Baylor College of Medicine researchers are part of a collaborative research group with AstraZeneca and Memorial Sloan ...
UCLA Health researchers have created a comprehensive map showing how eight different genetic mutations associated with autism ...
Structural variants (SVs) are alterations in the DNA sequence that involve large-scale changes, typically longer than 50 base pairs. Advances in long-read sequencing have significantly increased ...
By studying genetic data from nearly 140,000 IVF embryos, scientists have with unprecedented detail revealed why fewer than ...
Scientists have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect. Scientists at the Icahn School of Medicine at Mount Sinai and ...
Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study. Certain common genetic changes might make some people with ...
Researchers from Johns Hopkins University and the University of Copenhagen analyzed over 139,000 embryos and identified variants in key meiosis genes, such as SMC1B, that influence chromosomal ...
A virus that infects nearly all children early in life has, in rare cases, been present within human DNA for thousands of ...
The research, published in Science, argues that the true genetic contribution to the variation in human lifespan has been masked. A genetic contribution of 55% aligns far more closely with what has ...
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