Stopfer JE - Search Results

1

Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.

Maxwell KN, Wubbenhorst B, D'Andrea K, Garman B, Long JM, Powers J, Rathbun K, Stopfer JE, Zhu J, Bradbury AR, Simon MS, DeMichele A, Domchek SM, Nathanson KL. Maxwell KN, et al. Among authors: stopfer je. Genet Med. 2015 Aug;17(8):630-8. doi: 10.1038/gim.2014.176. Epub 2014 Dec 11. Genet Med. 2015. PMID: 25503501 Free PMC article.

2

Assessment and counseling for women with a family history of breast cancer. A guide for clinicians.

Hoskins KF, Stopfer JE, Calzone KA, Merajver SD, Rebbeck TR, Garber JE, Weber BL. Hoskins KF, et al. Among authors: stopfer je. JAMA. 1995 Feb 15;273(7):577-85. JAMA. 1995. PMID: 7837392

3

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer.

Couch FJ, DeShano ML, Blackwood MA, Calzone K, Stopfer J, Campeau L, Ganguly A, Rebbeck T, Weber BL. Couch FJ, et al. N Engl J Med. 1997 May 15;336(20):1409-15. doi: 10.1056/NEJM199705153362002. N Engl J Med. 1997. PMID: 9145677 Free article.

4

Anticipated versus actual emotional reactions to disclosure of results of genetic tests for cancer susceptibility: findings from p53 and BRCA1 testing programs.

Dorval M, Patenaude AF, Schneider KA, Kieffer SA, DiGianni L, Kalkbrenner KJ, Bromberg JI, Basili LA, Calzone K, Stopfer J, Weber BL, Garber JE. Dorval M, et al. Among authors: stopfer j. J Clin Oncol. 2000 May;18(10):2135-42. doi: 10.1200/JCO.2000.18.10.2135. J Clin Oncol. 2000. PMID: 10811679

5

Factors associated with decisions about clinical BRCA1/2 testing.

Armstrong K, Calzone K, Stopfer J, Fitzgerald G, Coyne J, Weber B. Armstrong K, et al. Cancer Epidemiol Biomarkers Prev. 2000 Nov;9(11):1251-4. Cancer Epidemiol Biomarkers Prev. 2000. PMID: 11097234

6

BRCA1 and BRCA2 mutation frequency in women evaluated in a breast cancer risk evaluation clinic.

Shih HA, Couch FJ, Nathanson KL, Blackwood MA, Rebbeck TR, Armstrong KA, Calzone K, Stopfer J, Seal S, Stratton MR, Weber BL. Shih HA, et al. J Clin Oncol. 2002 Feb 15;20(4):994-9. doi: 10.1200/JCO.2002.20.4.994. J Clin Oncol. 2002. PMID: 11844822

7

Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program.

Brose MS, Rebbeck TR, Calzone KA, Stopfer JE, Nathanson KL, Weber BL. Brose MS, et al. Among authors: stopfer je. J Natl Cancer Inst. 2002 Sep 18;94(18):1365-72. doi: 10.1093/jnci/94.18.1365. J Natl Cancer Inst. 2002. PMID: 12237282

8

Early use of clinical BRCA1/2 testing: associations with race and breast cancer risk.

Armstrong K, Weber B, Stopfer J, Calzone K, Putt M, Coyne J, Schwartz JS. Armstrong K, et al. Am J Med Genet A. 2003 Mar 1;117A(2):154-60. doi: 10.1002/ajmg.a.10928. Am J Med Genet A. 2003. PMID: 12567413

9

Application of breast cancer risk prediction models in clinical practice.

Domchek SM, Eisen A, Calzone K, Stopfer J, Blackwood A, Weber BL. Domchek SM, et al. J Clin Oncol. 2003 Feb 15;21(4):593-601. doi: 10.1200/JCO.2003.07.007. J Clin Oncol. 2003. PMID: 12586794 Review.

10

Characterization of two novel BRCA1 germ-line mutations involving splice donor sites.

Brose MS, Volpe P, Paul K, Stopfer JE, Colligon TA, Calzone KA, Weber BL. Brose MS, et al. Among authors: stopfer je. Genet Test. 2004 Summer;8(2):133-8. doi: 10.1089/gte.2004.8.133. Genet Test. 2004. PMID: 15345110

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