An oversight regarding the club cell? von Parad, Richard B.

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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report von Farrell, Philip M., MD, PhD, Rosenstein, Beryl J., MD, White, Terry B., PhD, Accurso, Frank J., MD, Castellani, Carlo, MD, Cutting, Garry R., MD, Durie, Peter R., MD, FRCP, LeGrys, Vicky A., DrA, CLS, Massie, John, MBBS, FRACP, PhD, Parad, Richard B., MD, MPH, Rock, Michael J., MD, Campbell, Preston W., MD

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Non-sedation of the neonate for radiologic procedures von Parad, Richard B.

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Diagnosis of Cystic Fibrosis in Screened Populations von Farrell, Philip M., MD, PhD, White, Terry B., PhD, Howenstine, Michelle S., MD, Munck, Anne, MD, Parad, Richard B., MD, MPH, Rosenfeld, Margaret, MD, MPH, Sommerburg, Olaf, MD, Accurso, Frank J., MD, Davies, Jane C., MBChB, FRCPCH, MD, Rock, Michael J., MD, Sanders, Don B., MD, MS, Wilschanski, Michael, MBBS, Sermet-Gaudelus, Isabelle, MD, PhD, Blau, Hannah, MBBS, Gartner, Silvia, MD, McColley, Susanna A., MD

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A curated gene list for reporting results of newborn genomic sequencing von Ceyhan-Birsoy, Ozge, Machini, Kalotina, Lebo, Matthew S., Yu, Tim W., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy, Green, Robert C., Beggs, Alan H., Rehm, Heidi L.

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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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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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Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield von Gubbels, Cynthia S., VanNoy, Grace E., Madden, Jill A., Copenheaver, Deborah, Yang, Sandra, Wojcik, Monica H., Gold, Nina B., Genetti, Casie A., Stoler, Joan, Parad, Richard B., Roumiantsev, Sergei, Bodamer, Olaf, Beggs, Alan H., Juusola, Jane, Agrawal, Pankaj B., Yu, Timothy W.

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Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis von Borowitz, Drucy, MD, Robinson, Karen A., PhD, Rosenfeld, Margaret, MD, MPH, Davis, Stephanie D., MD, Sabadosa, Kathryn A., MPH, Spear, Stephanie L., PhD, Michel, Suzanne H., MPH, RD, LDN, Parad, Richard B., MD, MPH, White, Terry B., PhD, Farrell, Philip M., MD, PhD, Marshall, Bruce C., MD, Accurso, Frank J., MD

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Implementation of Hospital-Based Supplemental Duchenne Muscular Dystrophy Newborn Screening (sDMDNBS): A Pathway to Broadening Adoption von Parad, Richard B., Sheldon, Yvonne, Bhattacharjee, Arindam

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Specificity of International Classification of Diseases codes for bronchopulmonary dysplasia: an investigation using electronic health record data and a large insurance database von Beam, Kristyn S., Lee, Matthew, Hirst, Keith, Beam, Andrew, Parad, Richard B.

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Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project von Green, Robert C., Shah, Nidhi, Genetti, Casie A., Yu, Timothy, Zettler, Bethany, Uveges, Melissa K., Ceyhan-Birsoy, Ozge, Lebo, Matthew S., Pereira, Stacey, Agrawal, Pankaj B., Parad, Richard B., McGuire, Amy L., Christensen, Kurt D., Schwartz, Talia S., Rehm, Heidi L., Holm, Ingrid A., Beggs, Alan H.

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Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Tw... von Borowitz, Drucy, MD, Parad, Richard B., MD, MPH, Sharp, Jack K., MD, CM, Sabadosa, Kathryn A., MPH, Robinson, Karen A., PhD, Rock, Michael J., MD, Farrell, Philip M., MD, PhD, Sontag, Marci K., PhD, Rosenfeld, Margaret, MD, MPH, Davis, Stephanie D., MD, Marshall, Bruce C., MD, Accurso, Frank J., MD

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Abdominal ultrasound findings contribute to a multivariable predictive risk score for surgical necrotizing enterocolitis: A pilot study von Lazow, Stefanie P., Tracy, Sarah A., Staffa, Steven J., Estroff, Judy A., Parad, Richard B., Castro-Aragon, Ilse M., Fujii, Alan M., Zurakowski, David, Chen, Catherine

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Genetic counseling access for parents of newborns who screen positive for cystic fibrosis: Consensus guidelines von Langfelder‐Schwind, Elinor, Raraigh, Karen S., Parad, Richard B., Balcom, Jessica R., Birnbaum, Virginia K., Darrah, Rebecca, Farrell, Philip M., Foil, Kimberly, Ghate, Sumedha, Greene, Lisa, Gutierrez, Hector, Hopfer, Sidney, McColley, Susanna A., Lurie, Robert H., Nasr, Samya Z., Ren, Clement L., Salinas, Danieli B., Siracusa, Christopher, Taylor, Erin, Temme, Renee, Tluczek, Audrey

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Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project von Pereira, Stacey, Gutierrez, Amanda M., Robinson, Jill Oliver, Christensen, Kurt D., Genetti, Casie A., Blout Zawatsky, Carrie L., Hsu, Rebecca L., Zettler, Bethany, Uveges, Melissa Kurtz, Parad, Richard B., Beggs, Alan H., Holm, Ingrid A., Green, Robert C., McGuire, Amy L.

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Development of DNA Confirmatory and High-Risk Diagnostic Testing for Newborns Using Targeted Next-Generation DNA Sequencing von Bhattacharjee, Arindam, Sokolsky, Tanya, Wyman, Stacia K., Reese, Martin G., Puffenberger, Erik, Strauss, Kevin, Morton, Holmes, Parad, Richard B., Naylor, Edwin W.

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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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Urine Proteomics for Noninvasive Monitoring of Biomarkers in Bronchopulmonary Dysplasia von Ahmed, Saima, Odumade, Oludare A., van Zalm, Patrick, Smolen, Kinga K., Fujimura, Kimino, Muntel, Jan, Rotunno, Melissa S., Winston, Abigail B., Steen, Judith A., Parad, Richard B., Van Marter, Linda J., Kourembanas, Stella, Steen, Hanno

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Differences in clinical and laboratory biomarkers for short and long‐term respiratory outcomes in preterm neonates von Parad, Richard B., Breeze, Janis L., Terrin, Norma, Rogers, Lynette K., Salafia, Carolyn M., Greenough, Anne, Davis, Jonathan M.

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