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Wenshu XiangWei

Peking University

13

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280

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A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.

2021 Frontiers in Genetics
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Citations (1)
Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy.

2020 Developmental Medicine & Child Neurology
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Negative allosteric modulation of GluN1/GluN3 NMDA receptors.

2020 Neuropharmacology
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The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.

2020 Movement Disorders
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Citations (3)
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies

2019 Brain
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Citations (15)
Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation

2019 Gene
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Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy

2019 Brain
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The absence of NIPA2 enhances neural excitability through BK (big potassium) channels

2019 CNS Neuroscience & Therapeutics
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Citations (4)
De novo mutations and rare variants occurring in NMDA receptors

2018 Current Opinion in Physiology
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A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia

2017 PLOS ONE
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Citations (35)