Systems, Devices, and Methods for Managing Operation of Diagnostic Testing Instruments von Basford, Eric Christopher, Bowie, Jason, Hyson, Regina, Davis, Craig Taylor, Douglass, Keith

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SYSTEMS, DEVICES AND METHODS FOR MANAGING OPERATION OF DIAGNOSTIC TESTING INSTRUMENTS von BASFORD, ERIC CHRISTOPHER, DOUGLASS, KEITH, BOWIE, JASON, DAVIS, CRAIG TAYLOR, HYSON, REGINA

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Methods and Systems for Determining Patient and Geographic Specific Medical Reports von BRAZELL ROBERT, AYERS JONATHAN, BASFORD ERIC CHRISTOPHER, DURGIN MATTHEW B, STAMARIS JOHN

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Methods and systems for determining patient and geographic specific medical reports von STAMARIS, JOHN, AYERS, JONATHAN W, DURGIN, MATTHEW B, BRAZELL, ROBERT B, BASFORD, ERIC CHRISTOPHER

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METHODS AND SYSTEMS FOR DETERMINING PATIENT AND GEOGRAPHIC SPECIFIC MEDICAL REPORTS von STAMARIS, JOHN, AYERS, JONATHAN W, DURGIN, MATTHEW B, BRAZELL, ROBERT B, BASFORD, ERIC CHRISTOPHER

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The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future von Gottesman, Omri, Kuivaniemi, Helena, Tromp, Gerard, Faucett, W. Andrew, Li, Rongling, Manolio, Teri A., Sanderson, Saskia C., Kannry, Joseph, Zinberg, Randi, Basford, Melissa A., Brilliant, Murray, Carey, David J., Chisholm, Rex L., Chute, Christopher G., Connolly, John J., Crosslin, David, Denny, Joshua C., Gallego, Carlos J., Haines, Jonathan L., Hakonarson, Hakon, Harley, John, Jarvik, Gail P., Kohane, Isaac, Kullo, Iftikhar J., Larson, Eric B., McCarty, Catherine, Ritchie, Marylyn D., Roden, Dan M., Smith, Maureen E., Böttinger, Erwin P., Williams, Marc S.

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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies von McCarty, Catherine A, Chisholm, Rex L, Chute, Christopher G, Kullo, Iftikhar J, Jarvik, Gail P, Larson, Eric B, Li, Rongling, Masys, Daniel R, Ritchie, Marylyn D, Roden, Dan M, Struewing, Jeffery P, Wolf, Wendy A

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Genome- and Phenome-Wide Analyses of Cardiac Conduction Identifies Markers of Arrhythmia Risk von RITCHIE, Marylyn D, DENNY, Joshua C, BRADFORD, Yuki, RASMUSSEN, Luke V, PATHAK, Jyotishman, CHUTE, Christopher G, KULLO, Iftikhar J, MCCARTY, Catherine A, CHISHOLM, Rex L, KHO, Abel N, CARLSON, Christopher S, LARSON, Eric B, ZUVICH, Rebecca L, JARVIK, Gail P, SOTOODEHNIA, Nona, MANOLIO, Teri A, RONGLING LI, MASYS, Daniel R, HAINES, Jonathan L, RODEN, Dan M, CRAWFORD, Dana C, SCHILDCROUT, Jonathan S, BASTARACHE, Lisa, RAMIREZ, Andrea H, MOSLEY, Jonathan D, PULLEY, Jill M, BASFORD, Melissa A

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Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data von Denny, Joshua C, Bastarache, Lisa, Ritchie, Marylyn D, Carroll, Robert J, Zink, Raquel, Mosley, Jonathan D, Field, Julie R, Pulley, Jill M, Ramirez, Andrea H, Bowton, Erica, Basford, Melissa A, Carrell, David S, Peissig, Peggy L, Kho, Abel N, Pacheco, Jennifer A, Rasmussen, Luke V, Crosslin, David R, Crane, Paul K, Pathak, Jyotishman, Bielinski, Suzette J, Pendergrass, Sarah A, Xu, Hua, Hindorff, Lucia A, Li, Rongling, Manolio, Teri A, Chute, Christopher G, Chisholm, Rex L, Larson, Eric B, Jarvik, Gail P, Brilliant, Murray H, McCarty, Catherine A, Kullo, Iftikhar J, Haines, Jonathan L, Crawford, Dana C, Masys, Daniel R, Roden, Dan M

