Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer von SCHWARTZ, Marc D, VALDIMARSDOTTIR, Heiddis B, MCKINNON, Wendy, GARBER, Judy, MCCORMICK, Shelley, KINNEY, Anita Y, LUTA, George, KELLEHER, Sarah, LEVENTHAL, Kara-Grace, VEGELLA, Patti, ANGIE TONG, LESLEY KING, PESHKIN, Beth N, MANDELBLATT, Jeanne, NUSBAUM, Rachel, HUANG, An-Tsun, YAOJEN CHANG, GRAVES, Kristi, ISAACS, Claudine, WOOD, Marie

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Attenuation of RNA polymerase II pausing mitigates BRCA1-associated R-loop accumulation and tumorigenesis von Zhang, Xiaowen, Chiang, Huai-Chin, Wang, Yao, Zhang, Chi, Smith, Sabrina, Zhao, Xiayan, Nair, Sreejith J., Michalek, Joel, Jatoi, Ismail, Lautner, Meeghan, Oliver, Boyce, Wang, Howard, Petit, Anna, Soler, Teresa, Brunet, Joan, Mateo, Francesca, Angel Pujana, Miguel, Poggi, Elizabeth, Chaldekas, Krysta, Isaacs, Claudine, Peshkin, Beth N., Ochoa, Oscar, Chedin, Frederic, Theoharis, Constantine, Sun, Lu-Zhe, Curiel, Tyler J., Elledge, Richard, Jin, Victor X., Hu, Yanfen, Li, Rong

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Characterization of BRCA1 and BRCA2 Mutations in a Large United States Sample von SINING CHEN, IVERSEN, Edwin S, CORIO, Camille, LEONDARIDIS, Leoni, TOMLINSON, Gail, DUTSON, Debra, KERBER, Rich, AMOS, Christopher I, STRONG, Louise C, BERRY, Donald A, EUHUS, David M, PARMIGIANI, Giovanni, FRIEBEL, Tara, FINKELSTEIN, Dianne, WEBER, Barbara L, EISEN, Andrea, PETERSON, Leif E, SCHILDKRAUT, Joellen M, ISAACS, Claudine, PESHKIN, Beth N

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Pharmacogenetics in Practice: Estimating the Clinical Actionability of Pharmacogenetic Testing in Perioperative and Ambulatory Settings von Smith, D. Max, Peshkin, Beth N., Springfield, T. Blaise, Brown, Ryan P., Hwang, Elizabeth, Kmiecik, Susanna, Shapiro, Richard, Eldadah, Zayd, Lundergan, Conor, McAlduff, Joel, Levin, Bonnie, Swain, Sandra M.

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Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers von Walker, Logan C, Marquart, Louise, Pearson, John F, Wiggins, George A R, O'Mara, Tracy A, Parsons, Michael T, Barrowdale, Daniel, McGuffog, Lesley, Dennis, Joe, Benitez, Javier, Slavin, Thomas P, Radice, Paolo, Frost, Debra, Godwin, Andrew K, Meindl, Alfons, Schmutzler, Rita Katharina, Isaacs, Claudine, Peshkin, Beth N, Caldes, Trinidad, Hogervorst, Frans Bl, Lazaro, Conxi, Jakubowska, Anna, Montagna, Marco, Chen, Xiaoqing, Offit, Kenneth, Hulick, Peter J, Andrulis, Irene L, Lindblom, Annika, Nussbaum, Robert L, Nathanson, Katherine L, Chenevix-Trench, Georgia, Antoniou, Antonis C, Couch, Fergus J, Spurdle, Amanda B

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Impact of BRCA1/BRCA2 Counseling and Testing on Newly Diagnosed Breast Cancer Patients von 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

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BRCAPRO Validation, Sensitivity of Genetic Testing of BRCA1/BRCA2, and Prevalence of Other Breast Cancer Susceptibility Genes von BERRY, Donald A, IVERSEN, Edwin S, RUBINSTEIN, Wendy S, HUGHES, Kevin S, PARMIGIANI, Giovanni, GUDBJARTSSON, Daniel F, HILLER, Elaine H, GARBER, Judy E, PESHKIN, Beth N, LERMAN, Caryn, WATSON, Patrice, LYNCH, Henry T, HILSENBECK, Susan G

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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 von 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.

