NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders by Kee Chan, Zhanzhi Hu, Lynn W. Bush, Heidi Cope, Ingrid A. Holm, Stephen F. Kingsmore, Kevin Wilhelm, Curt Scharfe, Amy Brower

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Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system by Erika T. Allred, Erika T. Allred, Elliot A. Perens, Nicole G. Coufal, Nicole G. Coufal, Erica Sanford Kobayashi, Erica Sanford Kobayashi, Stephen F. Kingsmore, David P. Dimmock

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Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting by Lauren Thompson, Austin Larson, Austin Larson, Lisa Salz, Regan Veith, John-Paul Tsai, Anuj Jayakar, Rachel Chapman, Rachel Chapman, Apeksha Gupta, Stephen F. Kingsmore, David Dimmock, Alan Bedrick, Alan Bedrick, Maureen Kelly Galindo, Kari Casas, Mohamed Mohamed, Lisa Straight, M. Akram Khan, Daria Salyakina

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Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit by Erica Sanford Kobayashi, Erica Sanford Kobayashi, Bryce Waldman, Branden M. Engorn, Katherine Perofsky, Katherine Perofsky, Erika Allred, Erika Allred, Benjamin Briggs, Chelsea Gatcliffe, Nanda Ramchandar, Nanda Ramchandar, Jeffrey J. Gold, Jeffrey J. Gold, Ami Doshi, Ami Doshi, Elizabeth G. Ingulli, Courtney D. Thornburg, Courtney D. Thornburg, Wendy Benson, Lauge Farnaes, Shimul Chowdhury, Seema Rego, Charlotte Hobbs, Stephen F. Kingsmore, David P. Dimmock, Nicole G. Coufal, Nicole G. Coufal, Nicole G. Coufal

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