Diversity and inclusion for the All of Us research program: A scoping review von Mapes, Brandy M, Foster, Christopher S, Kusnoor, Sheila V, Epelbaum, Marcia I, AuYoung, Mona, Jenkins, Gwynne, Lopez-Class, Maria, Richardson-Heron, Dara, Elmi, Ahmed, Surkan, Karl, Cronin, Robert M, Wilkins, Consuelo H, Pérez-Stable, Eliseo J, Dishman, Eric, Denny, Joshua C, Rutter, Joni L

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The IDeaS initiative: pilot study to assess the impact of rare diseases on patients and healthcare systems von Tisdale, Ainslie, Cutillo, Christine M., Nathan, Ramaa, Russo, Pierantonio, Laraway, Bryan, Haendel, Melissa, Nowak, Douglas, Hasche, Cindy, Chan, Chun-Hung, Griese, Emily, Dawkins, Hugh, Shukla, Oodaye, Pearce, David A., Rutter, Joni L., Pariser, Anne R.

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A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health von Khoury, Muin J, Feero, W Gregory, Chambers, David A, Brody, Lawrence C, Aziz, Nazneen, Green, Robert C, Janssens, A Cecile J W, Murray, Michael F, Rodriguez, Laura Lyman, Rutter, Joni L, Schully, Sheri D, Winn, Deborah M, Mensah, George A

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Advancing translational science education von Faupel‐Badger, Jessica M., Vogel, Amanda L., Austin, Christopher P., Rutter, Joni L.

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The “All of Us” Research Program von Denny, Joshua C, Rutter, Joni L, Goldstein, David B, Philippakis, Anthony, Smoller, Jordan W, Jenkins, Gwynne, Dishman, Eric

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A framework for assessing clinical trial site readiness von Buse, John B, Austin, Christopher P, Johnston, S Claiborne, Lewis-Hall, Freda, March, Andrew N, Shore, Carolyn K, Tenaerts, Pamela, Rutter, Joni L

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The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment von Haendel, Melissa A, Chute, Christopher G, Bennett, Tellen D, Eichmann, David A, Guinney, Justin, Kibbe, Warren A, Payne, Philip R O, Pfaff, Emily R, Robinson, Peter N, Saltz, Joel H, Spratt, Heidi, Suver, Christine, Wilbanks, John, Wilcox, Adam B, Williams, Andrew E, Wu, Chunlei, Blacketer, Clair, Bradford, Robert L, Cimino, James J, Clark, Marshall, Colmenares, Evan W, Francis, Patricia A, Gabriel, Davera, Graves, Alexis, Hemadri, Raju, Hong, Stephanie S, Hripscak, George, Jiao, Dazhi, Klann, Jeffrey G, Kostka, Kristin, Lee, Adam M, Lehmann, Harold P, Lingrey, Lora, Miller, Robert T, Morris, Michele, Murphy, Shawn N, Natarajan, Karthik, Palchuk, Matvey B, Sheikh, Usman, Solbrig, Harold, Visweswaran, Shyam, Walden, Anita, Walters, Kellie M, Weber, Griffin M, Zhang, Xiaohan Tanner, Zhu, Richard L, Amor, Benjamin, Girvin, Andrew T, Manna, Amin, Qureshi, Nabeel, Kurilla, Michael G, Michael, Sam G, Portilla, Lili M, Rutter, Joni L, Austin, Christopher P, Gersing, Ken R

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Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health von Khoury, Muin J, Feero, W Gregory, Chambers, David A, Brody, Lawrence C, Aziz, Nazneen, Green, Robert C, Janssens, A Cecile J W, Murray, Michael F, Rodriguez, Laura Lyman, Rutter, Joni L, Schully, Sheri D, Winn, Deborah M, Mensah, George A

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Accelerating evidence generation: Addressing critical challenges and charting a path forward von Rim, Jeeyon G., Jackman, Jennifer G., Hornik, Christoph P., Rutter, Joni L., Warraich, Haider, Wittes, Janet, Fleisher, Lee, Anderson, Brian S., Krofah, Ester, Kinter, Elizabeth, Locke, Trevan, Kehoe, Lindsay, Abbasi, Ali, Marston, Hilary, Meeker-O’Connell, Ann, Weber, Wendy, Wang, Tracy, Hernandez, Adrian F., Landray, Martin, Palmer, Scott M.

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Evidence generation and reproducibility in cell and gene therapy research: A call to action von Abou-el-Enein, Mohamed, Angelis, Aris, Appelbaum, Frederick R., Andrews, Nancy C., Bates, Susan E., Bierman, Arlene S., Brenner, Malcolm K., Cavazzana, Marina, Caligiuri, Michael A., Clevers, Hans, Cooke, Emer, Daley, George Q., Dzau, Victor J., Ellis, Lee M., Fineberg, Harvey V., Goldstein, Lawrence S.B., Gottschalk, Stephen, Hamburg, Margaret A., Ingber, Donald E., Kohn, Donald B., Krainer, Adrian R., Maus, Marcela V., Marks, Peter, Mummery, Christine L., Pettigrew, Roderic I., Rutter, Joni L., Teichmann, Sarah A., Terzic, Andre, Urnov, Fyodor D., Williams, David A., Wolchok, Jedd D., Lawler, Mark, Turtle, Cameron J., Bauer, Gerhard, Ioannidis, John P.A.