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Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report von 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.

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Bilateral Prophylactic Oophorectomy and Ovarian Cancer Screening Following BRCA1/BRCA2 Mutation Testing von SCHWARTZ, Marc D, KAUFMAN, Elizabeth, PESHKIN, Beth N, ISAACS, Claudine, HUGHES, Chanita, DEMARCO, Tiffani, FINCH, Clinton, LERMAN, Caryn

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Quality of Life After Contralateral Prophylactic Mastectomy in Newly Diagnosed High-Risk Breast Cancer Patients Who Underwent BRCA1/2 Gene Testing von TERCYAK, Kenneth P, PESHKIN, Beth N, BROGAN, Barbara M, DEMARCO, Tiffani, PENNANEN, Marie F, WILLEY, Shawna C, MAGNANT, Colette M, ROGERS, Sarah, ISAACS, Claudine, SCHWARTZ, Marc D

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Re: Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative von Peshkin, Beth N, Isaacs, Claudine, Schwartz, Marc D

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Understanding the Needs of Young Women Regarding Breast Cancer Risk Assessment and Genetic Testing: Convergence and Divergence among Patient-Counselor Perceptions and the Promise o... von Evans, Chalanda, Hamilton, Rebekah J, Tercyak, Kenneth P, Peshkin, Beth N, Rabemananjara, Kantoniony, Isaacs, Claudine, O'Neill, Suzanne C

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Long‐term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance von Schwartz, Marc D., Isaacs, Claudine, Graves, Kristi D., Poggi, Elizabeth, Peshkin, Beth N., Gell, Christy, Finch, Clinton, Kelly, Scott, Taylor, Kathryn L., Perley, Lauren

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Utilization of BRCA1/BRCA2 Mutation Testing in Newly Diagnosed Breast Cancer Patients von SCHWARTZ, Marc D, LERMAN, Caryn, BROGAN, Barbara, PESHKIN, Beth N, ISAACS, Claudine, DEMARCO, Tiffani, HALBERT, Chanita Hughes, PENNANEN, Marie, FINCH, Clinton

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Pharmacogenomic testing in oncology: a health system's approach to identify oncology provider perspectives von Bhatt, Meghna, Peshkin, Beth N, Kazi, Sadaf, Schwartz, Marc D, Ashai, Nadia, Swain, Sandra M, Smith, D Max

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The Essentials of Multiomics von Marshall, John L, Peshkin, Beth N, Yoshino, Takayuki, Vowinckel, Jakob, Danielsen, Håvard E, Melino, Gerry, Tsamardinos, Ioannis, Haudenschild, Christian, Kerr, David J, Sampaio, Carlos, Rha, Sun Young, FitzGerald, Kevin T, Holland, Eric C, Gallagher, David, Garcia-Foncillas, Jesus, Juhl, Hartmut

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Long-Term Adaptation Among Adolescent and Young Adult Children to Familial Cancer Risk von McDonnell, Glynnis A, Peshkin, Beth N, DeMarco, Tiffani A, Peterson, Susan K, Arun, Banu K, Miesfeldt, Susan, O'Neill, Suzanne C, Schneider, Katherine, Garber, Judy, Isaacs, Claudine, Luta, George, Tercyak, Kenneth P

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ClinGen and Genetic Testing von Peshkin, Beth N, Isaacs, Claudine

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Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling von Butrick, Morgan, Kelly, Scott, Peshkin, Beth N., Luta, George, Nusbaum, Rachel, Hooker, Gillian W., Graves, Kristi, Feeley, Lisa, Isaacs, Claudine, Valdimarsdottir, Heiddis B., Jandorf, Lina, DeMarco, Tiffani, Wood, Marie, McKinnon, Wendy, Garber, Judy, McCormick, Shelley R., Schwartz, Marc D.

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