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Neuroimaging provides a window into the living brain, and is an increasingly vital experimental medicine tool for neuro-psychiatric disease. With a particular focus on early and pre-clinical disease, we explore how the brain changes before symptoms take hold.

The Translational Neuroimaging Group retreat, 2016
The Translational Neuroimaging Group retreat, 2016

Dementia has long been recognised as a major healthcare problem, but the focus on the ageing population and ever-increasing costs of care have brought it to the top of the political agenda (G8 dementia summit, London, Dec 2013). The only way to significantly reduce the burden of dementia to individuals, carers and society as a whole is to intervene before significant damage to the brain has occurred. This poses two major challenges; development of neuroprotective therapy, and the means of identifying the individuals who will most benefit. Neuroimaging is the window into the living brain, and is thus a key methodology to provide sensitive and specific in vivo markers of dementia risk and dementia phenotypes. The specific contribution of our work is to develop sensitive imaging measures that will aid early diagnosis and contribute to clinical trials. We collaborate with the FMRIB analysis group to apply sophisticated imaging techniques to patients and groups of individuals at increased risk of neurodegenerative disease. Individual research projects are linked below. 

The G8 summit ambition to “develop a cure or disease modifying therapy for dementia by 2025” can only be met by sharing resources and expertise and creating integrative platforms and infrastructure for basic and clinical neuroscientists to work together effectively. The Translational Neuroimaging Group is proud to be an active contributor to local (OxDARE, OPDC, ARUK local network) and national (MRC UK Dementia Platform, NIHR Translational Research Collaboration for Dementia, TRC-D) collaborative initiatives. 

Selected publications

Reduced cerebrovascular reactivity in young adults carrying the APOE ε4 allele.

Journal article

Suri S. et al, (2015), Alzheimers Dement, 11, 648 - 57.e1

Using structural and diffusion magnetic resonance imaging to differentiate the dementias.

Journal article

Suri S. et al, (2014), Curr Neurol Neurosci Rep, 14

Functional connectivity in the basal ganglia network differentiates PD patients from controls.

Journal article

Szewczyk-Krolikowski K. et al, (2014), Neurology, 83, 208 - 214

Study protocol: The Whitehall II imaging sub-study.

Journal article

Filippini N. et al, (2014), BMC Psychiatry, 14

Resting functional connectivity reveals residual functional activity in Alzheimer's disease.

Journal article

Zamboni G. et al, (2013), J Neurol Neurosurg Psychiatry, 84

The effects of APOE on the functional architecture of the resting brain.

Journal article

Trachtenberg AJ. et al, (2012), Neuroimage, 59, 565 - 572

The APOE ɛ4 allele modulates brain white matter integrity in healthy adults.

Journal article

Heise V. et al, (2011), Mol Psychiatry, 16, 908 - 916

Distinct patterns of brain activity in young carriers of the APOE-epsilon4 allele.

Journal article

Filippini N. et al, (2009), Proc Natl Acad Sci U S A, 106, 7209 - 7214

Related research themes