Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility von Cassa, Christopher A, Savage, Sarah K, Taylor, Patrick L, Green, Robert C, McGuire, Amy L, Mandl, Kenneth D

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Short report: Twins with 20p13 duplication. Case report and comprehensive literature review von Kennedy, Benjamin J., Savage, Sarah K., Kaler, Stephen G.

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Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board von Holm, Ingrid A., Savage, Sarah K., Green, Robert C., Juengst, Eric, McGuire, Amy, Kornetsky, Susan, Brewster, Stephanie J., Joffe, Steven, Taylor, Patrick

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Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study von Walters, Nicole L., Lindsey-Mills, Zoe T., Brangan, Andrew, Savage, Sarah K., Schmidlen, Tara J., Morgan, Kelly M., Tricou, Eric P., Betts, Megan M., Jones, Laney K., Sturm, Amy C., Campbell-Salome, Gemme

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Using a chat-based informed consent tool in large-scale genomic research von Savage, Sarah K, LoTempio, Jonathan, Smith, Erica D, Andrew, E Hallie, Mas, Gloria, Kahn-Kirby, Amanda H, Délot, Emmanuèle, Cohen, Andrea J, Pitsava, Georgia, Nussbaum, Robert, Fusaro, Vincent A, Berger, Seth, Vilain, Eric

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Increased LIS1 expression affects human and mouse brain development von Lu, Xin-Yan, Horner, Michele, Day-Salvatore, Debra-Lynn, Sahoo, Trilochan, Withers, Marjorie A, Cheung, Sau Wai, Gunderson, Kevin L, Hunter, Jill V, Sapir, Tamar, Peiffer, Daniel A, Yanagawa, Yuchio, Reiner, Orly, Shchelochkov, Oleg A, Levy, Talia, Lupski, James R, Nezarati, Marjan M, Martinez, Salvador, Savage, Sarah K, Shinder, Vera, Harris, David J, Ann Shotts, Vern, Bi, Weimin, Amato, Stephen S, Beaudet, Arthur L, Zhang, Feng

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Development of a culturally targeted chatbot to inform living kidney donor candidates of African ancestry about APOL1 genetic testing: a mixed methods study von Gordon, Elisa J., Gacki-Smith, Jessica, Gooden, Matthew J., Waite, Preeya, Yacat, Rochell, Abubakari, Zenab R., Duquette, Debra, Agrawal, Akansha, Friedewald, John, Savage, Sarah K., Cooper, Matthew, Gilbert, Alexander, Muhammad, Lutfiyya N., Wicklund, Catherine

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Family health history reporting is sensitive to small changes in wording von Conway-Pearson, Liam S., Christensen, Kurt D., Savage, Sarah K., Huntington, Noelle L., Weitzman, Elissa R., Ziniel, Sonja I., Bacon, Phoebe, Cacioppo, Cara N., Green, Robert C., Holm, Ingrid A.

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The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository von Harris, Erin D., Ziniel, Sonja I., Amatruda, Jonathan G., Clinton, Catherine M., Savage, Sarah K., Taylor, Patrick L., Huntington, Noelle L., Green, Robert C., Holm, Ingrid A.

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Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples von Christensen, Kurt D., Savage, Sarah K., Huntington, Noelle L., Weitzman, Elissa R., Ziniel, Sonja I., Bacon, Phoebe L., Cacioppo, Cara N., Green, Robert C., Holm, Ingrid A.

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Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing? von Mitchell, Phoebe B., Ziniel, Sonja I., Savage, Sarah K., Christensen, Kurt D., Weitzman, Elissa R., Green, Robert C., Huntington, Noelle L., Mathews, Debra J., Holm, Ingrid A.

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Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research von Holm, Ingrid A., Iles, Brittany R., Ziniel, Sonja I., Bacon, Phoebe L., Savage, Sarah K., Christensen, Kurt D., Weitzman, Elissa R., Green, Robert C., Huntington, Noelle L.

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The Development of a Preference-Setting Model for the Return of Individual Genomic Research Results von Bacon, Phoebe L., Harris, Erin D., Ziniel, Sonja I., Savage, Sarah K., Weitzman, Elissa R., Green, Robert C., Huntington, Noelle L., Holm, Ingrid A.

