Critically Ill Neonates and Secondary Genomic Findings

This Perspective discusses whether secondary genomic findings in the clinical context of diagnostic genomic sequencing tests should be sought and reported.

Authors

Whitney S. Thompson (ORCID: https://orcid.org/0009-0000-5148-6379)
Bruce R. Korf (ORCID: https://orcid.org/0000-0001-8272-339X)
Laura M. Amendola (ORCID: https://orcid.org/0000-0002-5506-6168)
Monica A. Giovanni

Institutions

Mayo Clinic (US)
University of Alabama at Birmingham (US)

Publication Details

Journal: JAMA
Published: 2026-09-28
DOI: https://doi.org/10.1001/jama.2026.18687
Primary Topic: Genomics and Rare Diseases
Type: article
Field-Weighted Citation Impact: 0.00

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article

Critically Ill Neonates and Secondary Genomic Findings

Whitney S. Thompson, Bruce R. Korf, Laura M. Amendola, Monica A. Giovanni

Sep 28, 2026

JAMA

Genomics and Rare Diseases

article

Critically Ill Neonates and Secondary Genomic Findings

Whitney S. Thompson, Bruce R. Korf, Laura M. Amendola, Monica A. Giovanni

September 28, 2026article en

Abstract

This Perspective discusses whether secondary genomic findings in the clinical context of diagnostic genomic sequencing tests should be sought and reported.

JAMA

Mayo Clinic (US), University of Alabama at Birmingham (US)

Zero hunger

Openalex Percentile: Top 12%

Genomics and Rare Diseases

DOI Source OpenAlex

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