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Genomic data in the All of Us Research Program von Bick, Alexander G., Metcalf, Ginger A., Mayo, Kelsey R., Lichtenstein, Lee, Rura, Shimon, Carroll, Robert J., Musick, Anjene, Linder, Jodell E., Jordan, I. King, Nagar, Shashwat Deepali, Sharma, Shivam, Meller, Robert, Basford, Melissa, Boerwinkle, Eric, Cicek, Mine S., Doheny, Kimberly F., Eichler, Evan E., Gabriel, Stacey, Gibbs, Richard A., Glazer, David, Harris, Paul A., Jarvik, Gail P., Philippakis, Anthony, Rehm, Heidi L., Roden, Dan M., Thibodeau, Stephen N., Topper, Scott, Blegen, Ashley L., Wirkus, Samantha J., Wagner, Victoria A., Meyer, Jeffrey G., Muzny, Donna M., Venner, Eric, Mawhinney, Michelle Z., Griffith, Sean M. L., Hsu, Elvin, Ling, Hua, Adams, Marcia K., Walker, Kimberly, Hu, Jianhong, Doddapaneni, Harsha, Kovar, Christie L., Murugan, Mullai, Dugan, Shannon, Khan, Ziad, Lennon, Niall J., Austin-Tse, Christina, Banks, Eric, Gatzen, Michael, Gupta, Namrata, Henricks, Emma, Larsson, Katie, McDonough, Sheli, Harrison, Steven M., Kachulis, Christopher, Lebo, Matthew S., Neben, Cynthia L., Steeves, Marcie, Zhou, Alicia Y., Smith, Joshua D., Frazar, Christian D., Davis, Colleen P., Patterson, Karynne E., Wheeler, Marsha M., McGee, Sean, Lockwood, Christina M., Shirts, Brian H., Pritchard, Colin C., Murray, Mitzi L., Vasta, Valeria, Leistritz, Dru, Richardson, Matthew A., Buchan, Jillian G., Radhakrishnan, Aparna, Krumm, Niklas, Ehmen, Brenna W., Schwartz, Sophie, Aster, M. Morgan T., Cibulskis, Kristian, Haessly, Andrea, Asch, Rebecca, Cremer, Aurora, Degatano, Kylee, Shergill, Akum, Gauthier, Laura D., Lee, Samuel K., Hatcher, Aaron, Grant, George B., Brandt, Genevieve R., Covarrubias, Miguel, Able, Ashley, Green, Ashley E., Zhang, Jennifer, Condon, Henry R., Wang, Yuanyuan, Dillon, Moira K., Albach, C. H., Baalawi, Wail, Choi, Seung Hoan, Wang, Xin

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Genome-wide study of resistant hypertension identified from electronic health records von Dumitrescu, Logan, Ritchie, Marylyn D, Denny, Joshua C, El Rouby, Nihal M, McDonough, Caitrin W, Bradford, Yuki, Ramirez, Andrea H, Bielinski, Suzette J, Basford, Melissa A, Chai, High Seng, Peissig, Peggy, Carrell, David, Pathak, Jyotishman, Rasmussen, Luke V, Wang, Xiaoming, Pacheco, Jennifer A, Kho, Abel N, Hayes, M Geoffrey, Matsumoto, Martha, Smith, Maureen E, Li, Rongling, Cooper-DeHoff, Rhonda M, Kullo, Iftikhar J, Chute, Christopher G, Chisholm, Rex L, Jarvik, Gail P, Larson, Eric B, Carey, David, McCarty, Catherine A, Williams, Marc S, Roden, Dan M, Bottinger, Erwin, Johnson, Julie A, de Andrade, Mariza, Crawford, Dana C

