NEUROGENETICS
Silvia Paracchini Research GroupThe Neurogenetics group at the University of St Andrews is directed by Prof Silvia Paracchini. We are studying the genetic basis of complex cognitive and behavioural phenotypes. In particular we focus on the biology of dyslexia, a specific difficulty 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. We work with collaborators based in different countries and with expertise in different disciplines.
group2023
Recent news
New preprint!
Our study invesitgating the link between dyslexia and language impairment is out in preprint https://psyarxiv.com/74jsd . A collaboration led by Filippo and made possible thanks to our GenLang partners.
New Paper!
Check out our new study led by Judith on the heritability and parental effects of laterality measures https://www.nature.com/articles/s41398-022-01834-z/
New Paper!
New study led by Rebeca Diaz and Nils Krononberg reporting the characterisation of the KIAA0319 using a combination of biophotonics and cell biology assays is now out in Scientific Reports. Our work shows a role of this gene in cilia biology and in mediating...
New Paper!
The latest review on dyslexia genetics written with Florina Erbeli and Marianne Rice is now available at https://www.mdpi.com/2076-3425/12/1/27
New preprint!
The largest genetic screening for reading and language measures conducted to date is now out in preprint https://www.biorxiv.org/content/10.1101/2021.11.04.466897v1. The results report on data collected over decades by the GenLang consortium a truly international and...
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