Sheng Luo

620 total citations
39 papers, 331 citations indexed

About

Sheng Luo is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Sheng Luo has authored 39 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 13 papers in Molecular Biology and 9 papers in Psychiatry and Mental health. Recurrent topics in Sheng Luo's work include Genomics and Rare Diseases (21 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Epilepsy research and treatment (9 papers). Sheng Luo is often cited by papers focused on Genomics and Rare Diseases (21 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Epilepsy research and treatment (9 papers). Sheng Luo collaborates with scholars based in China, United Kingdom and United States. Sheng Luo's co-authors include Yi Wu, Zhenyang Gao, Wei‐Ping Liao, Yu Ouyang, Yong‐Hong Yi, Haowei Wang, Bing-Mei Li, Qiong‐Xiang Zhai, Yunyan He and Xiao‐Rong Liu and has published in prestigious journals such as Progress in Materials Science, Experimental Neurology and Epilepsia.

In The Last Decade

Sheng Luo

36 papers receiving 323 citations

Peers

Sheng Luo
Irene Mitchell United Kingdom
Xiaoxiao Cui China
Yongbo Gao China
Chang-Cheng Chen China
Weihao Xu China
Masami Saito Japan
Hankui Liu China
Hendrik van Egmond Belgium
Irene Mitchell United Kingdom
Sheng Luo
Citations per year, relative to Sheng Luo Sheng Luo (= 1×) peers Irene Mitchell

Countries citing papers authored by Sheng Luo

Since Specialization
Citations

This map shows the geographic impact of Sheng Luo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sheng Luo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sheng Luo more than expected).

Fields of papers citing papers by Sheng Luo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sheng Luo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sheng Luo. The network helps show where Sheng Luo may publish in the future.

Co-authorship network of co-authors of Sheng Luo

This figure shows the co-authorship network connecting the top 25 collaborators of Sheng Luo. A scholar is included among the top collaborators of Sheng Luo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sheng Luo. Sheng Luo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ren, Pingda, Yu Ouyang, Sheng Luo, et al.. (2025). Metal powder atomization preparation, modification, and reuse for additive manufacturing: A review. Progress in Materials Science. 152. 101449–101449. 14 indexed citations
2.
Liu, Wenhui, et al.. (2025). De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis. Frontiers in Genetics. 16. 1499716–1499716. 1 indexed citations
3.
Meng, Xianghong, Wuchen Wu, Jing Guo, et al.. (2025). De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum. Epilepsia. 67(2). 846–861.
4.
Luo, Sheng, Wenjun Zhang, Lei Liu, et al.. (2025). De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy. Epilepsia. 66(7). 2365–2378. 3 indexed citations
5.
Pan, Jullie W., et al.. (2025). De Novo ACTB Variant Associated With Juvenile‐Onset Temporal Lobe Epilepsy With Favorable Outcomes. Human Mutation. 2025(1). 9951922–9951922. 3 indexed citations
6.
Wen, Q. G., Yan Ding, Sheng Luo, et al.. (2025). MDN1 variants cause susceptibility to epilepsy. PubMed. 7(1). 17–17. 1 indexed citations
7.
Zhang, Wenjun, Sheng Luo, Yunhong Wu, et al.. (2024). CSMD1 as a causative gene of developmental and epileptic encephalopathy and generalized epilepsies. Genes & Diseases. 12(4). 101473–101473. 6 indexed citations
8.
He, Ye, Xiaoyu Liang, Siqi Zhang, et al.. (2024). CCDC22 variants caused X-linked focal epilepsy and focal cortical dysplasia. Seizure. 123. 1–8. 8 indexed citations
9.
Luo, Sheng, Qianglong Wei, Yu Ouyang, et al.. (2024). The impact of coaxial gas technology on the morphology of powder by gas atomisation and the additive manufactured mechanical performance. Virtual and Physical Prototyping. 19(1). 3 indexed citations
10.
Lin, Xiukun, Sheng Luo, Pengyu Wang, et al.. (2024). Variants of TSC1 are associated with developmental and epileptic encephalopathy and focal epilepsy without tuberous sclerosis. PubMed. 6(1). 41–41. 2 indexed citations
11.
Ouyang, Yu, Sheng Luo, Hongze Wang, et al.. (2023). Synchrotron X-ray computed tomography analysis of the morphological characterization of aluminum alloy powders produced by gas atomization. Powder Technology. 429. 118904–118904. 9 indexed citations
12.
Jin, Liang, Sheng Luo, Qian Peng, et al.. (2023). Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders. Seizure. 111. 172–177. 7 indexed citations
13.
Luo, Sheng, et al.. (2023). Understanding the breakup behaviors of liquid jet in gas atomization for powder production. Materials & Design. 227. 111793–111793. 23 indexed citations
14.
Luo, Sheng, et al.. (2023). 3D numerical modeling of gas atomization process for powder preparation based on similarity theory. Powder Technology. 433. 119244–119244. 11 indexed citations
15.
Li, Ren‐Ke, Huan Li, Sheng Luo, et al.. (2023). Investigation of FRMPD4 variants associated with X-linked epilepsy. Seizure. 116. 45–50. 7 indexed citations
16.
Luo, Sheng, Xingguang Ye, Liang Jin, et al.. (2023). SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation. Frontiers in Molecular Neuroscience. 16. 1162408–1162408. 11 indexed citations
17.
Luo, Sheng, Yunqing Ma, Xinguo Lu, et al.. (2023). NEXMIF variants are associated with epilepsy with or without intellectual disability. Seizure. 116. 93–99. 11 indexed citations
18.
Li, Zongjun, Jie Wang, Sheng Luo, et al.. (2022). SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges. Frontiers in Molecular Neuroscience. 15. 862480–862480. 5 indexed citations
19.
Luo, Sheng, Bin Li, Lihong Liu, et al.. (2022). PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation. Frontiers in Neurology. 13. 836048–836048. 2 indexed citations
20.
Luo, Sheng, et al.. (2021). Interaction between high-velocity gas and liquid in gas atomization revealed by a new coupled simulation model. Materials & Design. 212. 110264–110264. 62 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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