Further Considerations on the Value of Whole-Genome Sequencing in Critically Ill Infants-Reference-Cited by-同舟云学术

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Further Considerations on the Value of Whole-Genome Sequencing in Critically Ill Infants

Published:2022-04-01 Issue:4 Volume:176 Page:421
ISSN:2168-6203
Container-title:JAMA Pediatrics
language:en
Short-container-title:JAMA Pediatr

Author:

Bhardwaj Umang¹,Endrakanti Mounika²,Gupta Neerja²

Affiliation:

1. Division of Neonatology, Department of Pediatrics, All India Institute of Medical Sciences, All India Institute Of Medical Science, New Delhi

2. Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, All India Institute Of Medical Science, New Delhi

Publisher

American Medical Association (AMA)

Subject

Pediatrics, Perinatology and Child Health

Link

https://jamanetwork.com/journals/jamapediatrics/articlepdf/2788908/jamapediatrics_bhardwaj_2022_le_210048_1648672941.66936.pdf

Reference4 articles.

1. Effect of whole-genome sequencing on the clinical management of acutely ill infants with suspected genetic disease: a randomized clinical trial.;Krantz;JAMA Pediatr,2021

2. A randomized, controlled trial of the analytic and diagnostic performance of singleton and trio, rapid genome and exome sequencing in ill infants.;Kingsmore;Am J Hum Genet,2019

3. Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.;Gubbels;Genet Med,2020

4. Seymour? CA, Thomason? MJ, Chalmers? RA, . Newborn screening for inborn errors of metabolism: a systematic review. Database of Abstracts of Reviews of Effects (DARE): Quality-assessed Reviews. Published 1997. Accessed October 24, 2021. https://www.ncbi.nlm.nih.gov/books/NBK66943/

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