Rebbeck TR - Search Results

1

Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers.

Rebbeck TR, Levin AM, Eisen A, Snyder C, Watson P, Cannon-Albright L, Isaacs C, Olopade O, Garber JE, Godwin AK, Daly MB, Narod SA, Neuhausen SL, Lynch HT, Weber BL. Rebbeck TR, et al. J Natl Cancer Inst. 1999 Sep 1;91(17):1475-9. doi: 10.1093/jnci/91.17.1475. J Natl Cancer Inst. 1999. PMID: 10469748

2

Assessment and counseling for women with a family history of breast cancer. A guide for clinicians.

Hoskins KF, Stopfer JE, Calzone KA, Merajver SD, Rebbeck TR, Garber JE, Weber BL. Hoskins KF, et al. Among authors: rebbeck tr. JAMA. 1995 Feb 15;273(7):577-85. JAMA. 1995. PMID: 7837392

3

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. Among authors: rebbeck tr. Nat Genet. 1996 Mar;12(3):309-11. doi: 10.1038/ng0396-309. Nat Genet. 1996. PMID: 8589723

4

Genetic heterogeneity in hereditary breast cancer: role of BRCA1 and BRCA2.

Rebbeck TR, Couch FJ, Kant J, Calzone K, DeShano M, Peng Y, Chen K, Garber JE, Weber BL. Rebbeck TR, et al. Am J Hum Genet. 1996 Sep;59(3):547-53. Am J Hum Genet. 1996. PMID: 8751855 Free PMC article.

5

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families.

Tonin P, Weber B, Offit K, Couch F, Rebbeck TR, Neuhausen S, Godwin AK, Daly M, Wagner-Costalos J, Berman D, Grana G, Fox E, Kane MF, Kolodner RD, Krainer M, Haber DA, Struewing JP, Warner E, Rosen B, Lerman C, Peshkin B, Norton L, Serova O, Foulkes WD, Garber JE, et al. Tonin P, et al. Among authors: rebbeck tr. Nat Med. 1996 Nov;2(11):1179-83. doi: 10.1038/nm1196-1179. Nat Med. 1996. PMID: 8898735 Review. No abstract available.

6

Variability in loss of constitutional heterozygosity across loci and among individuals: association with candidate genes in ductal breast carcinoma.

Rebbeck TR, Godwin AK, Buetow KH. Rebbeck TR, et al. Mol Carcinog. 1996 Nov;17(3):117-25. doi: 10.1002/(SICI)1098-2744(199611)17:3<117::AID-MC3>3.0.CO;2-C. Mol Carcinog. 1996. PMID: 8944071

7

Defining etiologic heterogeneity in breast cancer using genetic biomarkers.

Rebbeck TR, Walker AH, Phelan CM, Godwin AK, Buetow KH, Garber JE, Narod SA, Weber BL. Rebbeck TR, et al. Prog Clin Biol Res. 1997;396:53-61. Prog Clin Biol Res. 1997. PMID: 9108589 Review.

8

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer.

Couch FJ, DeShano ML, Blackwood MA, Calzone K, Stopfer J, Campeau L, Ganguly A, Rebbeck T, Weber BL. Couch FJ, et al. N Engl J Med. 1997 May 15;336(20):1409-15. doi: 10.1056/NEJM199705153362002. N Engl J Med. 1997. PMID: 9145677 Free article.

9

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. Among authors: rebbeck tr. Am J Hum Genet. 1998 Mar;62(3):676-89. doi: 10.1086/301749. Am J Hum Genet. 1998. PMID: 9497246 Free PMC article.

10

BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing.

Rubin SC, Blackwood MA, Bandera C, Behbakht K, Benjamin I, Rebbeck TR, Boyd J. Rubin SC, et al. Among authors: rebbeck tr. Am J Obstet Gynecol. 1998 Apr;178(4):670-7. doi: 10.1016/s0002-9378(98)70476-4. Am J Obstet Gynecol. 1998. PMID: 9579428 Free article.

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