Complex trait genetics
We aim to dissect the genetic factors that cause or predispose people to brain diseases and conditions.
Pinpointing the genes
Our studies of the genetics of brain disorders are focussed around psychiatric disorders, brain vascular disease and neurodegenerative conditions (multiple sclerosis and motor neurone disease).
A key approach is to study multiply affected families and rare cases of autosomal dominant inheritance as an entry-point to the study of the genes and pathways involved in these multifactorial conditions.
Much of our work is performed in collaboration with other University of Edinburgh Centres, particularly the Centre for Genomic and Experimental Medicine (CGEM) and the Centre for Cognitive Ageing and Cognitive Epidemiology (CCACE).
CCBS investigators are members of the Generation Scotland Psychiatry Expert Working Group (McIntosh) and the Enhancing Neuroimaging Genetics through Meta-Analysis (ENIGMA) Consortium (Andrew McIntosh, Joanna Wardlaw, Stephen Lawrie, Heather Whalley and Ian Deary [Associate Member]).
|Mitochondrial DNA mutations in neuronal damage||multiple sclerosis||Don Mahad|
|Psychiatric genetics||psychiatric disorders||Andrew McIntosh|
|Genetics of stroke and its subtypes||brain vascular disease||Cathie Sudlow|
|Neuroimaging genetics||brain vascular disease||Joanna Wardlaw|