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

Whole-Genome Screening of Newborns? The Constitutional Boundaries of State Newborn Screening Programs.

Pediatrics - 1 Jan 2016

King Jaime S, Smith Monica E

Abstract excerpt

State newborn screening (NBS) programs routinely screen nearly all of the 4 million newborns in the United States each year for ∼30 primary conditions and a number of secondary conditions. NBS could be on the cusp of an unprecedented expansion as a result of advances in whole-genome sequencing (WGS). As WGS becomes cheaper and easier and as our knowledge and understanding of human genetics expand, the question of...

Read the complete abstract on PubMed

Topics

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

Share to Exome
Share to Genome, Human
Share to Health Policy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Nucleotide Sequencing

Share to Infant, Newborn

Share to Informed Consent

Share to Neonatal Screening

Share to United States

Source

Open in PubMed Open full text

Identifiers

PMID: 26729704
DOI: 10.1542/peds.2015-3731D
PMCID: PMC4939764

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole-Genome Screening of Newborns? The Constitutional Boundaries of State Newborn Screening Programs.PMID 26729704Read ↗

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

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

Genetics Professionals’ Opinions of Whole‐Genome Sequencing in the Newborn PeriodSemantic proximity Read ↗

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

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

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

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.Semantic proximity Read ↗

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

Genomic sequencing for newborn screening: current perspectives and challengesSemantic proximity Read ↗

Emerging Issues in Public Health GenomicsSemantic proximity Read ↗

Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be foundSemantic proximity Read ↗

Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates.Semantic proximity Read ↗

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