The small study in patients with a rare disorder that causes liver and lung damage showed the potential for precisely ...

A recent review published in the journal Engineering delves into the significant advancements and potential of CRISPR ...

In Nature Neuroscience, UConn School of Medicine researchers have revealed a new scientific clue that could unlock the key ...

CDKL5, one of the five members of the CDKL family of genes, is important for proper neurodevelopment and associated with seizures. However, the role ...

Creation of a comprehensive genetic representation for more than 2.5 billion people across the Middle East and South Asia ...

Researchers at Washington University School of Medicine in St. Louis have uncovered why some patients with a rare genetic ...

Discover how the UAE's Genome Programme is revolutionizing premarital genetic screening, with 2,400 couples tested and 92% ...

Researchers at the University of Washington and Seattle Children's found that using exclusion-based criteria to refer infants ...

Danon disease is a rare but serious cardiomyopathy that drastically reduces life expectancy. Male patients infrequently live ...

Creation of a comprehensive genetic representation for more than 2.5 billion people across the Middle East and South Asia could make a major contribution towards advancing precision medicine.

The challenge of the obesity epidemic is widespread and one that even pediatricians face constantly,” a Connecticut doctor ...

Johns Hopkins scientists develop mRNA "booster" as potential new way to treat rare genetic diseases marked by too low levels ...