Researchers led by the University of Vienna and Liège University Hospital Center have identified genetic variants associated ...

A double burial found in southern Italy more than 60 years ago has just yielded a striking new secret: ancient DNA has confirmed a rare inherited form of dwarfism in a teenage girl who lived around 12 ...

A "gene silencer" (technically known as small interfering RNA, or siRNA), locally delivered by nanoparticles embedded in an ...

Gene-editing tools like CRISPR have unlocked new treatments for previously uncurable diseases. Now, researchers at the ...

Explore the groundbreaking study on mini-stomach organoids that replicate human stomach regions for advanced research.

Editor’s note: This article has been updated to remove some incorrect statistics provided by the nonprofit n-Lorem regarding their treatment of the disease. MADISON, Ala. (WHNT) — As a parent, you ...

Two Virginia siblings share a rare genetic disorder. A National Institutes of Health doctor and a global donor network now give their family hope.

GOLDSBORO, N.C. (WITN) - A Goldsboro family is sharing their story and asking for community support as they raise their two-year-old son, diagnosed with a rare genetic disorder. Declan Newberry was ...

AlphaGenome is a DNA sequence model that advances regulatory variant-effect prediction to understand genome function.

The number of cases in Malaysia is very small. However, the risk still exists, particularly for parents with a family history ...

Add Yahoo as a preferred source to see more of our stories on Google. Maddox was born completely healthy, while his sister Emery is fighting an extremely rare genetic mutation. Mailbag: With Kayla ...