Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population von Martin, Christa Lese, Wain, Karen E, Oetjens, Matthew T, Tolwinski, Kasia, Palen, Emily, Hare-Harris, Abby, Habegger, Lukas, Maxwell, Evan K, Reid, Jeffrey G, Walsh, Lauren Kasparson, Myers, Scott M, Ledbetter, David H

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The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants von Wain, Karen E., Palen, Emily, Savatt, Juliann M., Shuman, Devin, Finucane, Brenda, Seeley, Andrea, Challman, Thomas D., Myers, Scott M., Martin, Christa Lese

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Expanding the KIF4A‐associated phenotype von Kalantari, Silvia, Carlston, Colleen, Alsaleh, Norah, Abdel‐Salam, Ghada M. H., Alkuraya, Fowzan, Kato, Mitsuhiro, Matsumoto, Naomichi, Miyatake, Satoko, Yamamoto, Tatsuya, Fares‐Taie, Lucas, Rozet, Jean‐Michel, Chassaing, Nicolas, Vincent‐Delorme, Catherine, Kang‐Bellin, Anjeung, McWalter, Kirsty, Bupp, Caleb, Palen, Emily, Wagner, Monisa D., Niceta, Marcello, Cesario, Claudia, Milone, Roberta, Kaplan, Julie, Wadman, Erin, Dobyns, William B., Filges, Isabel

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SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research von Feliciano, Pamela, Daniels, Amy M., Esler, Amy, Gutierrez, Anibal, Nicholson, Amy, Stephens, Alexandra N., Stedman, Amy, Finucane, Brenda, O’Roak, Brian J., Robertson, Beverly E., Rodriguez, Barbara, Van Metre, Bonnie, Bradley, Catherine, Erickson, Craig A., Harkins, Christina, Ochoa-Lubinoff, Cesar, Rosenberg, Cordelia R., Smith, Christopher J., Taylor, Cora M., White, Loran Casey, Walston, Corrie H., Amaral, David G., Coury, Daniel Lee, Sarver, Dustin E., Li, Deana, Berry-Kravis, Elizabeth, Fombonne, Eric J., Hofammann, Eugenia, Wodka, Ericka L., O’Connor, Eirene, Miller, Fiona, Stein, Gail, Hutter, Hanna, Li, Hai, Lechniak, Holly, Schneider, Hoa Lam, Zaydens, Hana, Arriaga, Ivette, Cubells, Joseph F., Cordova, Jeanette M., Gunderson, Jaclyn, McCracken, James T., Michaelson, Jacob J., Neely, Jason, Orobio, Jessica, Piven, Joseph, Tjernagel, Jennifer, Dent, Katherine, Schweers, Kathryn A., Law, J. Kiely, Lowe, Kathryn, O’Brien, Kaela, Smith, Kaitlin, Pawlowski, Katherine G., Pierce, Karen L., Roeder, Katherine, Coppola, Leigh A., Carpenter, Laura, Huang-Storms, Lark Y., Herbert, Lynette M., Simon, Laura, Soorya, Latha V., Wasserburg, Lucy, Lazar, Maya, Currin, Mary Hannah, Heyman, Michelle, Jones, Mark, Jordy, Michelle, Sahin, Mustafa, Siegel, Matthew S., Yinger, Meredith, Hanna, Nathan, Juarez, A. Pablo, Remington, Rick, Schultz, Robert T., Carpenter, Sarah, Eldred, Sara, Francis, Sunday, Horner, Susannah, Lee, Soo J., Mastel, Sarah A., Myers, Vincent J., Amatya, Alpha, Chatha, Ahmad S., Lash, Alex E., Ridenour, Curtis, Stock, Colleen M., Schmidt, Danielle, Butler, Martin E., Carriero, Nicholas, Volfovsky, Natalia, Edgar, Ron, Chin, Wubin, Jensen, William, Krentz, Anthony D., Astrovskaya, Irina, Gibbs, Richard A., Han, Xinwei, Shen, Yufeng, Reichardt, Louis F.

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BEYOND MEDICAL ACTIONABILITY: PERSONAL UTILITY OF KNOWING A GENETIC ETIOLOGY von Finucane, Brenda, Martin, Christa, Wain, Karen, Palen, Emily, Ledbetter, David

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Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry von Savatt, Juliann M., Azzariti, Danielle R., Ledbetter, David H., Palen, Emily, Rehm, Heidi L., Riggs, Erin Rooney, Martin, Christa Lese

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ClinGen's GenomeConnect registry enables patient‐centered data sharing von Savatt, Juliann M., Azzariti, Danielle R., Faucett, W. Andrew, Harrison, Steven, Hart, Jennifer, Kattman, Brandi, Landrum, Melissa J., Ledbetter, David H., Miller, Vanessa Rangel, Palen, Emily, Rehm, Heidi L., Rhode, Jud, Turner, Stefanie, Vidal, Jo Anne, Wain, Karen E., Riggs, Erin Rooney, Martin, Christa Lese

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IDENTIFICATION AND RESULTS DISCLOSURE: OF RARE, PATHOGENIC COPY NUMBER VARIANTS TO ADULT RESEARCH PARTICIPANTS WITH DEVELOPMENTAL BRAIN DISORDERS von Finucane, Brenda, Wain, Karen, Palen, Emily, Kasparson, Lauren, Hare-Harris, Abby, Overton, John, Habegger, Lukas, Maxwell, Evan, Reid, Jeffrey, Martin, Christa L., Ledbetter, David H.

