Wong N - Search Results

1

Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach.

Tischkowitz M, Hamel N, Carvalho MA, Birrane G, Soni A, van Beers EH, Joosse SA, Wong N, Novak D, Quenneville LA, Grist SA; kConFab; Nederlof PM, Goldgar DE, Tavtigian SV, Monteiro AN, Ladias JA, Foulkes WD. Tischkowitz M, et al. Among authors: wong n. Eur J Hum Genet. 2008 Jul;16(7):820-32. doi: 10.1038/ejhg.2008.13. Epub 2008 Feb 20. Eur J Hum Genet. 2008. PMID: 18285836 Free PMC article.

2

Survival of patients with breast cancer and BRCA1 mutations.

Foulkes WD, Wong N, Rozen F, Brunet JS, Narod SA. Foulkes WD, et al. Among authors: wong n. Lancet. 1998 May 2;351(9112):1359-60. doi: 10.1016/S0140-6736(05)79091-7. Lancet. 1998. PMID: 9643825 No abstract available.

3

BRCA mutations and survival in breast cancer.

Foulkes WD, Wong N, Brunet JS, Narod SA. Foulkes WD, et al. Among authors: wong n. J Clin Oncol. 1998 Sep;16(9):3206-8. doi: 10.1200/JCO.1998.16.9.3206. J Clin Oncol. 1998. PMID: 9738598 No abstract available.

4

Germ-line BRCA1 mutation is an adverse prognostic factor in Ashkenazi Jewish women with breast cancer.

Foulkes WD, Wong N, Brunet JS, Bégin LR, Zhang JC, Martinez JJ, Rozen F, Tonin PN, Narod SA, Karp SE, Pollak MN. Foulkes WD, et al. Among authors: wong n. Clin Cancer Res. 1997 Dec;3(12 Pt 1):2465-9. Clin Cancer Res. 1997. PMID: 9815648

5

A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.

Yuan ZQ, Wong N, Foulkes WD, Alpert L, Manganaro F, Andreutti-Zaugg C, Iggo R, Anthony K, Hsieh E, Redston M, Pinsky L, Trifiro M, Gordon PH, Lasko D. Yuan ZQ, et al. Among authors: wong n. J Med Genet. 1999 Oct;36(10):790-3. doi: 10.1136/jmg.36.10.792. J Med Genet. 1999. PMID: 10528862 Free PMC article. 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: wong n. 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. Among authors: wong n. 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: wong n. 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. Among authors: wong n. Dis Colon Rectum. 2001 Mar;44(3):437-46. doi: 10.1007/BF02234746. Dis Colon Rectum. 2001. PMID: 11289293 Review.

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