Liu X - Search Results

1

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.

Jiang Y, Zhang Y, Zhang P, Sang T, Zhang F, Ji T, Huang Q, Xie H, Du R, Cai B, Zhao H, Wang J, Wu Y, Wu H, Xu K, Liu X, Chan P, Wu X. Jiang Y, et al. Among authors: liu x. Hum Genet. 2012 Jul;131(7):1217-24. doi: 10.1007/s00439-012-1149-3. Epub 2012 Feb 26. Hum Genet. 2012. PMID: 22367439

2

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Lu J, Chen Y, Zhang Y, Pan H, Liu X, Jiang Y, Du W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Jun;19(3):183-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12048673 Chinese.

3

Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy.

Lu J, Chen Y, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Ding K, Shen Y, Wu X. Lu J, et al. Among authors: liu x. Neurosci Lett. 2002 Oct 31;332(2):75-8. doi: 10.1016/s0304-3940(02)00805-4. Neurosci Lett. 2002. PMID: 12384214 Clinical Trial.

4

Association between genetic variation of CACNA1H and childhood absence epilepsy.

Chen Y, Lu J, Pan H, Zhang Y, Wu H, Xu K, Liu X, Jiang Y, Bao X, Yao Z, Ding K, Lo WH, Qiang B, Chan P, Shen Y, Wu X. Chen Y, et al. Among authors: liu x. Ann Neurol. 2003 Aug;54(2):239-43. doi: 10.1002/ana.10607. Ann Neurol. 2003. PMID: 12891677

5

New variants in the CACNA1H gene identified in childhood absence epilepsy.

Liang J, Zhang Y, Wang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X. Liang J, et al. Among authors: liu x. Neurosci Lett. 2006 Oct 2;406(1-2):27-32. doi: 10.1016/j.neulet.2006.06.073. Epub 2006 Aug 14. Neurosci Lett. 2006. PMID: 16905256

6

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Wang J, Zhang Y, Liang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X. Wang J, et al. Among authors: liu x. Pediatr Neurol. 2006 Sep;35(3):187-90. doi: 10.1016/j.pediatrneurol.2006.03.006. Pediatr Neurol. 2006. PMID: 16939858

7

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Among authors: liu x. J Hum Genet. 2008;53(8):769-774. doi: 10.1007/s10038-008-0306-y. Epub 2008 Jun 20. J Hum Genet. 2008. PMID: 18566737

8

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.

Sun H, Zhang Y, Liu X, Ma X, Yang Z, Qin J, Jiang Y, Qi Y, Wu X. Sun H, et al. Among authors: liu x. J Hum Genet. 2010 Jul;55(7):421-7. doi: 10.1038/jhg.2010.39. Epub 2010 Apr 30. J Hum Genet. 2010. PMID: 20431604

9

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Zeng Q, Yang X, Zhang J, Liu A, Yang Z, Liu X, Wu Y, Wu X, Wei L, Zhang Y. Zeng Q, et al. Among authors: liu x, liu a. J Hum Genet. 2018 Jan;63(1):9-18. doi: 10.1038/s10038-017-0359-x. Epub 2017 Nov 13. J Hum Genet. 2018. PMID: 29215089 Free PMC article. Clinical Trial.

10

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population.

Chen Y, Lu J, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Zhou J, Liu W, Shi G, Shen Y, Wu X. Chen Y, et al. Among authors: liu x, liu w. Neurosci Lett. 2003 Apr 24;341(1):29-32. doi: 10.1016/s0304-3940(03)00124-1. Neurosci Lett. 2003. PMID: 12676336

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