Woods MO - Search Results

1

Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus.

Woods MO, Young TL, Parfrey PS, Hefferton D, Green JS, Davidson WS. Woods MO, et al. Genomics. 1999 Jan 1;55(1):2-9. doi: 10.1006/geno.1998.5626. Genomics. 1999. PMID: 9888993

2

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.

Young TL, Woods MO, Parfrey PS, Green JS, O'Leary E, Hefferton D, Davidson WS. Young TL, et al. Among authors: woods mo. Am J Med Genet. 1998 Aug 6;78(5):461-7. doi: 10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d. Am J Med Genet. 1998. PMID: 9714014

3

A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31.

Young TL, Penney L, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. Young TL, et al. Among authors: woods mo. Am J Hum Genet. 1999 Mar;64(3):900-4. doi: 10.1086/302301. Am J Hum Genet. 1999. PMID: 10053027 Free PMC article. No abstract available.

4

A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM.

Young TL, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. Young TL, et al. Among authors: woods mo. Am J Hum Genet. 1999 Dec;65(6):1680-7. doi: 10.1086/302686. Am J Hum Genet. 1999. PMID: 10577922 Free PMC article.

5

Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome.

Katsanis N, Beales PL, Woods MO, Lewis RA, Green JS, Parfrey PS, Ansley SJ, Davidson WS, Lupski JR. Katsanis N, et al. Among authors: woods mo. Nat Genet. 2000 Sep;26(1):67-70. doi: 10.1038/79201. Nat Genet. 2000. PMID: 10973251

6

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci.

Beales PL, Katsanis N, Lewis RA, Ansley SJ, Elcioglu N, Raza J, Woods MO, Green JS, Parfrey PS, Davidson WS, Lupski JR. Beales PL, et al. Among authors: woods mo. Am J Hum Genet. 2001 Mar;68(3):606-16. doi: 10.1086/318794. Epub 2001 Feb 1. Am J Hum Genet. 2001. PMID: 11179009 Free PMC article.

7

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. 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

8

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: woods mo. Fam Cancer. 2007;6(1):1-12. doi: 10.1007/s10689-006-0014-8. Fam Cancer. 2007. PMID: 17039271

9

Cytochrome P450 17A1 and catechol O-methyltransferase polymorphisms and age at Lynch syndrome colon cancer onset in Newfoundland.

Campbell PT, Edwards L, McLaughlin JR, Green J, Younghusband HB, Woods MO. Campbell PT, et al. Among authors: woods mo. Clin Cancer Res. 2007 Jul 1;13(13):3783-8. doi: 10.1158/1078-0432.CCR-06-2987. Clin Cancer Res. 2007. PMID: 17606708

10

Prediction of Lynch syndrome in consecutive patients with colorectal cancer.

Green RC, Parfrey PS, Woods MO, Younghusband HB. Green RC, et al. Among authors: woods mo. 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

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