Jiang H - Search Results

1

Identification of a de novo DYNC1H1 mutation via WES according to published guidelines.

Ding D, Chen Z, Li K, Long Z, Ye W, Tang Z, Xia K, Qiu R, Tang B, Jiang H. Ding D, et al. Among authors: jiang h. Sci Rep. 2016 Feb 5;6:20423. doi: 10.1038/srep20423. Sci Rep. 2016. PMID: 26846447 Free PMC article.

2

Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.

Long Z, Chen Z, Wang C, Huang F, Peng H, Hou X, Ding D, Ye W, Wang J, Pan Q, Li J, Xia K, Tang B, Ashizawa T, Jiang H. Long Z, et al. Among authors: jiang h. PLoS One. 2015 Feb 17;10(2):e0117488. doi: 10.1371/journal.pone.0117488. eCollection 2015. PLoS One. 2015. PMID: 25689313 Free PMC article.

3

Primary erythromelalgia: a review.

Tang Z, Chen Z, Tang B, Jiang H. Tang Z, et al. Among authors: jiang h. Orphanet J Rare Dis. 2015 Sep 30;10:127. doi: 10.1186/s13023-015-0347-1. Orphanet J Rare Dis. 2015. PMID: 26419464 Free PMC article. Review.

4

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective.

Chen Z, Ye W, Long Z, Ding D, Peng H, Hou X, Qiu R, Xia K, Tang B, Jiang H. Chen Z, et al. Among authors: jiang h. PLoS One. 2015 Oct 6;10(10):e0139738. doi: 10.1371/journal.pone.0139738. eCollection 2015. PLoS One. 2015. PMID: 26439923 Free PMC article.

5

Spinocerebellar ataxia type 21 exists in the Chinese Han population.

Zeng S, Zeng J, He M, Zeng X, Zhou Y, Liu Z, Xia K, Pan Q, Jiang H, Shen L, Yan X, Tang B, Wang J. Zeng S, et al. Among authors: jiang h. Sci Rep. 2016 Jan 27;6:19897. doi: 10.1038/srep19897. Sci Rep. 2016. PMID: 26813285 Free PMC article.

6

Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease.

Sun Z, Jia D, Shi Y, Hou X, Yang X, Guo J, Li N, Wang J, Sun Q, Zhang H, Lei L, Shen L, Yan X, Xia K, Jiang H, Tang B. Sun Z, et al. Among authors: jiang h. Sci Rep. 2016 Feb 12;6:21649. doi: 10.1038/srep21649. Sci Rep. 2016. PMID: 26867507 Free PMC article.

7

Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China.

Huang F, Long Z, Chen Z, Li J, Hu Z, Qiu R, Zhuang W, Tang B, Xia K, Jiang H. Huang F, et al. Among authors: jiang h. PLoS One. 2015 Jun 10;10(6):e0129052. doi: 10.1371/journal.pone.0129052. eCollection 2015. PLoS One. 2015. PMID: 26061495 Free PMC article.

8

Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China.

Wang C, Chen Z, Yang F, Jiao B, Peng H, Shi Y, Wang Y, Huang F, Wang J, Shen L, Xia K, Tang B, Ashizawa T, Jiang H. Wang C, et al. Among authors: jiang h. PLoS One. 2015 Jun 17;10(6):e0130336. doi: 10.1371/journal.pone.0130336. eCollection 2015. PLoS One. 2015. PMID: 26083476 Free PMC article.

9

Alleviating neurodegeneration in Drosophila models of PolyQ diseases.

Long Z, Tang B, Jiang H. Long Z, et al. Among authors: jiang h. Cerebellum Ataxias. 2014 Jul 4;1:9. doi: 10.1186/2053-8871-1-9. eCollection 2014. Cerebellum Ataxias. 2014. PMID: 26331033 Free PMC article. Review.

10

Polygenic determinants of Parkinson's disease in a Chinese population.

Guo JF, Li K, Yu RL, Sun QY, Wang L, Yao LY, Hu YC, Lv ZY, Luo LZ, Shen L, Jiang H, Yan XX, Pan Q, Xia K, Tang BS. Guo JF, et al. Among authors: jiang h. Neurobiol Aging. 2015 Apr;36(4):1765.e1-1765.e6. doi: 10.1016/j.neurobiolaging.2014.12.030. Epub 2015 Jan 6. Neurobiol Aging. 2015. PMID: 25623333

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