Feilong Meng

695 total citations
24 papers, 501 citations indexed

About

Feilong Meng is a scholar working on Molecular Biology, Clinical Biochemistry and Cancer Research. According to data from OpenAlex, Feilong Meng has authored 24 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Cancer Research. Recurrent topics in Feilong Meng's work include Mitochondrial Function and Pathology (17 papers), RNA modifications and cancer (12 papers) and RNA and protein synthesis mechanisms (12 papers). Feilong Meng is often cited by papers focused on Mitochondrial Function and Pathology (17 papers), RNA modifications and cancer (12 papers) and RNA and protein synthesis mechanisms (12 papers). Feilong Meng collaborates with scholars based in China, United States and Canada. Feilong Meng's co-authors include Min‐Xin Guan, Meng Wang, Yanchun Ji, Mi Zhou, Yun Xiao, Xiaohui Cang, Jing Zheng, Jun Qin Mo, Xiaoli Zhao and Juanjuan Zhang and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Investigative Ophthalmology & Visual Science.

In The Last Decade

Feilong Meng

24 papers receiving 497 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Feilong Meng China 16 462 80 66 44 25 24 501
Kim D. Falkenberg Netherlands 6 188 0.4× 32 0.4× 51 0.8× 29 0.7× 17 0.7× 9 253
Kevin Berendse Netherlands 8 301 0.7× 126 1.6× 28 0.4× 33 0.8× 47 1.9× 12 370
Robert B. Bentham United Kingdom 7 245 0.5× 16 0.2× 81 1.2× 23 0.5× 27 1.1× 10 286
Sakie Katsumura Japan 6 279 0.6× 29 0.4× 46 0.7× 38 0.9× 23 0.9× 8 359
Michael Martinez United States 6 243 0.5× 20 0.3× 28 0.4× 18 0.4× 12 0.5× 6 300
Dana Pearl Canada 2 226 0.5× 29 0.4× 38 0.6× 26 0.6× 17 0.7× 3 276
Marian León Spain 8 302 0.7× 28 0.3× 68 1.0× 13 0.3× 20 0.8× 14 365
Mariangela Corricelli Italy 5 202 0.4× 26 0.3× 33 0.5× 17 0.4× 4 0.2× 5 334
Shinsuke Ninomiya Japan 14 268 0.6× 41 0.5× 48 0.7× 10 0.2× 16 0.6× 31 444
Eveline M. Hogenhout Netherlands 6 407 0.9× 128 1.6× 58 0.9× 45 1.0× 21 0.8× 8 461

Countries citing papers authored by Feilong Meng

Since Specialization
Citations

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

Fields of papers citing papers by Feilong Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Feilong Meng

This figure shows the co-authorship network connecting the top 25 collaborators of Feilong Meng. A scholar is included among the top collaborators of Feilong 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 Feilong Meng. Feilong Meng 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.
Ji, Yanchun, Huanhuan Zhang, Kai Wang, et al.. (2025). Leber's hereditary optic neuropathy–associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasis. Journal of Biological Chemistry. 301(8). 110464–110464. 1 indexed citations
2.
Chen, Xiaowan, Feilong Meng, Chao Chen, et al.. (2024). Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity. Journal of Biological Chemistry. 300(5). 107235–107235. 6 indexed citations
3.
Meng, Feilong, Jing Zheng, Yanchun Ji, et al.. (2022). A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism. Nucleic Acids Research. 50(16). 9453–9469. 17 indexed citations
4.
Meng, Feilong, Xincheng Li, Xiao He, et al.. (2022). Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro. Nucleic Acids Research. 50(16). 9368–9381. 28 indexed citations
5.
Ji, Yanchun, Juanjuan Zhang, Min Liang, et al.. (2022). Mitochondrial tRNA variants in 811 Chinese probands with Leber’s hereditary optic neuropathy. Mitochondrion. 65. 56–66. 5 indexed citations
6.
Xu, Chengxian, Jia Rao, Qing Ye, et al.. (2022). Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia. JCI Insight. 7(11). 13 indexed citations
7.
Jin, Xiaofen, Zengming Zhang, Chenghui Wang, et al.. (2021). An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function. Journal of Biological Chemistry. 296. 100437–100437. 25 indexed citations
8.
Jin, Xiaofen, Juanjuan Zhang, Feilong Meng, et al.. (2021). Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations. Investigative Ophthalmology & Visual Science. 62(7). 22–22. 15 indexed citations
9.
Ji, Yanchun, Feilong Meng, Hui Chen, et al.. (2021). Mechanistic insights into mitochondrial tRNAAla 3’-end metabolism deficiency. Journal of Biological Chemistry. 297(1). 100816–100816. 21 indexed citations
10.
Xiao, Yun, Meng Wang, Lei Xu, et al.. (2020). Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts. Nucleic Acids Research. 48(19). 11113–11129. 15 indexed citations
11.
Ji, Yanchun, Juanjuan Zhang, Yuanyuan Lu, et al.. (2020). Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy. Journal of Biological Chemistry. 295(38). 13224–13238. 32 indexed citations
12.
Gong, Shasha, et al.. (2020). Novel Insights Into Triple-Negative Breast Cancer Prognosis by Comprehensive Characterization of Aberrant Alternative Splicing. Frontiers in Genetics. 11. 534–534. 9 indexed citations
13.
Zheng, Jing, Xiaohui Bai, Yun Xiao, et al.. (2020). Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss. Mitochondrion. 52. 163–172. 20 indexed citations
14.
Meng, Feilong, Mi Zhou, Yun Xiao, et al.. (2020). A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation. Nucleic Acids Research. 49(2). 1075–1093. 32 indexed citations
15.
Zhou, Qiyin, Hua Li, Yuanyuan Li, et al.. (2019). Inhibiting neddylation modification alters mitochondrial morphology and reprograms energy metabolism in cancer cells. JCI Insight. 4(4). 61 indexed citations
16.
Gong, Shasha, Xiaoqiong Wang, Feilong Meng, et al.. (2019). Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHismutation. Journal of Biological Chemistry. 295(4). 940–954. 16 indexed citations
17.
Meng, Feilong, Xiaowen Tang, Jing Zheng, et al.. (2018). Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation. Journal of Biological Chemistry. 293(9). 3321–3334. 33 indexed citations
18.
Zhou, Mi, Ling Xue, Yaru Chen, et al.. (2017). A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function. Journal of Biological Chemistry. 293(4). 1425–1438. 58 indexed citations
19.
20.

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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