Boshi Fu

1.6k total citations
40 papers, 1.1k citations indexed

About

Boshi Fu is a scholar working on Molecular Biology, Cancer Research and Materials Chemistry. According to data from OpenAlex, Boshi Fu has authored 40 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 7 papers in Cancer Research and 7 papers in Materials Chemistry. Recurrent topics in Boshi Fu's work include DNA and Nucleic Acid Chemistry (17 papers), Advanced biosensing and bioanalysis techniques (14 papers) and RNA modifications and cancer (13 papers). Boshi Fu is often cited by papers focused on DNA and Nucleic Acid Chemistry (17 papers), Advanced biosensing and bioanalysis techniques (14 papers) and RNA modifications and cancer (13 papers). Boshi Fu collaborates with scholars based in China, United States and Maldives. Boshi Fu's co-authors include Xiang Zhou, Shaoru Wang, Tian Tian, Yanyan Song, Jiaqi Wang, Guohua Xu, Xiaoe Zhang, Zhiyong He, Minjie Wei and Shengyong Yan and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Analytical Chemistry.

In The Last Decade

Boshi Fu

40 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Boshi Fu China 19 817 277 239 135 124 40 1.1k
Xiaolan Chen China 21 1.2k 1.4× 227 0.8× 424 1.8× 76 0.6× 239 1.9× 55 1.7k
Baixing Wu China 20 1.2k 1.5× 128 0.5× 368 1.5× 94 0.7× 64 0.5× 38 1.5k
Chiranjeevi Peetla United States 14 835 1.0× 145 0.5× 79 0.3× 72 0.5× 174 1.4× 15 1.3k
Ana M. Sánchez United States 22 853 1.0× 144 0.5× 150 0.6× 64 0.5× 137 1.1× 50 1.1k
Christine Saint‐Pierre France 18 721 0.9× 181 0.7× 71 0.3× 58 0.4× 74 0.6× 45 1.1k
Dacheng He China 21 883 1.1× 360 1.3× 99 0.4× 147 1.1× 33 0.3× 61 1.3k
Stefan Vogel Denmark 21 931 1.1× 81 0.3× 56 0.2× 35 0.3× 130 1.0× 52 1.2k
Virginie Gervais France 19 819 1.0× 140 0.5× 92 0.4× 59 0.4× 97 0.8× 36 1.1k
Qiong Yang China 16 431 0.5× 252 0.9× 55 0.2× 86 0.6× 86 0.7× 38 802

Countries citing papers authored by Boshi Fu

Since Specialization
Citations

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

Fields of papers citing papers by Boshi Fu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Boshi Fu

