Zhang W - Search Results

1

Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders.

Pang N, Li K, Tan S, Chen M, He F, Chen C, Yang L, Zhang C, Deng X, Yang L, Mao L, Wang G, Duan H, Wang X, Zhang W, Guo H, Peng J, Yin F, Xia K. Pang N, et al. Among authors: zhang c, zhang w. Gene. 2024 Mar 1;897:148071. doi: 10.1016/j.gene.2023.148071. Epub 2023 Dec 10. Gene. 2024. PMID: 38081334

2

Novel West syndrome candidate genes in a Chinese cohort.

Peng J, Wang Y, He F, Chen C, Wu LW, Yang LF, Ma YP, Zhang W, Shi ZQ, Chen C, Xia K, Guo H, Yin F, Pang N. Peng J, et al. Among authors: zhang w. CNS Neurosci Ther. 2018 Dec;24(12):1196-1206. doi: 10.1111/cns.12860. Epub 2018 Apr 17. CNS Neurosci Ther. 2018. PMID: 29667327 Free PMC article.

3

Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.

Kessi M, Xiong J, Wu L, Yang L, He F, Chen C, Pang N, Duan H, Zhang W, Arafat A, Yin F, Peng J. Kessi M, et al. Among authors: zhang w. Front Neurol. 2018 Nov 19;9:947. doi: 10.3389/fneur.2018.00947. eCollection 2018. Front Neurol. 2018. PMID: 30510536 Free PMC article.

4

A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel.

Xiong J, Chen S, Chen B, Zhang W, Chen C, Deng X, He F, Zhang C, Yang L, Wang Y, Peng J, Yin F. Xiong J, et al. Among authors: zhang c, zhang w. Clin Chim Acta. 2022 May 1;530:74-80. doi: 10.1016/j.cca.2022.03.001. Epub 2022 Mar 3. Clin Chim Acta. 2022. PMID: 35247435

5

Restoration of Sarco/Endoplasmic Reticulum Ca²⁺-ATPase Activity Functions as a Pivotal Therapeutic Target of Anti-Glutamate-Induced Excitotoxicity to Attenuate Endoplasmic Reticulum Ca²⁺ Depletion.

Zhang W, Ye F, Pang N, Kessi M, Xiong J, Chen S, Peng J, Yang L, Yin F. Zhang W, et al. Front Pharmacol. 2022 Apr 20;13:877175. doi: 10.3389/fphar.2022.877175. eCollection 2022. Front Pharmacol. 2022. PMID: 35517826 Free PMC article.

6

Splicing Interruption by Intron Variants in CSNK2B Causes Poirier-Bienvenu Neurodevelopmental Syndrome: A Focus on Genotype-Phenotype Correlations.

Zhang W, Ye F, Chen S, Peng J, Pang N, Yin F. Zhang W, et al. Front Neurosci. 2022 Jun 14;16:892768. doi: 10.3389/fnins.2022.892768. eCollection 2022. Front Neurosci. 2022. PMID: 35774559 Free PMC article.

7

The second-tier status of fragile X syndrome testing for unexplained intellectual disability/global developmental delay in the era of next-generation sequencing.

Zhang W, Li D, Pang N, Jiang L, Li B, Ye F, He F, Chen S, Liu F, Peng J, Yin J, Yin F. Zhang W, et al. Front Pediatr. 2022 Jul 22;10:911805. doi: 10.3389/fped.2022.911805. eCollection 2022. Front Pediatr. 2022. PMID: 35935362 Free PMC article.

8

Silencing of miR-132-3p protects against neuronal injury following status epilepticus by inhibiting IL-1β-induced reactive astrocyte (A1) polarization.

Zhang W, Ye F, Xiong J, He F, Yang L, Yin F, Peng J, Wang X. Zhang W, et al. FASEB J. 2022 Oct;36(10):e22554. doi: 10.1096/fj.202200110RR. FASEB J. 2022. PMID: 36111973

9

KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.

Cheng J, Wang Z, Tang M, Zhang W, Li G, Tan S, Mu C, Hu M, Zhang D, Jia X, Wen Y, Guo H, Xu D, Liu L, Li J, Xia K, Li F, Duan R, Xu Z, Yuan L. Cheng J, et al. Among authors: zhang w, zhang d. Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2315707121. doi: 10.1073/pnas.2315707121. Epub 2024 Mar 15. Proc Natl Acad Sci U S A. 2024. PMID: 38489388 Free PMC article.

10

Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in Patients and a Murine Model.

He H, Cao X, He F, Zhang W, Wang X, Peng P, Xie C, Yin F, Li D, Li J, Wang M, Klüssendorf M, Jentsch TJ, Stauber T, Peng J. He H, et al. Among authors: zhang w. Ann Neurol. 2024 Sep;96(3):608-624. doi: 10.1002/ana.27002. Epub 2024 Jun 15. Ann Neurol. 2024. PMID: 38877824

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