US infant KJ Muldoon makes history as first patient treated with personalized gene-editing, offering hope for rare illnesses.

Retinoblastoma is a rare eye cancer affecting young children, and early detection is the key to saving both vision and ...

Rapidly mutating DNA regions were mapped using a multi-generational family and advanced sequencing tools. Understanding how ...

After losing her two babies, Danielle Green wants genetic testing introduced in the post-mortem investigations of young ...

A groundbreaking genetic study traces the migration of Indigenous Americans from Asia, unveiling their ancestral origins and ...

A new AI model developed by researchers at the Eric and Wendy Schmidt Center at the Broad Institute and ETH Zurich's ...

As a researcher who studies the genetics of disease, I don’t fully disagree – lifestyle factors play a large role in ...

Two new studies found that a small, missing piece of DNA located next to a specific protein resulted in orange fur coloration ...

A CRISPR treatment seems to have been effective for a baby’s devastating disease, but it is not clear whether such bespoke ...

An infant with a rare urea cycle disorder became the first patient to receive a personalized gene-editing therapy. His care ...

Nine-and-a-half-month-old KJ Muldoon has a rare metabolic condition that meant he spent the first months of his life in ...