Xiaoli Cheng

446 total citations
31 papers, 325 citations indexed

About

Xiaoli Cheng is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Xiaoli Cheng has authored 31 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 7 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Xiaoli Cheng's work include Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (8 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers). Xiaoli Cheng is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (8 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers). Xiaoli Cheng collaborates with scholars based in China, United States and Germany. Xiaoli Cheng's co-authors include Xuetao Yan, Xianghu He, Wenzhong Zheng, Hu Chen, Akiko Seki, Yu Wang, John R. Yates, Wei-meng Zhao, Guowei Fang and Hu Chen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Cellular Physiology and Cancer Letters.

In The Last Decade

Xiaoli Cheng

28 papers receiving 323 citations

Peers

Xiaoli Cheng
Dianer Yang United States
Claudia M Weller Netherlands
Silvia Catricalà Italy
Yingwu Shi China
Jie Peng China
Yunhe Gu China
Elaine Lu Wang Japan
Xiaoyang Lu China
Jiming Han China
Dianer Yang United States
Xiaoli Cheng
Citations per year, relative to Xiaoli Cheng Xiaoli Cheng (= 1×) peers Dianer Yang

Countries citing papers authored by Xiaoli Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Xiaoli Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoli Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaoli Cheng. A scholar is included among the top collaborators of Xiaoli Cheng 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 Xiaoli Cheng. Xiaoli Cheng 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
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Fu, Yixiao, Zhiliang Long, Qinghua Luo, et al.. (2021). Functional and Structural Connectivity Between the Left Dorsolateral Prefrontal Cortex and Insula Could Predict the Antidepressant Effects of Repetitive Transcranial Magnetic Stimulation. Frontiers in Neuroscience. 15. 645936–645936. 26 indexed citations
4.
Chen, Guoliang, et al.. (2021). Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency. Acta Haematologica. 144(6). 712–716. 2 indexed citations
5.
Wang, Li, Xuefei Tian, Xiaoli Cheng, et al.. (2019). Protective effects of GPR120 agonist-programmed macrophages on renal interstitial fibrosis in unilateral ureteral obstruction (UUO) rats. Biomedicine & Pharmacotherapy. 117. 109172–109172. 13 indexed citations
6.
Wang, Liwen, et al.. (2018). [Association of polymorphisms of NAPE-PLD and FAAH genes with schizophrenia in Chinese Han population].. PubMed. 35(2). 215–218. 4 indexed citations
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Yan, Xuetao, Jing‐Min Lu, Yu Wang, et al.. (2018). XIST accelerates neuropathic pain progression through regulation of miR‐150 and ZEB1 in CCI rat models. Journal of Cellular Physiology. 233(8). 6098–6106. 54 indexed citations
8.
Wang, Mingshan, et al.. (2018). Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage. International Journal of Hematology. 107(4). 436–441. 2 indexed citations
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Cheng, Xiaoli, et al.. (2018). HO-1 Overexpressed Mesenchymal Stem Cells Ameliorate Sepsis-Associated Acute Kidney Injury by Activating JAK/stat3 Pathway. Cellular and Molecular Bioengineering. 11(6). 509–518. 15 indexed citations
10.
Yan, Xuetao, Ying Zhao, Xiaoli Cheng, et al.. (2017). Inhibition of miR‐200b/miR‐429 contributes to neuropathic pain development through targeting zinc finger E box binding protein‐1. Journal of Cellular Physiology. 233(6). 4815–4824. 29 indexed citations
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Cheng, Xiaoli, et al.. (2017). A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient. Blood Coagulation & Fibrinolysis. 29(1). 67–74. 3 indexed citations
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Yang, Lihong, et al.. (2016). Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese Patients. Acta Haematologica. 135(4). 238–240. 9 indexed citations
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Cheng, Xiaoli, et al.. (2016). Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s. Blood Coagulation & Fibrinolysis. 27(4). 461–463. 4 indexed citations
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Cheng, Xiaoli, et al.. (2016). A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families. Blood Coagulation & Fibrinolysis. 27(7). 838–844. 3 indexed citations
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Jin, Lu, et al.. (2013). Association of Single-Nucleotide Polymorphisms in the Cannabinoid Receptor 2 Gene with Schizophrenia in the Han Chinese Population. Journal of Molecular Neuroscience. 51(2). 454–460. 21 indexed citations
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Liu, Chunsheng, et al.. (2013). Accurate identification of Psammosilene tunicoides and its confused species by systematic identification method. China Journal of Chinese Materia Medica. 38(8). 1134–7. 1 indexed citations
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Wang, Liwen, et al.. (2013). [Association between ESR1 gene polymorphisms and haplotypes with schizophrenia].. PubMed. 30(1). 21–5. 1 indexed citations
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Chen, Ziping, et al.. (2010). Effects of selected genetic polymorphisms in xeroderma pigmentosum complementary group D on gastric cancer. Molecular Biology Reports. 38(3). 1507–1513. 11 indexed citations
20.
Cheng, Xiaoli, et al.. (2008). Clinicopathological evaluation of immunohistochemical Ki-67 and endothelial nitric oxide synthase expression in intracranial ependymoma. Clinical and investigative medicine. 31(4). E206–E211. 4 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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