Large international study uncovers genes involved in heart disease

3D render of a medical background with DNA strands

Over the past 15 years, more than 200 sites in the human genome have been linked to risk for coronary artery disease (CAD), the leading cause of death worldwide. Still, researchers don’t fully understand how those genomic variations alter the function of proteins, cells, or tissues to cause illness—knowledge that could inform the development of new treatments.

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