Local Culture and Community Through a Digital Lens: Viewpoint on Designing and Implementing a Virtual Second Look Event for Residency Applicants by Martindale, Jaclyn M, Carrasquillo, Rachel A, Otallah, Scott Ireland, Brooks, Amber K, Denizard-Thompson, Nancy, Pharr, Emily, Choate, Nakiea, Sokolosky, Mitchell, Strauss, Lauren Doyle

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284 Real World Data of Sequencing Immune Checkpoint Inhibitors (ICI) after Initial ICI by Gunturu, Krishna, Awidi, Muhammad, Ranjit, Rojer, Connell, Brendan, Carrasquillo, Rachel, Gil, Brigitte, Dalbo, Natalie, Maher, Lewena, Reilly, Seanna, McDonald, Stephanie, Tsoukas, Philip, Voner, Linda

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Low Birth Weight and Hypertension Severity in Youth Referred for Hypertension Disorders: A SUPERHERO Interim Analysis: TH-PO590 by Carrasquillo, Rachel A., Giammattei, Victoria, Lucas, Caroline, Sethna, Christine B., Vincent, Carol, Viviano, Irina, Weaver, Donald J., South, Andrew M.

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Abstract P093: Preterm Birth And Hypertension Severity In Youth Referred For Hypertension Disorders: A Superhero Interim Analysis by Carrasquillo, Rachel A, Giammattei, Victoria, Lucas, Caroline B, Sethna, Christine, Vincent, Carol, Viviano, Irina, Weaver, Donald, South, Andrew M

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Association between SARS-CoV-2 infection and select symptoms and conditions 31 to 150 days after testing among children and adults by Zhang, Yongkang, Romieu-Hernandez, Alfonso, Boehmer, Tegan K, Azziz-Baumgartner, Eduardo, Carton, Thomas W, Gundlapalli, Adi V, Fearrington, Julia, Nagavedu, Kshema, Dea, Katherine, Moyneur, Erick, Cowell, Lindsay G, Kaushal, Rainu, Mayer, Kenneth H, Puro, Jon, Rasmussen, Sonja A, Thacker, Deepika, Weiner, Mark G, Saydah, Sharon, Block, Jason P

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“Click and mortar” opportunities for digitization and consumerism in trials by Randell, Rachel L., Hornik, Christoph P., Curtis, Lesley, Hernandez, Adrian F., Denwood, Tom, Nebeker, Camille, Sugarman, Jeremy, Tyl, Benoit, Murakami, Masahiro, Oley Wilberforce, Leslie, Pagoto, Sherry, Vedin, Ola, Andersson, Tomas, Carrasquillo, Olveen, Dolor, Rowena, Kollins, Scott H., Pellegrino, Jill, Ranney, Megan L.

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Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care by Maghiro, AudreyStephannie, Tabor, Holly K., Acosta, Maria T., Amendola, Laura, Andrews, Ashley, Balasubramanyam, Ashok, Baldridge, Dustin, Bennett, Jimmy, Berg-Rood, Beverly, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Burke, Elizabeth A., Byers, Peter, Peter Chang, Ta Chen, Chanprasert, Sirisak, Clark, Gary D., Cobban, Laurel A., Cogan, Joy D., Sessions Cole, F., Colley, Heather A., Cope, Heidi, D'Souza, Precilla, Dasari, Surendra, Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Earl, Dawn, Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Goddard, Page C., Golden-Grant, Katie, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Introne, Wendy, Izumi, Kosuke, Jayadev, Suman, Kiley, Dana, Kobren, Shilpa N., Korrick, Susan, Krasnewich, Donna M., Lam, Christina, Lanza, Ian R., Lee, Brendan H., Loo, Sandra K., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Marth, Gabor, McConkie-Rosell, Allyn, Mefford, Heather, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Robertson, Amy K., Rossignol, Francis, Ruzhnikov, Maura, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Sisco, Kathy, Smith, Edward C., Solomon, Ben, Sullivan, Jennifer A., Sybert, Virginia, Tan, Amelia L.M., Tekin, Mustafa, Telischi, Fred, Toro, Camilo, Ungar, Rachel A., Vanderver, Adeline, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Worley, Kim, Xiao, Changrui, Yang, John

