Foulkes WD - Search Results

1

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: foulkes wd. Hum Mutat. 2009 Aug;30(8):E797-812. doi: 10.1002/humu.21056. Hum Mutat. 2009. PMID: 19459153

2

Family with Graves disease, multinodular goiter, nonmedullary thyroid carcinoma, and alveolar rhabdomyosarcoma.

Druker HA, Kasprzak L, Bégin LR, Jothy S, Narod SA, Foulkes WD. Druker HA, et al. Among authors: foulkes wd. Am J Med Genet. 1997 Oct 3;72(1):30-3. Am J Med Genet. 1997. PMID: 9295070

3

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.

4

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: foulkes wd. Clin Genet. 1998 Oct;54(4):368-70. doi: 10.1034/j.1399-0004.1998.5440421.x. Clin Genet. 1998. PMID: 9831355

5

Forth nightly review: hereditary ovarian carcinoma.

Kasprzak L, Foulkes WD, Shelling AN. Kasprzak L, et al. Among authors: foulkes wd. BMJ. 1999 Mar 20;318(7186):786-9. doi: 10.1136/bmj.318.7186.786. BMJ. 1999. PMID: 10082707 Free PMC article. Review. No abstract available.

6

The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer.

Yuan ZQ, Bégin LR, Wong N, Brunet JS, Trifiro M, Gordon PH, Pinsky L, Foulkes WD. Yuan ZQ, et al. Among authors: foulkes wd. Br J Cancer. 1999 Nov;81(5):850-4. doi: 10.1038/sj.bjc.6690775. Br J Cancer. 1999. PMID: 10555757 Free PMC article.

7

Primary node negative breast cancer in BRCA1 mutation carriers has a poor outcome.

Foulkes WD, Chappuis PO, Wong N, Brunet JS, Vesprini D, Rozen F, Yuan ZQ, Pollak MN, Kuperstein G, Narod SA, Bégin LR. Foulkes WD, et al. Ann Oncol. 2000 Mar;11(3):307-13. doi: 10.1023/a:1008340723974. Ann Oncol. 2000. PMID: 10811497 Free article.

8

Germline BRCA1/2 mutations and p27(Kip1) protein levels independently predict outcome after breast cancer.

Chappuis PO, Kapusta L, Bégin LR, Wong N, Brunet JS, Narod SA, Slingerland J, Foulkes WD. Chappuis PO, et al. Among authors: foulkes wd. J Clin Oncol. 2000 Dec 15;18(24):4045-52. doi: 10.1200/JCO.2000.18.24.4045. J Clin Oncol. 2000. PMID: 11118465

9

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. Dis Colon Rectum. 2001 Feb;44(2):271-9. doi: 10.1007/BF02234304. Dis Colon Rectum. 2001. PMID: 11227946 Review.

10

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. Dis Colon Rectum. 2001 Mar;44(3):437-46. doi: 10.1007/BF02234746. Dis Colon Rectum. 2001. PMID: 11289293 Review.

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