Developments in genomics are enabling the rise of personalised medicine, with therapies tailored specifically for individuals ...

Cutting-edge DNA mapping technology has identified new genetic information that can help researchers decipher more genetic ...

As the world heats up, vast numbers of microbes frozen in vast amounts of ice are set to thaw. We must prepare ...

Researchers from the Francis Crick Institute, UCL, Gustave Roussy and Memorial Sloan Kettering Cancer Center (MSK), have ...

DNA found in museum pieces could provide a unique opportunity to study the history and spread of infectious diseases, ...

In psychology, the term subjective well-being (SWB) is used to describe the extent to which different people feel happy and ...

Rare diseases affect 300 million globally, posing diagnostic challenges due to limited awareness and complex genetic factors. Addressing these gaps is crucial.

The genome database will open up the possibility of personalised medicine, and faster and efficient diagnostics. It will also ...

Valley parents are racing to find a treatment for their son's progressive genetic disorder that will eventually lead to him ...

Carrier screening, for example, can identify individuals who carry genes for certain genetic disorders, enabling parents to make informed choices about family planning. This early identification ...

A seminal study from researchers at the Icahn School of Medicine at Mount Sinai and their collaborators in the United Kingdom, Belgium, Spain, the Netherlands, and Iceland has uncovered a new genetic ...

They include conditions such as intellectual disability, autism spectrum disorder, and motor disorders. These NDDs, which often have a genetic basis, manifest in early childhood and can lead to ...