Joshua Hersheson
National Hospital for Neurology and Neurosurgery(GB)University College London(GB)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological disorders and treatments, Genetics and Neurodevelopmental Disorders, Neurological diseases and metabolism
Most-Cited Works
- → High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease(2006)1,563 cited
- → Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers(2014)195 cited
- → Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia(2012)178 cited
- → Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes(2014)121 cited
- → Extended phenotypic spectrum of KIF5A mutations(2014)112 cited
- → The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics(2012)104 cited
- → Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome(2014)100 cited
- → Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans(2016)98 cited
- → ADCY5 mutations are another cause of benign hereditary chorea(2015)90 cited
- → Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia(2014)62 cited