Search Results - "Bednar, Erica M."

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    Assessing relatives’ readiness for hereditary cancer cascade genetic testing by Bednar, Erica M., Sun, Charlotte C., McCurdy, Sheryl, Vernon, Sally W.

    Published in Genetics in medicine (01-04-2020)
    “…To explore the readiness of living, untested first-degree relatives (FDRs) to have cascade genetic testing (CGT) for a hereditary predisposition to cancer…”
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    Journal Article
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    Disparities in gynecologic cancer genetics evaluation by Hinchcliff, Emily M., Bednar, Erica M., Lu, Karen H., Rauh-Hain, J. Alejandro

    Published in Gynecologic oncology (01-04-2019)
    “…An estimated 2–5% of endometrial cancers and 15–20% of high-grade, non-mucinous epithelial ovarian cancers have an underlying hereditary cause. Appropriate…”
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    Interventions to improve delivery of cancer genetics services in the United States: A scoping review by Bednar, Erica M., Nitecki, Roni, Krause, Kate J., Rauh-Hain, Jose Alejandro

    Published in Genetics in medicine (01-06-2022)
    “…Interventions that decrease barriers and improve clinical processes can increase patient access to guideline-recommended cancer genetics services. We sought to…”
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    Clinical management among individuals with variant of uncertain significance in hereditary cancer: A systematic review and meta‐analysis by Makhnoon, Sukh, Bednar, Erica M., Krause, Kate J., Peterson, Susan K., Lopez‐Olivo, Maria A.

    Published in Clinical genetics (01-08-2021)
    “…Improper medical use of variant of uncertain significance (VUS) remains a concern in hereditary cancer genetic testing. The goal of this study was to assess…”
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    Factors impacting adolescent and young adult cancer patients’ decision to pursue genetic counseling and testing by Morand, Megan, Roth, Michael, Peterson, Susan K., Bednar, Erica M., Ramdaney, Aarti, Livingston, J. Andrew, Yarbrough, Angela, Corredor, Jessica

    Published in Supportive care in cancer (01-06-2022)
    “…Purpose Adolescent and young adult (AYA) cancer patients face challenges when navigating cancer treatment and survivorship. Many are at risk for cancer…”
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    A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment by Bednar, Erica M, Oakley, Holly D, Sun, Charlotte C, Burke, Catherine C, Munsell, Mark F, Westin, Shannon N, Lu, Karen H

    Published in Gynecologic oncology (01-08-2017)
    “…Highlights • < 25% of ovarian cancer patients in the U.S. receive recommended genetics services. • We increased the rates of genetic counseling and testing to…”
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    Cascade genetic testing: an underutilized pathway to equitable cancer care? by Wilke, Roni Nitecki, Bednar, Erica M., Pirzadeh-Miller, Sara, Lahiri, Sayoni, Scarinci, Isabel C., Leath III, Charles A., Frey, Melissa K., Lu, Karen H., Rauh-Hain, J. Alejandro

    Published in Familial cancer (01-06-2024)
    “…The Precision Medicine Initiative was launched upon the potential of genomic information to tailor medical care. Cascade genetic testing represents a powerful…”
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    Disseminating universal genetic testing to a diverse, indigent patient population at a county hospital gynecologic oncology clinic by Bednar, Erica M., Sun, Charlotte C., Camacho, Bethsaida, Terrell, John, Rieber, Alyssa G., Ramondetta, Lois M., Freedman, Ralph S., Lu, Karen H.

    Published in Gynecologic oncology (01-02-2019)
    “…The universal genetic testing initiative (UGTI) is a quality improvement effort to increase rates of guideline-based genetic counseling (GC) and genetic…”
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    Journal Article
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    Clinical applicability of proposed algorithm for identifying individuals at risk for hereditary hematologic malignancies by Clifford, Maggie, Bannon, Sarah, Bednar, Erica M., Czerwinski, Jennifer, Davis, Jessica, Dunnington, Leslie, Shahrukh Hashmi, S., DiNardo, Courtney D.

    Published in Leukemia & lymphoma (15-10-2019)
    “…Multiple genes have been identified to cause hereditary predispositions to hematologic malignancies, and characterized by an increased risk to develop…”
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    Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication by Makhnoon, Sukh, Smith, Hadley S., Bednar, Erica M., Bhatt, Arjun, Turner, Llaran, Arun, Banu, Volk, Robert J., Peterson, Susan K.

    Published in Journal of community genetics (01-07-2021)
    “…Familial communication of pathogenic genetic variants is necessary to maximize the clinical utility of genetic testing and its public health benefits. Insights…”
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    Journal Article
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