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Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies von Denny, Joshua C., Crawford, Dana C., Ritchie, Marylyn D., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Chai, High Seng, Bastarache, Lisa, Zuvich, Rebecca, Peissig, Peggy, Carrell, David, Ramirez, Andrea H., Pathak, Jyotishman, Wilke, Russell A., Rasmussen, Luke, Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Weston, Noah, Matsumoto, Martha, Kopp, Peter A., Newton, Katherine M., Jarvik, Gail P., Li, Rongling, Manolio, Teri A., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza

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Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network von Malinowski, Jennifer R, Denny, Joshua C, Bielinski, Suzette J, Basford, Melissa A, Bradford, Yuki, Peissig, Peggy L, Carrell, David, Crosslin, David R, Pathak, Jyotishman, Rasmussen, Luke, Pacheco, Jennifer, Kho, Abel, Newton, Katherine M, Li, Rongling, Kullo, Iftikhar J, Chute, Christopher G, Chisholm, Rex L, Jarvik, Gail P, Larson, Eric B, McCarty, Catherine A, Masys, Daniel R, Roden, Dan M, de Andrade, Mariza, Ritchie, Marylyn D, Crawford, Dana C

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Defining the role of common variation in the genomic and biological architecture of adult human height von Amin, Najaf, Croteau-Chonka, Damien C, Jackson, Anne U, Randall, Joshua C, Westra, Harm-Jan, Absher, Devin, Baron, Jeffrey, Feitosa, Mary F, Fischer, Krista, Kanoni, Stavroula, Leach, Irene Mateo, Palmer, Cameron D, Prokopenko, Inga, Ripke, Stephan, Stancáková, Alena, Sung, Yun Ju, Trompet, Stella, Blüher, Matthias, Bolton, Jennifer L, Claudi-Boehm, Simone, Cooper, Matthew, Daw, E Warwick, Dörr, Marcus, Folkersen, Lasse, Grönberg, Henrik, Hannemann, Anke, Helmer, Quinta, Hemani, Gibran, Hoffmann, Wolfgang, Holmen, Oddgeir, Kho, Abel N, Kratzer, Wolfgang, Magnusson, Patrik K E, McLaren, Paul J, Menni, Cristina, Merger, Sigrun, Milani, Lili, Nauck, Matthias, Oozageer, Laticia, Pilz, Stefan, Rayner, Nigel W, Renstrom, Frida, Scott, Robert A, Stringham, Heather M, Swertz, Morris A, Syvänen, Ann-Christine, van Dijk, Suzanne, Vonk, Judith M, Wennauer, Roman, Wilsgaard, Tom, Wong, Andrew, Wright, Alan F, Bergmann, Sven, Bornstein, Stefan R, Brambilla, Paolo, Brown, Morris J, Chakravarti, Aravinda, Danesh, John, de Faire, Ulf, Erbel, Raimund, Ferrières, Jean, Gejman, Pablo V, Heath, Andrew C, Hengstenberg, Christian, Hingorani, Aroon D, Kaprio, Jaakko, Madden, Pamela A F, Marette, André, Montgomery, Grant W, Nelis, Mari, Ong, Ken K, Peters, Annette, Qi, Lu, Rice, Treva K, Saramies, Jouko, Sebert, Sylvain, Steinthorsdottir, Valgerdur, Tardif, Jean-Claude, Tremblay, Angelo, Assimes, Themistocles L, Dedoussis, George, Franks, Paul W, Groop, Leif C, Hamsten, Anders, Kuh, Diana, Laakso, Markku, Munroe, Patricia B, Schlessinger, David, Slagboom, P Eline, Snieder, Harold, Spector, Tim D, Tuomilehto, Jaakko, Uusitupa, Matti, Walker, Mark, Thorsteinsdottir, Unnur, Barroso, Inês, Borecki, Ingrid B, McCarthy, Mark I, Visscher, Peter M, Frayling, Timothy M

