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

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.

Pediatrics - 1 Jan 2016

Joseph Galen, Chen Flavia, Harris-Wai Julie, Puck Jennifer M, Young Charlotte, Koenig Barbara A

Abstract excerpt

BACKGROUND AND OBJECTIVE: The potential application of whole-genome sequencing (WGS) to state-mandated standard newborn screening (NBS) challenges the traditional public health approach to NBS and raises ethical, policy, and clinical practice issues. This article examines the perspectives and values of diverse healthy pregnant women and parents of children diagnosed with a primary immunodeficiency disorder about...

Read the complete abstract on PubMed

Topics

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

Share to Attitude to Health
Share to Focus Groups
Share to Genetic Privacy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Storage and Retrieval

Share to Informed Consent

Share to Neonatal Screening

Share to Parents

Share to Patient Participation

Source

Open in PubMed Open full text

Identifiers

PMID: 26729702
DOI: 10.1542/peds.2015-3731H
PMCID: PMC4939888

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

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.PMID 26729702Read ↗

Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newbornsSemantic proximity Read ↗

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

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

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

Young Adults’ Attitudes Toward Pediatric Whole-Genome SequencingSemantic proximity Read ↗

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

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

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

Emerging Issues in Public Health GenomicsSemantic proximity Read ↗

Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?Semantic proximity Read ↗

Prenatal Whole Genome SequencingSemantic proximity Read ↗

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq StudySemantic proximity Read ↗

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