Deng S - Search Results

1

Genetic basis of human left-right asymmetry disorders.

Deng H, Xia H, Deng S. Deng H, et al. Among authors: deng s. Expert Rev Mol Med. 2015 Jan 27;16:e19. doi: 10.1017/erm.2014.22. Expert Rev Mol Med. 2015. PMID: 26258520 Review.

2

Genetic analysis of the NEUROG2 gene in patients with Parkinson's disease.

Deng S, Deng H, Le W, Xu H, Yang H, Deng X, Lv H, Xie W, Zhu S, Jankovic J. Deng S, et al. Among authors: deng h, deng x. Neurosci Lett. 2010 Jan 14;468(3):195-7. doi: 10.1016/j.neulet.2009.10.078. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879328

3

LINGO1 rs9652490 variant in Parkinson disease patients.

Guo Y, Jankovic J, Song Z, Yang H, Zheng W, Le W, Tang X, Deng X, Yang Y, Deng S, Luo Z, Deng H. Guo Y, et al. Among authors: deng x, deng h, deng s. Neurosci Lett. 2011 Jan 7;487(2):174-6. doi: 10.1016/j.neulet.2010.10.016. Epub 2010 Oct 15. Neurosci Lett. 2011. PMID: 20951767

4

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease.

Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H. Guo Y, et al. Among authors: deng x, deng h, deng s. Neurosci Lett. 2013 Oct 25;555:134-6. doi: 10.1016/j.neulet.2013.09.037. Epub 2013 Sep 25. Neurosci Lett. 2013. PMID: 24076007

5

Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease.

Deng S, Deng X, Yuan L, Song Z, Yang Z, Xiong W, Deng H. Deng S, et al. Among authors: deng x, deng h. Acta Neurol Belg. 2015 Sep;115(3):267-71. doi: 10.1007/s13760-014-0347-2. Epub 2014 Aug 5. Acta Neurol Belg. 2015. PMID: 25092551

6

Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson's Disease.

Deng S, Deng X, Song Z, Xiu X, Guo Y, Xiao J, Deng H. Deng S, et al. Among authors: deng x, deng h. Mol Neurobiol. 2016 Sep;53(7):5025-9. doi: 10.1007/s12035-015-9426-5. Epub 2015 Sep 16. Mol Neurobiol. 2016. PMID: 26377108

7

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

Deng H, Deng S, Xu H, Deng HX, Chen Y, Yuan L, Deng X, Yang S, Guan L, Zhang J, Yuan H, Guo Y. Deng H, et al. Among authors: deng hx, deng x, deng s. PLoS One. 2016 May 25;11(5):e0155180. doi: 10.1371/journal.pone.0155180. eCollection 2016. PLoS One. 2016. PMID: 27223613 Free PMC article.

8

Identification of TMEM230 mutations in familial Parkinson's disease.

Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T. Deng HX, et al. Among authors: deng h, deng s. Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6. Nat Genet. 2016. PMID: 27270108 Free PMC article.

9

Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.

Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Deng S, et al. Among authors: deng x, deng h. Indian J Med Res. 2016 Aug;144(2):200-205. doi: 10.4103/0971-5916.195026. Indian J Med Res. 2016. PMID: 27934798 Free PMC article.

10

A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy.

Chen Q, Yuan L, Deng X, Yang Z, Zhang S, Deng S, Lu H, Deng H. Chen Q, et al. Among authors: deng x, deng h, deng s. Mol Neurobiol. 2018 Jun;55(6):4911-4917. doi: 10.1007/s12035-017-0694-0. Epub 2017 Jul 31. Mol Neurobiol. 2018. PMID: 28762097

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