Zhimin Xiong - Search Results

Year	Number of Results
2010	2
2012	5
2013	2
2014	2
2015	1
2017	2
2018	1
2019	1
2020	1
2021	1
2024	0

1

AIBN-Induced Remote Trifluoromethyl-Alkynylation of Thioalkynes.

Xiong Z, Zhang F, Yu Y, Tan Z, Zhu G. Xiong Z, et al. Org Lett. 2020 Jun 5;22(11):4088-4092. doi: 10.1021/acs.orglett.0c01147. Epub 2020 May 19. Org Lett. 2020. PMID: 32427485

2

Lewis acid mediated cyclization: synthesis of 2 spirocyclohexylindolines.

Kong XK, Xiong ZM, Zhi X, Meng XL, Zhao JF, Chen W, Zhang H. Kong XK, et al. Org Biomol Chem. 2021 May 12;19(18):4043-4047. doi: 10.1039/d1ob00293g. Org Biomol Chem. 2021. PMID: 33885129

3

Visible-light induced three-component alkynyl-difluoroalkylation of unactivated alkenes.

Jin W , Wu M , Xiong Z , Zhu G . Jin W , et al. Among authors: xiong z. Chem Commun (Camb). 2018 Jul 12;54(57):7924-7927. doi: 10.1039/c8cc03105c. Chem Commun (Camb). 2018. PMID: 29951648

4

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: xiong z. Sci Rep. 2015 Feb 6;5:8296. doi: 10.1038/srep08296. Sci Rep. 2015. PMID: 25656819 Free PMC article.

5

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

Guo H, Peng Y, Hu Z, Li Y, Xun G, Ou J, Sun L, Xiong Z, Liu Y, Wang T, Chen J, Xia L, Bai T, Shen Y, Tian Q, Hu Y, Shen L, Zhao R, Zhang X, Zhang F, Zhao J, Zou X, Xia K. Guo H, et al. Among authors: xiong z. Sci Rep. 2017 Mar 10;7:44155. doi: 10.1038/srep44155. Sci Rep. 2017. PMID: 28281572 Free PMC article. Clinical Trial.

6

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: xiong z. 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

7

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

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: xiong z. 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

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: xiong z. Psychiatr Genet. 2010 Jun;20(3):113-7. doi: 10.1097/YPG.0b013e32833a216f. Psychiatr Genet. 2010. PMID: 20414140

10

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: xiong z. 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

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