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Plos One|July 21, 2009
Dissociated fear and spatial learning in mice with deficiency of ataxin-2Duong P Huynh, Marwan Maalouf, Alcino J Silva, et al.HGG Advances|April 12, 2026
Genetic contributions to mitochondrial dysfunction in amyotrophic lateral sclerosis etiologyNikki D Russell, Jonathan M Downie, Mark B Bromberg, et al.Experimental Neurology|November 14, 2006
Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell deathDuong P Huynh, Dung T Nguyen, Johannes B Pulst-Korenberg, et al.Journal of Neural Engineering|March 15, 2021
Computational investigation of the impact of deep brain stimulation contact size and shape on neural selectivityDaria Nesterovich Anderson, Alan D Dorval, John D Rolston, et al.Neurology. Genetics|May 8, 2024
Cerebellar Micro-RNA Profile in a Mouse Model of Spinocerebellar Ataxia Type 2Sharan Paul, Warunee Dansithong, Mandi Gandelman, et al.Neurology. Genetics|May 24, 2017
Genetic analysis of age at onset variation in spinocerebellar ataxia type 2K P Figueroa, Hilary Coon, Nieves Santos, et al.Brain Stimulation|April 13, 2020
Neural selectivity, efficiency, and dose equivalence in deep brain stimulation through pulse width tuning and segmented electrodesCollin J Anderson, Daria Nesterovich Anderson, Stefan M Pulst, et al.Annals of Neurology|March 21, 2021
Staufen1 in Human NeurodegenerationSharan Paul, Warunee Dansithong, Karla P Figueroa, et al.Neurology|December 6, 2013
Familial clustering of ALS in a population-based resourceSummer B Gibson, Karla P Figueroa, Mark B Bromberg, et al.Human Molecular Genetics|February 13, 2018
Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxiaRavi Chopra, Aaron H Wasserman, Stefan M Pulst, et al.Pageof 15