Foulkes W - Search Results

1

Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).

van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R. van der Klift H, et al. Among authors: foulkes w. Genes Chromosomes Cancer. 2005 Oct;44(2):123-38. doi: 10.1002/gcc.20219. Genes Chromosomes Cancer. 2005. PMID: 15942939

2

Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms.

Yuan ZQ, Gottlieb B, Beitel LK, Wong N, Gordon PH, Wang Q, Puisieux A, Foulkes WD, Trifiro M. Yuan ZQ, et al. Hum Mutat. 2002 Feb;19(2):108-13. doi: 10.1002/humu.10040. Hum Mutat. 2002. PMID: 11793469

3

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.

4

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred.

Thiffault I, Hamel N, Pal T, McVety S, Marcus VA, Farber D, Cowie S, Deschênes J, Meschino W, Odefrey F, Goldgar D, Graham T, Narod S, Watters AK, MacNamara E, Du Sart D, Chong G, Foulkes WD. Thiffault I, et al. Among authors: foulkes wd. Br J Cancer. 2004 Jan 26;90(2):483-91. doi: 10.1038/sj.bjc.6601424. Br J Cancer. 2004. PMID: 14735197 Free PMC article.

5

Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families.

Thiffault I, Foulkes WD, Marcus VA, Farber D, Kasprzak L, MacNamara E, Wong N, Hutter P, Radice P, Bertario L, Chong G. Thiffault I, et al. Among authors: foulkes wd. Clin Genet. 2004 Aug;66(2):137-43. doi: 10.1111/j.1399-0004.2004.00274.x. Clin Genet. 2004. PMID: 15253764

6

Double frameshift mutations in APC and MSH2 in the same individual.

Soravia C, DeLozier CD, Dobbie Z, Berthod CR, Arrigoni E, Bründler MA, Blouin JL, Foulkes WD, Hutter P. Soravia C, et al. Int J Colorectal Dis. 2005 Sep;20(5):466-470. doi: 10.1007/s00384-005-0764-z. Int J Colorectal Dis. 2005. PMID: 15834612 Corrected and republished.

7

Novel genomic insertion-- deletion in MLH1: possible mechanistic role for non-homologous end-joining DNA repair.

McVety S, Younan R, Li L, Gordon PH, Wong N, Foulkes WD, Chong G. McVety S, et al. Among authors: foulkes wd. Clin Genet. 2005 Sep;68(3):234-8. doi: 10.1111/j.1399-0004.2005.00486.x. Clin Genet. 2005. PMID: 16098012

8

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. BMC Med Genet. 2006 Mar 1;7:15. doi: 10.1186/1471-2350-7-15. BMC Med Genet. 2006. PMID: 16509964 Free PMC article.

9

The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing alone.

McVety S, Li L, Thiffault I, Gordon PH, Macnamara E, Wong N, Australie K, Kasprzak L, Chong G, Foulkes WD. McVety S, et al. Fam Cancer. 2006;5(1):21-8. doi: 10.1007/s10689-005-2572-6. Fam Cancer. 2006. PMID: 16528605

10

Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC).

Li L, McVety S, Younan R, Liang P, Du Sart D, Gordon PH, Hutter P, Hogervorst FB, Chong G, Foulkes WD. Li L, et al. Hum Mutat. 2006 Apr;27(4):388. doi: 10.1002/humu.9417. Hum Mutat. 2006. PMID: 16541406

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