Peshkin BN - Search Results

1

All in the family: evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results.

Hughes C, Lerman C, Schwartz M, Peshkin BN, Wenzel L, Narod S, Corio C, Tercyak KP, Hanna D, Isaacs C, Main D. Hughes C, et al. Among authors: peshkin bn. Am J Med Genet. 2002 Jan 15;107(2):143-50. doi: 10.1002/ajmg.10110. Am J Med Genet. 2002. PMID: 11807889

2

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families.

Tonin P, Weber B, Offit K, Couch F, Rebbeck TR, Neuhausen S, Godwin AK, Daly M, Wagner-Costalos J, Berman D, Grana G, Fox E, Kane MF, Kolodner RD, Krainer M, Haber DA, Struewing JP, Warner E, Rosen B, Lerman C, Peshkin B, Norton L, Serova O, Foulkes WD, Garber JE, et al. Tonin P, et al. Nat Med. 1996 Nov;2(11):1179-83. doi: 10.1038/nm1196-1179. Nat Med. 1996. PMID: 8898735 Review. No abstract available.

3

Genetic counseling and testing for breast-ovarian cancer susceptibility: what do women want?

Audrain J, Rimer B, Cella D, Garber J, Peshkin BN, Ellis J, Schildkraut J, Stefanek M, Vogel V, Lerman C. Audrain J, et al. Among authors: peshkin bn. J Clin Oncol. 1998 Jan;16(1):133-8. doi: 10.1200/JCO.1998.16.1.133. J Clin Oncol. 1998. PMID: 9440734

4

Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.

Frank TS, Manley SA, Olopade OI, Cummings S, Garber JE, Bernhardt B, Antman K, Russo D, Wood ME, Mullineau L, Isaacs C, Peshkin B, Buys S, Venne V, Rowley PT, Loader S, Offit K, Robson M, Hampel H, Brener D, Winer EP, Clark S, Weber B, Strong LC, Thomas A, et al. Frank TS, et al. J Clin Oncol. 1998 Jul;16(7):2417-25. doi: 10.1200/JCO.1998.16.7.2417. J Clin Oncol. 1998. PMID: 9667259

5

Psychological distress in women seeking genetic counseling for breast-ovarian cancer risk: the contributions of personality and appraisal.

Audrain J, Schwartz MD, Lerman C, Hughes C, Peshkin BN, Biesecker B. Audrain J, et al. Among authors: peshkin bn. Ann Behav Med. 1997 Fall;19(4):370-7. doi: 10.1007/BF02895156. Ann Behav Med. 1997. PMID: 9706364 Clinical Trial.

6

Genetic counselling for hereditary breast cancer.

Peshkin BN, Lerman C. Peshkin BN, et al. Lancet. 1999 Jun 26;353(9171):2176-7. doi: 10.1016/S0140-6736(99)90078-8. Lancet. 1999. PMID: 10392978 Free article. No abstract available.

7

Spiritual faith and genetic testing decisions among high-risk breast cancer probands.

Schwartz MD, Hughes C, Roth J, Main D, Peshkin BN, Isaacs C, Kavanagh C, Lerman C. Schwartz MD, et al. Among authors: peshkin bn. Cancer Epidemiol Biomarkers Prev. 2000 Apr;9(4):381-5. Cancer Epidemiol Biomarkers Prev. 2000. PMID: 10794482

8

BRCA1/2 testing: complex themes in result interpretation.

Peshkin BN, DeMarco TA, Brogan BM, Lerman C, Isaacs C. Peshkin BN, et al. J Clin Oncol. 2001 May 1;19(9):2555-65. doi: 10.1200/JCO.2001.19.9.2555. J Clin Oncol. 2001. PMID: 11331335 Review.

9

Cost of genetic counseling and testing for BRCA1 and BRCA2 breast cancer susceptibility mutations.

Lawrence WF, Peshkin BN, Liang W, Isaacs C, Lerman C, Mandelblatt JS. Lawrence WF, et al. Among authors: peshkin bn. Cancer Epidemiol Biomarkers Prev. 2001 May;10(5):475-81. Cancer Epidemiol Biomarkers Prev. 2001. PMID: 11352857 Clinical Trial.

10

Effects of coping style and BRCA1 and BRCA2 test results on anxiety among women participating in genetic counseling and testing for breast and ovarian cancer risk.

Tercyak KP, Lerman C, Peshkin BN, Hughes C, Main D, Isaacs C, Schwartz MD. Tercyak KP, et al. Among authors: peshkin bn. Health Psychol. 2001 May;20(3):217-22. Health Psychol. 2001. PMID: 11403219

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