Easton DF - Search Results

1

FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.

Udler MS, Meyer KB, Pooley KA, Karlins E, Struewing JP, Zhang J, Doody DR, MacArthur S, Tyrer J, Pharoah PD, Luben R, Bernstein L, Kolonel LN, Henderson BE, Le Marchand L, Ursin G, Press MF, Brennan P, Sangrajrang S, Gaborieau V, Odefrey F, Shen CY, Wu PE, Wang HC, Kang D, Yoo KY, Noh DY, Ahn SH, Ponder BA, Haiman CA, Malone KE, Dunning AM, Ostrander EA, Easton DF; SEARCH Collaborators. Udler MS, et al. Among authors: easton df. Hum Mol Genet. 2009 May 1;18(9):1692-703. doi: 10.1093/hmg/ddp078. Epub 2009 Feb 17. Hum Mol Genet. 2009. PMID: 19223389 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 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.

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

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.

8

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.

Gardner E, Papi L, Easton DF, Cummings T, Jackson CE, Kaplan M, Love DR, Mole SE, Moore JK, Mulligan LM, et al. Gardner E, et al. Among authors: easton df. Hum Mol Genet. 1993 Mar;2(3):241-6. doi: 10.1093/hmg/2.3.241. Hum Mol Genet. 1993. PMID: 8098977

9

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

10

An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes.

Easton DF, Ponder MA, Huson SM, Ponder BA. Easton DF, et al. Am J Hum Genet. 1993 Aug;53(2):305-13. Am J Hum Genet. 1993. PMID: 8328449 Free PMC article.

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