Pang N - 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. 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: pang n. 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: pang n. Front Neurol. 2018 Nov 19;9:947. doi: 10.3389/fneur.2018.00947. eCollection 2018. Front Neurol. 2018. PMID: 30510536 Free PMC article.

4

Synaptopathology Involved in Autism Spectrum Disorder.

Guang S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Guang S, et al. Among authors: pang n. Front Cell Neurosci. 2018 Dec 21;12:470. doi: 10.3389/fncel.2018.00470. eCollection 2018. Front Cell Neurosci. 2018. PMID: 30627085 Free PMC article. Review.

5

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes.

Xiong J, Chen S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Xiong J, et al. Among authors: pang n. Front Neurosci. 2019 Apr 11;13:349. doi: 10.3389/fnins.2019.00349. eCollection 2019. Front Neurosci. 2019. PMID: 31031587 Free PMC article.

6

[Mutations in aminoacyl-tRNA synthetase genes: an analysis of 10 cases].

Wu TH, Peng J, Zhang CL, Wu LW, Yang LF, Peng P, Pang N, Yin F, He F. Wu TH, et al. Among authors: pang n. Zhongguo Dang Dai Er Ke Za Zhi. 2020 Jun;22(6):595-601. doi: 10.7499/j.issn.1008-8830.1912040. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 32571458 Free PMC article. Chinese.

7

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. Among authors: pang n. Front Neurosci. 2022 Jun 14;16:892768. doi: 10.3389/fnins.2022.892768. eCollection 2022. Front Neurosci. 2022. PMID: 35774559 Free PMC article.

8

A presumed missense variant in the U2AF2 gene causes exon skipping in neurodevelopmental diseases.

Wang X, You B, Yin F, Chen C, He H, Liu F, Pan Z, Ni X, Pang N, Peng J. Wang X, et al. Among authors: pang n. J Hum Genet. 2023 Jun;68(6):375-382. doi: 10.1038/s10038-023-01128-2. Epub 2023 Feb 7. J Hum Genet. 2023. PMID: 36747105 Review.

9

The genotype-phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews.

Kessi M, Chen B, Pang N, Yang L, Peng J, He F, Yin F. Kessi M, et al. Among authors: pang n. Front Mol Neurosci. 2023 Jul 24;16:1222321. doi: 10.3389/fnmol.2023.1222321. eCollection 2023. Front Mol Neurosci. 2023. PMID: 37555011 Free PMC article.

10

Next-generation sequencing improves treatment efficacy and reduces hospitalization in children with drug-resistant epilepsy.

Peng J, Pang N, Wang Y, Wang XL, Chen J, Xiong J, Peng P, Zhu CH, Kessi MB, He F, Yin F. Peng J, et al. Among authors: pang n. CNS Neurosci Ther. 2019 Jan;25(1):14-20. doi: 10.1111/cns.12869. Epub 2018 Jun 22. CNS Neurosci Ther. 2019. PMID: 29933521 Free PMC article.

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