Narod SA - Search Results

1

Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers.

Cullinane CA, Lubinski J, Neuhausen SL, Ghadirian P, Lynch HT, Isaacs C, Weber B, Moller P, Offit K, Kim-Sing C, Friedman E, Randall S, Pasini B, Ainsworth P, Gershoni-Baruch R, Foulkes WD, Klijn J, Tung N, Rennert G, Olopade O, Couch F, Wagner T, Olsson H, Sun P, Weitzel JN, Narod SA. Cullinane CA, et al. Among authors: narod sa. Int J Cancer. 2005 Dec 20;117(6):988-91. doi: 10.1002/ijc.21273. Int J Cancer. 2005. PMID: 15986445 Free article.

2

Family history and risk of ovarian cancer.

Foulkes W, Glendon G, Narod S. Foulkes W, et al. JAMA. 1995 Aug 2;274(5):383. JAMA. 1995. PMID: 7616630 No abstract available.

3

An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.

Narod SA, Ford D, Devilee P, Barkardottir RB, Lynch HT, Smith SA, Ponder BA, Weber BL, Garber JE, Birch JM, et al. Narod SA, et al. Am J Hum Genet. 1995 Jan;56(1):254-64. Am J Hum Genet. 1995. PMID: 7825586 Free PMC article.

4

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening.

Shattuck-Eidens D, McClure M, Simard J, Labrie F, Narod S, Couch F, Hoskins K, Weber B, Castilla L, Erdos M, et al. Shattuck-Eidens D, et al. JAMA. 1995 Feb 15;273(7):535-41. JAMA. 1995. PMID: 7837387

5

Increasing incidence of breast cancer in family with BRCA1 mutation.

Narod S, Lynch H, Conway T, Watson P, Feunteun J, Lenoir G. Narod S, et al. Lancet. 1993 Apr 24;341(8852):1101-2. doi: 10.1016/0140-6736(93)92468-9. Lancet. 1993. PMID: 8097005 No abstract available.

6

Hereditary breast cancer and family cancer syndromes.

Lynch HT, Lynch J, Conway T, Watson P, Feunteun J, Lenoir G, Narod S, Fitzgibbons R Jr. Lynch HT, et al. World J Surg. 1994 Jan-Feb;18(1):21-31. doi: 10.1007/BF00348188. World J Surg. 1994. PMID: 8197773 Review.

7

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

8

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.

Serova O, Montagna M, Torchard D, Narod SA, Tonin P, Sylla B, Lynch HT, Feunteun J, Lenoir GM. Serova O, et al. Among authors: narod sa. Am J Hum Genet. 1996 Jan;58(1):42-51. Am J Hum Genet. 1996. PMID: 8554067 Free PMC article.

9

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE. Neuhausen SL, et al. Am J Hum Genet. 1996 Feb;58(2):271-80. Am J Hum Genet. 1996. PMID: 8571953 Free PMC article.

10

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: narod sa. Nat Genet. 1996 Mar;12(3):309-11. doi: 10.1038/ng0396-309. Nat Genet. 1996. PMID: 8589723

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