Li N - Search Results

1

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.

Cong PK, Bai WY, Li JC, Yang MY, Khederzadeh S, Gai SR, Li N, Liu YH, Yu SH, Zhao WW, Liu JQ, Sun Y, Zhu XW, Zhao PP, Xia JW, Guan PL, Qian Y, Tao JG, Xu L, Tian G, Wang PY, Xie SY, Qiu MC, Liu KQ, Tang BS, Zheng HF. Cong PK, et al. Among authors: li n, li jc. Nat Commun. 2022 May 26;13(1):2939. doi: 10.1038/s41467-022-30526-x. Nat Commun. 2022. PMID: 35618720 Free PMC article.

2

Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

Che XQ, Sun ZF, Mao X, Xia K, Yan XX, Jiang H, Shen L, Li N, Tang BS. Che XQ, et al. Among authors: li n. Int J Neurosci. 2017 Jan;127(1):10-13. doi: 10.3109/00207454.2015.1136886. Epub 2016 Apr 6. Int J Neurosci. 2017. PMID: 26954261

3

[PRRT2 gene-related paroxysmal disorders].

Li J, Mao X, Wang J, Li N, Tang B. Li J, et al. Among authors: li n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):595-9. doi: 10.3760/cma.j.issn.1003-9406.2014.01.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297589 Review. Chinese.

4

Exon dosage analysis of parkin gene in Chinese sporadic Parkinson's disease.

Guo JF, Dong XL, Xu Q, Li N, Yan XX, Xia K, Tang BS. Guo JF, et al. Among authors: li n. Neurosci Lett. 2015 Sep 14;604:47-51. doi: 10.1016/j.neulet.2015.07.046. Epub 2015 Aug 1. Neurosci Lett. 2015. PMID: 26240990

5

Novel mutation of SCN1A in familial generalized epilepsy with febrile seizures plus.

Li N, Zhang J, Guo JF, Yan XX, Xia K, Tang BS. Li N, et al. Neurosci Lett. 2010 Aug 23;480(3):211-4. doi: 10.1016/j.neulet.2010.06.040. Epub 2010 Jun 18. Neurosci Lett. 2010. PMID: 20600615

6

L10P mutation in DJ-1 gene induced oxidative stress and mitochondrial disfunction.

Guo J, He D, Wang L, Kang J, Li N, Yan X, Tang B. Guo J, et al. Among authors: li n. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2015 Dec;40(12):1285-91. doi: 10.11817/j.issn.1672-7347.2015.12.001. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2015. PMID: 26739068 Free article.

7

Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases.

Wang JL, Mao X, Hu ZM, Li JD, Li N, Guo JF, Jiang H, Shen L, Li J, Shi YT, Xia K, Liu JY, Liao WP, Tang BS. Wang JL, et al. Among authors: li j, li n, li jd. Neurosci Lett. 2013 Sep 27;552:40-5. doi: 10.1016/j.neulet.2013.07.020. Epub 2013 Jul 26. Neurosci Lett. 2013. PMID: 23896529

8

LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population.

Li K, Tang BS, Liu ZH, Kang JF, Zhang Y, Shen L, Li N, Yan XX, Xia K, Guo JF. Li K, et al. Among authors: li n. Neurobiol Aging. 2015 Oct;36(10):2908.e11-5. doi: 10.1016/j.neurobiolaging.2015.07.012. Epub 2015 Jul 11. Neurobiol Aging. 2015. PMID: 26234753

9

A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.

Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B. Li H, et al. Among authors: li n. Epilepsy Res. 2008 Mar;79(1):1-5. doi: 10.1016/j.eplepsyres.2007.12.005. Epub 2008 Feb 4. Epilepsy Res. 2008. PMID: 18249525

10

Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism.

Yang Y, Tang BS, Weng L, Li N, Shen L, Wang J, Zuo CT, Yan XX, Xia K, Guo JF. Yang Y, et al. Among authors: li n. PLoS One. 2015 Aug 21;10(8):e0136245. doi: 10.1371/journal.pone.0136245. eCollection 2015. PLoS One. 2015. PMID: 26295349 Free PMC article.

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