Mark P. DeAndrade

Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neurons

Jason Schapansky, Saurabh Khasnavis, Mark P. DeAndrade et al. · Neurobiology of Disease · 2017 · 138 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Familial Knockin Mutation +12

Lysosome and Inflammatory Defects in <i>GBA1</i>‐Mutant Astrocytes Are Normalized by LRRK2 Inhibition

Anwesha Sanyal, Mark P. DeAndrade, Hailey S. Novis et al. · Movement Disorders · 2020 · 98 citations · Full text

Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice

Mark P. DeAndrade, Russell L. Johnson, Erica L. Unger et al. · Human Molecular Genetics · 2012 · 94 citations · Full text

Sleep Disorders, Social Sciences, Rls Patients +17

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism

Mark P. DeAndrade, Fumiaki Yokoi, Thomas van Groen et al. · Behavioural Brain Research · 2010 · 81 citations

Atp1a3 Mutant Mice, Neurodegenerative Diseases, Molecular Neuroscience +11

Altered Dendritic Morphology of Purkinje cells in Dyt1 ΔGAG Knock-In and Purkinje Cell-Specific Dyt1 Conditional Knockout Mice

Lin Zhang, Fumiaki Yokoi, Yuan‐Hu Jin et al. · PLoS ONE · 2011 · 75 citations · Full text