Narod S - Search Results

1

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. Among authors: narod s. JAMA. 1995 Feb 15;273(7):535-41. JAMA. 1995. PMID: 7837387

2

Androgen receptor and familial prostate cancer.

Sun S, Narod SA, Aprikian A, Ghadirian P, Labrie F. Sun S, et al. Among authors: narod sa. Nat Med. 1995 Sep;1(9):848-9. doi: 10.1038/nm0995-848b. Nat Med. 1995. PMID: 7585194 No abstract available.

3

BRCA1 mutations in Ashkenazi Jewish women.

Tonin P, Serova O, Lenoir G, Lynch H, Durocher F, Simard J, Morgan K, Narod S. Tonin P, et al. Among authors: narod s. Am J Hum Genet. 1995 Jul;57(1):189. Am J Hum Genet. 1995. PMID: 7611288 Free PMC article. No abstract available.

4

Family history and risk of ovarian cancer.

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

5

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.

6

The gene for hereditary breast-ovarian cancer, BRCA1, maps distal to EDH17B2 in chromosome region 17q12-q21.

Tonin P, Serova O, Simard J, Lenoir G, Feunteun J, Morgan K, Lynch H, Narod S. Tonin P, et al. Among authors: narod s. Hum Mol Genet. 1994 Sep;3(9):1679-82. doi: 10.1093/hmg/3.9.1679. Hum Mol Genet. 1994. PMID: 7833928

7

Detection of polymorphisms in the estradiol 17 beta-hydroxysteroid dehydrogenase II gene at the EDH17B2 locus on 17q11-q21.

Normand T, Narod S, Labrie F, Simard J. Normand T, et al. Among authors: narod s. Hum Mol Genet. 1993 Apr;2(4):479-83. doi: 10.1093/hmg/2.4.479. Hum Mol Genet. 1993. PMID: 8389226

8

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

9

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.

10

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. Among authors: narod s. Am J Hum Genet. 1996 Feb;58(2):271-80. Am J Hum Genet. 1996. PMID: 8571953 Free PMC article.

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