Impact of Promotoras on Social Support and Glycemic Control Among Members of a Farmworker Community on the US-Mexico Border von Ingram, Maia, Torres, Emma, Redondo, Flor, Bradford, Gail, Wang, Chin, O'Toole, Mary L

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Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies von Amendola, Laura M., Muenzen, Kathleen, Biesecker, Leslie G., Bowling, Kevin M., Cooper, Greg M., Dorschner, Michael O., Driscoll, Catherine, Foreman, Ann Katherine M., Golden-Grant, Katie, Greally, John M., Hindorff, Lucia, Kanavy, Dona, Jobanputra, Vaidehi, Johnston, Jennifer J., Kenny, Eimear E., McNulty, Shannon, Murali, Priyanka, Ou, Jeffrey, Powell, Bradford C., Rehm, Heidi L., Rolf, Bradley, Roman, Tamara S., Van Ziffle, Jessica, Guha, Saurav, Abhyankar, Avinash, Crosslin, David, Venner, Eric, Yuan, Bo, Zouk, Hana, Jarvik, Gail P.

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The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations von Amendola, Laura M., Berg, Jonathan S., Horowitz, Carol R., Angelo, Frank, Bensen, Jeannette T., Biesecker, Barbara B., Biesecker, Leslie G., Cooper, Gregory M., East, Kelly, Filipski, Kelly, Fullerton, Stephanie M., Gelb, Bruce D., Goddard, Katrina A.B., Hailu, Benyam, Hart, Ragan, Hassmiller-Lich, Kristen, Joseph, Galen, Kenny, Eimear E., Koenig, Barbara A., Knight, Sara, Kwok, Pui-Yan, Lewis, Katie L., McGuire, Amy L., Norton, Mary E., Ou, Jeffrey, Parsons, Donald W., Powell, Bradford C., Risch, Neil, Robinson, Mimsie, Rini, Christine, Scollon, Sarah, Slavotinek, Anne M., Veenstra, David L., Wasserstein, Melissa P., Wilfond, Benjamin S., Hindorff, Lucia A., Plon, Sharon E., Jarvik, Gail P.

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Imputation and quality control steps for combining multiple genome-wide datasets von Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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Inflammation and immune-related candidate gene associations with acute lung injury susceptibility and severity: a validation study von O'Mahony, D Shane, Glavan, Bradford J, Holden, Tarah D, Fong, Christie, Black, R Anthony, Rona, Gail, Tejera, Paula, Christiani, David C, Wurfel, Mark M

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Marketing while Black: commentary on the Galak and Kahn 2019 Academic Marketing Climate Survey von Bradford, Tonya Williams, Perry, Vanessa Gail

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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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Behavioral Animal Model of the Emotional Response to Tinnitus and Hearing Loss von Lauer, Amanda M., Larkin, Gail, Jones, Aikeen, May, Bradford J.

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The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study von Rini, Christine, Khan, Cynthia M., Moore, Elizabeth, Roche, Myra I., Evans, James P., Berg, Jonathan S., Powell, Bradford C., Corbie-Smith, Giselle, Foreman, Ann Katherine M., Griesemer, Ida, Lee, Kristy, O’Daniel, Julianne M., Henderson, Gail E.

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Localisation of citrullinated proteins in normal appearing white matter and lesions in the central nervous system in multiple sclerosis von Bradford, Claire M, Ramos, Inês, Cross, Alison K, Haddock, Gail, McQuaid, Stephen, Nicholas, Anthony P, Woodroofe, M. Nicola

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Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project von Auer, Paul L, Nalls, Mike, Meschia, James F, Worrall, Bradford B, Longstreth, W. T, Seshadri, Sudha, Kooperberg, Charles, Burger, Kathleen M, Carlson, Christopher S, Carty, Cara L, Chen, Wei-Min, Cupples, L. Adrienne, DeStefano, Anita L, Fornage, Myriam, Hardy, John, Hsu, Li, Jackson, Rebecca D, Jarvik, Gail P, Kim, Daniel S, Lakshminarayan, Kamakshi, Lange, Leslie A, Manichaikul, Ani, Quinlan, Aaron R, Singleton, Andrew B, Thornton, Timothy A, Nickerson, Deborah A, Peters, Ulrike, Rich, Stephen S

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Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease von Rannikmäe, Kristiina, Davies, Gail, Thomson, Pippa A, Bevan, Steve, Devan, William J, Falcone, Guido J, Traylor, Matthew, Anderson, Christopher D, Battey, Thomas W.K, Radmanesh, Farid, Deka, Ranjan, Woo, Jessica G, Martin, Lisa J, Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L, Silliman, Scott L, Kidwell, Chelsea S, Montaner, Joan, Langefeld, Carl D, Slowik, Agnieszka, Hansen, Björn M, Lindgren, Arne G, Meschia, James F, Fornage, Myriam, Bis, Joshua C, Debette, Stéphanie, Ikram, Mohammad A, Longstreth, Will T, Schmidt, Reinhold, Zhang, Cathy R, Yang, Qiong, Sharma, Pankaj, Kittner, Steven J, Mitchell, Braxton D, Holliday, Elizabeth G, Levi, Christopher R, Attia, John, Rothwell, Peter M, Poole, Deborah L, Boncoraglio, Giorgio B, Psaty, Bruce M, Malik, Rainer, Rost, Natalia, Worrall, Bradford B, Dichgans, Martin, Van Agtmael, Tom, Woo, Daniel, Markus, Hugh S, Seshadri, Sudha, Rosand, Jonathan, Sudlow, Cathie L.M

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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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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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Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project[S] von Kim, Daniel Seung, Crosslin, David R., Auer, Paul L., Suzuki, Stephanie M., Marsillach, Judit, Burt, Amber A., Gordon, Adam S., Meschia, James F., Nalls, Mike A., Worrall, Bradford B., Longstreth, W.T., Gottesman, Rebecca F., Furlong, Clement E., Peters, Ulrike, Rich, Stephen S., Nickerson, Deborah A., Jarvik, Gail P.

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Factors influencing NCGENES research participants’ requests for non–medically actionable secondary findings von Roche, Myra I., Griesemer, Ida, Khan, Cynthia M., Moore, Elizabeth, Lin, Feng-Chang, O’Daniel, Julianne M., Foreman, Ann Katherine M., Lee, Kristy, Powell, Bradford C., Berg, Jonathan S., Evans, James P., Henderson, Gail E., Rini, Christine

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Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience von Muenzen, Kathleen D., Amendola, Laura M., Kauffman, Tia L., Mittendorf, Kathleen F., Bensen, Jeannette T., Chen, Flavia, Green, Richard, Powell, Bradford C., Kvale, Mark, Angelo, Frank, Farnan, Laura, Fullerton, Stephanie M., Robinson, Jill O., Li, Tianran, Murali, Priyanka, Lawlor, James M.J., Ou, Jeffrey, Hindorff, Lucia A., Jarvik, Gail P., Crosslin, David R.

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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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Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings von Christensen, Kurt D, Bernhardt, Barbara A, Jarvik, Gail P, Hindorff, Lucia A, Ou, Jeffrey, Biswas, Sawona, Powell, Bradford C, Grundmeier, Robert W, Machini, Kalotina, Karavite, Dean J, Pennington, Jeffrey W, Krantz, Ian D, Berg, Jonathan S, Goddard, Katrina A B

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Visual System Assessment in Infants, Children, and Young Adults by Pediatricians von Donahue, Sean, Nixon, Cynthia

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