Massive 32,000-Person study seeks genetic clues to common birth heart defects
NCT ID NCT01196182
Summary
This study aims to understand the genetic causes of congenital heart defects (CHD), which are common and serious birth abnormalities. Researchers are collecting DNA samples and detailed health information from 32,000 participants, including children with CHD and their families. The goal is to find genetic patterns linked to these heart conditions and see how genes influence a person's health journey, but this is an observational study and does not test treatments.
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Contacts and locations
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Locations
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Brigham & Women's Hospital
Boston, Massachusetts, 02115, United States
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Children's Healthcare of Atlanta
Atlanta, Georgia, 30342, United States
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Children's Hospital Boston
Boston, Massachusetts, 02115, United States
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Children's Hospital Los Angeles
Los Angeles, California, 90027, United States
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Children's Hospital Philadelphia
Philadelphia, Pennsylvania, 19104, United States
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Cohen Children's Medical Center New York
New Hyde Park, New York, 11040, United States
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Columbia University Medical Center
New York, New York, 10032, United States
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Mount Sinai School of Medicine
New York, New York, 10029, United States
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Stanford University
Palo Alto, California, 94304, United States
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University College London
London, WC1N3JH, United Kingdom
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University of California, San Francisco
San Francisco, California, 94158, United States
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University of Michigan Health
Ann Arbor, Michigan, 48109, United States
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University of Rochester
Rochester, New York, 14642, United States
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University of Utah
Salt Lake City, Utah, 84113, United States
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Yale University
New Haven, Connecticut, 06520, United States
Conditions
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