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De-black-boxing health AI: demonstrating reproducible machine learning computable phenotypes using the N3C-RECOVER Long COVID model in the All of Us data repository von Pfaff, Emily R, Girvin, Andrew T, Crosskey, Miles, Gangireddy, Srushti, Master, Hiral, Wei, Wei-Qi, Kerchberger, V Eric, Weiner, Mark, Harris, Paul A, Basford, Melissa, Lunt, Chris, Chute, Christopher G, Moffitt, Richard A, Haendel, Melissa

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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network von Venner, Eric, Muzny, Donna M., Abrams, Debra, Albertson-Junkans, Ladia, Ames, Darren C., Aronson, Samuel, Babb, Lawrence J., Balasubramanian, Adithya, Bastarache, Lisa, Behr, Meckenzie, Blout, Carrie, Bowser, Mark, Brilliant, Murray, Brodeur, Wendy, Caraballo, Pedro, Castro, Victor, Chisholm, Rex L., Chung, Wendy, Chute, Christopher G., City, Brittany, Connolly, John J., Crane, Paul, Crew, Katherine, De Andrade, Mariza, Denson, Shawn, Denny, Josh, DeSmet, Tim, Dikilitas, Ozan, Fullerton, Stephanie M., Gabriel, Stacey, Gainer, Vivian, Gharavi, Ali, Glazer, Andrew M., Goehringer, Jessica, Gordon, Adam S., Graham, Chet, Dayal, Jyoti, Hakonarson, Hakon, Harden, Maegan V., Harr, Margaret, Hayes, M. Geoffrey, Henrikson, Nora, Howell, Kayla M., Jiang, Yunyun, Joo, Yoonjung Yoonie, Justice, Anne E., Kalla, Sara E., Kalra, Divya, Kelly, Melissa A., Key, Dustin, Kiryluk, Krzysztof, Kullo, Iftikhar J., Larson, Eric B., Lin, Chiao-Feng, Linder, Jodell, Macbeth, Alyssa, Dinsmore, Michael J., Dodge, Sheila, Fasel, David, Fedotov, Alex, Feng, Qiping, McGowan, Michelle L., Meldrim, Jim, Mosley, Jonathan, Muniz, Jesse, Murdock, David R., Murugan, Mullai, Myers, Melanie F., Namjou, Bahram, Ni, Yizhao, Obeng, Aniwaa Owusu, Taylor, Casey Overby, Peterson, Josh F., Pratap, Siddharth, Prows, Cynthia A., Ralston, James D., Ramaprasan, Arvind, Rasmussen-Torvik, Laura, Schaid, Dan, Sengupta, Soumitra, Singh, Rajbir, Sleiman, Patrick M.A., Smoller, Jordan W., Stanaway, Ian B., Stroud, Mary, Tolwinski, Kasia, Van Driest, Sara L., Veenstra, David, Vicente, Gina, Wagner, Michael, Walunas, Theresa, Wells, Quinn, White, Peter S., Wiley, Ken L., Wilson, Michael W., Woolf, Betty, Yi, Victoria, Zhang, Ge, Zhang, Lan, Gibbs, Richard A.

