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Hereditary and familial ovarian cancer in southern Ontario.
Narod SA, Madlensky L, Bradley L, Cole D, Tonin P, Rosen B, Risch HA. Narod SA, et al. Cancer. 1994 Oct 15;74(8):2341-6. doi: 10.1002/1097-0142(19941015)74:8<2341::aid-cncr2820740819>3.0.co;2-z. Cancer. 1994. PMID: 7922985
Risk modifiers in carriers of BRCA1 mutations.
Narod SA, Goldgar D, Cannon-Albright L, Weber B, Moslehi R, Ives E, Lenoir G, Lynch H. Narod SA, et al. Int J Cancer. 1995 Dec 20;64(6):394-8. doi: 10.1002/ijc.2910640608. Int J Cancer. 1995. PMID: 8550241
Is hereditary site-specific ovarian cancer a distinct genetic condition?
Liede A, Tonin PN, Sun CC, Serruya C, Daly MB, Narod SA, Foulkes WD. Liede A, et al. Among authors: narod sa. Am J Med Genet. 1998 Jan 6;75(1):55-8. doi: 10.1002/(sici)1096-8628(19980106)75:1<55::aid-ajmg12>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9450858
Effect of smoking on breast cancer in carriers of mutant BRCA1 or BRCA2 genes.
Brunet JS, Ghadirian P, Rebbeck TR, Lerman C, Garber JE, Tonin PN, Abrahamson J, Foulkes WD, Daly M, Wagner-Costalas J, Godwin A, Olopade OI, Moslehi R, Liede A, Futreal PA, Weber BL, Lenoir GM, Lynch HT, Narod SA. Brunet JS, et al. Among authors: narod sa. J Natl Cancer Inst. 1998 May 20;90(10):761-6. doi: 10.1093/jnci/90.10.761. J Natl Cancer Inst. 1998. PMID: 9605646
A family with three germline mutations in BRCA1 and BRCA2.
Liede A, Metcalfe K, Offit K, Brown K, Miller S, Narod SA, Moslehi R. Liede A, et al. Among authors: narod sa. Clin Genet. 1998 Sep;54(3):215-8. doi: 10.1111/j.1399-0004.1998.tb04287.x. Clin Genet. 1998. PMID: 9788724
Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.
Warner E, Foulkes W, Goodwin P, Meschino W, Blondal J, Paterson C, Ozcelik H, Goss P, Allingham-Hawkins D, Hamel N, Di Prospero L, Contiga V, Serruya C, Klein M, Moslehi R, Honeyford J, Liede A, Glendon G, Brunet JS, Narod S. Warner E, et al. J Natl Cancer Inst. 1999 Jul 21;91(14):1241-7. doi: 10.1093/jnci/91.14.1241. J Natl Cancer Inst. 1999. PMID: 10413426
Intron variants of the p53 gene are associated with increased risk for ovarian cancer but not in carriers of BRCA1 or BRCA2 germline mutations.
Wang-Gohrke S, Weikel W, Risch H, Vesprini D, Abrahamson J, Lerman C, Godwin A, Moslehi R, Olipade O, Brunet JS, Stickeler E, Kieback DG, Kreienberg R, Weber B, Narod SA, Runnebaum IB. Wang-Gohrke S, et al. Among authors: narod sa. Br J Cancer. 1999 Sep;81(1):179-83. doi: 10.1038/sj.bjc.6690669. Br J Cancer. 1999. PMID: 10487631 Free PMC article.
888 results