Eliciting patient views on the allocation of limited healthcare resources: a deliberation on hepatitis C treatment in the Veterans Health Administration von Waljee, Akbar K., Ryan, Kerry A., Krenz, Chris D., Ioannou, George N., Beste, Lauren A., Tincopa, Monica A., Saini, Sameer D., Su, Grace L., Arasim, Maria E., Roman, Patti T., Nallamothu, Brahmajee K., De Vries, Raymond

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Patient and Provider Perspectives on Enrollment in Precision Oncology Research: Qualitative Ethical Analysis von Spector-Bagdady, Kayte, Kent, Madison, Krenz, Chris D, Brummel, Collin, Swiecicki, Paul L, Brenner, J Chad, Shuman, Andrew G

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Reported Interest in Notification Regarding Use of Health Information and Biospecimens von Spector-Bagdady, Kayte, Trinidad, Grace, Kardia, Sharon, Krenz, Chris D, Nong, Paige, Raj, Minakshi, Platt, Jodyn E

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“My Research Is Their Business, but I'm Not Their Business”: Patient and Clinician Perspectives on Commercialization of Precision Oncology Data von Spector‐Bagdady, Kayte, Krenz, Chris D., Brummel, Collin, Brenner, J. Chad, Bradford, Carol R., Shuman, Andrew G.

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“Extremely slow and capricious”: A qualitative exploration of genetic researcher priorities in selecting shared data resources von Trinidad, M. Grace, Ryan, Kerry A., Krenz, Chris D., Roberts, J. Scott, McGuire, Amy L., De Vries, Raymond, Zikmund-Fisher, Brian J., Kardia, Sharon, Marsh, Erica, Forman, Jane, Kent, Madison, Wilborn, David, Spector-Bagdady, Kayte

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"A Double-Edged Sword": A Brief History of Genomic Data Governance and Genetic Researcher Perspectives on Data Sharing von Spector-Bagdady, Kayte, Ryan, Kerry A, McGuire, Amy L, Krenz, Chris D, Trinidad, M Grace, Jaffe, Kaitlyn, Greene, Amanda, Denard Thomas, J, Kent, Madison, Morain, Stephanie, Wilborn, David, Scott Roberts, J

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Biobanks and the Moral Concerns of Donors: A Democratic Deliberation von De Vries, Raymond G., Ryan, Kerry A., Gordon, Linda, Krenz, Chris D., Tomlinson, Tom, Jewell, Scott, Kim, Scott Y. H.

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Effect of deliberation on the public's attitudes toward consent policies for biobank research von Tomlinson, Tom, De Vries, Raymond G, Kim, H Myra, Gordon, Linda, Ryan, Kerry A, Krenz, Chris D, Jewell, Scott, Kim, Scott Y H

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Health Data Sharing Perspectives of Patients Receiving Care in CancerLinQ-Participating Oncology Practices von Jagsi, Reshma, Suresh, Krithika, Krenz, Chris D, Jones, Rochelle D, Griffith, Kent A, Perry, Lydia, Hawley, Sarah T, Zikmund-Fisher, Brian, Spector-Bagdady, Kayte, Platt, Jodyn, De Vries, Raymond, Bradbury, Angela R, Bansal, Pranshu, Kaime, Melissa, Patel, Monaliben, Schilsky, Richard L, Miller, Robert S, Spence, Rebecca

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The moral concerns of biobank donors: the effect of non-welfare interests on willingness to donate von De Vries, Raymond G., Tomlinson, Tom, Kim, H. Myra, Krenz, Chris D., Ryan, Kerry A., Lehpamer, Nicole, Kim, Scott Y. H.

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Workplace Harassment, Cyber Incivility, and Climate in Academic Medicine von Jagsi, Reshma, Griffith, Kent, Krenz, Chris, Jones, Rochelle D, Cutter, Christina, Feldman, Eva L, Jacobson, Clare, Kerr, Eve, Paradis, Kelly, Singer, Kanakadurga, Spector, Nancy, Stewart, Abby, Telem, Dana, Ubel, Peter, Settles, Isis

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Effect of Public Deliberation on Patient Attitudes Regarding Consent and Data Use in a Learning Health Care System for Oncology von Jagsi, Reshma, Griffith, Kent A, Jones, Rochelle D, Krenz, Chris, Gornick, Michele, Spence, Rebecca, De Vries, Raymond, Hawley, Sarah T, Zon, Robin, Bolte, Sage, Sadeghi, Navid, Schilsky, Richard L, Bradbury, Angela R

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The Most Valuable Resource Is Time: Insights From a Novel National Program to Improve Retention of Physician–Scientists With Caregiving Responsibilities von Jones, Rochelle D, Miller, Jacquelyn, Vitous, C Ann, Krenz, Chris, Brady, Kathleen T, Brown, Ann J, Daumit, Gail L, Drake, Amelia F, Fraser, Victoria J, Hartmann, Katherine E, Hochman, Judith S, Girdler, Susan, Libby, Anne M, Mangurian, Christina, Regensteiner, Judith G, Yonkers, Kimberly, Jagsi, Reshma

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Tu1496 – Democratic Deliberation to Assess Veteran Preferences on Allocation of Healthcare Resources for Chronic Hepatitis C Treatment von Waljee, Akbar K., Ryan, Kerry A., Konerman, Monica A., Beste, Lauren, Ioannou, George N., Su, Grace L., Saini, Sameer D., Hughes, Maria, Ellis, Amanda, Roman, Pia, Krenz, Chris, De Vries, Raymond

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From Stigma to Validation: A Qualitative Assessment of a Novel National Program to Improve Retention of Physician-Scientists with Caregiving Responsibilities von Jones, Rochelle D., Miller, Jacquelyn, Vitous, C. Ann, Krenz, Chris, Brady, Kathleen T., Brown, Ann J., Daumit, Gail L., Drake, Amelia F., Fraser, Victoria J., Hartmann, Katherine E., Hochman, Judith S., Girdler, Susan, Kalet, Adina L., Libby, Anne M., Mangurian, Christina, Regensteiner, Judith G., Yonkers, Kimberly, Jagsi, Reshma

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Patient Experiences, Trust, and Preferences for Health Data Sharing von Jones, Rochelle D, Krenz, Chris, Griffith, Kent A, Spence, Rebecca, Bradbury, Angela R, De Vries, Raymond, Hawley, Sarah T, Zon, Robin, Bolte, Sage, Sadeghi, Navid, Schilsky, Richard L, Jagsi, Reshma

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Governance of a Learning Health Care System for Oncology: Patient Recommendations von Jones, Rochelle D., Krenz, Chris, Griffith, Kent A., Spence, Rebecca, Bradbury, Angela R., De Vries, Raymond, Hawley, Sarah T., Zon, Robin, Bolte, Sage, Sadeghi, Navid, Schilsky, Richard L., Jagsi, Reshma

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Patient Preferences Regarding Informed Consent Models for Participation in a Learning Health Care System for Oncology von Jones, Rochelle D., Krenz, Chris, Gornick, Michele, Griffith, Kent A., Spence, Rebecca, Bradbury, Angela R., De Vries, Raymond, Hawley, Sarah T., Hayward, Rodney A., Zon, Robin, Bolte, Sage, Sadeghi, Navid, Schilsky, Richard L., Jagsi, Reshma

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