Easton DF - Search Results

1

Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Wang X, Pankratz VS, Fredericksen Z, Tarrell R, Karaus M, McGuffog L, Pharaoh PD, Ponder BA, Dunning AM, Peock S, Cook M, Oliver C, Frost D; EMBRACE; Sinilnikova OM, Stoppa-Lyonnet D, Mazoyer S, Houdayer C; GEMO; Hogervorst FB, Hooning MJ, Ligtenberg MJ; HEBON; Spurdle A, Chenevix-Trench G; kConFab; Schmutzler RK, Wappenschmidt B, Engel C, Meindl A, Domchek SM, Nathanson KL, Rebbeck TR, Singer CF, Gschwantler-Kaulich D, Dressler C, Fink A, Szabo CI, Zikan M, Foretova L, Claes K, Thomas G, Hoover RN, Hunter DJ, Chanock SJ, Easton DF, Antoniou AC, Couch FJ. Wang X, et al. Among authors: easton df. Hum Mol Genet. 2010 Jul 15;19(14):2886-97. doi: 10.1093/hmg/ddq174. Epub 2010 Apr 23. Hum Mol Genet. 2010. PMID: 20418484 Free PMC article.

2

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome.

Smith SA, Easton DF, Evans DG, Ponder BA. Smith SA, et al. Among authors: easton df. Nat Genet. 1992 Oct;2(2):128-31. doi: 10.1038/ng1092-128. Nat Genet. 1992. PMID: 1303261

3

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome.

Wooster R, Mangion J, Eeles R, Smith S, Dowsett M, Averill D, Barrett-Lee P, Easton DF, Ponder BA, Stratton MR. Wooster R, et al. Among authors: easton df. Nat Genet. 1992 Oct;2(2):132-4. doi: 10.1038/ng1092-132. Nat Genet. 1992. PMID: 1303262

4

Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative Group.

Mathew CG, Easton DF, Nakamura Y, Ponder BA. Mathew CG, et al. Among authors: easton df. Lancet. 1991 Jan 5;337(8732):7-11. doi: 10.1016/0140-6736(91)93329-8. Lancet. 1991. PMID: 1670689

5

[The genetics of medullary cancer of the thyroid].

Ponder BA, Easton DF, Mathew CG. Ponder BA, et al. Among authors: easton df. Ann Endocrinol (Paris). 1988;49(1):4-9. Ann Endocrinol (Paris). 1988. PMID: 2900621 Review. French.

6

Localisation of the breast-ovarian cancer susceptibility gene (BRCA1) on 17q12-21 to an interval of < or = 1 cM.

Smith SA, DiCioccio RA, Struewing JP, Easton DF, Gallion HH, Albertsen H, Mazoyer S, Johansson B, Steichen-Gersdorf E, Stratton M, et al. Smith SA, et al. Among authors: easton df. Genes Chromosomes Cancer. 1994 May;10(1):71-6. doi: 10.1002/gcc.2870100112. Genes Chromosomes Cancer. 1994. PMID: 7519878

7

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

Easton DF, Ford D, Bishop DT. Easton DF, et al. Am J Hum Genet. 1995 Jan;56(1):265-71. Am J Hum Genet. 1995. PMID: 7825587 Free PMC article.

8

Familial site-specific ovarian cancer is linked to BRCA1 on 17q12-21.

Steichen-Gersdorf E, Gallion HH, Ford D, Girodet C, Easton DF, DiCioccio RA, Evans G, Ponder MA, Pye C, Mazoyer S, et al. Steichen-Gersdorf E, et al. Among authors: easton df. Am J Hum Genet. 1994 Nov;55(5):870-5. Am J Hum Genet. 1994. PMID: 7977348 Free PMC article.

9

The genetics of familial breast cancer and their practical implications.

Eeles RA, Stratton MR, Goldgar DE, Easton DF. Eeles RA, et al. Among authors: easton df. Eur J Cancer. 1994;30A(9):1383-90. doi: 10.1016/0959-8049(94)90190-2. Eur J Cancer. 1994. PMID: 7999429 Review.

10

Human familial and sporadic breast cancer: analysis of the coding regions of the 17 beta-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assay.

Mannermaa A, Peltoketo H, Winqvist R, Ponder BA, Kiviniemi H, Easton DF, Poutanen M, Isomaa V, Vihko R. Mannermaa A, et al. Among authors: easton df. Hum Genet. 1994 Mar;93(3):319-24. doi: 10.1007/BF00212030. Hum Genet. 1994. PMID: 8125484

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