Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementation
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference5 articles.
1. Sources of unease about the use of genome sequencing for diagnosing rare diseases in children;Lantos;J Pediatr,2021
2. Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care;Dimmock;Am J Hum Genet,2021
3. Implementing rapid whole-genome sequencing in critical care: a qualitative study of facilitators and barriers to new technology adoption;Franck;J Pediatr,2021
4. An RCT of rapid genomic sequencing among seriously ill infants results in high clinical utility, changes in management, and low perceived harm;Dimmock;Am J Hum Genet,2020
5. A prospective study of parental perceptions of rapid whole-genome and -exome sequencing among seriously ill infants;Cakici;Am J Hum Genet,2020
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1. Rapid Whole-Genome Sequencing in Acutely Ill Children: A Single Pediatric Center Experience;Journal of Pediatric Intensive Care;2024-09-11
2. A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care Unit;2024-07-07
3. Perspectives of Rare Disease Experts on Newborn Genome Sequencing;JAMA Network Open;2023-05-08
4. Rapid Genetic Testing in Pediatric and Neonatal Critical Care: A Scoping Review of Emerging Ethical Issues;Hospital Pediatrics;2022-09-26
5. Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children;Genetics in Medicine;2022-05
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