Li J - Search Results

1

Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.

Li B, Zhao G, Li K, Wang Z, Fang Z, Wang X, Luo T, Zhang Y, Wang Y, Chen Q, Huang Y, Dong L, Guo J, Tang B, Li J. Li B, et al. Among authors: li j, li k. Front Neurosci. 2021 Apr 1;15:629156. doi: 10.3389/fnins.2021.629156. eCollection 2021. Front Neurosci. 2021. PMID: 33867917 Free PMC article.

2

VarCards: an integrated genetic and clinical database for coding variants in the human genome.

Li J, Shi L, Zhang K, Zhang Y, Hu S, Zhao T, Teng H, Li X, Jiang Y, Ji L, Sun Z. Li J, et al. Among authors: li x. Nucleic Acids Res. 2018 Jan 4;46(D1):D1039-D1048. doi: 10.1093/nar/gkx1039. Nucleic Acids Res. 2018. PMID: 29112736 Free PMC article.

3

A comparative study of the genetic components of three subcategories of autism spectrum disorder.

Li J, Hu S, Zhang K, Shi L, Zhang Y, Zhao T, Wang L, He X, Xia K, Liu C, Sun Z. Li J, et al. Mol Psychiatry. 2019 Nov;24(11):1720-1731. doi: 10.1038/s41380-018-0081-x. Epub 2018 Jun 6. Mol Psychiatry. 2019. PMID: 29875476

4

Performance evaluation of pathogenicity-computation methods for missense variants.

Li J, Zhao T, Zhang Y, Zhang K, Shi L, Chen Y, Wang X, Sun Z. Li J, et al. Nucleic Acids Res. 2018 Sep 6;46(15):7793-7804. doi: 10.1093/nar/gky678. Nucleic Acids Res. 2018. PMID: 30060008 Free PMC article.

5

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy.

Zeng S, Zhang MY, Wang XJ, Hu ZM, Li JC, Li N, Wang JL, Liang F, Yang Q, Liu Q, Fang L, Hao JW, Shi FD, Ding XB, Teng JF, Yin XM, Jiang H, Liao WP, Liu JY, Wang K, Xia K, Tang BS. Zeng S, et al. J Med Genet. 2019 Apr;56(4):265-270. doi: 10.1136/jmedgenet-2018-105484. Epub 2018 Sep 7. J Med Genet. 2019. PMID: 30194086

6

Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.

Zhao G, Li K, Li B, Wang Z, Fang Z, Wang X, Zhang Y, Luo T, Zhou Q, Wang L, Xie Y, Wang Y, Chen Q, Xia L, Tang Y, Tang B, Xia K, Li J. Zhao G, et al. Among authors: li j, li k, li b. Nucleic Acids Res. 2020 Jan 8;48(D1):D913-D926. doi: 10.1093/nar/gkz923. Nucleic Acids Res. 2020. PMID: 31642496 Free PMC article.

7

Mutation analysis of GLT8D1 and ARPP21 genes in amyotrophic lateral sclerosis patients from mainland China.

Li W, Liu Z, Sun W, Yuan Y, Hu Y, Ni J, Jiao B, Fang L, Li J, Shen L, Tang B, Wang J. Li W, et al. Among authors: li j. Neurobiol Aging. 2020 Jan;85:156.e1-156.e4. doi: 10.1016/j.neurobiolaging.2019.09.013. Epub 2019 Sep 25. Neurobiol Aging. 2020. PMID: 31653410

8

Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.

Sun QY, Xu Q, Tian Y, Hu ZM, Qin LX, Yang JX, Huang W, Xue J, Li JC, Zeng S, Wang Y, Min HX, Chen XY, Wang JP, Xie B, Liang F, Zhang HN, Wang CY, Lei LF, Yan XX, Xu HW, Duan RH, Xia K, Liu JY, Jiang H, Shen L, Guo JF, Tang BS. Sun QY, et al. Among authors: li jc. Brain. 2020 Jan 1;143(1):222-233. doi: 10.1093/brain/awz372. Brain. 2020. PMID: 31819945

9

Genetic evidence of gender difference in autism spectrum disorder supports the female-protective effect.

Zhang Y, Li N, Li C, Zhang Z, Teng H, Wang Y, Zhao T, Shi L, Zhang K, Xia K, Li J, Sun Z. Zhang Y, et al. Among authors: li c, li j, li n. Transl Psychiatry. 2020 Jan 15;10(1):4. doi: 10.1038/s41398-020-0699-8. Transl Psychiatry. 2020. PMID: 32066658 Free PMC article.

10

Identification of Alzheimer's disease-associated rare coding variants in the ECE2 gene.

Liao X, Cai F, Sun Z, Zhang Y, Wang J, Jiao B, Guo J, Li J, Liu X, Guo L, Zhou Y, Wang J, Yan X, Jiang H, Xia K, Li J, Tang B, Shen L, Song W. Liao X, et al. Among authors: li j. JCI Insight. 2020 Feb 27;5(4):e135119. doi: 10.1172/jci.insight.135119. JCI Insight. 2020. PMID: 32102983 Free PMC article.

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