Research

 
 

Our overall aim is to understand the role of the neural mechanisms involved in emotional behaviour in the development of psychotic symptoms and psychotic disorders such as schizophrenia, and to investigate whether targeting these mechanisms can help design new therapeutic strategies for psychosis. We do this through three interrelated research themes:

 
 

Emotion circuit-based studies of the extended psychosis phenotype

We use neuroimaging methods and behavioural assays to characterise the neural correlates of social and emotional information processing across the psychosis spectrum (schizotypy, clinical high risk of psychosis, first-episode psychosis).

From Modinos et al. 2010 Schizophr Res; 2012 Neuroimage; 2015 SCAN; 2020 JAMA Psychiatry.

From Modinos et al. 2010 Schizophr Res; 2012 Neuroimage; 2015 SCAN; 2020 JAMA Psychiatry.


 

The role of GABA/glutamate balance in emotion brain circuits in psychosis pathophysiology

We combine molecular imaging methods in rodent models of psychosis and in patients in the early stages of psychosis to link molecular mechanisms to functional and behavioural observations.

Cross-species molecular imaging of the GABAergic system in rodent and human.

Cross-species molecular imaging of the GABAergic system in rodent and human.


 

Can we modulate emotion brain circuits to design new disease-modifying drugs?

We use state-of-the-art translational in vivo imaging methods across species (rodents and humans) to allow a detailed analysis of the effects of pharmacological intervention on emotional brain circuits in the development of psychosis-like phenotypes.

Cross-species MR spectroscopy in rodent and human (rodent image courtesy of the BRAIN Centre).

Cross-species MR spectroscopy in rodent and human (rodent image courtesy of the BRAIN Centre).


Further research interests - ENIGMA Schizotypy

The aim of the ENIGMA Schizotypy working group is to bring together worldwide schizotypy researchers towards large scale meta-analyses of neuroimaging data across many different studies and datasets, in order to delineate the neural signature of the expression of subclinical psychotic-like experiences in healthy individuals.

Our consortium involves 30+ sites worldwide.

Our consortium involves 30+ sites worldwide.