Meili Lv

1.5k total citations
68 papers, 1.1k citations indexed

About

Meili Lv is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Meili Lv has authored 68 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 25 papers in Genetics and 13 papers in Cancer Research. Recurrent topics in Meili Lv's work include Molecular Biology Techniques and Applications (26 papers), Forensic and Genetic Research (24 papers) and MicroRNA in disease regulation (8 papers). Meili Lv is often cited by papers focused on Molecular Biology Techniques and Applications (26 papers), Forensic and Genetic Research (24 papers) and MicroRNA in disease regulation (8 papers). Meili Lv collaborates with scholars based in China, United States and Germany. Meili Lv's co-authors include Weibo Liang, Linbo Gao, Lin Zhang, Wei Dong, Zhaobo Wang, Xiaowei Su, Bin Zhou, Lin Zhang, Fan Yang and Peng Wang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer and Chemical Engineering Journal.

In The Last Decade

Meili Lv

62 papers receiving 1.1k citations

Peers

Meili Lv
Valérie Marchi France
Yun Zhou China
Min A Kim South Korea
Shuyang Wang China
Caiyun Zhou China
Swati Gupta United States
In-Hoo Kim South Korea
Hongling Huang China
Catherine Phelan United States
Carmela Dell’Aversana Italy
Valérie Marchi France
Meili Lv
Citations per year, relative to Meili Lv Meili Lv (= 1×) peers Valérie Marchi

Countries citing papers authored by Meili Lv

Since Specialization
Citations

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

Fields of papers citing papers by Meili Lv

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meili Lv

This figure shows the co-authorship network connecting the top 25 collaborators of Meili Lv. A scholar is included among the top collaborators of Meili Lv 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 Meili Lv. Meili Lv 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.
Xue, Jiaming, Guihong Liu, Yuanyuan Xiao, et al.. (2025). Explainable artificial intelligence in forensic DNA analysis: Alleles identification in challenging electropherograms using supervised machine learning methods. Forensic Science International Genetics. 78. 103289–103289.
2.
Sun, Yihan, Xiao Zhang, Meili Lv, et al.. (2024). From degraded to deciphered: ATAC-seq’s application potential in forensic diagnosis. International Journal of Legal Medicine. 138(4). 1273–1285.
3.
Yang, Qiuyun, Jinyuan Liu, Yang Xu, et al.. (2023). Intermittent fasting ameliorates neuronal ferroptosis and cognitive impairment in mice after traumatic brain injury. Nutrition. 109. 111992–111992. 15 indexed citations
4.
Zhang, Ranran, Jiaming Xue, Dezhi Chen, et al.. (2023). An MPS-Based 50plex Microhaplotype Assay for Forensic DNA Analysis. Genes. 14(4). 865–865. 10 indexed citations
5.
Liu, Guihong, Tao Feng, Dan Chen, et al.. (2023). Assessment of ForenSeq mtDNA Whole Genome Kit for forensic application. International Journal of Legal Medicine. 137(6). 1693–1703. 3 indexed citations
6.
Chen, Xiameng, Qiuyun Yang, Shuqiang Cao, et al.. (2023). Single-nucleus profiling of adult mice sub-ventricular zone after blast-related traumatic brain injury. Scientific Data. 10(1). 13–13. 4 indexed citations
7.
Jian, Hui, Li Wang, Meili Lv, et al.. (2021). A Novel SNP-STR System Based on a Capillary Electrophoresis Platform. Frontiers in Genetics. 12. 636821–636821. 8 indexed citations
8.
Zhu, Jing, Lu Yin, Meili Lv, et al.. (2019). Establishing a second-tier panel of 18 ancestry informative markers to improve ancestry distinctions among Asian populations. Forensic Science International Genetics. 41. 159–167. 11 indexed citations
9.
Zhu, Jing, Meili Lv, Nan Zhou, et al.. (2018). Genotyping polymorphic microhaplotype markers through the Illumina® MiSeq platform for forensics. Forensic Science International Genetics. 39. 1–7. 27 indexed citations
10.
Li, Yali, Meili Lv, Chien‐Wen Su, et al.. (2017). p40phox-Deficient Mice Exhibit Impaired Bacterial Clearance and Enhanced Pro-inflammatory Responses during Salmonella enterica serovar Typhimurium Infection. Frontiers in Immunology. 8. 1270–1270. 8 indexed citations
11.
Wang, Li, Meili Lv, Lushun Zhang, et al.. (2015). A comparative study of insertion/deletion polymorphisms applied among Southwest, South and Northwest Chinese populations using Investigator® DIPplex. Forensic Science International Genetics. 21. 10–14. 23 indexed citations
12.
Yuan, Fang, et al.. (2013). Influence of Angiotensin I-Converting Enzyme Gene Polymorphism on Hepatocellular Carcinoma Risk in China. DNA and Cell Biology. 32(5). 268–273. 19 indexed citations
13.
Lv, Meili, Wei Dong, Lijuan Li, et al.. (2013). Association between genetic variants in pre-miRNA and colorectal cancer risk in a Chinese population. Journal of Cancer Research and Clinical Oncology. 139(8). 1405–1410. 57 indexed citations
14.
Su, Xiaowei, Yang Yan, Meili Lv, et al.. (2011). Association Between Single-Nucleotide Polymorphisms in Pre-miRNAs and the Risk of Asthma in a Chinese Population. DNA and Cell Biology. 30(11). 919–923. 29 indexed citations
15.
Liang, Weibo, Meili Lv, Xiaowei Su, et al.. (2010). Association of Tumor Necrosis Factor Gene Polymorphisms with Susceptibility to Dilated Cardiomyopathy in a Han Chinese Population. DNA and Cell Biology. 29(10). 625–628. 14 indexed citations
16.
Deng, Wei, Weibo Liang, Linbo Gao, et al.. (2010). Association of ADAM33 Polymorphisms and Susceptibility to Psoriasis. DNA and Cell Biology. 29(8). 435–439. 9 indexed citations
17.
Li, Yi, Weibo Liang, Li Cui, et al.. (2009). The Association Between Interleukin-23 Receptor Gene Polymorphisms and Systemic Lupus Erythematosus. DNA and Cell Biology. 29(2). 79–82. 17 indexed citations
18.
Gao, Linbo, Bin Zhou, Lin Zhang, et al.. (2008). R497K polymorphism in epidermal growth factor receptor gene is associated with the risk of acute coronary syndrome. BMC Medical Genetics. 9(1). 74–74. 15 indexed citations
19.
20.
Zhu, Yinhua, Bing Du, Zhihui Yang, et al.. (2007). Association of transforming growth factor-β1 gene polymorphisms with genetic susceptibility to nasopharyngeal carcinoma. Clinica Chimica Acta. 380(1-2). 165–169. 39 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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