Peng Y - Search Results

1

Association of genetic variants of GRIN2B with autism.

Pan Y, Chen J, Guo H, Ou J, Peng Y, Liu Q, Shen Y, Shi L, Liu Y, Xiong Z, Zhu T, Luo S, Hu Z, Zhao J, Xia K. Pan Y, et al. Among authors: peng y. Sci Rep. 2015 Feb 6;5:8296. doi: 10.1038/srep08296. Sci Rep. 2015. PMID: 25656819 Free PMC article.

2

[Mapping of pathogenic genes in two families with autosomal dominant ichthyosis vulgaris].

Gong HY, Zhang J, Hu ZM, Wu LQ, Liang DS, Xie ZG, Pan Q, Bu FX, Peng Y, Xia K, Xia JH. Gong HY, et al. Among authors: peng y. Yi Chuan. 2008 Jul;30(7):843-50. doi: 10.3724/sp.j.1005.2008.00843. Yi Chuan. 2008. PMID: 18779126 Chinese.

3

[Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus].

Bu FX, Peng Y, Wang SH, Pan Q, Hu ZM, Gong HY, Zhang J, Wu LQ, Liang DS, Pan Q, Feng Y, Xia K, Xia JH. Bu FX, et al. Among authors: peng y. Yi Chuan. 2009 Jan;31(1):43-9. doi: 10.3724/sp.j.1005.2009.00043. Yi Chuan. 2009. PMID: 19138900 Chinese.

4

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.

Li X, Hu Z, He Y, Xiong Z, Long Z, Peng Y, Bu F, Ling J, Xun G, Mo X, Pan Q, Zhao J, Xia K. Li X, et al. Among authors: peng y. Psychiatr Genet. 2010 Jun;20(3):113-7. doi: 10.1097/YPG.0b013e32833a216f. Psychiatr Genet. 2010. PMID: 20414140

5

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: peng y. Mol Vis. 2010 Dec 8;16:2653-8. Mol Vis. 2010. PMID: 21179243 Free PMC article.

6

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: peng y. 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

7

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: peng y. Hum Genet. 2012 Jul;131(7):1269-74. doi: 10.1007/s00439-012-1155-5. Epub 2012 Mar 11. Hum Genet. 2012. PMID: 22407025

8

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: peng y. Gene. 2012 Sep 1;505(2):201-5. doi: 10.1016/j.gene.2012.06.051. Epub 2012 Jun 28. Gene. 2012. PMID: 22750301

9

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. Among authors: peng y. 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

10

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia.

Guo H, Jin X, Zhu T, Wang T, Tong P, Tian L, Peng Y, Sun L, Wan A, Chen J, Liu Y, Li Y, Tian Q, Xia L, Zhang L, Pan Y, Lu L, Liu Q, Shen L, Li Y, Xiong W, Li J, Tang B, Feng Y, Zhang X, Zhang Z, Pan Q, Hu Z, Xia K. Guo H, et al. Among authors: peng y. J Med Genet. 2014 Aug;51(8):518-25. doi: 10.1136/jmedgenet-2014-102351. Epub 2014 Jun 2. J Med Genet. 2014. PMID: 24891338 Free PMC article.

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