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PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy by Panneerselvam, Sugi, Wang, Julia, Zhu, Wenmiao, Dai, Hongzheng, Pappas, John G., Rabin, Rachel, Low, Karen J., Rosenfeld, Jill A., Emrick, Lisa, Xiao, Rui, Xia, Fan, Yang, Yaping, Eng, Christine M., Anderson, Anne, Chau, Vann, Soler‐Alfonso, Claudia, Streff, Haley, Lalani, Seema R., Mercimek‐Andrews, Saadet, Bi, Weimin

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De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities by Benke, Paul J., Emrick, Lisa, Fisher, Kristen, Adam, Margaret, Alvarez, Raquel L., Alvey, Justin, Ashley, Euan A., Bacino, Carlos A., Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Beggs, Alan H., Bejerano, Gill, Bennett, Jimmy, Bernstein, Jonathan A., Blue, Elizabeth, Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Cassini, Thomas, Chang, Ta Chen Peter, Coakley, Terra R., Cobban, Laurel A., Cole, F. Sessions, Colley, Heather A., Corona, Rosario, Crouse, Andrew B., Dai, Hongzheng, Davis, Joie, Dell'Angelica, Esteban C., Dickson, Patricia, Douine, Emilie D., Eckstein, David J., Emrick, Lisa T., Hadley, Don, Hamid, Rizwan, Hassey, Kelly, Hayes, Nichole, Horike‐Pyne, Martha, Huang, Alden, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Jean‐Marie, Orpa, Jobanputra, Vaidehi, Karaviti, Lefkothea, Korrick, Susan, Krasnewich, Donna M., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Liu, Pengfei, Longo, Nicola, Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Maghiro, Audrey Stephannie, Manolio, Teri A., Marwaha, Shruti, McConkie‐Rosell, Allyn, Mirzaa, Ghayda, Morava, Eva, Nicholas, Sarah K., Nickerson, Deborah, Pallais, J. Carl, Phillips, John A., Raskind, Wendy, Rosenfeld, Jill A., Rosenwasser, Natalie, Sampson, Jacinda B., Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Solnica‐Krezel, Lilianna, Solomon, Ben, Sullivan, Kathleen, Sweetser, David A., Tan, Amelia L. M., Tarakad, Arjun, Vanderver, Adeline, Velinder, Matt, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Hubshman, Monika Weisz, Yamamoto, Shinya, Zhang, Zhe, Zuchner, Stephan, Glaser, Kimberly, Murdock, David R., Rohena, Luis, Diderich, Karin E. M., Lee, Brendan

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The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities by Venner, Eric, Patterson, Karynne, Kalra, Divya, Wheeler, Marsha M., Chen, Yi-Ju, Kalla, Sara E., Yuan, Bo, Karnes, Jason H., Walker, Kimberly, Smith, Joshua D., McGee, Sean, Radhakrishnan, Aparna, Haddad, Andrew, Empey, Philip E., Wang, Qiaoyan, Lichtenstein, Lee, Toledo, Diana, Jarvik, Gail, Musick, Anjene, Gibbs, Richard A.

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Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities by Venner, Eric, Patterson, Karynne, Kalra, Divya, Wheeler, Marsha M., Chen, Yi-Ju, Kalla, Sara E., Yuan, Bo, Karnes, Jason H., Walker, Kimberly, Smith, Joshua D., McGee, Sean, Radhakrishnan, Aparna, Haddad, Andrew, Empey, Philip E., Wang, Qiaoyan, Lichtenstein, Lee, Toledo, Diana, Jarvik, Gail, Musick, Anjene, Gibbs, Richard A.

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