Varun Kannan

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria

Andrew E. Fry, Katherine A. Fawcett, Nathanel Zelnik et al. · Brain · 2017 · 99 citations · Full text

Neurogenomics, Brain Development, Genetics +18

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

De novo<i>GRIN</i>variants in NMDA receptor M2 channel pore‐forming loop are associated with neurological diseases

Jia Li, Jin Zhang, Weiting Tang et al. · Human Mutation · 2019 · 66 citations · Full text

Nmdar Subunits, Synaptic Transmission, Neurotransmitter +23

Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype

Varun Kannan, Alexander J. Sandweiss, Timothy A. Erickson et al. · Pediatric Neurology · 2023 · 16 citations

Neurological Disorder, Medicine, Case Series +6

Infectious profiles in pediatric anti-N-methyl-d-aspartate receptor encephalitis

Alexander J. Sandweiss, Timothy A. Erickson, Yike Jiang et al. · Journal of Neuroimmunology · 2023 · 11 citations · Full text