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S

Sheng Luo

guangzhou medical university

15H指数
63论文数
620被引数
收录论文 29
发表时间
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RLIM variant associated with X-linked epilepsy with neurodevelopmental disorders and the molecular sub-regional effects与X连锁癫痫伴神经发育障碍相关的RLIM变异及其分子亚区效应
errSeizure: European Journal of Epilepsy
IF0
err2026-06-14
err0
PREAI
errSi-Qi Zhang; Zhi-Hong Lao; Wen-Hui Liu; Sheng Luo; Peng-Yu Wang; Bing-Mei Li; Jie Wang; Xiao-Rong Liu; Yi-Bo Qu; Qian-Ru Wen; Heng Meng; Yan Ding
err分享
err收藏
Correction: Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report更正：晚发型Krabbe病以全身强直-阵挛性癫痫发作作为首发症状：一个病例报告
errFrontiers in Behavioral Neuroscience
IF2.9
err2025-12-02
err0
errOAAI
errSifen Xie†; Zuying Kuang†; Mengqiu Pan; Kanghua Zhang; Jinlong Ye; Bo Li; Sheng Luo; Zhanhang Wang
err分享
err收藏
Identification of writers and erasers in tomato and their response to drought stress and hormones在番茄中鉴定writers和erasers及其对干旱胁迫和激素的响应
errPlant Cell Reports
IF4.5
err2025-12-02
err0
PREAI
errYushi Lu; Sheng Luo; Jing Cui; Yuxia Yao; Yuna Pan; Wenjin Yu; Changxia Li
err分享
err收藏
Evaluation of reflective ring facilities in different segments of highway tunnels based on factor analysis基于因子分析对高速公路隧道不同区段反射环设施的评价
errTransportation Safety and Environment
IF3
err2025-11-14
err0
errOAAI
errHonglin Mu; Xinyuan Wang; Wenhua Ma; Yanqun Yang; Sheng Luo; Yan Jiang
err分享
err收藏
De novo truncating variant in the FBRSL1 gene caused neurodevelopmental disorders, epilepsy, congenital heart disease, and facial dysmorphismFBRSL1基因中的全新截断变异导致神经发育障碍、癫痫、先天性心脏病和面部畸形。
errExperimental Neurology
IF4.2
err2025-11-11
err0
PREAI
errDan Xu; Xiao-Li Zhang; Peng-Yu Wang; Man-Man Chu; Jia-Yang Xie; Meng-Yue Wang; Xiao-Li Li; Yun-Fei Xu; Jin Liu; Qian-Ru Wen; Yang Fang; Jin-Shuang Gao; Fa-Lin Xu; Sheng Luo
err分享
err收藏
Generalized tonic-clonic seizures as the initial symptom of late-onset Krabbe disease: a Case Report全身强直-阵挛性癫痫发作作为迟发性Krabbe病的首发症状：病例报告
errFrontiers in Behavioral Neuroscience
IF2.9
err2025-11-06
err0
errOAAI
errSifen Xie†; Zuying Kuang†; Mengqiu Pan; Kanghua Zhang; Jinlong Ye; Bo Li; Sheng Luo; Zhanhang Wang
err分享
err收藏
De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum新生的SRCAP基因变异导致发育性癫痫性脑病及其表型谱
errEpilepsia
IF6.6
err2025-10-27
err0
PREAI
errXiao-Yu Liang; Xiang-Hong Meng; Wu-Chen Wu; Jing Guo; Sheng Luo; Peng-Yu Wang; Dong-Ming Zhang; Zi-Sheng Lin; Jin-Jie Liang; Su-Li He; Bing-Mei Li; Jie Wang; Yong-Hong Yi; Na He; Wei-Ping Liao; for the China Epilepsy Gene 1.0 Project
err分享
err收藏
Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny回复：USP25在遗传性全身性癫痫中的作用：一个备受关注的基因
errBrain
IF11.7
err2025-10-27
err0
PREAI
errZi-Long Ye; Wen-Bin Li; Cui-Xia Fan; Jie Wang; Bin Li; Sheng Luo; Zi-Sheng Lin; Liang-Di Gao; Tao Su; Yong-Hong Yi; Yi-Wu Shi; Wei-Ping Liao
err分享
err收藏
Metal powder atomization preparation, modification, and reuse for additive manufacturing: A review金属粉末雾化制备、改性及在增材制造中的回收利用：综述
errPROGRESS IN MATERIALS SCIENCE
IF40
err2025-06-01
err4
PREAI
errRen, Pengyuan; Ouyang, Yu; Mu, Jierui; Luo, Sheng; Tang, Zijue; Wu, Yi; Leung, Chu Lun Alex; Oliveira, J. P.; Zou, Yu; Wang, Haowei; Wang, Hongze
err分享
err收藏
Protective effect of CACNA1A deficiency in oligogenic refractory epilepsy with CACNA1A-CELSR2 digenic mutationsCACNA1A缺乏在携带CACNA1A-CELSR2双基因突变的寡基因难治性癫痫中的保护作用
errEPILEPSIA
IF6.6
err2025-04-04
err0
PREAI
errChu-Qiao Liu; Mei-Zhen Sun; Yong-Miao Lin; Xi-Xing Zhang; Rui-Na Huang; Ming-Feng He; Sheng Luo; Si-Yuan Luo; Tao Huang; Nan Jiang; Jie Luo; Jia-Xin Zhang
err分享
err收藏
De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy新生TANC2基因变异导致发育性癫痫性脑病和癫痫
