Hamel N - Search Results

1

Circulating tumor DNA is readily detectable among Ghanaian breast cancer patients supporting non-invasive cancer genomic studies in Africa.

Ahuno ST, Doebley AL, Ahearn TU, Yarney J, Titiloye N, Hamel N, Adjei E, Clegg-Lamptey JN, Edusei L, Awuah B, Song X, Vanderpuye V, Abubakar M, Duggan M, Stover DG, Nyarko K, Bartlett JMS, Aitpillah F, Ansong D, Gardner KL, Boateng FA, Bowcock AM, Caldas C, Foulkes WD, Wiafe S, Wiafe-Addai B, Garcia-Closas M, Kwarteng A, Ha G, Figueroa JD, Polak P; Ghana Breast Health Study Team. Ahuno ST, et al. Among authors: hamel n. NPJ Precis Oncol. 2021 Sep 17;5(1):83. doi: 10.1038/s41698-021-00219-7. NPJ Precis Oncol. 2021. PMID: 34535742 Free PMC article.

2

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.

3

The prognostic implication of the basal-like (cyclin E high/p27 low/p53+/glomeruloid-microvascular-proliferation+) phenotype of BRCA1-related breast cancer.

Foulkes WD, Brunet JS, Stefansson IM, Straume O, Chappuis PO, Bégin LR, Hamel N, Goffin JR, Wong N, Trudel M, Kapusta L, Porter P, Akslen LA. Foulkes WD, et al. Among authors: hamel n. Cancer Res. 2004 Feb 1;64(3):830-5. doi: 10.1158/0008-5472.can-03-2970. Cancer Res. 2004. PMID: 14871808

4

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.

5

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

6

[A role for PALB2/FANCN in breast cancer predisposition?].

Hamel N, Tischkowitz M, Foulkes WD. Hamel N, et al. Med Sci (Paris). 2008 Feb;24(2):120-1. doi: 10.1051/medsci/2008242120. Med Sci (Paris). 2008. PMID: 18272064 Free article. French. No abstract available.

7

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: hamel 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.

8

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.

9

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.

10

A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.

Yilmaz A, Hamel N, Schwartz CE, Houlston RS, Harper JI, Foulkes WD. Yilmaz A, et al. Among authors: hamel n. J Hum Genet. 2010 Sep;55(9):627-30. doi: 10.1038/jhg.2010.70. Epub 2010 Jun 17. J Hum Genet. 2010. PMID: 20555334

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