Expanding newborn screening through genomics

WGS in NBS has the potential to improve outcomes for children and families by enabling earlier diagnosis and intervention. Nurse practitioners, as frontline providers in primary care and pediatrics, are uniquely positioned to support families through genomic education, ethical decision making, and care navigation. Building workforce genomic competency and advocating for equitable policies are critical to realizing the promise of genomic NBS in clinical practice.

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Publication Details

Journal
Journal of the American Association of Nurse Practitioners
Published
2026-02-01
DOI
https://doi.org/10.1097/jxx.0000000000001235
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Expanding newborn screening through genomics

Laurie M. Connors
Journal of the American Association of Nurse Practitioners
Genomics and Rare Diseases
article

Expanding newborn screening through genomics

Laurie M. Connors
article en

Abstract

WGS in NBS has the potential to improve outcomes for children and families by enabling earlier diagnosis and intervention. Nurse practitioners, as frontline providers in primary care and pediatrics, are uniquely positioned to support families through genomic education, ethical decision making, and care navigation. Building workforce genomic competency and advocating for equitable policies are critical to realizing the promise of genomic NBS in clinical practice.

Journal of the American Association of Nurse PractitionersVol. 38(2)
University of South Florida (US)
Openalex Percentile: Top 62%
Genomics and Rare Diseases
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Expanding newborn screening through genomics — Laurie M. Connors · Journal of the American Association of Nurse Practitioners (2026) | TGRS Research Map | TGRS