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

Genomic sequencing for newborn screening: current perspectives and challenges

1 Jun 2024

Abstract excerpt

Traditional newborn screening (NBS) serves as a critical tool in identifying conditions that may impact a child's health from an early stage. Newborn sequencing (NBSeq), the comprehensive analysis of an infant's genome, holds immense promise for revolutionizing health care throughout the lifespan. NBSeq allows for early detection of genetic disease risk and precision personalized medicine. The rapid evolution of...

Read the complete abstract on PubMed

Topics

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

Share to Cancer Genomics and Diagnostics
Share to Ethics in Clinical Research
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38868972
DOI: 10.3325/cmj.2024.65.261

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic sequencing for newborn screening: current perspectives and challengesPMID 38868972Read ↗

Newborn Screening by Genomic Sequencing: Opportunities and ChallengesSemantic proximity Read ↗

Genomic newborn screening: public health policy considerations and recommendations.Semantic proximity Read ↗

Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmesSemantic proximity Read ↗

From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programsSemantic proximity Read ↗

The Future of Newborn Genomic ScreeningSemantic proximity Read ↗

Whole-genome sequencing in newborn screening programs.Semantic proximity Read ↗

[Genomic newborn screening-research approaches, challenges, and opportunities].Semantic proximity Read ↗

A Genomic Sequencing Approach to Newborn Mass Screening and Its OpportunitiesSemantic proximity Read ↗

Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?Semantic proximity Read ↗

Ethical and Psychosocial Implications of Genomic Newborn ScreeningSemantic proximity Read ↗

Analytical Validation of a Genomic Newborn Screening WorkflowSemantic proximity Read ↗

Newborn screening and the era of medical genomics.Semantic proximity Read ↗

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