Bian WJ - Search Results

1

BCOR variants are associated with X-linked recessive partial epilepsy.

Li X, Bian WJ, Liu XR, Wang J, Luo S, Li BM, Yi YH, Wu QY, Zhai QX, Gao LD, Zhang HF, He N, Liao WP; China Epilepsy Gene 1.0 Project. Li X, et al. Among authors: bian wj. Epilepsy Res. 2022 Nov;187:107036. doi: 10.1016/j.eplepsyres.2022.107036. Epub 2022 Oct 19. Epilepsy Res. 2022. PMID: 36279688

2

UNC13B variants associated with partial epilepsy with favourable outcome.

Wang J, Qiao JD, Liu XR, Liu DT, Chen YH, Wu Y, Sun Y, Yu J, Ren RN, Mei Z, Liu YX, Shi YW, Jiang M, Lin SM, He N, Li B, Bian WJ, Li BM, Yi YH, Su T, Liu HK, Gu WY, Liao WP. Wang J, et al. Among authors: bian wj. Brain. 2021 Nov 29;144(10):3050-3060. doi: 10.1093/brain/awab164. Brain. 2021. PMID: 33876820 Free PMC article.

3

SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges.

Bian WJ, Li ZJ, Wang J, Luo S, Li BM, Gao LD, He N, Yi YH. Bian WJ, et al. Front Mol Neurosci. 2022 May 17;15:862480. doi: 10.3389/fnmol.2022.862480. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35663265 Free PMC article.

4

CELSR1 variants are associated with partial epilepsy of childhood.

Chen Z, Luo S, Liu ZG, Deng YC, He SL, Liu XR, Yi YH, Wang J, Gao LD, Li BM, Wu ZJ, Ye ZL, Liang DH, Bian WJ, Liao WP; China Epilepsy Gene 1.0 Project. Chen Z, et al. Among authors: bian wj. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):247-256. doi: 10.1002/ajmg.b.32916. Epub 2022 Aug 12. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 36453712

5

Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome.

He N, Li BM, Li ZX, Wang J, Liu XR, Meng H, Tang B, Bian WJ, Shi YW, Liao WP. He N, et al. Among authors: bian wj. J Neurodev Disord. 2018 Mar 20;10(1):10. doi: 10.1186/s11689-018-9229-x. J Neurodev Disord. 2018. PMID: 29558884 Free PMC article.

6

Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.

Liu XR, Bian WJ, Wang J, Ye TT, Li BM, Liu DT, Tang B, Deng WW, Shi YW, Su T, Yi YH, Liao WP. Liu XR, et al. Among authors: bian wj. Front Genet. 2020 Oct 15;11:559080. doi: 10.3389/fgene.2020.559080. eCollection 2020. Front Genet. 2020. PMID: 33193641 Free PMC article.

7

CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications.

Li XL, Li ZJ, Liang XY, Liu DT, Jiang M, Gao LD, Li H, Tang XQ, Shi YW, Li BM, He N, Li B, Bian WJ, Yi YH, Cheng CF, Wang J. Li XL, et al. Among authors: bian wj. Front Mol Neurosci. 2022 May 4;15:860662. doi: 10.3389/fnmol.2022.860662. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35600082 Free PMC article.

8

ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities.

Zhou P, Meng H, Liang X, Lei X, Zhang J, Bian W, He N, Lin Z, Song X, Zhu W, Hu B, Li B, Yan L, Tang B, Su T, Liu H, Mao Y, Zhai Q, Yi Y. Zhou P, et al. Front Mol Neurosci. 2022 Jun 23;15:864074. doi: 10.3389/fnmol.2022.864074. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35813073 Free PMC article.

9

A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug.

Gao QW, Hua LD, Wang J, Fan CX, Deng WY, Li B, Bian WJ, Shao CX, He N, Zhou P, Liao WP, Shi YW. Gao QW, et al. Among authors: bian wj. Mol Neurobiol. 2017 May;54(4):2428-2434. doi: 10.1007/s12035-016-9800-y. Epub 2016 Mar 11. Mol Neurobiol. 2017. PMID: 26969601

10

Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation.

Chen ZR, Liu DT, Meng H, Liu L, Bian WJ, Liu XR, Zhu WW, He Y, Wang J, Tang B, Su T, Yi YH. Chen ZR, et al. Among authors: bian wj. Seizure. 2019 Jul;69:180-185. doi: 10.1016/j.seizure.2018.08.027. Epub 2018 Sep 2. Seizure. 2019. PMID: 31059981 Free article.

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