Should all healthy newborns get their DNA screened? study investigates
NCT ID NCT05161169
First seen Nov 12, 2025 · Last updated Jun 08, 2026 · Updated 34 times
Summary
This study looked at whether whole genome sequencing can help screen healthy babies for genetic health risks. Researchers enrolled 500 infants and their parents from three U.S. cities, took a small blood sample from each baby, and sequenced the DNA of half the group. After three months, they shared the results with families and doctors to study the medical, emotional, and financial effects of this approach.
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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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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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