Mengnan Xu

1.7k total citations
60 papers, 1.1k citations indexed

About

Mengnan Xu is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Mengnan Xu has authored 60 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Surgery, 11 papers in Pediatrics, Perinatology and Child Health and 11 papers in Genetics. Recurrent topics in Mengnan Xu's work include Prenatal Screening and Diagnostics (11 papers), Calcium signaling and nucleotide metabolism (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Mengnan Xu is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Calcium signaling and nucleotide metabolism (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Mengnan Xu collaborates with scholars based in China, Canada and United States. Mengnan Xu's co-authors include David S. Cram, Xian‐Ping Dong, Peng Huang, Xiaosi Qi, Wei Zhong, Chak‐Tong Au, Fuli Yu, Hongmin Zhu, Huaiyu Sun and Feng Tian and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Scientific Reports and Chemical Engineering Journal.

In The Last Decade

Mengnan Xu

54 papers receiving 1.0k citations

Peers

Mengnan Xu
Mengnan Xu
Citations per year, relative to Mengnan Xu Mengnan Xu (= 1×) peers Xiaojin He

Countries citing papers authored by Mengnan Xu

Since Specialization
Citations

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

Fields of papers citing papers by Mengnan Xu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mengnan Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Mengnan Xu. A scholar is included among the top collaborators of Mengnan Xu 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 Mengnan Xu. Mengnan Xu 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
2.
Xu, Mengnan, Lina Yang, Hong Song, et al.. (2025). Preparation of size-controlled soy hull polysaccharide nanomicelles and evaluation of hypoglycaemic activity in type 2 diabetes zebrafish. International Journal of Biological Macromolecules. 321(Pt 4). 146587–146587. 1 indexed citations
3.
Liu, Ying, Mengnan Xu, Jing Zhang, et al.. (2025). Long-Term Efficacy of Repeated Endoscopic Incision Combined with Triamcinolone Injection in Patients with Recurrent Benign Esophageal Stricture. Digestive Diseases and Sciences. 70(9). 3077–3088.
4.
Song, Xinxin, Shuyue Zhang, Mengnan Xu, et al.. (2025). Experimental investigation on dynamic adhesion characteristics of wheel-rail under various media conditions at a large slip ratio range. Wear. 580-581. 206217–206217.
6.
Xue, Sen, et al.. (2024). The screening of α-glucosidase inhibitory peptides from β-conglycinin and hypoglycemic mechanism in HepG2 cells and zebrafish larvae. International Journal of Biological Macromolecules. 278(Pt 1). 134678–134678. 6 indexed citations
7.
Zheng, Xiaohua, et al.. (2024). Construction of novel dual Z-scheme g-C3N4/Ag2MoO4/AgBr heterojunction for efficient degradations of RhB dye and tetracycline hydrochloride under visible-light. Inorganic Chemistry Communications. 162. 112227–112227. 9 indexed citations
8.
Zheng, Xiaohua, et al.. (2024). Enhanced photocatalytic activity of BiOCl/BiOBr/SnS2 heterojunction using a superfine SnS2 and double S-scheme. Journal of Alloys and Compounds. 980. 173630–173630. 13 indexed citations
9.
Sui, Li, Mengnan Xu, Jianfeng Liu, et al.. (2024). Insect hypovirulence-associated mycovirus confers entomopathogenic fungi with enhanced resistance against phytopathogens. Virulence. 15(1). 2401978–2401978. 4 indexed citations
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11.
Huang, Peng, et al.. (2022). Lysosomal Potassium Channels. Handbook of experimental pharmacology. 278. 127–152. 3 indexed citations
12.
Xu, Mengnan, et al.. (2022). Lysosomal potassium channels. Cell Calcium. 102. 102536–102536. 13 indexed citations
14.
Huang, Peng, et al.. (2020). Multiple facets of TRPML1 in autophagy. Cell Calcium. 88. 102196–102196. 15 indexed citations
15.
Sun, Xue, Mengnan Xu, Qi Cao, et al.. (2020). A lysosomal K+ channel regulates large particle phagocytosis by facilitating lysosome Ca2+ release. Scientific Reports. 10(1). 1038–1038. 37 indexed citations
16.
Zhang, Rui, Xiangbin Chen, Dong Wang, et al.. (2019). Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders. Journal of International Medical Research. 47(3). 1169–1178. 20 indexed citations
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18.
Wang, Qian, et al.. (2019). The mTOR Signal Pathway Is Overactivated in Human Lymphatic Malformations. Lymphatic Research and Biology. 17(6). 624–629. 4 indexed citations
19.
Cram, David S., Hu Tan, Siyuan Linpeng, et al.. (2019). Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes. Genetics in Medicine. 21(9). 1998–2006. 167 indexed citations
20.
Han, Mingyu, Zhifeng Li, Wenlu Wang, et al.. (2017). A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations. Genetics in Medicine. 19(12). 1309–1316. 27 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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