The role of exome sequencing in newborn screening for inborn errors of metabolism von Adhikari, Aashish N., Gallagher, Renata C., Wang, Yaqiong, Currier, Robert J., Amatuni, George, Bassaganyas, Laia, Chen, Flavia, Kundu, Kunal, Kvale, Mark, Mooney, Sean D., Nussbaum, Robert L., Randi, Savanna S., Sanford, Jeremy, Shieh, Joseph T., Srinivasan, Rajgopal, Sunderam, Uma, Tang, Hao, Vaka, Dedeepya, Zou, Yangyun, Koenig, Barbara A., Kwok, Pui-Yan, Risch, Neil, Puck, Jennifer M., Brenner, Steven E.

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Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies von Johnston, Josephine, Lantos, John D., Goldenberg, Aaron, Chen, Flavia, Parens, Erik, Koenig, Barbara A.

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Wang Wei e o Mistério do Musgo Verde Azulado von Menezes Junior, Antônio José Bezerra de, Chen Chen, Flávia

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Wang Wei e o Mistério do Musgo Verde Azulado von Menezes Junior, Antônio José Bezerra de, Chen Chen, Flávia

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Wang Wei and the Mistery of the Blue-Green Moss von Antônio José Bezerra de Menezes Junior, Flávia Chen Chen

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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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Newborn Sequencing in Genomic Medicine and Public Health von Berg, Jonathan S, Agrawal, Pankaj B, Bailey, Jr, Donald B, Beggs, Alan H, Brenner, Steven E, Brower, Amy M, Cakici, Julie A, Ceyhan-Birsoy, Ozge, Chan, Kee, Chen, Flavia, Currier, Robert J, Dukhovny, Dmitry, Green, Robert C, Harris-Wai, Julie, Holm, Ingrid A, Iglesias, Brenda, Joseph, Galen, Kingsmore, Stephen F, Koenig, Barbara A, Kwok, Pui-Yan, Lantos, John, Leeder, Steven J, Lewis, Megan A, McGuire, Amy L, Milko, Laura V, Mooney, Sean D, Parad, Richard B, Pereira, Stacey, Petrikin, Joshua, Powell, Bradford C, Powell, Cynthia M, Puck, Jennifer M, Rehm, Heidi L, Risch, Neil, Roche, Myra, Shieh, Joseph T, Veeraraghavan, Narayanan, Watson, Michael S, Willig, Laurel, Yu, Timothy W, Urv, Tiina, Wise, Anastasia L

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Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing von Joseph, Galen, Chen, Flavia, Harris-Wai, Julie, Puck, Jennifer M, Young, Charlotte, Koenig, Barbara A

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904: Agreement to secondary findings with exome sequencing in pre- and postnatal settings von Sparks, Teresa N., Chen, Flavia, Rego, Shannon, Lianoglou, Billie R., Patel, Sachi, Slavotinek, Anne M., Koenig, Barbara, Norton, Mary E.

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Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification von Bassaganyas, Laia, Freedman, George, Vaka, Dedeepya, Wan, Eunice, Lao, Richard, Chen, Flavia, Kvale, Mark, Currier, Robert J., Puck, Jennifer M., Kwok, Pui‐Yan

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Preference for secondary findings in prenatal and pediatric exome sequencing von Swanson, Kate, Sparks, Teresa N., Lianoglou, Billie R., Chen, Flavia, Downum, Sarah, Patel, Sachi, Rego, Shannon, Yip, Tiffany, Ziffle, Jessica, Koenig, Barbara A., Slavotinek, Anne M., Norton, Mary E.

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Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach von Rego, Shannon, Hoban, Hannah, Outram, Simon, Zamora, Astrid N., Chen, Flavia, Sahin-Hodoglugil, Nuriye, Anguiano, Beatriz, Norstad, Matthew, Yip, Tiffany, Lianoglou, Billie, Sparks, Teresa N., Norton, Mary E., Koenig, Barbara A., Slavotinek, Anne M., Ackerman, Sara L.

