Xiang-Wei WS - Search Results

1

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

Liu NN, Xie H, Xiang-Wei WS, Gao K, Wang TS, Jiang YW. Liu NN, et al. Among authors: xiang wei ws. CNS Neurosci Ther. 2019 Aug;25(8):865-875. doi: 10.1111/cns.13119. Epub 2019 Mar 20. CNS Neurosci Ther. 2019. PMID: 30895737 Free PMC article.

2

A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.

Gao K, Tankovic A, Zhang Y, Kusumoto H, Zhang J, Chen W, XiangWei W, Shaulsky GH, Hu C, Traynelis SF, Yuan H, Jiang Y. Gao K, et al. PLoS One. 2017 Feb 9;12(2):e0170818. doi: 10.1371/journal.pone.0170818. eCollection 2017. PLoS One. 2017. PMID: 28182669 Free PMC article.

3

De Novo Mutations and Rare Variants Occurring in NMDA Receptors.

XiangWei W, Jiang Y, Yuan H. XiangWei W, et al. Curr Opin Physiol. 2018 Apr;2:27-35. doi: 10.1016/j.cophys.2017.12.013. Epub 2017 Dec 27. Curr Opin Physiol. 2018. PMID: 29756080 Free PMC article.

4

SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.

Vlaskamp DRM, Shaw BJ, Burgess R, Mei D, Montomoli M, Xie H, Myers CT, Bennett MF, XiangWei W, Williams D, Maas SM, Brooks AS, Mancini GMS, van de Laar IMBH, van Hagen JM, Ware TL, Webster RI, Malone S, Berkovic SF, Kalnins RM, Sicca F, Korenke GC, van Ravenswaaij-Arts CMA, Hildebrand MS, Mefford HC, Jiang Y, Guerrini R, Scheffer IE. Vlaskamp DRM, et al. Neurology. 2019 Jan 8;92(2):e96-e107. doi: 10.1212/WNL.0000000000006729. Epub 2018 Dec 12. Neurology. 2019. PMID: 30541864 Free PMC article.

5

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.

Li J, Gao K, Yan H, Xiangwei W, Liu N, Wang T, Xu H, Lin Z, Xie H, Wang J, Wu Y, Jiang Y. Li J, et al. Gene. 2019 Jun 5;700:168-175. doi: 10.1016/j.gene.2019.03.037. Epub 2019 Mar 21. Gene. 2019. PMID: 30904718

6

Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Hernandez CC, XiangWei W, Hu N, Shen D, Shen W, Lagrange AH, Zhang Y, Dai L, Ding C, Sun Z, Hu J, Zhu H, Jiang Y, Macdonald RL. Hernandez CC, et al. Brain. 2019 Jul 1;142(7):1938-1954. doi: 10.1093/brain/awz123. Brain. 2019. PMID: 31056671 Free PMC article.

7

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

XiangWei W, Kannan V, Xu Y, Kosobucki GJ, Schulien AJ, Kusumoto H, Moufawad El Achkar C, Bhattacharya S, Lesca G, Nguyen S, Helbig KL, Cuisset JM, Fenger CD, Marjanovic D, Schuler E, Wu Y, Bao X, Zhang Y, Dirkx N, Schoonjans AS, Syrbe S, Myers SJ, Poduri A, Aizenman E, Traynelis SF, Lemke JR, Yuan H, Jiang Y. XiangWei W, et al. Brain. 2019 Oct 1;142(10):3009-3027. doi: 10.1093/brain/awz232. Brain. 2019. PMID: 31504254 Free PMC article.

8

Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy.

Yang Y, Xiangwei W, Zhang X, Xiao J, Chen J, Yang X, Jia T, Yang Z, Jiang Y, Zhang Y. Yang Y, et al. Dev Med Child Neurol. 2020 Oct;62(10):1213-1220. doi: 10.1111/dmcn.14614. Epub 2020 Jul 20. Dev Med Child Neurol. 2020. PMID: 32686847 Free article.

9

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

Yang Y, Zeng Q, Cheng M, Niu X, Xiangwei W, Gong P, Li W, Ma J, Zhang X, Yang X, Yang Z, Sun D, Zhou S, Liao J, Jiang Y, Zhang Y. Yang Y, et al. J Neurol. 2022 May;269(5):2649-2665. doi: 10.1007/s00415-021-10834-w. Epub 2021 Oct 26. J Neurol. 2022. PMID: 34698933

10

Clinical and functional consequences of GRIA variants in patients with neurological diseases.

XiangWei W, Perszyk RE, Liu N, Xu Y, Bhattacharya S, Shaulsky GH, Smith-Hicks C, Fatemi A, Fry AE, Chandler K, Wang T, Vogt J, Cohen JS, Paciorkowski AR, Poduri A, Zhang Y, Wang S, Wang Y, Zhai Q, Fang F, Leng J, Garber K, Myers SJ, Jauss RT, Park KL, Benke TA, Lemke JR, Yuan H, Jiang Y, Traynelis SF. XiangWei W, et al. Cell Mol Life Sci. 2023 Nov 3;80(11):345. doi: 10.1007/s00018-023-04991-6. Cell Mol Life Sci. 2023. PMID: 37921875 Free PMC article.

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