Chen YP - Search Results

1

Association analysis of single-nucleotide polymorphisms of USP24 and USP40 with Parkinson's disease in the Han Chinese population.

Zhao B, Song W, Chen YP, Huang R, Chen K, Cao B, Yang Y, Shang HF. Zhao B, et al. Among authors: chen k, chen yp. Eur Neurol. 2012;68(3):181-4. doi: 10.1159/000339641. Epub 2012 Aug 24. Eur Neurol. 2012. PMID: 22923019

2

Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort.

Chen Y, Burgunder JM, Song W, Huang R, Shang HF. Chen Y, et al. Eur J Neurol. 2012 Jun;19(6):924-6. doi: 10.1111/j.1468-1331.2011.03582.x. Epub 2011 Nov 7. Eur J Neurol. 2012. PMID: 22054283

3

Analysis of the genotype of diacylglycerol kinase delta single-nucleotide polymorphisms in Parkinson disease in the Han Chinese population.

Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF. Song W, et al. Among authors: chen k, chen yp. Neurol India. 2012 Jan-Feb;60(1):82-5. doi: 10.4103/0028-3886.93607. Neurol India. 2012. PMID: 22406787 Free article.

4

GLIS1 rs797906: an increased risk factor for late-onset Parkinson's disease in the Han Chinese population.

Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF. Song W, et al. Among authors: chen k, chen yp. Eur Neurol. 2012;68(2):89-92. doi: 10.1159/000337955. Epub 2012 Jul 3. Eur Neurol. 2012. PMID: 22759478

5

Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.

Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake W, Toda T, Shang HF. Chen K, et al. Among authors: chen yp. Neurol Res. 2012 Sep;34(7):725-9. doi: 10.1179/1743132812Y.0000000075. Neurol Res. 2012. PMID: 22889673

6

PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China.

Chen YP, Song W, Yang J, Zheng ZZ, Huang R, Chen K, Zhao B, Chen XP, Burgunder JM, Shang HF. Chen YP, et al. Among authors: chen k, chen xp. Eur J Neurol. 2014;21(1):174-6. doi: 10.1111/ene.12122. Epub 2013 Mar 16. Eur J Neurol. 2014. PMID: 23496026

7

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.

Chen YP, Song W, Huang R, Chen K, Zhao B, Li J, Yang Y, Shang HF. Chen YP, et al. Among authors: chen k. J Clin Neurosci. 2013 Jun;20(6):880-3. doi: 10.1016/j.jocn.2012.07.011. Epub 2013 Apr 23. J Clin Neurosci. 2013. PMID: 23618683

8

SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.

Guo XY, Chen YP, Song W, Zhao B, Cao B, Wei QQ, Ou RW, Yang Y, Yuan LX, Shang HF. Guo XY, et al. Among authors: chen yp. Neurobiol Aging. 2014 Dec;35(12):2882.e1-2882.e6. doi: 10.1016/j.neurobiolaging.2014.07.014. Epub 2014 Jul 18. Neurobiol Aging. 2014. PMID: 25129240

9

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy.

Chen YP, Zhao B, Cao B, Song W, Guo X, Wei QQ, Yang Y, Yuan LX, Shang HF. Chen YP, et al. Neurobiol Aging. 2015 Feb;36(2):1222.e7-11. doi: 10.1016/j.neurobiolaging.2014.09.010. Epub 2014 Sep 18. Neurobiol Aging. 2015. PMID: 25442117

10

Genetic Analysis of Prosaposin, the Lysosomal Storage Disorder Gene in Parkinson's Disease.

Chen YP, Gu XJ, Ou RW, Zhang LY, Hou YB, Liu KC, Cao B, Wei QQ, Song W, Zhao B, Wu Y, Cheng JQ, Shang HF. Chen YP, et al. Mol Neurobiol. 2021 Apr;58(4):1583-1592. doi: 10.1007/s12035-020-02218-4. Epub 2020 Nov 20. Mol Neurobiol. 2021. PMID: 33219486

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