Principal Investigator: Professor Patrick Chinnery
Department: Clinical Neurosciences
Institution: University of CambridgeTags: 18794, cardiovascular disease, deafness, Dementia, featured, glaucoma, Mitochondrial DNA
Lead Collaborators: 1) Dr Gavin Hudson
Collaborating Institutions and Addresses: 1) Newcastle University, Institute of Genetic Medicine, International Center for Life, Central Parkway, Newcastle upon Tyne NE1 3BZ, United Kingdom.
Funding: Wellcome Trust
1a: Genetic variation of maternally inherited mitochondrial DNA (mtDNA) has been associated with several common human diseases, including hypertension, cardiovascular disease, dementia, diabetes, deafness, glaucoma and stroke. However, many of the published studies are under-powered, and only some have been independently replicated. We helped design the UK BIobank Axiom Array by adding the main mtDNA variants. Our aim is to validate or refute the published genetic associations between mtDNA and common human diseases phenotyped through UK Biobank, and preform exploratory analysis to look for new associations with mtDNA variation.
1b: This work will determine whether inherited variation of mtDNA makes an important contribution to the pathogenesis of these common human diseases.
1c: We will compare the frequency of the genetic variants in different groups based on the phenotype data to determine whether mtDNA is associated with these phenotypes.
1d: Full cohort.
Last updated Jul 7, 2016