Li W - Search Results

1

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: li w. 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

2

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

3

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

4

Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese population.

Mo X, Liu D, Li W, Hu Z, Hu Y, Li J, Guo J, Tang B, Zhang Z, Bai Y, Xia K. Mo X, et al. Among authors: li j, li w. Parkinsonism Relat Disord. 2010 Mar;16(3):222-4. doi: 10.1016/j.parkreldis.2009.09.001. Epub 2009 Oct 2. Parkinsonism Relat Disord. 2010. PMID: 19800834

5

Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports.

Xiong Z, Lu Y, Xue J, Luo S, Xu X, Zhang L, Peng H, Li W, Chen D, Hu Z, Xia K. Xiong Z, et al. Among authors: li w. J Med Case Rep. 2013 Mar 8;7:63. doi: 10.1186/1752-1947-7-63. J Med Case Rep. 2013. PMID: 23497705 Free PMC article.

6

AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis.

Li W, Li Y, Zhang L, Guo H, Tian D, Li Y, Peng Y, Zheng Y, Dai Y, Xia K, Lan X, Wang B, Hu Z. Li W, et al. Among authors: li y. J Med Genet. 2016 Jul;53(7):488-93. doi: 10.1136/jmedgenet-2015-103684. Epub 2016 Mar 17. J Med Genet. 2016. PMID: 26989089 Free PMC article.

7

[Novel mutation of Y271H in EXT1 gene causes multiple exostoses].

Li W, Hu ZM, Xie ZG, He HB, Pan Q, Xia K, Xia JH. Li W, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Aug;32(4):546-50. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007. PMID: 17767039 Chinese.

8

Evaluation of the Genetic Variation Spectrum Related to Corneal Dystrophy in a Large Cohort.

Li W, Qu N, Li JK, Li YX, Han DM, Chen YX, Tian L, Shao K, Yang W, Wang ZS, Chen X, Jin XY, Wang ZW, Liang C, Qian WP, Wang LS, He W. Li W, et al. Among authors: li yx, li jk. Front Cell Dev Biol. 2021 Mar 18;9:632946. doi: 10.3389/fcell.2021.632946. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33816482 Free PMC article.

9

Association study confirms two susceptibility loci for breast cancer in Chinese Han women.

Xu M, Xu Y, Chen M, Li Y, Li W, Zhu J, Zhang M, Chen Z, Zhang X, Liu J, Zhang B. Xu M, et al. Among authors: li y, li w. Breast Cancer Res Treat. 2016 Oct;159(3):433-42. doi: 10.1007/s10549-016-3952-3. Epub 2016 Aug 29. Breast Cancer Res Treat. 2016. PMID: 27572337

10

[Identification of a novel mutation in the ATP2C1 gene in a Chinese pedigree with Hailey-Hailey disease].

Zhang ZZ, Li W, Zhou FS, Gao M, Xiao FL, Fang QY, Shen YJ, Du WH, Sui WC, Yang S, Zhang XJ. Zhang ZZ, et al. Among authors: li w. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Apr;29(2):163-6. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007. PMID: 17536260 Chinese.

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