News
Researchers at the University of Essex have shown that a genetic variant could make some people more sensitive to their emotional environment - and more susceptible to anxiety disorders - than others. 13/01/12
The discovery of a gene that causes a form of hereditary spastic paraplegia may provide an important insight into what causes axons, the stems of our nerve cells, to degenerate in conditions such as multiple sclerosis. 10/01/12
A rare genetic disorder has given researchers a surprising insight into how the pancreas develops. The finding provides a clue to how it may be possible to 'programme' stem cells to become pancreatic cells. 12/12/11
The first patient to receive gene therapy for an incurable type of blindness was treated at the John Radcliffe Hospital in Oxford this week as part of a trial funded by the Health Innovation Challenge Fund. 31/10/11
Researchers in South-east Asia have identified two genetic variants associated with increased susceptibility to severe dengue. The study offers clues to how the body responds to dengue infection. 17/10/11
Your genes, your health
and your future
A free resource allowing you to explore the human genome, your health and your future.
Features and backgrounds
To mark the 75th anniversary of the death of Henry Wellcome and the founding of the Wellcome Trust, we are publishing a series of 14 features on people who have been significant in the Trust's history. In our second piece, Mark Henderson (Science Editor of 'The Times') looks at Sir John Sulston, a Nobel Prize winner and the first Director of the Wellcome Trust Sanger Institute.
A pathologist drawn into molecular biology in the mid-1980s and now Director of the Wellcome Trust Sanger Institute, Professor Mike Stratton tells Chrissie Giles how he'll never stop being fascinated by cells.
What does Britishness mean to a scientist? How does a person from Kent differ from one from the Hebrides? People of the British Isles is a project cataloguing the genetic basis of the entire UK.
It's been a decade since the draft human genome sequence was announced. What impact has it had on genetics, genomics and science in general?
























