A deeper understanding of how DNA changes over generations helps scientists learn why people differ and how diseases develop. Until recently, many fast-changing parts of the human genome remained ...
For many scientists, the first glimpse of a DNA sequence—those colored peaks marking A, T, C, and G—sparked a lifelong fascination with the code that shapes us all. That same spirit of discovery ...
The number of people who have the gene that causes Huntington's disease in Northern Scotland has been accurately counted for the first time in 35 years in new research from the University of Aberdeen ...
Scientists at the Icahn School of Medicine at Mount Sinai and collaborators have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.
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