Easton DF - Search Results

1

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations.

Lakhani SR, Jacquemier J, Sloane JP, Gusterson BA, Anderson TJ, van de Vijver MJ, Farid LM, Venter D, Antoniou A, Storfer-Isser A, Smyth E, Steel CM, Haites N, Scott RJ, Goldgar D, Neuhausen S, Daly PA, Ormiston W, McManus R, Scherneck S, Ponder BA, Ford D, Peto J, Stoppa-Lyonnet D, Bignon YJ, Struewing JP, Spurr NK, Bishop DT, Klijn JG, Devilee P, Cornelisse CJ, Lasset C, Lenoir G, Barkardottir RB, Egilsson V, Hamann U, Chang-Claude J, Sobol H, Weber B, Stratton MR, Easton DF. Lakhani SR, et al. Among authors: easton df. J Natl Cancer Inst. 1998 Aug 5;90(15):1138-45. doi: 10.1093/jnci/90.15.1138. J Natl Cancer Inst. 1998. PMID: 9701363

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

No evidence for germline mutations in exons 5-9 of the p53 gene in 25 breast cancer families.

Warren W, Eeles RA, Ponder BA, Easton DF, Averill D, Ponder MA, Anderson K, Evans AM, DeMars R, Love R, et al. Warren W, et al. Among authors: easton df. Oncogene. 1992 May;7(5):1043-6. Oncogene. 1992. PMID: 1570151

5

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

6

The study of nevi in British twins: study design and description of the data set.

Easton DF, Cox GM, Macdonald AM, Ponder BA. Easton DF, et al. Cytogenet Cell Genet. 1992;59(2-3):165-6. doi: 10.1159/000133233. Cytogenet Cell Genet. 1992. PMID: 1737488 No abstract available.

7

Is the genetics of moliness simply the genetics of sun exposure? A path analysis of nevus counts and risk factors in British twins.

Duffy DL, Macdonald AM, Easton DF, Ponder BA, Martin NG. Duffy DL, et al. Among authors: easton df. Cytogenet Cell Genet. 1992;59(2-3):194-6. doi: 10.1159/000133243. Cytogenet Cell Genet. 1992. PMID: 1737498 No abstract available.

8

Genetic susceptibility to naevi--a twin study.

Easton DF, Cox GM, Macdonald AM, Ponder BA. Easton DF, et al. Br J Cancer. 1991 Dec;64(6):1164-7. doi: 10.1038/bjc.1991.483. Br J Cancer. 1991. PMID: 1764382 Free PMC article.

9

Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2A.

Telenius H, Mathew CG, Nakamura Y, Easton DF, Clark J, Neumann HP, Ziegler WH, Schinzel A, Ponder BA. Telenius H, et al. Among authors: easton df. Eur J Surg Oncol. 1990 Apr;16(2):134-40. Eur J Surg Oncol. 1990. PMID: 1969807

10

[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.

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