Foulkes WD - Search Results

1

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations.

Rudkin TM, Hamel N, Galvez M, Hogervorst F, Gille JJ, Møller P, Apold J, Foulkes WD. Rudkin TM, et al. Among authors: foulkes wd. BMC Med Genet. 2006 Mar 1;7:15. doi: 10.1186/1471-2350-7-15. BMC Med Genet. 2006. PMID: 16509964 Free PMC article.

2

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.

Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC, Dole K, Karimi S, Foulkes W, Lounis H, Warner E, Goss P, Anderson D, Larsson C, Narod SA, Futreal PA. Phelan CM, et al. Nat Genet. 1996 May;13(1):120-2. doi: 10.1038/ng0596-120. Nat Genet. 1996. PMID: 8673090

3

Increased incidence of cancer in first degree relatives of women with double primary carcinomas of the breast and colon.

Foulkes WD, Bolduc N, Lambert D, Ginsburg O, Olien L, Yandell DW, Tonin PN, Narod SA. Foulkes WD, et al. J Med Genet. 1996 Jul;33(7):534-9. doi: 10.1136/jmg.33.7.534. J Med Genet. 1996. PMID: 8818936 Free PMC article.

4

Pancreatic adenocarcinoma: epidemiology and genetics.

Flanders TY, Foulkes WD. Flanders TY, et al. Among authors: foulkes wd. J Med Genet. 1996 Nov;33(11):889-98. doi: 10.1136/jmg.33.11.889. J Med Genet. 1996. PMID: 8950667 Free PMC article. Review.

5

Is hereditary site-specific ovarian cancer a distinct genetic condition?

Liede A, Tonin PN, Sun CC, Serruya C, Daly MB, Narod SA, Foulkes WD. Liede A, et al. Among authors: foulkes wd. Am J Med Genet. 1998 Jan 6;75(1):55-8. doi: 10.1002/(sici)1096-8628(19980106)75:1<55::aid-ajmg12>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9450858

6

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.

Tonin PN, Mes-Masson AM, Futreal PA, Morgan K, Mahon M, Foulkes WD, Cole DE, Provencher D, Ghadirian P, Narod SA. Tonin PN, et al. Among authors: foulkes wd. Am J Hum Genet. 1998 Nov;63(5):1341-51. doi: 10.1086/302099. Am J Hum Genet. 1998. PMID: 9792861 Free PMC article.

7

Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.

Warner E, Foulkes W, Goodwin P, Meschino W, Blondal J, Paterson C, Ozcelik H, Goss P, Allingham-Hawkins D, Hamel N, Di Prospero L, Contiga V, Serruya C, Klein M, Moslehi R, Honeyford J, Liede A, Glendon G, Brunet JS, Narod S. Warner E, et al. J Natl Cancer Inst. 1999 Jul 21;91(14):1241-7. doi: 10.1093/jnci/91.14.1241. J Natl Cancer Inst. 1999. PMID: 10413426

8

An absence of founder BRCA2 mutations in individuals with squamous cell carcinoma of the head and neck.

Hamel N, Manning A, Black MJ, Tonin PN, Foulkes WD. Hamel N, et al. Among authors: foulkes wd. Int J Cancer. 1999 Dec 10;83(6):803-4. doi: 10.1002/(sici)1097-0215(19991210)83:6<803::aid-ijc17>3.0.co;2-n. Int J Cancer. 1999. PMID: 10597198 No abstract available.

9

No association between P53 codon 72 polymorphism and risk of squamous cell carcinoma of the head and neck.

Hamel N, Black MJ, Ghadirian P, Foulkes WD. Hamel N, et al. Among authors: foulkes wd. Br J Cancer. 2000 Feb;82(4):757-9. doi: 10.1054/bjoc.1999.0993. Br J Cancer. 2000. PMID: 10732740 Free PMC article.

10

A rapid fluorescent multiplexed-PCR analysis (FMPA) for founder mutations in the BRCA1 and BRCA2 genes.

Kuperstein G, Foulkes WD, Ghadirian P, Hakimi J, Narod SA. Kuperstein G, et al. Among authors: foulkes wd. Clin Genet. 2000 Mar;57(3):213-20. doi: 10.1034/j.1399-0004.2000.570307.x. Clin Genet. 2000. PMID: 10782928

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