Gordon PH - Search Results

1

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA. Foulkes WD, et al. Among authors: gordon ph. Am J Hum Genet. 2002 Dec;71(6):1395-412. doi: 10.1086/345075. Epub 2002 Nov 26. Am J Hum Genet. 2002. PMID: 12454801 Free PMC article.

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. Among authors: gordon ph. Hum Mutat. 2002 Feb;19(2):108-13. doi: 10.1002/humu.10040. Hum Mutat. 2002. PMID: 11793469

3

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. Among authors: gordon ph. Fam Cancer. 2006;5(1):21-8. doi: 10.1007/s10689-005-2572-6. Fam Cancer. 2006. PMID: 16528605

4

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. Among authors: gordon ph. Hum Mutat. 2006 Apr;27(4):388. doi: 10.1002/humu.9417. Hum Mutat. 2006. PMID: 16541406

5

High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.

Chong G, Jarry J, Marcus V, Thiffault I, Winocour S, Monczak Y, Drouin R, Latreille J, Australie K, Bapat B, Gordon PH, Giguère Y, Gologan A, Galiatsatos P, Jass JR, Wong N, Zaor S, Palma L, Kasprzak L, Tischkowitz M, Foulkes WD. Chong G, et al. Among authors: gordon ph. Hum Mutat. 2009 Aug;30(8):E797-812. doi: 10.1002/humu.21056. Hum Mutat. 2009. PMID: 19459153

6

Genetic counseling and interpretation of genetic tests in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.

Wong N, Lasko D, Rabelo R, Pinsky L, Gordon PH, Foulkes W. Wong N, et al. Among authors: gordon ph. Dis Colon Rectum. 2001 Feb;44(2):271-9. doi: 10.1007/BF02234304. Dis Colon Rectum. 2001. PMID: 11227946 Review.

7

Role of molecular diagnostic testing in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer families.

Rabelo R, Foulkes W, Gordon PH, Wong N, Yuan ZQ, MacNamara E, Chong G, Pinsky L, Lasko D. Rabelo R, et al. Among authors: gordon ph. Dis Colon Rectum. 2001 Mar;44(3):437-46. doi: 10.1007/BF02234746. Dis Colon Rectum. 2001. PMID: 11289293 Review.

8

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: gordon ph. Clin Genet. 2005 Sep;68(3):234-8. doi: 10.1111/j.1399-0004.2005.00486.x. Clin Genet. 2005. PMID: 16098012

9

I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer.

Yuan ZQ, Kasprzak L, Gordon PH, Pinsky L, Foulkes WD. Yuan ZQ, et al. Among authors: gordon ph. Clin Genet. 1998 Oct;54(4):368-70. doi: 10.1034/j.1399-0004.1998.5440421.x. Clin Genet. 1998. PMID: 9831355

10

Multimodal molecular screening is required to improve the sensitivity of MLH1 and MSH2 mutation analysis.

Andermann A, Thiffault I, Wong N, Gordon P, MacNamara E, Chong G, Foulkes W. Andermann A, et al. J Clin Oncol. 2002 Mar 15;20(6):1705-7. doi: 10.1200/JCO.2002.20.6.1705. J Clin Oncol. 2002. PMID: 11896123 No abstract available.

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