As the first personalized cell and gene therapies are approved from small clinical trials, researchers propose the creation of publicly accessible databases to pull together real-world results.  

With few resources and hesitant investors, basic scientists must rely on clinicians, patient advocates, and their own keen eye for biological connections.

Teenager Lauren Bendesky turned her cancer diagnosis on its head, using herself as a research subject to test potential therapies.

A study has shown that less than half of the outcomes of some clinical trials are publicly available.

The pharmaceutical industry has agreed to share data from clinical trials with researchers, patients, and the public.

Leading medical and research centers around the world announce a plan to share massive amounts of genetic and clinical information.

NIH Director Francis Collins and colleagues announce plans to create a health-care research network to connect patients, doctors, and clinical researchers.

Despite increasing use of electronic medical records, much patient data remains in text form, requiring text-mining techniques to make full use of patient information.

Tailoring ethical oversight to participant-led research