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Heterozygous variants in SPTBN1 cause intellectual disability and autism von Rosenfeld, Jill A., Xiao, Rui, Bekheirnia, Mir Reza, Kanani, Farah, Parker, Michael J., Koenig, Mary K., Haeringen, Arie, Ruivenkamp, Claudia, Rosmaninho‐Salgado, Joana, Almeida, Pedro M., Sá, Joaquim, Pinto Basto, Jorge, Palen, Emily, Oetjens, Kathryn F., Burrage, Lindsay C., Xia, Fan, Liu, Pengfei, Eng, Christine M., Yang, Yaping, Posey, Jennifer E., Lee, Brendan H.

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Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3 von Schirwani, Schaida, Albaba, Shadi, Carere, Deanna Alexis, Guillen Sacoto, Maria J., Milan Zamora, Francisca, Si, Yue, Rabin, Rachel, Pappas, John, Renaud, Deborah L., Hauser, Natalie, Reid, Evan, Blanchet, Patricia, Foulds, Nichola, Dixit, Abhijit, Fisher, Richard, Armstrong, Ruth, Isidor, Bertrand, Cogne, Benjamin, Schrier Vergano, Samantha, Demirdas, Serwet, Dykzeul, Natalie, Cohen, Julie S., Grand, Katheryn, Morel, Dayna, Slavotinek, Anne, Albassam, Hessa F., Naik, Swati, Dean, John, Ragge, Nicola, Cinzia, Costa, Tedesco, Maria Giovanna, Harrison, Rachel E., Bouman, Arjan, Palen, Emily, Challman, Thomas D., Willemsen, Marjolein H., Vogt, Julie, Cunniff, Christopher, Bergstrom, Katherine, Walia, Jagdeep S., Bruel, Ange‐Line, Kini, Usha, Alkuraya, Fowzan S., Slegesky, Valerie, Meeks, Naomi, Girotto, Paula, Johnson, Diana, Newbury‐Ecob, Ruth, Ockeloen, Charlotte W., Prontera, Paolo, Lynch, Sally Ann, Li, Dong, Graham, John M., Balasubramanian, Meena

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Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses von Wain, Karen E., Tolwinski, Kasia, Palen, Emily, Heidlebaugh, Alexis R., Holdren, Karahlyn, Walsh, Lauren Kasparson, Oetjens, Matthew T., Ledbetter, David H., Martin, Christa Lese

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STING agonist inflames the pancreatic cancer immune microenvironment and reduces tumor burden in mouse models von Jing, Weiqing, McAllister, Donna, Vonderhaar, Emily P, Palen, Katie, Riese, Matthew J, Gershan, Jill, Johnson, Bryon D, Dwinell, Michael B

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Patients’ perspectives of tuberculosis treatment challenges and barriers to treatment adherence in Ukraine: a qualitative study von Aibana, Omowunmi, Dauria, Emily, Kiriazova, Tetiana, Makarenko, Olena, Bachmaha, Mariya, Rybak, Natasha, Flanigan, Timothy Palen, Petrenko, Vasyl, Becker, Anne E, Murray, Megan B

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Ideology in U.S. Foreign Relations: New Histories von Nichols, Christopher McKnight, Milne, David

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Views on Parent-Child Connectedness Among English- and Spanish-Speaking Parents of High-Risk Youth von Scarborough, Megan, Kulkarni, Shanti, Lewis, Carol M., Palen, Lori-Ann, Wade, Emily, Pierce, Amy

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Additional file 2: of STING agonist inflames the pancreatic cancer immune microenvironment and reduces tumor burden in mouse models von Weiqing Jing, McAllister, Donna, Vonderhaar, Emily, Palen, Katie, Riese, Matthew, Gershan, Jill, Johnson, Bryon, Dwinell, Michael

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Additional file 3: of STING agonist inflames the pancreatic cancer immune microenvironment and reduces tumor burden in mouse models von Weiqing Jing, McAllister, Donna, Vonderhaar, Emily, Palen, Katie, Riese, Matthew, Gershan, Jill, Johnson, Bryon, Dwinell, Michael

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