Understanding the molecular mechanism of complex I and its roles in human disease

Programme Leader

Mitochondrial genomics and human diseases

Mass Spectrometry Facility

Identifying and characterising mitochondrial proteins and their associations

Programme Leader

Understanding transport processes in mitochondria

Programme Leader

Mitochondrial genome engineering to unravel the genetic links between mitochondrial gene regulation and human disease for future mechanism-based therapies

Programme Leader

Targeting therapeutic and probe molecules to mitochondria, mitochondrial radical production and redox signalling

Programme Leader

Interactions between mitochondria and the endoplasmic reticulum in cell physiology and disease

Bioinformatics Facility

Understanding mitochondria using computer modelling

Wellcome Clinical Research Career Development Fellow

Molecular mechanisms of tissue specificity in mitochondrial disease

Emeritus Director

Understanding the molecular mechanism of how ATP is made

Programme Leader

Genetic models of neurodegenerative disease