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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1983 2
1986 2
1988 1
1989 2
1991 2
1992 1
1993 1
1994 1
1996 2
2002 3
2003 5
2004 10
2005 10
2006 10
2007 7
2008 15
2009 17
2010 21
2011 25
2012 17
2013 23
2014 15
2015 23
2016 26
2017 32
2018 30
2019 33
2020 33
2021 41
2022 35
2023 58
2024 55
2025 52
2026 45

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597 results

Results by year

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Page 1
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.
Luo S, Wang PY, Zhou P, Zhang WJ, Gu YJ, Liang XY, Zhang JW, Luo JX, Zhang HW, Lan S, Zhang TT, Yang JH, Sun SZ, Guo XY, Wang JL, Deng LF, Xu ZH, Jin L, He YY, Ye ZL, Gu WY, Li BM, Shi YW, Liu XR, Yan HJ, Yi YH, Jiang YW, Mao X, Li WL, Meng H, Liao WP. Luo S, et al. Among authors: liu xr. Am J Hum Genet. 2025 Jan 2;112(1):87-105. doi: 10.1016/j.ajhg.2024.11.010. Epub 2024 Dec 20. Am J Hum Genet. 2025. PMID: 39708813 Free PMC article.
Systemic immune activity occurs during human immune system maturation.
He S, Luo CL, Luo T, Chen HT, Zhang SF, Jiang JX, Wang XY, Ma D, Zhao SL, Xu AY, He JJ, Ruan ZH, Yan WX, Xu ZH, Liu Y, Huang QT, Gan YJ, Wang TL, Tang YH, Liu XR, Zhu CX, Li L, Wang ZL, Guo ZY, Bei JX, He XS. He S, et al. Among authors: liu xr. Cell. 2025 Dec 11;188(25):7291-7308.e23. doi: 10.1016/j.cell.2025.10.003. Epub 2025 Oct 28. Cell. 2025. PMID: 41161316 Free article.
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia.
Liu XR, Ye TT, Zhang WJ, Guo X, Wang J, Huang SP, Xie LS, Song XW, Deng WW, Li BM, He N, Wu QY, Zhuang MZ, Xu M, Shi YW, Su T, Yi YH, Liao WP; China Epilepsy Gene 1.0 Project. Liu XR, et al. CNS Neurosci Ther. 2021 Oct;27(10):1146-1156. doi: 10.1111/cns.13692. Epub 2021 Jun 9. CNS Neurosci Ther. 2021. PMID: 34109749 Free PMC article.
Editorial: Sub-molecular mechanism of genetic epilepsy.
Liao WP, Chen Q, Jiang YW, Luo S, Liu XR. Liao WP, et al. Among authors: liu xr. Front Mol Neurosci. 2022 Jul 26;15:958747. doi: 10.3389/fnmol.2022.958747. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35959103 Free PMC article. No abstract available.
Heterozygous variants in USP25 cause genetic generalized epilepsy.
Fan CX, Liu XR, Mei DQ, Li BM, Li WB, Xie HC, Wang J, Shen NX, Ye ZL, You QL, Li LY, Qu XC, Chen LZ, Liang JJ, Zhang MR, He N, Li J, Gao JY, Deng WY, Liu WZ, Wang WT, Liao WP, Chen Q, Shi YW. Fan CX, et al. Among authors: liu xr. Brain. 2024 Oct 3;147(10):3442-3457. doi: 10.1093/brain/awae191. Brain. 2024. PMID: 38875478 Free article.
Role of oral microbiota in atherosclerosis.
Liu XR, Xu Q, Xiao J, Deng YM, Tang ZH, Tang YL, Liu LS. Liu XR, et al. Clin Chim Acta. 2020 Jul;506:191-195. doi: 10.1016/j.cca.2020.03.033. Epub 2020 Mar 24. Clin Chim Acta. 2020. PMID: 32220421 Review.
UNC13B variants associated with partial epilepsy with favourable outcome.
Wang J, Qiao JD, Liu XR, Liu DT, Chen YH, Wu Y, Sun Y, Yu J, Ren RN, Mei Z, Liu YX, Shi YW, Jiang M, Lin SM, He N, Li B, Bian WJ, Li BM, Yi YH, Su T, Liu HK, Gu WY, Liao WP. Wang J, et al. Among authors: liu xr. Brain. 2021 Nov 29;144(10):3050-3060. doi: 10.1093/brain/awab164. Brain. 2021. PMID: 33876820 Free PMC article.
597 results