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Items: 9

1.

Breast cancer risks for BRCA1/2 carriers.

Easton DF, Hopper JL, Thomas DC, Antoniou A, Pharoah PD, Whittemore AS, Haile RW.

Science. 2004 Dec 24;306(5705):2187-91; author reply 2187-91. No abstract available.

PMID:
15622557
2.

Susceptibility to breast cancer: hereditary syndromes and low penetrance genes.

Nusbaum R, Vogel KJ, Ready K.

Breast Dis. 2006-2007;27:21-50. Review.

PMID:
17917139
3.

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations.

Fackenthal JD, Olopade OI.

Nat Rev Cancer. 2007 Dec;7(12):937-48. Review.

PMID:
18034184
4.

Bias in intervention studies that enroll patients from high-risk clinics.

Wacholder S.

J Natl Cancer Inst. 2004 Aug 18;96(16):1204-7. Review.

PMID:
15316055
5.

Update on genetic predisposition to breast cancer.

Ahmed M, Lalloo F, Evans DG.

Expert Rev Anticancer Ther. 2009 Aug;9(8):1103-13. doi: 10.1586/era.09.38. Review.

PMID:
19671030
6.

Bilateral risk-reducing oophorectomy in BRCA1 and BRCA2 mutation carriers.

Domchek SM, Stopfer JE, Rebbeck TR.

J Natl Compr Canc Netw. 2006 Feb;4(2):177-82. Review.

PMID:
16451773
7.

Use of association studies to define genetic modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Hughes DJ.

Fam Cancer. 2008;7(3):233-44. doi: 10.1007/s10689-008-9181-0. Epub 2008 Feb 19. Review.

PMID:
18283561
8.

Hormonal and genetic risk factors for breast cancer.

Clamp A, Danson S, Clemons M.

Surgeon. 2003 Feb;1(1):23-31. Review.

PMID:
15568421
9.

Hormone replacement and breast cancer.

Castiglione-Gertsch M.

Ann Oncol. 2004;15 Suppl 4:iv275-7. Review. No abstract available.

PMID:
15477320

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