Neurogenetics Research Group

Silvia Paracchini

Royal Society University Research Fellow

We are studying the genetic basis of complex cognitive and behavioural phenotypes. In particular we focus on the biology of dyslexia, a specific impairment in learning to read which is caused in large part by genetic factors. We are also interested in cognitive traits related to dyslexia such as general reading and language abilities. More recently we have become interested in handedness and in a complex link between dyslexia and laterality. We are using large scale screening involving genome-wide and functional genomics approaches to identify candidate genes or loci underlying these phenotypes. In parallel we are developing functional assays to understand the biological mechanisms that mediate genetic differences to phenotypic variation.

Recent News


Silvia will chair a symposium on language genetics at the forthcoming BNA2017 conference, Birmingham 10-13 March.. The aim of the symposium is to cover the most recent advances in language genetic research going from phenotype definitions to the functional dissection of genetic associations using different animal models. The symposium is sponsored by the Genetics Society.

  1. New grant!
  2. New publication