Anthony J. Schulien

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers

Dong Li, Hongjie Yuan, Xilma R. Ortiz‐González et al. · The American Journal of Human Genetics · 2016 · 176 citations · Full text

Neurophysiology, Experimental Neuropathology, Neuropharmacology +6

Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology

Kevin K. Ogden, Wenjuan Chen, Sharon A. Swanger et al. · PLoS Genetics · 2017 · 127 citations · Full text

Brain Development, Different Subunits, Neurotransmitter +19

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy

Wenshu XiangWei, Varun Kannan, Yuchen Xu et al. · Brain · 2019 · 87 citations · Full text

Receptor Surface Expression, Grin2d-related Developmental, Nmdar Subunits +25

Targeted disruption of Kv2.1-VAPA association provides neuroprotection against ischemic stroke in mice by declustering Kv2.1 channels

Anthony J. Schulien, Chung‐Yang Yeh, Bailey N. Orange et al. · Science Advances · 2020 · 39 citations · Full text

Cyclin E1 Regulates Kv2.1 Channel Phosphorylation and Localization in Neuronal Ischemia

Niyathi H. Shah, Anthony J. Schulien, Katerina Clemens et al. · Journal of Neuroscience · 2014 · 20 citations · Full text