Zhang J - Search Results

1

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.

Yang X, Gao H, Zhang J, Xu X, Liu X, Wu X, Wei L, Zhang Y. Yang X, et al. Among authors: zhang j, zhang y. PLoS One. 2014 May 19;9(5):e97274. doi: 10.1371/journal.pone.0097274. eCollection 2014. PLoS One. 2014. PMID: 24842602 Free PMC article.

2

Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.

Zhao Y, Zhang X, Bao X, Zhang Q, Zhang J, Cao G, Zhang J, Li J, Wei L, Pan H, Wu X. Zhao Y, et al. Among authors: zhang q, zhang j, zhang x. BMC Med Genet. 2014 Feb 25;15:24. doi: 10.1186/1471-2350-15-24. BMC Med Genet. 2014. PMID: 24564546 Free PMC article.

3

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.

Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Zhou WZ, et al. Among authors: zhang j. Hum Mutat. 2019 Jun;40(6):801-815. doi: 10.1002/humu.23724. Epub 2019 Apr 29. Hum Mutat. 2019. PMID: 30763456 Free PMC article.

4

Molecular characteristics of Chinese patients with Rett syndrome.

Zhang X, Bao X, Zhang J, Zhao Y, Cao G, Pan H, Zhang J, Wei L, Wu X. Zhang X, et al. Among authors: zhang j. Eur J Med Genet. 2012 Dec;55(12):677-81. doi: 10.1016/j.ejmg.2012.08.009. Epub 2012 Aug 27. Eur J Med Genet. 2012. PMID: 22982301

5

AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder.

Yang C, Li J, Wu Q, Yang X, Huang AY, Zhang J, Ye AY, Dou Y, Yan L, Zhou WZ, Kong L, Wang M, Ai C, Yang D, Wei L. Yang C, et al. Among authors: zhang j. Database (Oxford). 2018 Jan 1;2018:bay106. doi: 10.1093/database/bay106. Database (Oxford). 2018. PMID: 30339214 Free PMC article.

6

Autism prevalence in China is comparable to Western prevalence.

Sun X, Allison C, Wei L, Matthews FE, Auyeung B, Wu YY, Griffiths S, Zhang J, Baron-Cohen S, Brayne C. Sun X, et al. Among authors: zhang j. Mol Autism. 2019 Feb 28;10:7. doi: 10.1186/s13229-018-0246-0. eCollection 2019. Mol Autism. 2019. PMID: 30858963 Free PMC article.

7

Clinical features and surgical outcomes in young children with focal cortical dysplasia type II.

Wang TS, Liu QZ, Liu M, Zhang Q, Wang RF, Wu CW, Zhang J, Wang W, Ji TY, Liu XY, Wang S, Cai LX, Jiang YW, Wu Y. Wang TS, et al. Among authors: zhang q, zhang j. CNS Neurosci Ther. 2020 Feb;26(2):270-277. doi: 10.1111/cns.13205. Epub 2019 Aug 1. CNS Neurosci Ther. 2020. PMID: 31368639 Free PMC article.

8

Natural history and genotype-phenotype correlation of pantothenate kinase-associated neurodegeneration.

Chang X, Zhang J, Jiang Y, Wang J, Wu Y. Chang X, et al. Among authors: zhang j. CNS Neurosci Ther. 2020 Jul;26(7):754-761. doi: 10.1111/cns.13294. Epub 2020 Feb 11. CNS Neurosci Ther. 2020. PMID: 32043823 Free PMC article. Review.

9

Functional Connectivity of Anterior Insula Predicts Recovery of Patients With Disorders of Consciousness.

Zhang L, Luo L, Zhou Z, Xu K, Zhang L, Liu X, Tan X, Zhang J, Ye X, Gao J, Luo B. Zhang L, et al. Among authors: zhang j. Front Neurol. 2018 Nov 30;9:1024. doi: 10.3389/fneur.2018.01024. eCollection 2018. Front Neurol. 2018. PMID: 30555407 Free PMC article.

10

Reference intervals for plasma pro-gastrin releasing peptide (ProGRP) levels in healthy adults of Chinese Han ethnicity.

Zhang J, Zhao Y, Chen Y. Zhang J, et al. Int J Biol Markers. 2014 Dec 9;29(4):e436-9. doi: 10.5301/jbm.5000084. Int J Biol Markers. 2014. PMID: 24723213 Free article.

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