Ding D - Search Results

1

Rare GCH1 heterozygous variants contributing to Parkinson's disease.

Xu Q, Li K, Sun Q, Ding D, Zhao Y, Yang N, Luo Y, Liu Z, Zhang Y, Wang C, Xia K, Yan X, Jiang H, Shen L, Tang B, Guo J. Xu Q, et al. Among authors: ding d. Brain. 2017 Jul 1;140(7):e41. doi: 10.1093/brain/awx110. Brain. 2017. PMID: 28582483 No abstract available.

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: ding d. 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

Posterior reversible encephalopathy syndrome following paroxysmal nocturnal hemoglobinuria: a case report and literature review.

Ding D, Li K, Li G, Long X. Ding D, et al. Int J Clin Exp Med. 2015 Jul 15;8(7):11617-20. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26379993 Free PMC article.

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: ding d. 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

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. Sci Rep. 2016 Feb 5;6:20423. doi: 10.1038/srep20423. Sci Rep. 2016. PMID: 26846447 Free PMC article.

6

(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.

Chen Z, Zheng C, Long Z, Cao L, Li X, Shang H, Yin X, Zhang B, Liu J, Ding D, Peng Y, Wang C, Peng H, Ye W, Qiu R, Pan Q, Xia K, Chen S, Sequeiros J, Ashizawa T, Klockgether T, Tang B, Jiang H; Chinese Clinical Research Cooperative Group for Spinocerebellar Ataxias (CCRCG-SCA). Chen Z, et al. Among authors: ding d. Brain. 2016 Aug;139(Pt 8):e41. doi: 10.1093/brain/aww087. Epub 2016 Apr 16. Brain. 2016. PMID: 27085188 No abstract available.

7

ATXN2 polymorphism modulates age at onset in Machado-Joseph disease.

Ding D, Li K, Wang C, Chen Z, Long Z, Peng Y, Zhou X, Peng H, Qiu R, Xia K, Tang B, Jiang H. Ding D, et al. Brain. 2016 Oct 1;139(10):e59. doi: 10.1093/brain/aww176. Brain. 2016. PMID: 27452601 No abstract available.

8

Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD.

Wang C, Peng H, Li J, Ding D, Chen Z, Long Z, Peng Y, Zhou X, Ye W, Li K, Xu Q, Ai S, Song C, Weng L, Qiu R, Xia K, Tang B, Jiang H. Wang C, et al. Among authors: ding d. Neurobiol Aging. 2017 May;53:192.e5-192.e10. doi: 10.1016/j.neurobiolaging.2016.12.014. Epub 2016 Dec 24. Neurobiol Aging. 2017. PMID: 28094059

9

Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.

Chen Z, Wang C, Zheng C, Long Z, Cao L, Li X, Shang H, Yin X, Zhang B, Liu J, Ding D, Peng Y, Peng H, Ye W, Qiu R, Pan Q, Xia K, Chen S, Sequeiros J, Ashizawa T, Tang B, Jiang H; Chinese Clinical Research Cooperative Group for Spinocerebellar Ataxias (CCRCG-SCA). Chen Z, et al. Among authors: ding d. Brain. 2017 Apr 1;140(4):e25. doi: 10.1093/brain/awx028. Brain. 2017. PMID: 28334945 No abstract available.

10

Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines.

Mao X, Li K, Tang B, Luo Y, Ding D, Zhao Y, Wang C, Zhou X, Liu Z, Zhang Y, Wang P, Xu Q, Sun Q, Xia K, Yan X, Jiang H, Lu S, Guo J. Mao X, et al. Among authors: ding d. Sci Rep. 2017 May 9;7(1):1625. doi: 10.1038/s41598-017-01637-z. Sci Rep. 2017. PMID: 28487569 Free PMC article.

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