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Times Cited
Times Co-cited
Similarity
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Dong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, Eric D Marsh, Lifeng Tian, Elizabeth M McCormick, Gabrielle J Kosobucki, Wenjuan Chen, Anthony J Schulien, Rosetta Chiavacci,[...]. Am J Hum Genet 2016
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Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
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GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
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GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
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GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
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NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease.
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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
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Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.
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Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.
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SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
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10
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.