Incidence, demographic characteristics, and geographic distribution of sickle cell trait and sickle cell anemia births in Michigan, 1997–2014 by Sarah L. Reeves, Hannah K. Jary, Jennifer P. Gondhi, Mary Kleyn, Kayte Spector‐Bagdady, Kevin J. Dombkowski

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

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3313 “My research is their business, but I’m not their business”: Patient and Oncologist Perspectives on the Commercialization of Research Data by Kayte Spector-Bagdady, Chris Krenz, Michele Gornick, Collin Brummel, Madison Kent, J. Chad Brenner, J. Scott Roberts, Andrew G. Shuman

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Genomic testing in voluntary workplace wellness programs in the US: Evidence and challenges by Betty Cohn, Kerry A. Ryan, Katherine Hendy, Katherine Callahan, J. Scott Roberts, Kayte Spector‐Bagdady, Debra J. H. Mathews, the INSIGHT @ Work Consortium

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Public Deliberation Process on Patient Perspectives on Health Information Sharing: Evaluative Descriptive Study by Minakshi Raj, Kerry Ryan, Paige Nong, Karen Calhoun, M Grace Trinidad, Raymond De Vries, Melissa Creary, Kayte Spector-Bagdady, Sharon L R Kardia, Jodyn Platt

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Policy Preferences Regarding Health Data Sharing Among Patients With Cancer: Public Deliberations by Minakshi Raj, Kerry Ryan, Philip Sahr Amara, Paige Nong, Karen Calhoun, M Grace Trinidad, Daniel Thiel, Kayte Spector-Bagdady, Raymond De Vries, Sharon Kardia, Jodyn Platt

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