Foulkes WD - Search Results

1

[A role for PALB2/FANCN in breast cancer predisposition?].

Hamel N, Tischkowitz M, Foulkes WD. Hamel N, et al. Among authors: foulkes wd. Med Sci (Paris). 2008 Feb;24(2):120-1. doi: 10.1051/medsci/2008242120. Med Sci (Paris). 2008. PMID: 18272064 Free article. French. No abstract available.

2

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

3

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.

4

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.

5

Polymorphisms in GSTM1, GSTT1 and CYP1A1 and risk of pancreatic adenocarcinoma.

Liu G, Ghadirian P, Vesprini D, Hamel N, Paradis AJ, Lal G, Gallinger S, Narod SA, Foulkes WD. Liu G, et al. Among authors: foulkes wd. Br J Cancer. 2000 May;82(10):1646-9. doi: 10.1054/bjoc.2000.1221. Br J Cancer. 2000. PMID: 10817498 Free PMC article.

6

Increased risk of head and neck cancer in association with GSTT1 nullizygosity for individuals with low exposure to tobacco.

Hamel N, Karimi S, Hébert-Blouin MN, Brunet JS, Gilfix B, Ghadirian P, Black MJ, Narod SA, Foulkes WD. Hamel N, et al. Among authors: foulkes wd. Int J Cancer. 2000 Aug 1;87(3):452-4. Int J Cancer. 2000. PMID: 10897054 No abstract available.

7

Re: Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients.

Chappuis PO, Hamel N, Paradis AJ, Deschênes J, Tonin PN, Ghadirian P, Foulkes WD. Chappuis PO, et al. Among authors: foulkes wd. J Natl Cancer Inst. 2001 Jan 17;93(2):152-4. doi: 10.1093/jnci/93.2.152-a. J Natl Cancer Inst. 2001. PMID: 11208888 No abstract available.

8

TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: distinctive spectrum and structural distribution.

Greenblatt MS, Chappuis PO, Bond JP, Hamel N, Foulkes WD. Greenblatt MS, et al. Among authors: foulkes wd. Cancer Res. 2001 May 15;61(10):4092-7. Cancer Res. 2001. PMID: 11358831

9

Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer.

Chappuis PO, Hamel N, Paradis AJ, Deschênes J, Robidoux A, Potvin C, Cantin J, Tonin P, Ghadirian P, Foulkes WD. Chappuis PO, et al. Among authors: foulkes wd. Clin Genet. 2001 Jun;59(6):418-23. doi: 10.1034/j.1399-0004.2001.590606.x. Clin Genet. 2001. PMID: 11453973

10

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1.

Hutter P, Wijnen J, Rey-Berthod C, Thiffault I, Verkuijlen P, Farber D, Hamel N, Bapat B, Thibodeau SN, Burn J, Wu J, MacNamara E, Heinimann K, Chong G, Foulkes WD. Hutter P, et al. Among authors: foulkes wd. J Med Genet. 2002 May;39(5):323-7. doi: 10.1136/jmg.39.5.323. J Med Genet. 2002. PMID: 12011148 Free PMC article.

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