Xu X - Search Results

1

Common and rare variants of the THBS1 gene associated with the risk for autism.

Lu L, Guo H, Peng Y, Xun G, Liu Y, Xiong Z, Tian D, Liu Y, Li W, Xu X, Zhao J, Hu Z, Xia K. Lu L, et al. Among authors: xu x. Psychiatr Genet. 2014 Dec;24(6):235-40. doi: 10.1097/YPG.0000000000000054. Psychiatr Genet. 2014. PMID: 25304225

2

Mutation analysis of the NRXN1 gene in a Chinese autism cohort.

Liu Y, Hu Z, Xun G, Peng Y, Lu L, Xu X, Xiong Z, Xia L, Liu D, Li W, Zhao J, Xia K. Liu Y, et al. Among authors: xu x. J Psychiatr Res. 2012 May;46(5):630-4. doi: 10.1016/j.jpsychires.2011.10.015. Epub 2012 Mar 9. J Psychiatr Res. 2012. PMID: 22405623

3

Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population.

Hu Z, Xiong Z, Xu X, Li F, Lu L, Li W, Su J, Liu Y, Liu D, Xie Z, Peng Y, Kuang Y, Wu L, Zhang J, Pan Q, Tang B, Chen X, Xia K. Hu Z, et al. Among authors: xu x. Hum Genet. 2012 Jul;131(7):1269-74. doi: 10.1007/s00439-012-1155-5. Epub 2012 Mar 11. Hum Genet. 2012. PMID: 22407025

4

Disruption of Contactin 4 in two subjects with autism in Chinese population.

Guo H, Xun G, Peng Y, Xiang X, Xiong Z, Zhang L, He Y, Xu X, Liu Y, Lu L, Long Z, Pan Q, Hu Z, Zhao J, Xia K. Guo H, et al. Among authors: xu x. Gene. 2012 Sep 1;505(2):201-5. doi: 10.1016/j.gene.2012.06.051. Epub 2012 Jun 28. Gene. 2012. PMID: 22750301

5

Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.

Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z. Xu X, et al. Mol Biol Rep. 2014 Jun;41(6):4133-40. doi: 10.1007/s11033-014-3284-5. Epub 2014 Feb 26. Mol Biol Rep. 2014. PMID: 24570023

6

AMPD1 functional variants associated with autism in Han Chinese population.

Zhang L, Ou J, Xu X, Peng Y, Guo H, Pan Y, Chen J, Wang T, Peng H, Liu Q, Tian D, Pan Q, Zou X, Zhao J, Hu Z, Xia K. Zhang L, et al. Among authors: xu x. Eur Arch Psychiatry Clin Neurosci. 2015 Sep;265(6):511-7. doi: 10.1007/s00406-014-0524-6. Epub 2014 Aug 26. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25155876

7

A novel nonsense mutation in the NDP gene in a Chinese family with Norrie disease.

Liu D, Hu Z, Peng Y, Yu C, Liu Y, Mo X, Li X, Lu L, Xu X, Su W, Pan Q, Xia K. Liu D, et al. Among authors: xu x. Mol Vis. 2010 Dec 8;16:2653-8. Mol Vis. 2010. PMID: 21179243 Free PMC article.

8

Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.

Xu X, Hu Z, Zhang L, Liu H, Cheng Y, Xia K, Zhang X. Xu X, et al. Brain Behav. 2017 Aug 14;7(9):e00793. doi: 10.1002/brb3.793. eCollection 2017 Sep. Brain Behav. 2017. PMID: 28948087 Free PMC article.

9

Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population.

Guo H, Peng D, Xu M, Xue J, Lu L, Xu X, Liu Y, Xiong Z, Pan Q, Hu Z, Xia K. Guo H, et al. Among authors: xu m, xu x. Clin Dysmorphol. 2010 Oct;19(4):206-208. doi: 10.1097/MCD.0b013e32833986c8. Clin Dysmorphol. 2010. PMID: 20736820 No abstract available.

10

GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing.

Peng H, Xu X, Zhang L, Zhang X, Peng H, Zheng Y, Luo S, Guo H, Xia K, Li J, Yao H, Hu Z. Peng H, et al. Among authors: xu x. Gene. 2016 Jan 10;575(2 Pt 1):363-7. doi: 10.1016/j.gene.2015.09.088. Epub 2015 Oct 9. Gene. 2016. PMID: 26456105 Clinical Trial.

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