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Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods von Ferket, Bart S., Baldwin, Zach, Murali, Priyanka, Pai, Akila, Mittendorf, Kathleen F., Russell, Heidi V., Chen, Flavia, Lynch, Frances L., Lich, Kristen Hassmiller, Hindorff, Lucia A., Savich, Renate, Slavotinek, Anne, Smith, Hadley Stevens, Gelb, Bruce D., Veenstra, David L.

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Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies von Johnston, Josephine, Lantos, John D., Goldenberg, Aaron, Chen, Flavia, Parens, Erik, Koenig, Barbara A.

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Characteristics of upper-extremity reactions to sudden lateral loss of balance in persons with stroke von Handelzalts, Shirley, Steinberg-Henn, Flavia, Soroker, Nachum, Shani, Guy, Melzer, Itshak

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Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population von Slavotinek, Anne, Rego, Shannon, Sahin-Hodoglugil, Nuriye, Kvale, Mark, Lianoglou, Billie, Yip, Tiffany, Hoban, Hannah, Outram, Simon, Anguiano, Beatrice, Chen, Flavia, Michelson, Jeremy, Cilio, Roberta M., Curry, Cynthia, Gallagher, Renata C., Gardner, Marisa, Kuperman, Rachel, Mendelsohn, Bryce, Sherr, Elliott, Shieh, Joseph, Strober, Jonathan, Tam, Allison, Tenney, Jessica, Weiss, William, Whittle, Amy, Chin, Garrett, Faubel, Amanda, Prasad, Hannah, Mavura, Yusuph, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Sparks, Teresa N., Koenig, Barbara, Ackerman, Sara, Risch, Neil, Kwok, Pui-Yan, Norton, Mary E.

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Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium von Gutierrez, Amanda M, Robinson, Jill O, Outram, Simon M, Smith, Hadley S, Kraft, Stephanie A, Donohue, Katherine E, Biesecker, Barbara B, Brothers, Kyle B, Chen, Flavia, Hailu, Benyam, Hindorff, Lucia A, Hoban, Hannah, Hsu, Rebecca L, Knight, Sara J, Koenig, Barbara A, Lewis, Katie L, Lich, Kristen Hassmiller, O'Daniel, Julianne M, Okuyama, Sonia, Tomlinson, Gail E, Waltz, Margaret, Wilfond, Benjamin S, Ackerman, Sara L, Majumder, Mary A

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Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population von Slavotinek, Anne, Rego, Shannon, Sahin-Hodoglugil, Nuriye, Kvale, Mark, Lianoglou, Billie, Yip, Tiffany, Hoban, Hannah, Outram, Simon, Anguiano, Beatrice, Chen, Flavia, Michelson, Jeremy, Cilio, Roberta M., Curry, Cynthia, Gallagher, Renata C., Gardner, Marisa, Kuperman, Rachel, Mendelsohn, Bryce, Sherr, Elliott, Shieh, Joseph, Strober, Jonathan, Tam, Allison, Tenney, Jessica, Weiss, William, Whittle, Amy, Chin, Garrett, Faubel, Amanda, Prasad, Hannah, Mavura, Yusuph, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Sparks, Teresa N., Koenig, Barbara, Ackerman, Sara, Risch, Neil, Kwok, Pui-Yan, Norton, Mary E.

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Surrogate Pregnancy After Prenatal Diagnosis of Spina Bifida von Mazur, Lynnette J, Kisthardt, Mary Kay, Kim, Helen H, Rosas, Laura M, Lantos, John D

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FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation von Milko, Laura V, Chen, Flavia, Chan, Kee, Brower, Amy M, Agrawal, Pankaj B, Beggs, Alan H, Berg, Jonathan S, Brenner, Steven E, Holm, Ingrid A, Koenig, Barbara A, Parad, Richard B, Powell, Cynthia M, Kingsmore, Stephen F

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