errEPILEPSIA
IF6.6
err2025-03-20
err0
PREAI
errSheng Luo; Wen-Jun Zhang; Mi Jiang; Rong-Na Ren; Lei Liu; Yu-Lan Li; Wen-Hui Liu; Peng-Yu Wang; Yu-Jie Gu; Li-Zhi Chen; Li-Ping Shen; Yang Tian
err分享
err收藏
De Novo ACTB Variant Associated With Juvenile-Onset Temporal Lobe Epilepsy With Favorable Outcomes
errHUMAN MUTATION
IF3.7
err2025-02-12
err1
errOAAI
errYan, Hong-Jun; Wang, Peng-Yu; Liu, Wen-Hui; Gu, Yu-Jie; Pan, Jia-Cheng; Li, Hua; Luo, Sheng
err分享
err收藏
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disordersEP400中的变体，编码染色质重塑物，导致神经发育障碍的癫痫
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-01-01
err9
PREAI
errLuo, Sheng; Wang, Peng-Yu; Zhou, Peng; Zhang, Wen-Jun; Gu, Yu-Jie; Liang, Xiao-Yu; Zhang, Jing-Wen; Luo, Jun-Xia; Zhang, Hong-Wei; Lan, Song; Zhang, Ting-Ting; Yang, Jie-Hua; Sun, Su-Zhen; Guo, Xiang-Yang; Wang, Ju-Li; Deng, Lin-Fan; Xu, Ze-Hai; Jin, Liang; He, Yun-Yan; Ye, Zi-Long; Gu, Wei-Yue; Li, Bing-Mei; Shi, Yi-Wu; Liu, Xiao-Rong; Yan, Hong-Jun; Yi, Yong-Hong; Jiang, Yu-Wu; Mao, Xiao; Li, Wen-Ling; Meng, Heng; Liao, Wei-Ping
err分享
err收藏
The impact of coaxial gas technology on the morphology of powder by gas atomisation and the additive manufactured mechanical performance
errVIRTUAL AND PHYSICAL PROTOTYPING
IF8.8
err2024-07-22
err0
errOAAI
errLuo, Sheng; Wei, Qianglong; Yu, Ouyang; Wang, An; Tang, Zijue; Sun, Hua; Wang, Shimao; Wu, Yi; Wang, Haowei; Wang, Hongze
err分享
err收藏
The Impact of Different Ventilation Conditions on Electric Bus Fires
errFIRE-SWITZERLAND
IF2.7
err2024-05-25
err1
errOAAI
errYao, Haowei; Xing, Mengyang; Song, Huaitao; Zhang, Yang; Luo, Sheng; Bai, Zhenpeng
err分享
err收藏
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2024-03-20
err11
errOAAI
errHe, Ming-Feng; Liu, Li-Hong; Luo, Sheng; Wang, Juan; Guo, Jia-Jun; Wang, Peng-Yu; Zhai, Qiong-Xiang; He, Su-Li; Zou, Dong-Fang; Liu, Xiao-Rong; Li, Bing-Mei; Ma, Hai-Yan; Qiao, Jing-Da; Zhou, Peng; He, Na; Yi, Yong-Hong; Liao, Wei-Ping
err分享
err收藏
ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus (vol 15, 889534, 2022)ATP6V0C与热性惊厥和癫痫伴热性惊厥plus (vol 15，889534，2022) 相关
errFRONTIERS IN MOLECULAR NEUROSCIENCE
IF3.8
err2024-03-01
err0
errOAAI
errTian, Yang; Zhai, Qiong-Xiang; Li, Xiao-Jing; Shi, Zhen; Cheng, Chuan-Fang; Fan, Cui-Xia; Tang, Bin; Zhang, Ying; He, Yun-Yan; Li, Wen-Bin; Luo, Sheng; Hou, Chi; Chen, Wen-Xiong; Liao, Wei-Ping; Wang, Jie
err分享
err收藏
De novo GABRA1 variants in childhood epilepsies and the molecular subregional effects
errFRONTIERS IN MOLECULAR NEUROSCIENCE
IF3.8
err2024-01-10
err8
errOAAI
errLiu, Wen-Hui; Luo, Sheng; Zhang, Dong-Ming; Lin, Zi-Sheng; Lan, Song; Li, Xin; Shi, Yi-Wu; Su, Tao; Yi, Yong-Hong; Zhou, Peng; Li, Bing-Mei
err分享
err收藏
A new neurodevelopmental disorder linked to heterozygous variants in UNC79
errGENETICS IN MEDICINE
IF6.2
err2023-09-01
err7
PREAI
errBayat, Allan; Liu, Zhenjiang; Luo, Sheng; Fenger, Christina D.; Hojte, Anne F.; Isidor, Bertrand; Cogne, Benjamin; Larson, Austin; Zanus, Caterina; Faletra, Flavio; Keren, Boris; Musante, Luciana; Gourfikel-An, Isabelle; Perrine, Charles; Demily, Caroline; Lesca, Gaeton; Liao, Weiping; Ren, Dejian
err分享
err收藏
SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation与部分性癫痫或癫痫性脑病相关的SZT2变异及其基因型-表型相关性
errFRONTIERS IN MOLECULAR NEUROSCIENCE
IF3.8
err2023-05-05
err12
errOAAI
errLuo, Sheng; Ye, Xing-Guang; Jin, Liang; Li, Huan; He, Yun-Yan; Guan, Bao-Zhu; Gao, Liang-Di; Liang, Xiao-Yu; Wang, Peng-Yu; Lu, Xin-Guo; Yan, Hong-Jun; Li, Bing-Mei; Chen, Yong-Jun; Liu, Zhi-Gang
err分享
err收藏

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