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The Bespoke Gene Therapy Consortium: facilitating development of AAV gene therapies for rare diseases von Brooks, P. J., Miller, Timothy M., Revah, Frédéric, Suh, Junghae, Garrison, Bradley R., Starke, Lawrence C., MacLachlan, Timothy K., Neilan, Edward G., Raychaudhuri, Gopa, Kassim, Sadik H., Dehdashti, Jean, Rutter, Joni L.

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Data use under the NIH GWAS Data Sharing Policy and future directions von Paltoo, Dina N, Rodriguez, Laura Lyman, Feolo, Michael, Gillanders, Elizabeth, Ramos, Erin M, Rutter, Joni L, Sherry, Stephen, Wang, Vivian Ota, Bailey, Alice, Baker, Rebecca, Caulder, Mark, Harris, Emily L, Langlais, Kristofor, Leeds, Hilary, Luetkemeier, Erin, Paine, Taunton, Roomian, Tamar, Tryka, Kimberly, Patterson, Amy, Green, Eric D

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The All of Us Research Program is an opportunity to enhance the diversity of US biomedical research von Bianchi, Diana W., Brennan, Patricia Flatley, Chiang, Michael F., Criswell, Lindsey A., D’Souza, Rena N., Gibbons, Gary H., Gilman, James K., Gordon, Joshua A., Green, Eric D., Gregurick, Susan, Hodes, Richard J., Kilmarx, Peter H., Koob, George F., Koroshetz, Walter J., Langevin, Helene M., Lorsch, Jon R., Marrazzo, Jeanne M., Pérez-Stable, Eliseo J., Rathmell, W. Kimryn, Rodgers, Griffin P., Rutter, Joni L., Simoni, Jane M., Tromberg, Bruce J., Tucci, Debara L., Volkow, Nora D., Woychik, Rick, Zenk, Shannon N., Kozlowski, Elyse, Peterson, Rachele S., Ginsburg, Geoffrey S., Denny, Joshua C.

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Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm von Saccone, Scott F, Bierut, Laura J, Chesler, Elissa J, Kalivas, Peter W, Lerman, Caryn, Saccone, Nancy L, Uhl, George R, Li, Chuan-Yun, Philip, Vivek M, Edenberg, Howard J, Sherry, Stephen T, Feolo, Michael, Moyzis, Robert K, Rutter, Joni L

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Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes von Sigurdson, Alice J, Hauptmann, Michael, Chatterjee, Nilanjan, Alexander, Bruce H, Doody, Michele Morin, Rutter, Joni L, Struewing, Jeffery P

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National Trends in Anticoagulation Therapy for COVID-19 Hospitalized Adults in the United States: Analyses of the National COVID Cohort Collaborative von Lee, Eileen, Bates, Benjamin, Kuhrt, Nathaniel, Andersen, Kathleen M, Visaria, Aayush, Patel, Rachel, Setoguchi, Soko

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Vaccination Against SARS-CoV-2 Decreases Risk of Adverse Events in Patients who Develop COVID-19 Following Cancer Surgery von Verhagen, Nathaniel B., Koerber, Nicolas K., Szabo, Aniko, Taylor, Bradley, Wainaina, J. Njeri, Evans, Douglas B., Kothari, Anai N.

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Associations of County-Level Social Determinants of Health with COVID-19 Related Hospitalization Among People with HIV: A Retrospective Analysis of the U.S. National COVID Cohort C... von Islam, Jessica Y., Hurwitz, Eric, Li, Dongmei, Camacho-Rivera, Marlene, Sun, Jing, Safo, Sandra, Ross, Jennifer M., Wilkins, Kenneth, Hassan, Shukri, Hill, Elaine L., Nosyk, Bohdan, Varley, Cara, Fadul, Nada, Madlock-Brown, Charisse, Patel, Rena C.

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The Intersections of COVID-19, HIV, and Race/Ethnicity: Machine Learning Methods to Identify and Model Risk Factors for Severe COVID-19 in a Large U.S. National Dataset von Kunz, Miranda, Rott, Kollin W., Hurwitz, Eric, Kunisaki, Ken, Sun, Jing, Wilkins, Kenneth J., Islam, Jessica Y., Patel, Rena, Safo, Sandra E.

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Demonstrating an approach for evaluating synthetic geospatial and temporal epidemiologic data utility: results from analyzing >1.8 million SARS-CoV-2 tests in the United States Nat... von Thomas, Jason A, Foraker, Randi E, Zamstein, Noa, Morrow, Jon D, Payne, Philip R O, Wilcox, Adam B

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