Integrating primary care, shared decision making, and community engagement to facilitate equitable access to multi-cancer early detection clinical trials von Thompson, Cheryl L, Buchanan, Adam H, Myers, Ronald, Weinberg, David S

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Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists von Hallquist, Miranda L G, Borensztein, Maia J, Coughlin, 2nd, Curtis R, Buchanan, Adam H, Andrew Faucett, W, Peay, Holly L, Smith, Maureen E, Tricou, Eric P, Uhlmann, Wendy R, Wain, Karen E, Ormond, Kelly E

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Real-time evaluation and adaptation to facilitate rapid recruitment in a large, prospective cohort study von Honushefsky, Ashley, Wagner, Eric S, Sheridan, Kathleen, Spickard, Kathleen M, LeMasters, William R, Walter, Carroll N, Beaver, Taryn, Lennon, Anne Marie, Papadopoulos, Nickolas, Rahm, Alanna Kulchak, Buchanan, Adam H

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Pre-malignant conditions diagnosed following a positive cancer signal from a multi-cancer early detection test von Choudhry, Omair A, Kharge, Angana B, Rego, Seema P, Elias, Paul Z, Buchanan, Adam H, Lennon, Anne Marie, Papadopoulos, Nickolas, Diehl, Frank, Beer, Tomasz M

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Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort von Savatt, Juliann M, Ortiz, Nicole M, Thone, Gretchen M, McDonald, Whitney S, Kelly, Melissa A, Berry, Alexander S F, Alvi, Madiha M, Hallquist, Miranda L G, Malinowski, Jennifer, Purdy, Nicholas C, Williams, Marc S, Sturm, Amy C, Buchanan, Adam H

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A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System von Jones, Laney K, Strande, Natasha T, Calvo, Evan M, Chen, Jingheng, Rodriguez, Gabriela, McCormick, Cara Z, Hallquist, Miranda L G, Savatt, Juliann M, Rocha, Heather, Williams, Marc S, Sturm, Amy C, Buchanan, Adam H, Glasgow, Russell E, Martin, Christa L, Rahm, Alanna Kulchak

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Application of a framework to guide genetic testing communication across clinical indications von Hallquist, Miranda L G, Tricou, Eric P, Ormond, Kelly E, Savatt, Juliann M, Coughlin, 2nd, Curtis R, Faucett, W Andrew, Hercher, Laura, Levy, Howard P, O'Daniel, Julianne M, Peay, Holly L, Stosic, Melissa, Smith, Maureen, Uhlmann, Wendy R, Wand, Hannah, Wain, Karen E, Buchanan, Adam H

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Cancer Genetic Counseling and Testing in an Era of Rapid Change von Hooker, Gillian W., Clemens, Keelia Rhoads, Quillin, John, Vogel Postula, Kristen J., Summerour, Pia, Nagy, Rebecca, Buchanan, Adam H.

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Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention von Lennon, Anne Marie, Buchanan, Adam H, Kinde, Isaac, Warren, Andrew, Honushefsky, Ashley, Cohain, Ariella T, Ledbetter, David H, Sanfilippo, Fred, Sheridan, Kathleen, Rosica, Dillenia, Adonizio, Christian S, Hwang, Hee Jung, Lahouel, Kamel, Cohen, Joshua D, Douville, Christopher, Patel, Aalpen A, Hagmann, Leonardo N, Rolston, David D, Malani, Nirav, Zhou, Shibin, Bettegowda, Chetan, Diehl, David L, Urban, Bobbi, Still, Christopher D, Kann, Lisa, Woods, Julie I, Salvati, Zachary M, Vadakara, Joseph, Leeming, Rosemary, Bhattacharya, Prianka, Walter, Carroll, Parker, Alex, Lengauer, Christoph, Klein, Alison, Tomasetti, Cristian, Fishman, Elliot K, Hruban, Ralph H, Kinzler, Kenneth W, Vogelstein, Bert, Papadopoulos, Nickolas

