Liu Y - Search Results

1

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: liu 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

2

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: liu y. Clin Dysmorphol. 2010 Oct;19(4):206-208. doi: 10.1097/MCD.0b013e32833986c8. Clin Dysmorphol. 2010. PMID: 20736820 No abstract available.

3

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

4

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.

Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Feng Y. Men M, et al. Among authors: liu y. Acta Otolaryngol. 2011 Sep;131(9):970-5. doi: 10.3109/00016489.2011.575794. Epub 2011 Apr 19. Acta Otolaryngol. 2011. PMID: 21504270

5

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

Jiang L, Chen H, Jiang W, Hu Z, Mei L, Xue J, He C, Liu Y, Xia K, Feng Y. Jiang L, et al. Among authors: liu y. Biochem Biophys Res Commun. 2011 May 20;408(4):620-4. doi: 10.1016/j.bbrc.2011.04.072. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531202

6

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.

Jiang L, Liu Y, Feng Y, Hu Z, Mei L, Long L, Chen H, Xue J, Xia K, He C. Jiang L, et al. Among authors: liu y. Acta Otolaryngol. 2011 Oct;131(10):1061-8. doi: 10.3109/00016489.2011.591822. Epub 2011 Jun 8. Acta Otolaryngol. 2011. PMID: 21651318

7

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: liu d. 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

8

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

9

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: liu 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

10

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: liu y. Psychiatr Genet. 2014 Dec;24(6):235-40. doi: 10.1097/YPG.0000000000000054. Psychiatr Genet. 2014. PMID: 25304225

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