Baby Badger Network ECHO Resources

Session Resources

• Didactic Presentation Slides
• Indications for ES-GS in Critically Ill Neonates

Articles

• Diaby, V, et al. Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United State.
• Dimmock, D, et al. Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children’s hospitals demonstrates improved clinical outcomes and reduced costs of care.
• Gubbels, CS, et al. Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.
• Kingsmore, SF, et al. Rapid genome sequencing for genetic disease diagnosis and therapy in intensive care units: a review.
• Kingsmore, SF & Sessions Cole, F. The Role of Genome Sequencing in Neonatal Intensive Care Units.
• Lemke, AA, et al. Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit.
• Muriello, M. Exome and Whole Genome Sequencing in the Neonatal Intensive Care Unit.
• Muriello, M & Basel, D. Rapid Exome and Genome Sequencing in the Intensive Care Unit.
• Sanford Kobayashi, E, et al. Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit.
• Smith, EE, et al. Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
• Srivastava, S, et al. Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.

Session Resources

• Didactic Presentation Slides
• Center for Special Children Brochure
• Plain Community Health Consortium
• Amish, Mennonite and Hutterite Genetic Disorder Database
• Windows of Hope Project

Other Resources

• • Evidence-Based Guidelines Webinar Series 101: Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disabilities – Murugu Manickam MD, MPH, FACGMG