Benjamin Munro

Benjamin Munro is a Researcher at Newcastle University, contributing to studies on mitochondrial diseases and genetic disorders. His work focuses on molecular mechanisms underlying neurological and metabolic conditions, particularly involving RNA processing, mitochondrial dysfunction, and genetic mutations.

Research Interests: Mr. Munro’s research explores the intersection of genetics and neurology, with a focus on mitochondrial disorders such as Leigh Syndrome and pontocerebellar hypoplasia. His studies investigate how genetic mutations disrupt cellular processes like ribosome biogenesis and metabolic pathways, leading to neurological deficits.

Publications Highlight: His work spans topics from TARS2-related mitochondrial disease mechanisms to nucleoside supplementation therapies in zebrafish models. The 2020 studies on TACO1 and RNA exosome mutations underscore his focus on identifying genetic causes of neurodegenerative diseases and developing potential therapeutic strategies.