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

Rapid genomic sequencing in the NICU: Who to test and why

6 Aug 2026

Abstract excerpt

Accessibility of rapid genomic sequencing (rGS), including rapid whole-exome sequencing (rWES) and rapid whole-genome sequencing (rWGS), is transforming care in neonatal intensive care units (NICUs) by enabling timely and precise diagnoses of genetic disorders with high diagnostic yield and significant impact on clinical management. However, determining which infants should undergo sequencing remains a major...

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 42562942
DOI: 10.1038/s41431-026-02207-6

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

Rapid genomic sequencing in the NICU: Who to test and whyPMID 42562942Read ↗

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

Clinical Utility of Rapid Whole Genome Sequencing in Neonatal Patients Receiving Extracorporeal Membrane Oxygenation (ECMO)Semantic proximity Read ↗

Integrating rapid exome sequencing into NICU clinical care after a pilot research studySemantic proximity Read ↗

Rapid genome sequencing for critically ill infants: an inaugural pilot study from TurkeySemantic proximity Read ↗

Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseasesSemantic proximity Read ↗

The NSIGHT1 Randomized Controlled Trial: Rapid Whole Genome Sequencing for Accelerated Etiologic Diagnosis in Critically Ill InfantsSemantic proximity Read ↗

Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder.Semantic proximity Read ↗

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

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseasesSemantic proximity Read ↗

Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.Semantic proximity Read ↗

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

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

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