Search Results - "Peshkin, N."

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    BRCA1/2 mutations and triple negative breast cancers by Peshkin, Beth N, Alabek, Michelle L, Isaacs, Claudine

    Published in Breast disease (2010)
    “…Identifying breast cancer patients at increased risk for carrying a mutation in the BRCA1 and BRCA2 genes is an important objective in clinical practice…”
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    Journal Article
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    Impact of BRCA1/BRCA2 Counseling and Testing on Newly Diagnosed Breast Cancer Patients by SCHWARTZ, Marc D, CARYN LERMAN, PENNANEN, Marie, TSANGARIS, Theodore, WILLEY, Shawna, ISAACS, Claudine, BROGAN, Barbara, PESHKIN, Beth N, HALBERT, Chanita Hughes, DEMARCO, Tiffani, LAWRENCE, William, MAIN, David, FINCH, Clinton, MAGNANT, Colette

    Published in Journal of clinical oncology (15-05-2004)
    “…Approximately 5% to 10% of newly diagnosed breast cancer patients carry a BRCA1 or BRCA2 mutation. Given these patients' high risk for contralateral breast…”
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    Journal Article
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    Results of a randomized controlled trial of a decision support intervention for disclosing maternal BRCA genetic test results to children and adolescents by Tercyak, Kenneth P., DeMarco, Tiffani A., Schneider, Katherine A., Luta, George, Isaacs, Claudine, Garber, Judy E., Sleiman, Marcelo M., Yockel, Mary Rose, Peshkin, Beth N.

    Published in PEC innovation (01-12-2023)
    “…Evaluate the impact of a targeted family communication intervention for mothers undergoing genetic counseling and testing (GCT) for BRCA gene alterations…”
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    Journal Article
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    Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report by O'Neill, Suzanne C, Hamilton, Jada G, Conley, Claire C, Peshkin, Beth N, Sacca, Rosalba, McDonnell, Glynnis A, Isaacs, Claudine, Robson, Mark E, Tercyak, Kenneth P

    Published in Hereditary cancer in clinical practice (26-09-2021)
    “…Consensus and evidence suggest that cascade testing is critical to achieve the promise of cancer genetic testing. However, barriers to cascade testing include…”
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    Journal Article
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    Bilateral Prophylactic Oophorectomy and Ovarian Cancer Screening Following BRCA1/BRCA2 Mutation Testing by SCHWARTZ, Marc D, KAUFMAN, Elizabeth, PESHKIN, Beth N, ISAACS, Claudine, HUGHES, Chanita, DEMARCO, Tiffani, FINCH, Clinton, LERMAN, Caryn

    Published in Journal of clinical oncology (01-11-2003)
    “…Despite the widespread availability of genetic testing for BRCA1/BRCA2 mutations, little is known about the impact of testing on ovarian cancer prevention and…”
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    A Brief Assessment of Concerns Associated With Genetic Testing for Cancer: The Multidimensional Impact of Cancer Risk Assessment (MICRA) Questionnaire by Cella, David, Hughes, Chanita, Peterman, Amy, Chang, Chih-Hung, Peshkin, Beth N, Schwartz, Marc D, Wenzel, Lari, Lemke, Amy, Marcus, Alfred C, Lerman, Caryn

    Published in Health psychology (01-11-2002)
    “…The Multidimensional Impact of Cancer Risk Assessment (MICRA) is a new tool to measure the specific impact of result disclosure after genetic testing. The…”
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    Utilization of BRCA1/BRCA2 Mutation Testing in Newly Diagnosed Breast Cancer Patients by SCHWARTZ, Marc D, LERMAN, Caryn, BROGAN, Barbara, PESHKIN, Beth N, ISAACS, Claudine, DEMARCO, Tiffani, HALBERT, Chanita Hughes, PENNANEN, Marie, FINCH, Clinton

    “…Background: Among newly diagnosed breast cancer patients who are at risk for carrying a BRCA1 or BRCA2 mutation, knowledge of mutation status can influence…”
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    Journal Article
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    Diffusion tensor tomography with tractography in assessment of the pyramidal system in patients with highly active multiple sclerosis by Peshkin, A. N., Toniya, G. T., Stepanova, E. A., Lizhdvoi, V. Yu, Kotov, S. V.

    “…Objective : to study the pyramidal tract in patients with highly active multiple sclerosis (HAMS) during treatment switching from first-line MS therapy to…”
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    What Would You Do? Specialists’ Perspectives on Cancer Genetic Testing, Prophylactic Surgery, and Insurance Discrimination by MATLOFF, E. T, SHAPPELL, H, BRIERLEY, K, BERNHARDT, B. A, MCKINNON, W, PESHKIN, B. N

    Published in Journal of clinical oncology (01-06-2000)
    “…To examine what cancer genetics specialists predict they would do personally if they were at 50% risk of carrying a mutation that predisposes to hereditary…”
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    Journal Article
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