Green RC. Stuckless S, et al. Among authors: parfrey ps. Fam Cancer. 2007;6(1):1-12. doi: 10.1007/s10689-006-0014-8. Fam Cancer. 2007. PMID: 17039271

2

High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

Woods MO, Hyde AJ, Curtis FK, Stuckless S, Green JS, Pollett AF, Robb JD, Green RC, Croitoru ME, Careen A, Chaulk JA, Jegathesan J, McLaughlin JR, Gallinger SS, Younghusband HB, Bapat BV, Parfrey PS. Woods MO, et al. Among authors: parfrey ps. Clin Cancer Res. 2005 Oct 1;11(19 Pt 1):6853-61. doi: 10.1158/1078-0432.CCR-05-0726. Clin Cancer Res. 2005. PMID: 16203774

3

Prediction of Lynch syndrome in consecutive patients with colorectal cancer.

Green RC, Parfrey PS, Woods MO, Younghusband HB. Green RC, et al. Among authors: parfrey ps. J Natl Cancer Inst. 2009 Mar 4;101(5):331-40. doi: 10.1093/jnci/djn499. Epub 2009 Feb 24. J Natl Cancer Inst. 2009. PMID: 19244167

4

Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.

Clarke E, Green RC, Green JS, Mahoney K, Parfrey PS, Younghusband HB, Woods MO. Clarke E, et al. Among authors: parfrey ps. Hum Mutat. 2012 Jul;33(7):1056-8. doi: 10.1002/humu.22088. Epub 2012 Apr 9. Hum Mutat. 2012. PMID: 22461326

5

Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation.

Green J, O'Driscoll M, Barnes A, Maher ER, Bridge P, Shields K, Parfrey PS. Green J, et al. Among authors: parfrey ps. Dis Colon Rectum. 2002 Sep;45(9):1223-32. doi: 10.1007/s10350-004-6397-4. Dis Colon Rectum. 2002. PMID: 12352241

6

Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

Green RC, Green JS, Buehler SK, Robb JD, Daftary D, Gallinger S, McLaughlin JR, Parfrey PS, Younghusband HB. Green RC, et al. Among authors: parfrey ps. Fam Cancer. 2007;6(1):53-62. doi: 10.1007/s10689-006-9104-x. Fam Cancer. 2007. PMID: 17039269

7

Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation.

Stuckless S, Green JS, Morgenstern M, Kennedy C, Green RC, Woods MO, Fitzgerald W, Cox J, Parfrey PS. Stuckless S, et al. Among authors: parfrey ps. Clin Genet. 2012 Nov;82(5):439-45. doi: 10.1111/j.1399-0004.2011.01802.x. Epub 2011 Nov 15. Clin Genet. 2012. PMID: 22011075

8

Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation.

Stuckless S, Green J, Dawson L, Barrett B, Woods MO, Dicks E, Parfrey PS. Stuckless S, et al. Among authors: parfrey ps. Clin Genet. 2013 Apr;83(4):359-64. doi: 10.1111/j.1399-0004.2012.01929.x. Epub 2012 Aug 7. Clin Genet. 2013. PMID: 22775459

9

Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study.

Moore SJ, Green JS, Fan Y, Bhogal AK, Dicks E, Fernandez BA, Stefanelli M, Murphy C, Cramer BC, Dean JC, Beales PL, Katsanis N, Bassett AS, Davidson WS, Parfrey PS. Moore SJ, et al. Among authors: parfrey ps. Am J Med Genet A. 2005 Feb 1;132A(4):352-60. doi: 10.1002/ajmg.a.30406. Am J Med Genet A. 2005. PMID: 15637713 Free PMC article.

10

Increased cancer predisposition in family members of colorectal cancer patients harboring the p.V600E BRAF mutation: a population-based study.

Wish TA, Hyde AJ, Parfrey PS, Green JS, Younghusband HB, Simms MI, Fontaine DG, Dicks EL, Stuckless SN, Gallinger S, McLaughlin JR, Woods MO, Green RC. Wish TA, et al. Among authors: parfrey ps. Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1831-9. doi: 10.1158/1055-9965.EPI-10-0055. Epub 2010 Jun 22. Cancer Epidemiol Biomarkers Prev. 2010. PMID: 20570909

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