Ward BE - Search Results

1

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer.

Hall MJ, Reid JE, Burbidge LA, Pruss D, Deffenbaugh AM, Frye C, Wenstrup RJ, Ward BE, Scholl TA, Noll WW. Hall MJ, et al. Among authors: ward be. Cancer. 2009 May 15;115(10):2222-33. doi: 10.1002/cncr.24200. Cancer. 2009. PMID: 19241424 Free PMC article.

2

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.

Frank TS, Deffenbaugh AM, Reid JE, Hulick M, Ward BE, Lingenfelter B, Gumpper KL, Scholl T, Tavtigian SV, Pruss DR, Critchfield GC. Frank TS, et al. Among authors: ward be. J Clin Oncol. 2002 Mar 15;20(6):1480-90. doi: 10.1200/JCO.2002.20.6.1480. J Clin Oncol. 2002. PMID: 11896095

3

Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families.

Hendrickson BC, Judkins T, Ward BD, Eliason K, Deffenbaugh AE, Burbidge LA, Pyne K, Leclair B, Ward BE, Scholl T. Hendrickson BC, et al. Among authors: ward be. Genes Chromosomes Cancer. 2005 Jul;43(3):309-13. doi: 10.1002/gcc.20189. Genes Chromosomes Cancer. 2005. PMID: 15846789

4

Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.

Judkins T, Hendrickson BC, Deffenbaugh AM, Eliason K, Leclair B, Norton MJ, Ward BE, Pruss D, Scholl T. Judkins T, et al. Among authors: ward be. Cancer Res. 2005 Nov 1;65(21):10096-103. doi: 10.1158/0008-5472.CAN-05-1241. Cancer Res. 2005. PMID: 16267036

5

Prediction of MLH1 and MSH2 mutations in Lynch syndrome.

Balmaña J, Stockwell DH, Steyerberg EW, Stoffel EM, Deffenbaugh AM, Reid JE, Ward B, Scholl T, Hendrickson B, Tazelaar J, Burbidge LA, Syngal S. Balmaña J, et al. JAMA. 2006 Sep 27;296(12):1469-78. doi: 10.1001/jama.296.12.1469. JAMA. 2006. PMID: 17003395

6

A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets.

Ward BD, Hendrickson BC, Judkins T, Deffenbaugh AM, Leclair B, Ward BE, Scholl T. Ward BD, et al. Among authors: ward be. J Mol Diagn. 2005 Feb;7(1):139-42. doi: 10.1016/S1525-1578(10)60020-7. J Mol Diagn. 2005. PMID: 15681486 Free PMC article.

7

A characterization of genetic variants in BRCA1 intron 8 identifies a mutation and a polymorphism.

Pyne MT, Pruss D, Ward BE, Scholl T. Pyne MT, et al. Among authors: ward be. Mutat Res. 1999 Aug;406(2-4):101-7. doi: 10.1016/s1383-5726(99)00006-0. Mutat Res. 1999. PMID: 10479726

8

Biochemical and genetic characterisation shows that the BRCA1 IVS20 insertion is a polymorphism.

Scholl T, Pyne MT, Ward B, Pruss D. Scholl T, et al. J Med Genet. 1999 Jul;36(7):571-2. J Med Genet. 1999. PMID: 10424822 Free PMC article. No abstract available.

9

The BRCA2 genetic variant IVS7 + 2T-->G is a mutation.

Pyne MT, Brothman AR, Ward B, Pruss D, Hendrickson BC, Scholl T. Pyne MT, et al. J Hum Genet. 2000;45(6):351-7. doi: 10.1007/s100380070007. J Hum Genet. 2000. PMID: 11185744

10

BRCA1 IVS16+6T-->C is a deleterious mutation that creates an aberrant transcript by activating a cryptic splice donor site.

Scholl T, Pyne MT, Russo D, Ward BE. Scholl T, et al. Among authors: ward be. Am J Med Genet. 1999 Jul 16;85(2):113-6. Am J Med Genet. 1999. PMID: 10406662

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