Green JS - 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: green rc, green js. Fam Cancer. 2007;6(1):1-12. doi: 10.1007/s10689-006-0014-8. Fam Cancer. 2007. PMID: 17039271

2

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. Dis Colon Rectum. 2002 Sep;45(9):1223-32. doi: 10.1007/s10350-004-6397-4. Dis Colon Rectum. 2002. PMID: 12352241

3

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: green rc, green js. 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

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: green rc, green js. Hum Mutat. 2012 Jul;33(7):1056-8. doi: 10.1002/humu.22088. Epub 2012 Apr 9. Hum Mutat. 2012. PMID: 22461326

5

Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

Evans DR, Green JS, Woods MO. Evans DR, et al. Among authors: green js. Fam Cancer. 2018 Apr;17(2):205-208. doi: 10.1007/s10689-017-0016-8. Fam Cancer. 2018. PMID: 28660566

6

Impact of colonoscopic screening in Familial Colorectal Cancer Type X.

Hatfield E, Green JS, Woods MO, Warden G, Parfrey PS. Hatfield E, et al. Among authors: green js. Mol Genet Genomic Med. 2018 Nov;6(6):1021-1030. doi: 10.1002/mgg3.478. Epub 2018 Oct 9. Mol Genet Genomic Med. 2018. PMID: 30300963 Free PMC article.

7

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. 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

8

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: green js. Fam Cancer. 2007;6(1):53-62. doi: 10.1007/s10689-006-9104-x. Fam Cancer. 2007. PMID: 17039269

9

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: green rc, green js. 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

10

Estimating successive cancer risks in Lynch Syndrome families using a progressive three-state model.

Choi YH, Briollais L, Green J, Parfrey P, Kopciuk K. Choi YH, et al. Stat Med. 2014 Feb 20;33(4):618-38. doi: 10.1002/sim.5938. Epub 2013 Aug 15. Stat Med. 2014. PMID: 23946183

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