Chen DF - Search Results

1

TMEM151A variants cause paroxysmal kinesigenic dyskinesia.

Li HF, Chen YL, Zhuang L, Chen DF, Ke HZ, Luo WJ, Liu GL, Wu SN, Zhou WH, Xiong ZQ, Wu ZY. Li HF, et al. Among authors: chen df, chen yl. Cell Discov. 2021 Sep 13;7(1):83. doi: 10.1038/s41421-021-00322-w. Cell Discov. 2021. PMID: 34518509 Free PMC article. No abstract available.

2

Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing.

Jiang B, Zhou J, Li HL, Chen YG, Cheng HR, Ye LQ, Liu DS, Chen DF, Tao QQ, Wu ZY. Jiang B, et al. Among authors: chen yg, chen df. Neurobiol Aging. 2019 Apr;76:215.e15-215.e21. doi: 10.1016/j.neurobiolaging.2018.11.024. Epub 2018 Dec 6. Neurobiol Aging. 2019. PMID: 30598257

3

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders.

Zhao SY, Li LX, Chen YL, Chen YJ, Liu GL, Dong HL, Chen DF, Li HF, Wu ZY. Zhao SY, et al. Among authors: chen yj, chen df, chen yl. CNS Neurosci Ther. 2020 Jan;26(1):39-46. doi: 10.1111/cns.13147. Epub 2019 May 23. CNS Neurosci Ther. 2020. PMID: 31124310 Free PMC article.

4

The discriminative capacity of CSF β-amyloid 42 and Tau in neurodegenerative diseases in the Chinese population.

Ye LQ, Li XY, Zhang YB, Cheng HR, Ma Y, Chen DF, Tao QQ, Li HL, Wu ZY. Ye LQ, et al. Among authors: chen df. J Neurol Sci. 2020 May 15;412:116756. doi: 10.1016/j.jns.2020.116756. Epub 2020 Feb 22. J Neurol Sci. 2020. PMID: 32142967

5

TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study.

Cheng HL, Dong HL, Liu DS, Ni W, Ma Y, Yang L, Du YC, Chen DF, Dong Y, Wu ZY. Cheng HL, et al. Among authors: chen df. Gene. 2021 May 5;779:145495. doi: 10.1016/j.gene.2021.145495. Epub 2021 Feb 13. Gene. 2021. PMID: 33588035

6

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.

Dong HL, Ma Y, Yu H, Wei Q, Li JQ, Liu GL, Li HF, Chen L, Chen DF, Bai G, Wu ZY. Dong HL, et al. Among authors: chen l, chen df. Brain. 2021 Sep 4;144(8):2457-2470. doi: 10.1093/brain/awab135. Brain. 2021. PMID: 33751098

7

Clinical and genetic characteristics of Chinese patients with reducing body myopathy.

Chen L, Lin HX, Yang XX, Chen DF, Dong HL, Yu H, Liu GL, Wu ZY. Chen L, et al. Among authors: chen df. Neuromuscul Disord. 2021 May;31(5):442-449. doi: 10.1016/j.nmd.2021.02.009. Epub 2021 Feb 12. Neuromuscul Disord. 2021. PMID: 33846077

8

A novel frameshift ACTN2 variant causes a rare adult-onset distal myopathy with multi-minicores.

Chen L, Chen DF, Dong HL, Liu GL, Wu ZY. Chen L, et al. Among authors: chen df. CNS Neurosci Ther. 2021 Oct;27(10):1198-1205. doi: 10.1111/cns.13697. Epub 2021 Jun 25. CNS Neurosci Ther. 2021. PMID: 34170073 Free PMC article.

9

Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia.

Li HF, Chen YL, Zhuang L, Chen DF, Ke HZ, Luo WJ, Liu GL, Wu SN, Zhou WH, Xiong ZQ, Wu ZY. Li HF, et al. Among authors: chen df, chen yl. Cell Discov. 2021 Oct 28;7(1):102. doi: 10.1038/s41421-021-00345-3. Cell Discov. 2021. PMID: 34711800 Free PMC article. No abstract available.

10

Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions.

Chen Y, Chen D, Zhao S, Liu G, Li H, Wu ZY. Chen Y, et al. Front Med. 2021 Dec;15(6):877-886. doi: 10.1007/s11684-021-0863-4. Epub 2021 Nov 26. Front Med. 2021. PMID: 34825340

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