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陈倩，主任医师，医学博士，教授，博士研究生导师。首都医科大学附属首都儿童医学中心癫痫中心科主任，工作方向为儿童癫痫、神经发育与认知的机制与临床研究，发表学术论文150余篇，其中SCI论文40余篇，任职中国抗癫痫协会理事、北京抗癫痫协会常务理事、北京转化医学学会儿童全生命周期健康管理分会会长、北京神经病学会癫痫专病委员会副主任委员等。
代表性论著如下：
1.Wu F, Ji X, Shen M, Cheng P, Feng S, Gao Y, Liu W, Chen J, Li S, Zhang X, Chen Q. Whole exome sequencing identifies KCNH7 variants associated with epilepsy in children. Genes Dis. 2024 May 9;12(2):101322.
2.Han Y, Ge Y, Liu H, Liu L, Xie L, Chen X, Chen Q. A novel compound heterozygous mutation of UFC1 in a patient with neurodevelopmental disorder. Genes Genomics. 2024 Sep;46(9):1037-1043.
3.Shen M, Chen Q, Gao Y, Yan H, Feng S, Ji X, Zhang X. A de novo heterozygous variant in ACOX1 gene cause Mitchell syndrome: the first case in China and literature review. BMC Med Genomics. 2023 Jul 3;16(1):156.
4.Shen M, Fan S, Wu F, Cheng P, Gao Y, Zheng P, Feng S, Ji X, Chen Q, Zhang X. Generation of a human iPSC line CIPi003-A from a patient with focal epilepsy harboring a heterozygous mutation in DEPDC5 gene. Stem Cell Res. 2023 Oct;72:103195.
5.Zhang JZ, Zheng P, Sun HM, Dong JJ, Li SL, Fan SY, Ren HT, Wu HL, Guan HZ, Chen Q. Next-generation sequencing combined with routine methods to detect the pathogens of encephalitis/meningitis from a Chinese tertiary pediatric neurology center. J Infect. 2019 May;78(5):409-421.
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