Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project von Pereira, Stacey, Robinson, Jill Oliver, Gutierrez, Amanda M, Petersen, Devan K, Hsu, Rebecca L, Lee, Caroline H, Schwartz, Talia S, Holm, Ingrid A, Beggs, Alan H, Green, Robert C, McGuire, Amy L

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Rediscovering Apollo Biomedical Data to Support Artemis: The Apollo Records Synthesis Project von Beaton, Robert S, Wheeler, Brenna K, Jorgensen, Sara C, Charvat, Jacqueline M, Petersen, Devan K, Keune, Jessica A

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Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project von Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Guiterrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

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Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project von Wojcik, Monica H., Zhang, Tian, Ceyhan-Birsoy, Ozge, Genetti, Casie A., Lebo, Matthew S., Yu, Timothy W., Parad, Richard B., Holm, Ingrid A., Rehm, Heidi L., Beggs, Alan H., Green, Robert C., Agrawal, Pankaj B., Agrawal, Pankaj B., Betting, Wendi N., Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Graham, Chet, Guiterrez, Amanda M., Harden, Maegan, Krier, Joel B., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E.

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Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project von Genetti, Casie A., Schwartz, Talia S., Robinson, Jill O., VanNoy, Grace E., Petersen, Devan, Pereira, Stacey, Fayer, Shawn, Peoples, Hayley A., Agrawal, Pankaj B., Betting, Wendi N., Holm, Ingrid A., McGuire, Amy L., Waisbren, Susan E., Yu, Timothy W., Green, Robert C., Beggs, Alan H., Parad, Richard B.

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The BabySeq project: implementing genomic sequencing in newborns von Holm, Ingrid A, Agrawal, Pankaj B, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Fayer, Shawn, Frankel, Leslie A, Genetti, Casie A, Krier, Joel B, LaMay, Rebecca C, Levy, Harvey L, McGuire, Amy L, Parad, Richard B, Park, Peter J, Pereira, Stacey, Rehm, Heidi L, Schwartz, Talia S, Waisbren, Susan E, Yu, Timothy W, Green, Robert C, Beggs, Alan H

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Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project von Holm, Ingrid A, McGuire, Amy, Pereira, Stacey, Rehm, Heidi, Green, Robert C, Beggs, Alan H

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Family genetic risk communication and reverse cascade testing in the BabySeq project von Uveges, Melissa K., Smith, Hadley Stevens, Pereira, Stacey, Genetti, Casie, McGuire, Amy L., Beggs, Alan H., Green, Robert C., Holm, Ingrid A., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Gutierrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Lee, Kaitlyn B., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen Dolphyn, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill Oliver, Roumiantsev, Sergei, Schwartz, Talia S., Smith, Hadley Stevens, Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W., Blout Zawatsky, Carrie L., Zettler, Bethany

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Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study von Armstrong, Brittan, Christensen, Kurt D, Genetti, Casie A, Parad, Richard B, Robinson, Jill Oliver, Blout Zawatsky, Carrie L, Zettler, Bethany, Beggs, Alan H, Holm, Ingrid A, Green, Robert C, McGuire, Amy L, Smith, Hadley Stevens, Pereira, Stacey

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Challenging the Current Recommendations for Carrier Testing in Children von VanNoy, Grace E, Genetti, Casie A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Holm, Ingrid A

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Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report von Murry, Jaclyn B, Machini, Kalotina, Ceyhan-Birsoy, Ozge, Kritzer, Amy, Krier, Joel B, Lebo, Matthew S, Fayer, Shawn, Genetti, Casie A, VanNoy, Grace E, Yu, Timothy W, Agrawal, Pankaj B, Parad, Richard B, Holm, Ingrid A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Rehm, Heidi L

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