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Phenotype delineation of ZNF462 related syndrome von Kruszka, Paul, Hu, Tommy, Hong, Sungkook, Signer, Rebecca, Cogné, Benjamin, Isidor, Betrand, Mazzola, Sarah E., Giltay, Jacques C., Gassen, Koen L. I., England, Eleina M., Pais, Lynn, Ockeloen, Charlotte W., Sanchez‐Lara, Pedro A., Kinning, Esther, Adams, Darius J., Treat, Kayla, Torres‐Martinez, Wilfredo, Bedeschi, Maria F., Iascone, Maria, Blaney, Stephanie, Bell, Oliver, Tan, Tiong Y., Delrue, Marie‐Ange, Jurgens, Julie, Barry, Brenda J., Engle, Elizabeth C., Savage, Sarah K., Fleischer, Nicole, Martinez‐Agosto, Julian A., Boycott, Kym, Zackai, Elaine H., Muenke, Maximilian

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Turner syndrome in diverse populations von Kruszka, Paul, Addissie, Yonit A., Tekendo‐Ngongang, Cedrik, Jones, Kelly L., Savage, Sarah K., Gupta, Neerja, Sirisena, Nirmala D., Dissanayake, Vajira H. W., Paththinige, C. Sampath, Aravena, Teresa, Nampoothiri, Sheela, Yesodharan, Dhanya, Girisha, Katta M., Patil, Siddaramappa Jagdish, Jamuar, Saumya Shekhar, Goh, Jasmine Chew‐Yin, Utari, Agustini, Sihombing, Nydia, Mishra, Rupesh, Chitrakar, Neer Shoba, Iriele, Brenda C., Lulseged, Ezana, Megarbane, Andre, Uwineza, Annette, Oyenusi, Elizabeth Eberechi, Olopade, Oluwarotimi Bolaji, Fasanmade, Olufemi Adetola, Duenas‐Roque, Milagros M., Thong, Meow‐Keong, Tung, Joanna Y. L., Mok, Gary T. K., Fleischer, Nicole, Rwegerera, Godfrey M., Herreros, María Beatriz, Watts, Johnathan, Fieggen, Karen, Huckstadt, Victoria, Moresco, Angélica, Obregon, María Gabriela, Hussen, Dalia Farouk, Ashaat, Neveen A., Ashaat, Engy A., Chung, Brian H. Y., Badoe, Eben, Faradz, Sultana M. H., El Ruby, Mona O., Shotelersuk, Vorasuk, Wonkam, Ambroise, Ekure, Ekanem Nsikak, Phadke, Shubha R., Richieri‐Costa, Antonio, Muenke, Maximilian

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Parents’ Preferences for Return of Results in Pediatric Genomic Research von Ziniel, S.I., Savage, S.K., Huntington, N., Amatruda, J., Green, R.C., Weitzman, E.R., Taylor, P., Holm, I.A.

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Family Health History Reporting is Sensitive to Small Changes in Wording von Conway-Pearson, Liam S, Christensen, Kurt D, Savage, Sarah K, Huntington, Noelle L, Weitzman, Elissa R, Ziniel, Sonja I, Bacon, Phoebe, Cacioppo, Cara N, Green, Robert C, Holm, Ingrid A

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Increased LIS1 expression affects human and mouse brain development: Making diversity count von WEIMIN BI, SAPIR, Tamar, NEZARATI, Marjan M, SHOTTS, Vern Ann, AMATO, Stephen S, SAVAGE, Sarah K, HARRIS, David J, DAY-SALVATORE, Debra-Lynn, HORNER, Michele, LU, Xin-Yan, SAHOO, Trilochan, YANAGAWA, Yuchio, SHCHELOCHKOV, Oleg A, BEAUDET, Arthur L, SAU WAI CHEUNG, MARTINEZ, Salvador, LUPSKI, James R, REINER, Orly, FENG ZHANG, WITHERS, Marjorie A, HUNTER, Jill V, LEVY, Talia, SHINDER, Vera, PEIFFER, Daniel A, GUNDERSON, Kevin L

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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease von Wightman, Douglas P., Jansen, Iris E., Savage, Jeanne E., Shadrin, Alexey A., Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S., Drange, Ole Kristian, Martinsen, Amy E., Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G., Thomas, Laurent F., Pedersen, Linda M., Gabrielsen, Maiken E., Johnsen, Marianne Bakke, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Hodges, Angela, Dobson, Richard, Velayudhan, Latha, Heilbron, Karl, Auton, Adam, Sealock, Julia M., Davis, Lea K., Pedersen, Nancy L., Reynolds, Chandra A., Karlsson, Ida K., Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V., Snaedal, Jon, Zettergren, Anna, Skoog, Ingmar, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Hveem, Kristian, Zwart, John-Anker, Athanasiu, Lavinia, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B., Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Selbæk, Geir, Ripke, Stephan, Stefansson, Kari, Andreassen, Ole A., Posthuma, Danielle

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Quantifying antibody kinetics and RNA detection during early-phase SARS-CoV-2 infection by time since symptom onset von Borremans, Benny, Gamble, Amandine, Prager, K C, Helman, Sarah K, McClain, Abby M, Cox, Caitlin, Savage, Van, Lloyd-Smith, James O

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