Lingchao Meng

1.3k total citations
81 papers, 603 citations indexed

About

Lingchao Meng is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Lingchao Meng has authored 81 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 16 papers in Neurology. Recurrent topics in Lingchao Meng's work include Hereditary Neurological Disorders (19 papers), Muscle Physiology and Disorders (15 papers) and Genetic Neurodegenerative Diseases (13 papers). Lingchao Meng is often cited by papers focused on Hereditary Neurological Disorders (19 papers), Muscle Physiology and Disorders (15 papers) and Genetic Neurodegenerative Diseases (13 papers). Lingchao Meng collaborates with scholars based in China, United States and Romania. Lingchao Meng's co-authors include Yun Yuan, Zhaoxia Wang, Wei Zhang, He Lv, Wenbiao Liao, Sixing Yang, Yunhe Xiong, Meng Yu, Chao Song and Jianwen Deng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Annals of Neurology and The FASEB Journal.

In The Last Decade

Lingchao Meng

74 papers receiving 599 citations

Peers

Lingchao Meng

CMN

NEURO

SURGE

GENET

Saki Kondo Japan

Patrick L. Leslie United States

Kang Guo China

Zishan Wang China

Francesca Saladino Italy

Holly Martinson United States

Chunyu Cai United States

Edith Rian Norway

Julia Schreml Germany

Karin Ackermann Germany

Saki Kondo Japan

Lingchao Meng

375 ×1.1

41 ×0.3

CMN

17 ×0.2

NEURO

134 ×1.9

SURGE

121 ×1.9

GENET

Citations per year, relative to Lingchao Meng Lingchao Meng (= 1×) peers Saki Kondo

Countries citing papers authored by Lingchao Meng

Since Specialization

Citations

This map shows the geographic impact of Lingchao Meng'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 Lingchao Meng with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lingchao Meng more than expected).

Fields of papers citing papers by Lingchao Meng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lingchao Meng. 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 Lingchao Meng. The network helps show where Lingchao Meng may publish in the future.

Co-authorship network of co-authors of Lingchao Meng

This figure shows the co-authorship network connecting the top 25 collaborators of Lingchao Meng. A scholar is included among the top collaborators of Lingchao Meng 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 Lingchao Meng. Lingchao Meng is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Shao, Yiming, Xiaobei Zhang, Ping Li, et al.. (2024). Targeted nuclear degranulation of neutrophils promotes the progression of pneumonia in ulcerative colitis. Precision Clinical Medicine. 7(4). pbae028–pbae028. 2 indexed citations

Sun, Chengyue, Yilin Liu, Lingchao Meng, et al.. (2024). Single‐Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy. Annals of Neurology. 96(6). 1070–1085. 2 indexed citations

Zhang, Bing, Huapan Xiao, Wei Liu, et al.. (2024). Rapid prediction of electrohydrodynamically printed polyethylene oxide (PEO) fiber width by using response surface methodology. Journal of Mechanical Science and Technology. 38(11). 6169–6179.

Xie, Zhiying, Chang Liu, Haiyan Yu, et al.. (2024). Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies. Orphanet Journal of Rare Diseases. 19(1). 123–123. 2 indexed citations

Yu, Meng, Zhiying Xie, Lingchao Meng, et al.. (2024). Multiomics analysis reveals serine catabolism as a potential therapeutic target for MELAS. The FASEB Journal. 38(12). e23742–e23742. 1 indexed citations

Liu, Jing, Feng Gao, Hong-Jun Hao, et al.. (2023). CIDP/autoimmune nodopathies with nephropathy: a case series study. Annals of Clinical and Translational Neurology. 10(5). 706–718. 9 indexed citations

Li, Zhenyu, Yize Li, Kang Du, et al.. (2023). Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa. Neuropathology. 44(2). 87–95. 3 indexed citations

Song, Chao, Wenbiao Liao, Qianlin Song, et al.. (2023). An overview of global research landscape in etiology of urolithiasis based on bibliometric analysis. Urolithiasis. 51(1). 71–71. 9 indexed citations

Lü, Yanyu, Yunlong Lu, Li Bai, et al.. (2023). Clinical, pathological, and genetic characterization in a large Chinese cohort with female dystrophinopathy. Neuromuscular Disorders. 33(10). 728–736. 3 indexed citations

10.

Wang, Hui, Yilei Zheng, Jiaxi Yu, et al.. (2023). Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress. Neurobiology of Disease. 190. 106391–106391. 2 indexed citations

11.

Xie, Zhiying, Chang Liu, Chengyue Sun, et al.. (2023). Cryptic exon activation caused by a novel deep‐intronic splice‐altering variant in Becker muscular dystrophy. Journal of Clinical Laboratory Analysis. 37(21-22). e24987–e24987. 1 indexed citations

12.

Zheng, Yiming, Yikang Wang, Chengli Que, et al.. (2022). Thigh MRI in antisynthetase syndrome, and comparisons with dermatomyositis and immune-mediated necrotizing myopathy. Lara D. Veeken. 62(1). 310–320. 12 indexed citations

13.

Ma, Zhixing, He Lv, Hongwei Zhang, et al.. (2022). Clinicopathological features in two families with MARS‐related Charcot–Marie–Tooth disease. Neuropathology. 42(6). 505–511. 2 indexed citations

14.

Li, Yuxi, Lin Wu, Lingchao Meng, et al.. (2022). Case Report: Systemic Amyloidosis Involving the Heart and Skeletal Muscle. Frontiers in Cardiovascular Medicine. 9. 816236–816236.

15.

Xie, Zhiying, Chengyue Sun, Chang Liu, et al.. (2022). First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy. Frontiers in Pediatrics. 10. 900280–900280. 1 indexed citations

16.

Yu, Meng, Yawen Zhao, Yiming Zheng, et al.. (2022). Circulating cell-free mtDNA release is associated with the activation of cGAS-STING pathway and inflammation in mitochondrial diseases. Journal of Neurology. 269(9). 4985–4996. 25 indexed citations

17.

Nan, Haitian, Yunqing Wu, Jiawei Wang, et al.. (2022). Coexistence of Charcot-Marie-Tooth 1A and nondystrophic myotonia due to PMP22 duplication and SCN4A pathogenic variants: a case report. BMC Neurology. 22(1). 17–17. 1 indexed citations

18.

Wang, Hui, Jiaxi Yu, Meng Yu, et al.. (2021). GGC Repeat Expansion in the NOTCH2NLC Gene Is Associated With a Phenotype of Predominant Motor–Sensory and Autonomic Neuropathy. Frontiers in Genetics. 12. 694790–694790. 18 indexed citations

19.

Meng, Lingchao, et al.. (2015). [The clinical and muscular pathological features of statin-induced myopathy].. PubMed. 54(8). 716–20.

20.

Liao, Wenbiao, Sixing Yang, Chao Song, et al.. (2012). Tissue-engineered tubular graft for urinary diversion after radical cystectomy in rabbits. Journal of Surgical Research. 182(2). 185–191. 23 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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