Similar articles for PMID: 15744044

Year	Number of Results
2001	1
2002	2
2003	2
2004	3
2005	6
2006	6
2007	6
2008	5
2009	4
2010	5
2012	2
2013	2
2014	4
2015	2
2017	2
2018	2
2019	1
2024	0

1

Complete allelic analysis of BRCA1 and BRCA2 variants in young Nigerian breast cancer patients.

Fackenthal JD, Sveen L, Gao Q, Kohlmeir EK, Adebamowo C, Ogundiran TO, Adenipekun AA, Oyesegun R, Campbell O, Rotimi C, Akang EE, Das S, Olopade OI. Fackenthal JD, et al. J Med Genet. 2005 Mar;42(3):276-81. doi: 10.1136/jmg.2004.020446. J Med Genet. 2005. PMID: 15744044 Free PMC article. No abstract available.

2

Screening for common mutations in BRCA1 and BRCA2 genes: interest in genetic testing of Tunisian families with breast and/or ovarian cancer.

Fourati A, Louchez MM, Fournier J, Gamoudi A, Rahal K, El May MV, El May A, Revillion F, Peyrat JP. Fourati A, et al. Bull Cancer. 2014 Nov;101(11):E36-40. doi: 10.1684/bdc.2014.2049. Bull Cancer. 2014. PMID: 25418591

3

Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent.

Yarden RI, Friedman E, Metsuyanim S, Olender T, Ben-Asher E, Papa MZ. Yarden RI, et al. Mol Carcinog. 2010 Jun;49(6):545-55. doi: 10.1002/mc.20618. Mol Carcinog. 2010. PMID: 20306497

4

Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patients.

Pastrello C, Polesel J, Della Puppa L, Viel A, Maestro R. Pastrello C, et al. Carcinogenesis. 2010 Dec;31(12):2124-6. doi: 10.1093/carcin/bgq184. Epub 2010 Sep 1. Carcinogenesis. 2010. PMID: 20810544

5

Molecular and in silico analysis of BRCA1 and BRCA2 variants.

Tommasi S, Pilato B, Pinto R, Monaco A, Bruno M, Campana M, Digennaro M, Schittulli F, Lacalamita R, Paradiso A. Tommasi S, et al. Mutat Res. 2008 Sep 26;644(1-2):64-70. doi: 10.1016/j.mrfmmm.2008.07.005. Epub 2008 Jul 18. Mutat Res. 2008. PMID: 18694767

6

Q356R and S1512I are BRCA1 variants that may be associated with breast cancer in a Cypriot family.

Hadjisavvas A, Adamou A, O'Dowd Phanis C, Todd CM, Kitsios P, Kyriacou K, Christodoulou CG. Hadjisavvas A, et al. Oncol Rep. 2002 Mar-Apr;9(2):383-6. Oncol Rep. 2002. PMID: 11836613

7

Use of genetic testing and prophylactic mastectomy and oophorectomy in women with breast or ovarian cancer from families with a BRCA1 or BRCA2 mutation.

Meijers-Heijboer H, Brekelmans CT, Menke-Pluymers M, Seynaeve C, Baalbergen A, Burger C, Crepin E, van den Ouweland AW, van Geel B, Klijn JG. Meijers-Heijboer H, et al. J Clin Oncol. 2003 May 1;21(9):1675-81. doi: 10.1200/JCO.2003.09.052. J Clin Oncol. 2003. PMID: 12721241

8

ATM allelic variants associated to hereditary breast cancer in 94 Chilean women: susceptibility or ethnic influences?

Tapia T, Sanchez A, Vallejos M, Alvarez C, Moraga M, Smalley S, Camus M, Alvarez M, Carvallo P. Tapia T, et al. Breast Cancer Res Treat. 2008 Jan;107(2):281-8. doi: 10.1007/s10549-007-9544-5. Epub 2007 Mar 10. Breast Cancer Res Treat. 2008. PMID: 17351744

9

Similar contributions of BRCA1 and BRCA2 germline mutations to early-onset breast cancer in Germany.

Hamann U, Liu X, Bungardt N, Ulmer HU, Bastert G, Sinn HP. Hamann U, et al. Eur J Hum Genet. 2003 Jun;11(6):464-7. doi: 10.1038/sj.ejhg.5200988. Eur J Hum Genet. 2003. PMID: 12774040

10

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers.

Hughes DJ, Ginolhac SM, Coupier I, Corbex M, Bressac-de-Paillerets B, Chompret A, Bignon YJ, Uhrhammer N, Lasset C, Giraud S, Hardouin A, Berthet P, Peyrat JP, Fournier J, Nogues C, Lidereau R, Muller D, Fricker JP, Longy M, Toulas C, Guimbaud R, Maugard C, Olschwang S, Yannoukakos D, Durocher F, Moisan AM, Simard J, Mazoyer S, Lynch HT, Szabo C, Lenoir GM, Goldgar DE, Stoppa-Lyonnet D, Sinilnikova OM. Hughes DJ, et al. Cancer Epidemiol Biomarkers Prev. 2005 Jan;14(1):265-7. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 15668505

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