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The All of Us Research Program: Data quality, utility, and diversity von Ramirez, Andrea H., Halvorson, Alese, Qian, Jun, Mayo, Kelsey, Basford, Melissa, Deflaux, Nicole, Muthuraman, Karthik N., Xu, Hua, Wilkins, Consuelo, Anton-Culver, Hoda, Boerwinkle, Eric, Cohn, Elizabeth, Schully, Sheri D., Argos, Maria, Cronin, Robert M., O’Donnell, Christopher, Fouad, Mona, Greenland, Philip, Hebbring, Scott J., Karlson, Elizabeth W., Khatri, Parinda, Korf, Bruce, Sodeke, Stephen, Wilbanks, John, Hentges, Justin, Mockrin, Stephen, Lunt, Christopher, Devaney, Stephanie A., Gebo, Kelly, Denny, Joshua C., Harris, Paul A., Roden, Dan M., Ahmedani, Brian, Cole Johnson, Christine D., Ahsan, Habib, Antoine-LaVigne, Donna, Anton-Culver, Hoda, Topol, Eric, Jain, Praduman, Korf, Bruce, Behringer, Melissa, Gharavi, Ali G., Hripcsak, George, Bier, Louise, Hebbring, Scott Joseph, Burnside, Elizabeth, Drezner, Marc K., Channamsetty, Veena, Montalvo, Wanda, Chinea, Carmen, Jenks, Nancy, Cicek, Mine, Thibodeau, Steve, Collier, Ever, Winkler, Joyce, Corcoran, John, Daviglus, Martha, Denny, Joshua, Doheny, Kim, Eichler, Evan, Lennon, Niall, Gabriel, Stacey, Gibbs, Richard, Gil Rico, Edgar M., Glazer, David, Greenland, Philip, Hogan, William R., Pollan, Cliff, Okun, Sally, Karlson, Elizabeth W., Smoller, Jordan, Ross, Margaret Elizabeth, Kaushal, Rainu, Khatri, Parinda, Kheterpal, Vik, Ojo, Akinlolu, Moreno, Francisco A., Menon, Usha, Malik-Gagnon, Lynda, Mangravite, Lara, Marallo, Adria, Visweswaran, Shyam, Reis, Steven, Moore, John, Talavera, Gregory, O'Donnell, Christopher, Ohno-Machado, Lucila, Randal, Fornessa, Theodorou, Andreas A., Roxas-Murray, Mercedita, Stark, Louisa, Tepp, Ronnie, Topper, Scott, Weidman, Lisa, Weiss, Scott T., Wellis, David, Whittle, Jeffrey, Wilson, Amanda, Zuchner, Stephan, Zwick, Michael E.

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The All of Us Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research von Mayo, Kelsey R, Basford, Melissa A, Carroll, Robert J, Dillon, Moira, Fullen, Heather, Leung, Jesse, Master, Hiral, Rura, Shimon, Sulieman, Lina, Kennedy, Nan, Banks, Eric, Bernick, David, Gauchan, Asmita, Lichtenstein, Lee, Mapes, Brandy M, Marginean, Kayla, Nyemba, Steve L, Ramirez, Andrea, Rotundo, Charissa, Wolfe, Keri, Xia, Weiyi, Azuine, Romuladus E, Cronin, Robert M, Denny, Joshua C, Kho, Abel, Lunt, Christopher, Malin, Bradley, Natarajan, Karthik, Wilkins, Consuelo H, Xu, Hua, Hripcsak, George, Roden, Dan M, Philippakis, Anthony A, Glazer, David, Harris, Paul A

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing von Hu, Jianhong, Korchina, Viktoriya, Zouk, Hana, Harden, Maegan V, Murdock, David, Macbeth, Alyssa, Harrison, Steven M, Lennon, Niall, Kovar, Christie, Balasubramanian, Adithya, Zhang, Lan, Chandanavelli, Gauthami, Pasham, Divya, Rowley, Robb, Wiley, Ken, Smith, Maureen E, Gordon, Adam, Jarvik, Gail P, Sleiman, Patrick, Kelly, Melissa A, Bland, Harris T, Murugan, Mullai, Venner, Eric, Boerwinkle, Eric, Prows, Cynthia, Mahanta, Lisa, Rehm, Heidi L, Gibbs, Richard A, Muzny, Donna M

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Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk von Ritchie, Marylyn D., Denny, Joshua C., Zuvich, Rebecca L., Crawford, Dana C., Schildcrout, Jonathan S., Bastarache, Lisa, Ramirez, Andrea H., Mosley, Jonathan D., Pulley, Jill M., Basford, Melissa A., Bradford, Yuki, Rasmussen, Luke V., Pathak, Jyotishman, Chute, Christopher G., Kullo, Iftikhar J., McCarty, Catherine A., Chisholm, Rex L., Kho, Abel N., Carlson, Christopher S., Larson, Eric B., Jarvik, Gail P., Sotoodehnia, Nona, Manolio, Teri A., Li, Rongling, Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.

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