Hamel N - Search Results

1

Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish men with prostate cancer.

Hamel N, Kotar K, Foulkes WD. Hamel N, et al. BMC Med Genet. 2003 Aug 11;4:7. doi: 10.1186/1471-2350-4-7. BMC Med Genet. 2003. PMID: 12911837 Free PMC article.

2

Impact of germline BRCA1 mutations and overexpression of p53 on prognosis and response to treatment following breast carcinoma: 10-year follow up data.

Goffin JR, Chappuis PO, Bégin LR, Wong N, Brunet JS, Hamel N, Paradis AJ, Boyd J, Foulkes WD. Goffin JR, et al. Among authors: hamel n. Cancer. 2003 Feb 1;97(3):527-36. doi: 10.1002/cncr.11080. Cancer. 2003. PMID: 12548593 Free article.

3

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

4

Mixed ovarian germ cell tumor in a BRCA2 mutation carrier.

Hamel N, Wong N, Alpert L, Galvez M, Foulkes WD. Hamel N, et al. Int J Gynecol Pathol. 2007 Apr;26(2):160-4. doi: 10.1097/01.pgp.0000228142.52054.0f. Int J Gynecol Pathol. 2007. PMID: 17413983

5

Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer.

Tischkowitz MD, Yilmaz A, Chen LQ, Karyadi DM, Novak D, Kirchhoff T, Hamel N, Tavtigian SV, Kolb S, Bismar TA, Aloyz R, Nelson PS, Hood L, Narod SA, White KA, Ostrander EA, Isaacs WB, Offit K, Cooney KA, Stanford JL, Foulkes WD. Tischkowitz MD, et al. Among authors: hamel n. Cancer Lett. 2008 Oct 18;270(1):173-80. doi: 10.1016/j.canlet.2008.05.006. Epub 2008 Jun 20. Cancer Lett. 2008. PMID: 18571837 Free PMC article.

6

Identification of a novel CHEK2 variant and assessment of its contribution to the risk of breast cancer in French Canadian women.

Novak DJ, Chen LQ, Ghadirian P, Hamel N, Zhang P, Rossiny V, Cardinal G, Robidoux A, Tonin PN, Rousseau F, Narod SA, Foulkes WD. Novak DJ, et al. Among authors: hamel n. BMC Cancer. 2008 Aug 15;8:239. doi: 10.1186/1471-2407-8-239. BMC Cancer. 2008. PMID: 18706089 Free PMC article.

7

How old is this mutation? - a study of three Ashkenazi Jewish founder mutations.

Greenwood CM, Sun S, Veenstra J, Hamel N, Niell B, Gruber S, Foulkes WD. Greenwood CM, et al. Among authors: hamel n. BMC Genet. 2010 May 14;11:39. doi: 10.1186/1471-2156-11-39. BMC Genet. 2010. PMID: 20470408 Free PMC article.

8

Germline DICER1 mutations and familial cystic nephroma.

Bahubeshi A, Bal N, Rio Frio T, Hamel N, Pouchet C, Yilmaz A, Bouron-Dal Soglio D, Williams GM, Tischkowitz M, Priest JR, Foulkes WD. Bahubeshi A, et al. Among authors: hamel n. J Med Genet. 2010 Dec;47(12):863-6. doi: 10.1136/jmg.2010.081216. Epub 2010 Oct 29. J Med Genet. 2010. PMID: 21036787

9

On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations.

Hamel N, Feng BJ, Foretova L, Stoppa-Lyonnet D, Narod SA, Imyanitov E, Sinilnikova O, Tihomirova L, Lubinski J, Gronwald J, Gorski B, Hansen Tv, Nielsen FC, Thomassen M, Yannoukakos D, Konstantopoulou I, Zajac V, Ciernikova S, Couch FJ, Greenwood CM, Goldgar DE, Foulkes WD. Hamel N, et al. Eur J Hum Genet. 2011 Mar;19(3):300-6. doi: 10.1038/ejhg.2010.203. Epub 2010 Dec 1. Eur J Hum Genet. 2011. PMID: 21119707 Free PMC article.

10

Contribution of the PALB2 c.2323C>T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent.

Tischkowitz M, Sabbaghian N, Hamel N, Pouchet C, Foulkes WD, Mes-Masson AM, Provencher DM, Tonin PN. Tischkowitz M, et al. Among authors: hamel n. BMC Med Genet. 2013 Jan 9;14:5. doi: 10.1186/1471-2350-14-5. BMC Med Genet. 2013. PMID: 23302520 Free PMC article.

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