Wenstrup RJ - Search Results

1

Erratum to: Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry.

Rosenthal E, Moyes K, Arnell C, Evans B, Wenstrup RJ. Rosenthal E, et al. Among authors: wenstrup rj. Breast Cancer Res Treat. 2015 May;151(1):233. doi: 10.1007/s10549-015-3361-z. Breast Cancer Res Treat. 2015. PMID: 25850536

2

Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry.

Rosenthal E, Moyes K, Arnell C, Evans B, Wenstrup RJ. Rosenthal E, et al. Among authors: wenstrup rj. Breast Cancer Res Treat. 2015 Jan;149(1):223-7. doi: 10.1007/s10549-014-3218-x. Epub 2014 Dec 6. Breast Cancer Res Treat. 2015. PMID: 25476495

3

Clinical significance of large rearrangements in BRCA1 and BRCA2.

Judkins T, Rosenthal E, Arnell C, Burbidge LA, Geary W, Barrus T, Schoenberger J, Trost J, Wenstrup RJ, Roa BB. Judkins T, et al. Among authors: wenstrup rj. Cancer. 2012 Nov 1;118(21):5210-6. doi: 10.1002/cncr.27556. Epub 2012 Apr 27. Cancer. 2012. PMID: 22544547 Free PMC article.

4

Hereditary cancer-associated mutations in women diagnosed with two primary cancers: an opportunity to identify hereditary cancer syndromes after the first cancer diagnosis.

Saam J, Moyes K, Landon M, Williams K, Kaldate RR, Arnell C, Wenstrup R. Saam J, et al. Oncology. 2015;88(4):226-33. doi: 10.1159/000368836. Epub 2014 Dec 11. Oncology. 2015. PMID: 25503195 Free article.

5

Lynch Syndrome Patients with Limited Family History Identified in a Laboratory Setting: A Descriptive Study.

Landon M, Saam J, Brown KL, Moyes K, Evans B, Wenstrup R. Landon M, et al. Oncology. 2015;89(4):221-6. doi: 10.1159/000430097. Epub 2015 Jun 6. Oncology. 2015. PMID: 26393997 Free article.

6

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes.

Eggington JM, Bowles KR, Moyes K, Manley S, Esterling L, Sizemore S, Rosenthal E, Theisen A, Saam J, Arnell C, Pruss D, Bennett J, Burbidge LA, Roa B, Wenstrup RJ. Eggington JM, et al. Among authors: wenstrup rj. Clin Genet. 2014 Sep;86(3):229-37. doi: 10.1111/cge.12315. Epub 2013 Dec 20. Clin Genet. 2014. PMID: 24304220

7

Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases.

Vail PJ, Morris B, van Kan A, Burdett BC, Moyes K, Theisen A, Kerr ID, Wenstrup RJ, Eggington JM. Vail PJ, et al. Among authors: wenstrup rj. J Community Genet. 2015 Oct;6(4):351-9. doi: 10.1007/s12687-015-0220-x. Epub 2015 Mar 18. J Community Genet. 2015. PMID: 25782689 Free PMC article.

8

Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories.

Saam J, Arnell C, Theisen A, Moyes K, Marino I, Roundy KM, Wenstrup RJ. Saam J, et al. Among authors: wenstrup rj. Oncology. 2015;89(5):288-93. doi: 10.1159/000437307. Epub 2015 Aug 28. Oncology. 2015. PMID: 26315041 Free article.

9

BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study.

Zhen DB, Rabe KG, Gallinger S, Syngal S, Schwartz AG, Goggins MG, Hruban RH, Cote ML, McWilliams RR, Roberts NJ, Cannon-Albright LA, Li D, Moyes K, Wenstrup RJ, Hartman AR, Seminara D, Klein AP, Petersen GM. Zhen DB, et al. Among authors: wenstrup rj. Genet Med. 2015 Jul;17(7):569-77. doi: 10.1038/gim.2014.153. Epub 2014 Nov 20. Genet Med. 2015. PMID: 25356972 Free PMC article.

10

Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes.

Kerr ID, Cox HC, Moyes K, Evans B, Burdett BC, van Kan A, McElroy H, Vail PJ, Brown KL, Sumampong DB, Monteferrante NJ, Hardman KL, Theisen A, Mundt E, Wenstrup RJ, Eggington JM. Kerr ID, et al. Among authors: wenstrup rj. J Community Genet. 2017 Apr;8(2):87-95. doi: 10.1007/s12687-016-0289-x. Epub 2017 Jan 3. J Community Genet. 2017. PMID: 28050887 Free PMC article.

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