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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: liao wp. 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
CELSR1 variants are associated with partial epilepsy of childhood.
Chen Z, Luo S, Liu ZG, Deng YC, He SL, Liu XR, Yi YH, Wang J, Gao LD, Li BM, Wu ZJ, Ye ZL, Liang DH, Bian WJ, Liao WP; China Epilepsy Gene 1.0 Project. Chen Z, et al. Among authors: liao wp. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):247-256. doi: 10.1002/ajmg.b.32916. Epub 2022 Aug 12. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 36453712
Epilepsy-associated genes.
Wang J, Lin ZJ, Liu L, Xu HQ, Shi YW, Yi YH, He N, Liao WP. Wang J, et al. Among authors: liao wp. Seizure. 2017 Jan;44:11-20. doi: 10.1016/j.seizure.2016.11.030. Epub 2016 Dec 6. Seizure. 2017. PMID: 28007376 Free article. 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: liao wp. Brain. 2021 Nov 29;144(10):3050-3060. doi: 10.1093/brain/awab164. Brain. 2021. PMID: 33876820 Free PMC article.
146 results