The A1 astrocyte paradigm: New avenues for pharmacological intervention in neurodegeneration.Mov Disord.(2019).
Assessment of APOE in atypical parkinsonism syndromes.Neurobiol Dis.(2019).
Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.Jama Neurol.(2016).
GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease.Mov Disord.(2015).
Lysosomal Enzyme Glucocerebrosidase Protects against Aβ1-42 Oligomer-Induced Neurotoxicity.Plos One10, e0143854.(2015).
Parkin loss leads to PARIS-dependent declines in mitochondrial mass and respiration.Proc Natl Acad Sci U S A.(2015).
Genetic deficiency of the mitochondrial protein PGAM5 causes a Parkinson's-like movement disorder.Nat Commun5, 4930.(2014).
The interplay of microRNA and neuronal activity in health and disease.Front Cell Neurosci7, 136.(2013).