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Unlocking the code through genomics

Our hope for the future is to find the right treatment, for example the right drug, at the right dosage, from the point of diagnosis. Genomic medicine has the potential to transform the way we care for people with epilepsy, and we believe that whole genome sequencing will help us to unravel the genetic architecture underlying the different types of epilepsy.

Read how we are working to understand the genetic architecture of each individual person's epilepsy through our world leading genomics research programme.