[HTML][HTML] Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse …

CCY Chung, SPY Hue, NYT Ng, PHL Doong… - Genetics in …, 2023 - Elsevier
Purpose This meta-analysis aims to compare the diagnostic and clinical utility of exome
sequencing (ES) vs genome sequencing (GS) in pediatric and adult patients with rare …

Rapid genomic testing for critically ill children: time to become standard of care?

Z Stark, S Ellard - European Journal of Human Genetics, 2022 - nature.com
Rapid genomic testing in critically ill neonatal and paediatric patients has transformed the
paradigm of rare disease diagnosis, delivering results in real time to inform patient …

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American …

K Manickam, MR McClain, LA Demmer, S Biswas… - Genetics in …, 2021 - nature.com
Purpose To develop an evidence-based clinical practice guideline for the use of exome and
genome sequencing (ES/GS) in the care of pediatric patients with one or more congenital …

[HTML][HTML] A randomized, controlled trial of the analytic and diagnostic performance of singleton and trio, rapid genome and exome sequencing in ill infants

SF Kingsmore, JA Cakici, MM Clark… - The American Journal of …, 2019 - cell.com
The second Newborn Sequencing in Genomic Medicine and Public Health study was a
randomized, controlled trial of the effectiveness of rapid whole-genome or-exome …

An RCT of rapid genomic sequencing among seriously ill infants results in high clinical utility, changes in management, and low perceived harm

DP Dimmock, MM Clark, M Gaughran, JA Cakici… - The American Journal of …, 2020 - cell.com
Summary The second Newborn Sequencing in Genomic Medicine and Public Health
(NSIGHT2) study was a randomized, controlled trial of rapid whole-genome sequencing …

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

MM Clark, A Hildreth, S Batalov, Y Ding… - Science translational …, 2019 - science.org
By informing timely targeted treatments, rapid whole-genome sequencing can improve the
outcomes of seriously ill children with genetic diseases, particularly infants in neonatal and …

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

CE French, I Delon, H Dolling, A Sanchis-Juan… - Intensive care …, 2019 - Springer
Purpose With growing evidence that rare single gene disorders present in the neonatal
period, there is a need for rapid, systematic, and comprehensive genomic diagnoses in ICUs …

Feasibility of ultra-rapid exome sequencing in critically ill infants and children with suspected monogenic conditions in the Australian public health care system

S Lunke, S Eggers, M Wilson, C Patel, CP Barnett… - Jama, 2020 - jamanetwork.com
Importance Widespread adoption of rapid genomic testing in pediatric critical care requires
robust clinical and laboratory pathways that provide equitable and consistent service across …

Rapid whole genome sequencing has clinical utility in children in the PICU

EF Sanford, MM Clark, L Farnaes… - Pediatric Critical Care …, 2019 - journals.lww.com
Objectives: Genetic disorders are a leading contributor to mortality in the neonatal ICU and
PICU in the United States. Although individually rare, there are over 6,200 single-gene …

[HTML][HTML] Integrating genomics into healthcare: a global responsibility

Z Stark, L Dolman, TA Manolio, B Ozenberger… - The American Journal of …, 2019 - cell.com
Genomic sequencing is rapidly transitioning into clinical practice, and implementation into
healthcare systems has been supported by substantial government investment, totaling over …