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Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric... von Savatt, Juliann M, Wagner, Jennifer K, Joffe, Steven, Rahm, Alanna Kulchak, Williams, Marc S, Bradbury, Angela R, Davis, F Daniel, Hergenrather, Julie, Hu, Yirui, Kelly, Melissa A, Kirchner, H Lester, Meyer, Michelle N, Mozersky, Jessica, O'Dell, Sean M, Pervola, Josie, Seeley, Andrea, Sturm, Amy C, Buchanan, Adam H

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Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system von Orlando, Lori A, Hauser, Elizabeth R, Christianson, Carol, Powell, Karen P, Buchanan, Adam H, Chesnut, Blair, Agbaje, Astrid B, Henrich, Vincent C, Ginsburg, Geoffrey

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Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource von Strande, Natasha T., Riggs, Erin Rooney, Buchanan, Adam H., Ceyhan-Birsoy, Ozge, DiStefano, Marina, Dwight, Selina S., Goldstein, Jenny, Ghosh, Rajarshi, Seifert, Bryce A., Sneddon, Tam P., Wright, Matt W., Milko, Laura V., Cherry, J. Michael, Giovanni, Monica A., Murray, Michael F., O’Daniel, Julianne M., Ramos, Erin M., Santani, Avni B., Scott, Alan F., Plon, Sharon E., Rehm, Heidi L., Martin, Christa L., Berg, Jonathan S.

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Clinical outcomes of a genomic screening program for actionable genetic conditions von Buchanan, Adam H., Lester Kirchner, H., Schwartz, Marci L. B., Kelly, Melissa A., Schmidlen, Tara, Jones, Laney K., Hallquist, Miranda L. G., Rocha, Heather, Betts, Megan, Schwiter, Rachel, Butry, Loren, Lazzeri, Amanda L., Frisbie, Lauren R., Rahm, Alanna Kulchak, Hao, Jing, Willard, Huntington F., Martin, Christa L., Ledbetter, David H., Williams, Marc S., Sturm, Amy C.

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A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort von Schwartz, Marci L.B., McCormick, Cara Zayac, Lazzeri, Amanda L., Lindbuchler, D’Andra M., Hallquist, Miranda L.G., Manickam, Kandamurugu, Buchanan, Adam H., Rahm, Alanna Kulchak, Giovanni, Monica A., Frisbie, Lauren, Flansburg, Carroll N., Davis, F. Daniel, Sturm, Amy C., Nicastro, Christine, Lebo, Matthew S., Mason-Suares, Heather, Mahanta, Lisa Marie, Carey, David J., Williams, Janet L., Williams, Marc S., Ledbetter, David H., Faucett, W. Andrew, Murray, Michael F.

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Health Care Transition Programs for Adolescents and Young Adults With Hereditary Cancer Predisposition: A Scoping Review von Gabriel, Jazmine, Lyons, Tierney, Schlieder, Victoria, Zultevicz, Sarah, Frasch, Bryel, Davis, Thomas W, Buchanan, Adam H, Campbell-Salome, Gemme

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A New Agenda for Implementing Population Genomic Screening von Buchanan, Adam H, Kulchak Rahm, Alanna, Sturm, Amy C

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Establishing the Medical Actionability of Genomic Variants von Goddard, Katrina A.B, Lee, Kristy, Buchanan, Adam H, Powell, Bradford C, Hunter, Jessica Ezzell

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Uncertainty management for individuals with Lynch Syndrome: Identifying and responding to healthcare barriers von Campbell-Salome, Gemme, Buchanan, Adam H., Hallquist, Miranda L.G., Rahm, Alanna K., Rocha, Heather, Sturm, Amy C.

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Low adenoma burden in unselected patients with a pathogenic APC variant von Schwiter, Rachel, Rocha, Heather, Johns, Alicia, Savatt, Juliann M., Diehl, David L., Kelly, Melissa A., Williams, Marc S., Buchanan, Adam H.

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Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance von Buchanan, Adam H., Datta, Santanu K., Skinner, Celette Sugg, Hollowell, Gail P., Beresford, Henry F., Freeland, Thomas, Rogers, Benjamin, Boling, John, Marcom, P. Kelly, Adams, Martha B.

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