Chen YP - Search Results

1

Loss of CHCHD2 Stability Coordinates with C1QBP/CHCHD2/CHCHD10 Complex Impairment to Mediate PD-Linked Mitochondrial Dysfunction.

Ren YL, Jiang Z, Wang JY, He Q, Li SX, Gu XJ, Qi YR, Zhang M, Yang WJ, Cao B, Li JY, Wang Y, Chen YP. Ren YL, et al. Among authors: chen yp. Mol Neurobiol. 2024 Oct;61(10):7968-7988. doi: 10.1007/s12035-024-04090-y. Epub 2024 Mar 7. Mol Neurobiol. 2024. PMID: 38453793

2

Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population.

Chen Y, Chen K, Burgunder JM, Song W, Huang R, Zhao B, Cao B, Chen X, Jiang Y, Shang HF. Chen Y, et al. J Neurol Sci. 2012 Dec 15;323(1-2):228-31. doi: 10.1016/j.jns.2012.09.025. Epub 2012 Oct 9. J Neurol Sci. 2012. PMID: 23058565

3

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF. Chen Y, et al. Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20. Neurobiol Aging. 2013. PMID: 23261770

4

Association of the Val66Met polymorphism of the BDNF gene with primary cranial-cervical dystonia patients from South-west China.

Chen Y, Song W, Yang J, Chen K, Huang R, Zhao B, Cao B, Burgunder J, Shang HF. Chen Y, et al. Parkinsonism Relat Disord. 2013 Nov;19(11):1043-5. doi: 10.1016/j.parkreldis.2013.06.004. Epub 2013 Jun 29. Parkinsonism Relat Disord. 2013. PMID: 23816543

5

Camptocormia in Chinese patients with Parkinson's disease.

Song W, Guo X, Chen K, Huang R, Zhao B, Cao B, Chen Y, Shang HF. Song W, et al. J Neurol Sci. 2014 Feb 15;337(1-2):173-5. doi: 10.1016/j.jns.2013.12.004. Epub 2013 Dec 11. J Neurol Sci. 2014. PMID: 24360186

6

An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.

Yuan X, Chen Y, Cao B, Zhao B, Wei Q, Guo X, Yang Y, Yuan L, Shang H. Yuan X, et al. Parkinsonism Relat Disord. 2015 Feb;21(2):147-9. doi: 10.1016/j.parkreldis.2014.11.022. Epub 2014 Dec 3. Parkinsonism Relat Disord. 2015. PMID: 25511328

7

Assessment of TREM2 rs75932628 association with amyotrophic lateral sclerosis in a Chinese population.

Chen X, Chen Y, Wei Q, Guo X, Cao B, Ou R, Zhao B, Shang HF. Chen X, et al. J Neurol Sci. 2015 Aug 15;355(1-2):193-5. doi: 10.1016/j.jns.2015.05.010. Epub 2015 May 16. J Neurol Sci. 2015. PMID: 26026943

8

Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.

Chen Y, Chen X, Guo X, Song W, Cao B, Wei Q, Ou R, Zhao B, Shang HF. Chen Y, et al. Neurol Sci. 2015 Oct;36(10):1903-6. doi: 10.1007/s10072-015-2279-x. Epub 2015 Jun 10. Neurol Sci. 2015. PMID: 26058955

9

Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.

Chen Y, Wei QQ, Ou R, Cao B, Chen X, Zhao B, Guo X, Yang Y, Chen K, Wu Y, Song W, Shang HF. Chen Y, et al. PLoS One. 2015 Jul 24;10(7):e0133776. doi: 10.1371/journal.pone.0133776. eCollection 2015. PLoS One. 2015. PMID: 26208350 Free PMC article.

10

No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson's disease in a Chinese Han population.

Chen Y, Yuan X, Cao B, Wei Q, Ou R, Yang J, Chen X, Zhao B, Song W, Wu Y, Shang H. Chen Y, et al. J Neural Transm (Vienna). 2015 Nov;122(11):1547-52. doi: 10.1007/s00702-015-1430-4. Epub 2015 Jul 30. J Neural Transm (Vienna). 2015. PMID: 26224037

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