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

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions

26 Apr 2020

Abstract excerpt

No abstract is available from the source.

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 Metabolism and Genetic Disorders
Share to Neurogenetic and Muscular Disorders Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32336750
DOI: 10.1038/s41436-020-0798-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditionsPMID 32336750Read ↗

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

Rapid exome sequencing in critically ill children impacts acute and long-term management of patients and their families: A retrospective regional evaluationSemantic proximity Read ↗

The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill ChildrenSemantic proximity Read ↗

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

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

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

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testingSemantic proximity Read ↗

Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the NetherlandsSemantic proximity Read ↗

Whole-Exome Sequencing in Critically Ill Neonates and Infants: Diagnostic Yield and Predictability of Monogenic Diagnosis.Semantic proximity Read ↗

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

Singleton rapid long-read genome sequencing as first tier genetic test for critically Ill children with suspected genetic diseasesSemantic proximity Read ↗

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disordersSemantic proximity Read ↗

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