Baby DNA screening study aims to predict future health
NCT ID NCT05161169
First seen Nov 12, 2025 · Last updated May 25, 2026 · Updated 31 times
Summary
This study looked at whether whole genome sequencing can be used to screen healthy babies for genetic risks. Researchers enrolled 500 infants and their families from three U.S. cities. Half of the babies had their DNA sequenced, and results were shared with parents and doctors. The goal was to understand the medical, emotional, and financial impacts of this type of screening in routine care.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Beaumont - Corewell Health East
Royal Oak, Michigan, 48073, United States
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Boston Children's Hospital
Boston, Massachusetts, 02115, United States
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Icahn School of Medicine at Mount Sinai
New York, New York, 10029, United States
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University of Alabama at Birmingham
Birmingham, Alabama, 35294, United States
Conditions
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