Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?

12 Jun 2018

Abstract excerpt

Diagnostic genome-wide sequencing (exome or genome sequencing and data analysis for high-penetrance disease-causing variants) in acutely ill infants appears to be clinically useful, but the value of this diagnostic test should be rigorously demonstrated before it is accepted as a standard of care. This white paper was developed by the Paediatric Task Team of the Global Alliance for Genomics and Health's...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genomics and Rare Diseases
Share to Neonatal Respiratory Health Research
Share to Neurogenetic and Muscular Disorders Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29895853
DOI: 10.1038/s41436-018-0055-z

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?PMID 29895853Read ↗

Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.Semantic proximity Read ↗

Rapid Whole Genome Sequencing in Critically Ill Neonates Enables Precision Medicine PipelineSemantic proximity Read ↗

Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a reviewSemantic proximity Read ↗

Rapid genomic sequencing in the NICU: Who to test and whySemantic proximity Read ↗

Rapid Whole Genome Sequencing Decreases Morbidity and Healthcare Cost of Hospitalized InfantsSemantic proximity Read ↗

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditionsSemantic proximity Read ↗

Genome sequencing as a first-line diagnostic test for hospitalized newbornsSemantic proximity Read ↗

Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infantSemantic proximity Read ↗

The Future of Newborn Genomic ScreeningSemantic proximity Read ↗

Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic EvaluationSemantic proximity Read ↗

The Role of Genome Sequencing in Neonatal Intensive Care UnitsSemantic proximity Read ↗

Use of Exome Sequencing for Infants in Intensive Care UnitsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.