Chen J - Search Results

1

Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations.

Zhang J, Chen J, Zeng Q, Zhang L, Tian X, Yang X, Yang Z, Wu Y, Wu X, Zhang Y. Zhang J, et al. Among authors: chen j. Seizure. 2019 Jul;69:228-234. doi: 10.1016/j.seizure.2019.05.010. Epub 2019 May 13. Seizure. 2019. PMID: 31112829 Free article.

2

ATP1A3 mosaicism in families with alternating hemiplegia of childhood.

Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Among authors: chen j. Clin Genet. 2019 Jul;96(1):43-52. doi: 10.1111/cge.13539. Epub 2019 Apr 3. Clin Genet. 2019. PMID: 30891744 Free PMC article.

3

The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet Syndrome.

Tian X, Chen J, Zhang J, Yang X, Ji T, Zhang Y, Wu Y, Fang F, Wu X, Zhang Y. Tian X, et al. Among authors: chen j. Front Neurol. 2019 Jun 13;10:625. doi: 10.3389/fneur.2019.00625. eCollection 2019. Front Neurol. 2019. PMID: 31249551 Free PMC article.

4

CHD2-related epilepsy: novel mutations and new phenotypes.

Chen J, Zhang J, Liu A, Zhang L, Li H, Zeng Q, Yang Z, Yang X, Wu X, Zhang Y. Chen J, et al. Dev Med Child Neurol. 2020 May;62(5):647-653. doi: 10.1111/dmcn.14367. Epub 2019 Nov 1. Dev Med Child Neurol. 2020. PMID: 31677157 Free article.

5

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. Among authors: chen j. 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.

6

Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABA_A receptors.

Hernandez CC, Tian X, Hu N, Shen W, Catron MA, Yang Y, Chen J, Jiang Y, Zhang Y, Macdonald RL. Hernandez CC, et al. Among authors: chen j. Brain Commun. 2021 Mar 11;3(2):fcab033. doi: 10.1093/braincomms/fcab033. eCollection 2021. Brain Commun. 2021. PMID: 34095830 Free PMC article.

7

Phenotypes of GNAO1 Variants in a Chinese Cohort.

Yang X, Niu X, Yang Y, Cheng M, Zhang J, Chen J, Yang Z, Zhang Y. Yang X, et al. Among authors: chen j. Front Neurol. 2021 May 28;12:662162. doi: 10.3389/fneur.2021.662162. eCollection 2021. Front Neurol. 2021. PMID: 34122306 Free PMC article.

8

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.

Zeng Q, Yang Y, Duan J, Niu X, Chen Y, Wang D, Zhang J, Chen J, Yang X, Li J, Yang Z, Jiang Y, Liao J, Zhang Y. Zeng Q, et al. Among authors: chen j, chen y. Front Mol Neurosci. 2022 Mar 30;15:809951. doi: 10.3389/fnmol.2022.809951. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35431799 Free PMC article.

9

PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.

Chen Y, Yang X, Chen J, Yang X, Yang Y, Liu A, Zhang X, Wu W, Sun D, Yang Z, Jiang Y, Zhang Y. Chen Y, et al. Among authors: chen j. Front Neurol. 2022 Nov 3;13:1041509. doi: 10.3389/fneur.2022.1041509. eCollection 2022. Front Neurol. 2022. PMID: 36408521 Free PMC article.

10

Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing.

Chen J, Chen Y, Yang Y, Niu X, Zhang J, Zeng Q, Liu A, Xu X, Yang X, Li S, Yang X, Wang Y, Zhang Y. Chen J, et al. Among authors: chen y. J Hum Genet. 2023 Feb;68(2):73-80. doi: 10.1038/s10038-022-01103-3. Epub 2022 Dec 8. J Hum Genet. 2023. PMID: 36482122

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

128,762 results

Search Page