孟珩

医学博士，主任医师，副教授，硕士研究生导师。暨南大学附属第一医院癫痫中心副主任。本科毕业于中南大学湘雅医学院，博士就读于广州医科大学神经科学研究所。长期从事癫痫、脑血管病及神经遗传病学研究，国家自然科学基金和广东省自然科学基金通讯评审专家。

2014-2016年广东省优秀博士论文获得者；2015-2017年度梁仲景医学科研奖二等奖；2018年荣获首批广东省医学杰出青年医学人才2018年荣获广东省最强科室实力中青年医生称号； 2018年获得广东省“好医生好故事仁心奖”；2018年“卒中菁莘计划”全国总决赛优胜奖；2020年广东省青年五四奖章个人奖项；2020年“暨南大学青年榜样”；2020年所在援鄂医疗队荣获了中宣部十大“时代楷模”光荣称号

[1] Heng Meng#, Hai-Qing Xu, Lu Yu, Guo-Wang Lin, Na He, Tao Su, Yi-Wu Shi, Xiao-Rong Liu, Bin Tang, Yue-Sheng Long, Yong-Hong Yi, and Wei-Ping Liao*. The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype. Human Mutation, 2015, 36(6):573-580.[2] Heng Meng#, Bin Tang, Yong-Hong Yi, and Wei-Ping Liao*. Splice-site Mutations in SCN1A Cause Epilepsies with Febrile Seizures: Mechanisms and Correlations with Clinical Severity. Epilepsia. 2013. 54(Suppl.3): 192. [3] Liu XR#, Wu M, He N, Heng Meng, Wen L, Wang JL, Zhang MP, Li WB, Mao X, Qin JM, Li BM, Tang B, Deng YH, Shi YW, Su T, Yi YH, Tang BS, Wei-Ping Liao*. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes. Genes Brain Behav. 2013 Mar;12(2):234-40. [4] Shi YW#, Yu MJ, Long YS, Qin B, He N, Heng Meng, Liu XR, Deng WY, Gao MM, Yi YH, Li BM, Wei-Ping Liao*. Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures. Genes Brain Behav. 2012 Mar;11(2):170-6..[5]张美品#，孟珩#（并列第一作者），何娜，高曲文，秦兵，陈勇军，石奕武，陈亮，易咏红，廖卫平，黎冰梅*。热性惊厥附加症伴孤独症与临床及SCN1A基因突变的相关性分析。实用医学杂志，2014，30（05）：729-731。[6]孟珩#，余璐，李斌，况耀鋆，徐安定，郑金瓯，廖卫平*。SCN1A基因突变导致部分性癫痫伴热性惊厥附加征的分子特性分析。癫痫杂志，2015，1（2）：101-105.[7] Xiao-Rong Liu#, Dan Huang, Jie Wang, Yi-Fan Wang, Hui Sun, Bin Tang, Wen Li, Jin-Xing Lai, Na He, Mei Wu, Tao Su, Heng Meng, Yi-Wu Shi, Bing-Mei Li, Bei-Sha Tang, Wei-Ping Liao*, Paroxysmal hypnogenic dyskinesia is associated with mutations in the RRT2 gene. Neurol Genet. 2016, 2(2), e66. [8] Jing-Yang Wang#, Peng Zhou, Jie Wang, Bin Tang, Tao Su, Xiao-Rong Liu, Bing-Mei Li, Heng Meng, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao*. ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation. Neurogenetics, 2018, 19(1): 1-8.[9]Zefeng Tan#, Heng Meng#, Xiufeng Xing, Ying Zhao, Anding Xu*. Blood pressure variability estimated by average real variability predicts stroke in progression of acute ischemic stroke. Biomedical Research, 2018; 29(5):1001-1007.[10] P. Zhou#, N. He, J.-W. Zhang, Z.-J. Lin, J. Wang, L.-M. Yan, H. Meng, B. Tang, B.-M. Li, X.-R. Liu, Y.-W. Shi, Q.-X. Zhai, Y.-H. Yi, W.-P. Liao*. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies. Genes, Brain and Behavior, 2018, 8;e12456.[11] Na He, Zhi-Jian Lin, Jie Wang, Feng Wei, Heng Meng, Xiao-Rong Liu, Qian Chen, Tao Su, Yi-Wu Shi, Yong-Hong Yi, Wei-Ping Liao. Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies. Genetics in Medicine, 2019 01;21(1)[12]Zefeng Tan, Heng Meng, Dawei Dong, Ying Zhao, Anding Xu. Blood pressure variability estimated by ARV is a predictor of poor short-term outcomes in a prospective cohort of minor ischemic stroke. PLoS One, 2018, 13(8): e0202317.[13] Wen Li, Yifan Wang, Bin Li, Bin Tang, Hui Sun, Jinxing Lai, Na He, Bingmei Li, Heng Meng, Weiping Liao, Xiaorong Liu. 16p11.2 deletion in patients with paroxysmal kinesigenic dyskinesia but without intellectual disability. Brain and Behavior, 2018:e01134.[14]Liu L, Chen ZR, Xu HQ, Liu DT, Mao Y, Liu HK, Liu XR, Zhou P, Lin SM, Li B, He N, Su T, Zhai QX, Meng H, Liao WP, Yi YH, DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect. Front Neurosci.2020 Aug 11;14:821.[15]Yang WY, Tan ZF, Dong DW, Ding Y, Meng H, Zhao Y, Xin XF, Bi W, Association of aquaporin 1 with tumor migration, invasion and vasculogenic mimicry in glioblastoma multiforme. Mol Med Rep. 2018 Feb;17(2):3206-3211.[16]Chen ZR, Liu DT, Meng H, Liu L, Bian WJ, Liu XR, Zhu WW, He Y, Wang J, Tang B, Su T, Yi YH, Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation. Seizure2019 Jul;69:180-185.[17]He N, Li BM, Li ZX, Wang J, Liu XR, Meng H, Tang B, Bian WJ, Shi YW, Liao WP, Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome J Neurodev Disord. 2018 Mar 20;10(1):10.[18]癫痫综合征及临床治疗(第二版)。CP Panayiotopoulos (参与译著)[19]参加2012中国抗癫痫协会举办的第二届癫痫夏令营及2019年国际癫痫夏令营，并获得由国际抗癫痫协会及亚太癫痫协会联合签发的合格证书。2019年拿到国际抗癫痫协会认证的脑电图ASEPA资格证书[20]参加2013中国抗癫痫协会举办的“广州国际癫痫综合征学术研讨会”，并担任大会外籍教授授课随声翻译。

目前担任中国抗癫痫学会青年委员会委员，中国抗癫痫学会精准医疗与药物不良反应分会常务，广东省精准医学应用学会静脉血栓分会常委，广东省医师协会神经内科医师分会委员兼秘书，广东省医学会神经病学分会第九届委员会癫痫学组委员，广东省抗癫痫协会常务理事。欧洲癫痫杂志《Seizure: European Journal of Epilepsy》特约审稿人。获得国际抗癫痫协会脑电图ASEPA资格认证。同时也是国家卫健委脑防委卒中中心检查专家组成员。首批广东省医学杰出青年医学人才。

擅长癫痫、脑血管病、头晕及神经遗传学疾病。

癫痫、脑血管病、头晕及神经遗传学疾病。