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Year Number of Results
1994 2
1996 1
1997 2
1998 2
2001 1
2004 1
2020 0
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9 results
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Page 1
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, Bishop DT, Weber B, Lenoir G, Chang-Claude J, Sobol H, Teare MD, Struewing J, Arason A, Scherneck S, Peto J, Rebbeck TR, Tonin P, Neuhausen S, Barkardottir R, Eyfjord J, Lynch H, Ponder BA, Gayther SA, Zelada-Hedman M, et al. Ford D, et al. Am J Hum Genet. 1998 Mar;62(3):676-89. doi: 10.1086/301749. Am J Hum Genet. 1998. PMID: 9497246 Free PMC article.
Mutation testing of early-onset breast cancer genes BRCA1 and BRCA2.
Neuhausen SL, Ostrander EA. Neuhausen SL, et al. Genet Test. 1997;1(2):75-83. doi: 10.1089/gte.1997.1.75. Genet Test. 1997. PMID: 10464630 Review.
Breast-feeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
Jernström H, Lubinski J, Lynch HT, Ghadirian P, Neuhausen S, Isaacs C, Weber BL, Horsman D, Rosen B, Foulkes WD, Friedman E, Gershoni-Baruch R, Ainsworth P, Daly M, Garber J, Olsson H, Sun P, Narod SA. Jernström H, et al. J Natl Cancer Inst. 2004 Jul 21;96(14):1094-8. doi: 10.1093/jnci/djh211. J Natl Cancer Inst. 2004. PMID: 15265971
BRCA1 mutations in primary breast and ovarian carcinomas.
Futreal PA, Liu Q, Shattuck-Eidens D, Cochran C, Harshman K, Tavtigian S, Bennett LM, Haugen-Strano A, Swensen J, Miki Y, et al. Futreal PA, et al. Science. 1994 Oct 7;266(5182):120-2. doi: 10.1126/science.7939630. Science. 1994. PMID: 7939630
Modification of BRCA1- and BRCA2-associated breast cancer risk by AIB1 genotype and reproductive history.
Rebbeck TR, Wang Y, Kantoff PW, Krithivas K, Neuhausen SL, Godwin AK, Daly MB, Narod SA, Brunet JS, Vesprini D, Garber JE, Lynch HT, Weber BL, Brown M. Rebbeck TR, et al. Cancer Res. 2001 Jul 15;61(14):5420-4. Cancer Res. 2001. PMID: 11454686 Free article.
Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
Gao Q, Neuhausen S, Cummings S, Luce M, Olopade OI. Gao Q, et al. Am J Hum Genet. 1997 May;60(5):1233-6. Am J Hum Genet. 1997. PMID: 9150171 Free PMC article. No abstract available.
A large kindred with 17q-linked breast and ovarian cancer: genetic, phenotypic, and genealogical analysis.
Goldgar DE, Fields P, Lewis CM, Tran TD, Cannon-Albright LA, Ward JH, Swensen J, Skolnick MH. Goldgar DE, et al. J Natl Cancer Inst. 1994 Feb 2;86(3):200-9. doi: 10.1093/jnci/86.3.200. J Natl Cancer Inst. 1994. PMID: 8283492
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, Lenoir GM, Stratton MR, Easton DF, Ponder BA, Cannon-Albright L, Larsson C, Goldgar DE, Narod SA. Phelan CM, et al. Nat Genet. 1996 Mar;12(3):309-11. doi: 10.1038/ng0396-309. Nat Genet. 1996. PMID: 8589723
Response to radiation therapy and prognosis in breast cancer patients with BRCA1 and BRCA2 mutations.
Gaffney DK, Brohet RM, Lewis CM, Holden JA, Buys SS, Neuhausen SL, Steele L, Avizonis V, Stewart JR, Cannon-Albright LA. Gaffney DK, et al. Radiother Oncol. 1998 May;47(2):129-36. doi: 10.1016/s0167-8140(98)00023-1. Radiother Oncol. 1998. PMID: 9683359
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