Applying Genomic Medicine to Critically Ill Children, Science and Fiction
- PMID: 39101801
- DOI: 10.1097/PCC.0000000000003548
Applying Genomic Medicine to Critically Ill Children, Science and Fiction
Conflict of interest statement
The authors have disclosed that they do not have any potential conflicts of interest.
References
-
- Collins FS, McKusick VA: Implications of the Human Genome Project for medical science. JAMA. 2001; 285:540–544
-
- Krantz ID, Medne L, Weatherly JM, et al.; NICUSeq Study Group: Effect of whole-genome sequencing on the clinical management of acutely ill infants with suspected genetic disease: A randomized clinical trial [published correction appears in JAMA Pediatr . 2021 December 1;175(12):1295]. JAMA Pediatr. 2021; 175:1218–1226
-
- Rodriguez KM, Vaught J, Salz L, et al.: Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multi-Center Cohort, 2016–2023. Pediatr Crit Care Med. 2024; 25:699–709
-
- Wu ET, Hwu WL, Chien YH, et al.: Critical trio exome benefits in-time decision-making for pediatric patients with severe illnesses. Pediatr Crit Care Med. 2019; 20:1021–1026
-
- Lunke S, Eggers S, Wilson M, et al.; Australian Genomics Health Alliance Acute Care Flagship: Feasibility of ultra-rapid exome sequencing in critically ill infants and children with suspected monogenic conditions in the Australian public health care system. JAMA. 2020; 323:2503–2511
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