This figure shows the co-authorship network connecting the top 25 collaborators of Boshi Fu. A scholar is included among the top collaborators of Boshi Fu 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 Boshi Fu. Boshi Fu 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.
Sun, Yuqing, Haixin Yu, Shaoqing Han, et al.. (2023). Method for the extraction of circulating nucleic acids based on MOF reveals cell-free RNA signatures in liver cancer. National Science Review. 11(1). nwae022–nwae022. 8 indexed citations
2.
Liu, Min, Subo Zhang, Heng Zhou, et al.. (2023). The interplay between non-coding RNAs and alternative splicing: from regulatory mechanism to therapeutic implications in cancer. Theranostics. 13(8). 2616–2631. 22 indexed citations
3.
Du, Cheng, Xinli Liu, Yi Zhao, et al.. (2022). Analysis of 5-Methylcytosine Regulators and DNA Methylation-Driven Genes in Colon Cancer. Frontiers in Cell and Developmental Biology. 9. 657092–657092. 8 indexed citations
4.
Hu, Xiao, Qiuchen Chen, Hao Guo, et al.. (2021). Identification of Target PTEN-Based miR-425 and miR-576 as Potential Diagnostic and Immunotherapeutic Biomarkers of Colorectal Cancer With Liver Metastasis. Frontiers in Oncology. 11. 657984–657984. 8 indexed citations
5.
Sun, Tong, Zhikun Wu, Xiufang Wang, et al.. (2020). LNC942 promoting METTL14-mediated m6A methylation in breast cancer cell proliferation and progression. Oncogene. 39(31). 5358–5372. 154 indexed citations
6.
Wu, Huizhe, Xiao Hu, Yalun Li, et al.. (2020). LNC473 Regulating APAF1 IRES-Dependent Translation via Competitive Sponging miR574 and miR15b: Implications in Colorectal Cancer. Molecular Therapy — Nucleic Acids. 21. 764–779. 5 indexed citations
7.
Fu, Boshi, Cheng Du, Zhikun Wu, et al.. (2020). Analysis of DNA methylation-driven genes for predicting the prognosis of patients with colorectal cancer. Aging. 12(22). 22814–22839. 11 indexed citations
8.
Wang, Shaoru, Jiaqi Wang, Guohua Xu, et al.. (2018). The Cucurbit[7]Uril‐Based Supramolecular Chemistry for Reversible B/Z‐DNA Transition. Advanced Science. 5(7). 1800231–1800231. 23 indexed citations
9.
Wang, Shaoru, Jiaqi Wang, Boshi Fu, et al.. (2018). Supramolecular Coordination-Directed Reversible Regulation of Protein Activities at Epigenetic DNA Marks. Journal of the American Chemical Society. 140(46). 15842–15849. 12 indexed citations
10.
Fu, Boshi, Ki Tae Kim, Kun Chen, et al.. (2018). A novel nucleic acid aptamer tag: a rapid fluorescence strategy using a self-constructing G-quadruplex from AGG trinucleotide repeats. Chemical Communications. 54(81). 11487–11490. 5 indexed citations
11.
Tian, Tian, Yanyan Song, Lai Wei, et al.. (2017). Reversible manipulation of the G-quadruplex structures and enzymatic reactions through supramolecular host–guest interactions. Nucleic Acids Research. 45(5). gkx025–gkx025. 37 indexed citations
12.
Chen, Xu, Jinjun Wu, Wenting Liu, et al.. (2016). Detecting 5-methylcytosine using an enzyme-free DNA strand exchange reaction without pretreatment under physiological conditions. Chemical Communications. 52(41). 6833–6836. 5 indexed citations
13.
Wang, Shaoru, Jiaqi Wang, Xiaoe Zhang, et al.. (2015). N 6-Methyladenine hinders RNA- and DNA-directed DNA synthesis: application in human rRNA methylation analysis of clinical specimens. Chemical Science. 7(2). 1440–1446. 61 indexed citations
14.
Tian, Tian, Shuang Peng, Heng Xiao, et al.. (2013). 5-Methyldeoxycytidine enhances the substrate activity of DNA polymerase. Chemical Communications. 49(86). 10085–10085. 8 indexed citations
15.
Wang, Changcheng, Shengyong Yan, Rong Huang, et al.. (2013). A turn-on fluorescent probe for detection of tyrosinase activity. The Analyst. 138(10). 2825–2825. 47 indexed citations
16.
Huang, Rong, et al.. (2013). A novel combined bisulfite UDG assay for selective 5-methylcytosine detection. Talanta. 117. 445–448. 3 indexed citations
17.
Tian, Tian, Boshi Fu, Shuang Peng, et al.. (2013). Systematic investigation of DNAs with modified cytosines under hot alkali treatment. Chemical Communications. 49(85). 9968–9968. 3 indexed citations
18.
Wang, Shaoru, Boshi Fu, Shuang Peng, et al.. (2013). The G-triplex DNA could function as a new variety of DNA peroxidase. Chemical Communications. 49(72). 7920–7920. 31 indexed citations
19.
Huang, Rong, Shengyong Yan, Xiaolong Zheng, et al.. (2012). Development of a pH-activatable fluorescent probe and its application for visualizing cellular pH change. The Analyst. 137(19). 4418–4418. 25 indexed citations
20.
Yan, Shengyong, Rong Huang, Changcheng Wang, et al.. (2012). A Two‐photon Fluorescent Probe for Intracellular Detection of Tyrosinase Activity. Chemistry - An Asian Journal. 7(12). 2782–2785. 42 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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