Baoshan Chen

1.7k total citations
51 papers, 1.2k citations indexed

About

Baoshan Chen is a scholar working on Plant Science, Endocrinology and Molecular Biology. According to data from OpenAlex, Baoshan Chen has authored 51 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Plant Science, 24 papers in Endocrinology and 19 papers in Molecular Biology. Recurrent topics in Baoshan Chen's work include Plant and Fungal Interactions Research (24 papers), Plant Virus Research Studies (21 papers) and Plant Disease Resistance and Genetics (16 papers). Baoshan Chen is often cited by papers focused on Plant and Fungal Interactions Research (24 papers), Plant Virus Research Studies (21 papers) and Plant Disease Resistance and Genetics (16 papers). Baoshan Chen collaborates with scholars based in China, United States and Australia. Baoshan Chen's co-authors include Donald L. Nuss, Gil H. Choi, Lynn M. Geletka, Nobuhiro Suzuki, Todd B. Parsley, Jinzi Wang, Qingfeng Chen, Qi Chen, Jianxin Wang and Wei Lan and has published in prestigious journals such as Science, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Baoshan Chen

49 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Baoshan Chen China 20 983 690 288 177 71 51 1.2k
Dimitar Douchkov Germany 18 1.4k 1.4× 117 0.2× 614 2.1× 169 1.0× 70 1.0× 33 1.6k
Chenlei Hua China 21 1.4k 1.4× 126 0.2× 532 1.8× 181 1.0× 49 0.7× 31 1.5k
Cheng‐Guo Duan China 30 2.6k 2.6× 249 0.4× 1.4k 5.0× 46 0.3× 118 1.7× 58 2.9k
Mikhail Schepetilnikov France 19 1.3k 1.3× 168 0.2× 810 2.8× 28 0.2× 114 1.6× 25 1.6k
Azeddine Si‐Ammour Italy 14 1.2k 1.2× 184 0.3× 624 2.2× 99 0.6× 109 1.5× 21 1.4k
Naoki Kadotani Japan 10 695 0.7× 173 0.3× 537 1.9× 132 0.7× 42 0.6× 11 937
Yùzhēn Shí China 22 1.1k 1.1× 160 0.2× 370 1.3× 52 0.3× 27 0.4× 68 1.2k
Yun Jin China 17 1.5k 1.6× 110 0.2× 999 3.5× 57 0.3× 44 0.6× 36 2.0k
Dongwei Hu China 13 817 0.8× 122 0.2× 315 1.1× 165 0.9× 103 1.5× 36 889
Stéphanie Boutet France 13 2.0k 2.0× 209 0.3× 1.3k 4.5× 23 0.1× 86 1.2× 29 2.3k

Countries citing papers authored by Baoshan Chen

Since Specialization
Citations

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

Fields of papers citing papers by Baoshan Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Baoshan Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Baoshan Chen. A scholar is included among the top collaborators of Baoshan Chen 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 Baoshan Chen. Baoshan Chen 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.
Zhang, Jinxu, Shaoli Zhou, Shuo Jiang, et al.. (2025). Genome-wide identification of sugarcane SINA family proteins reveals that SsSINA1a positively regulates drought tolerance. Industrial Crops and Products. 226. 120746–120746. 1 indexed citations
2.
Li, Yihan, Shuangyu Li, Xiuting Hua, et al.. (2025). Mitochondrial genome structural variants and candidate cytoplasmic male sterility-related gene in sugarcane. BMC Genomics. 26(1). 28–28. 4 indexed citations
3.
4.
Chen, Baoshan, et al.. (2024). Functional Characterization of the Gibberellin (GA) Receptor ScGID1 in Sugarcane. International Journal of Molecular Sciences. 25(19). 10688–10688. 1 indexed citations
5.
Wang, Jinzi, Rui Quan, Qiang Fu, et al.. (2023). Hypovirus infection induces proliferation and perturbs functions of mitochondria in the chestnut blight fungus. Frontiers in Microbiology. 14. 1206603–1206603. 2 indexed citations
6.
Li, Wenyan, et al.. (2022). Gene-coexpression network analysis identifies specific modules and hub genes related to cold stress in rice. BMC Genomics. 23(1). 251–251. 29 indexed citations
7.
8.
Deng, Yizhen, et al.. (2019). The Farnesyltransferase β-Subunit Ram1 Regulates Sporisorium scitamineum Mating, Pathogenicity and Cell Wall Integrity. Frontiers in Microbiology. 10. 976–976. 19 indexed citations
9.
Xu, Shiqiang, Jihua Wang, Haixuan Wang, et al.. (2019). Molecular characterization of carbendazim resistance of Fusarium species complex that causes sugarcane pokkah boeng disease. BMC Genomics. 20(1). 115–115. 31 indexed citations
10.
Li, Ru, et al.. (2018). Comparative Methylome Analysis Reveals Perturbation of Host Epigenome in Chestnut Blight Fungus by a Hypovirus. Frontiers in Microbiology. 9. 1026–1026. 17 indexed citations
11.
Lu, Shan, et al.. (2017). Development of an efficient vector system for gene knock-out and near in-cis gene complementation in the sugarcane smut fungus. Scientific Reports. 7(1). 3113–3113. 27 indexed citations
12.
Wang, Jinzi, et al.. (2016). Comparative Secretome Analysis Reveals Perturbation of Host Secretion Pathways by a Hypovirus. Scientific Reports. 6(1). 34308–34308. 17 indexed citations
13.
Yao, Ziting, et al.. (2013). Δ1-Pyrroline-5-Carboxylate/Glutamate Biogenesis Is Required for Fungal Virulence and Sporulation. PLoS ONE. 8(9). e73483–e73483. 14 indexed citations
14.
Li, Youzhi, et al.. (2013). Complexity of roles and regulation of the PMK1-MAPK pathway in mycelium development, conidiation and appressorium formation in Magnaporthe oryzae. Gene Expression Patterns. 13(5-6). 133–141. 17 indexed citations
15.
Wang, Jinzi, et al.. (2012). Comparative vesicle proteomics reveals selective regulation of protein expression in chestnut blight fungus by a hypovirus. Journal of Proteomics. 78. 221–230. 17 indexed citations
16.
Feng, Youjun, et al.. (2011). MoDUO1, a Duo1-like gene, is required for full virulence of the rice blast fungus Magnaporthe oryzae. Current Genetics. 57(6). 409–420. 6 indexed citations
17.
Huang, Dongliang, Dong‐Jie Tang, Qing Liao, et al.. (2008). The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters. Nucleic Acids Research. 36(13). 4295–4309. 51 indexed citations
18.
Yao, Ziting, et al.. (2007). Deletion of the cpku80 gene in the chestnut blight fungus, Cryphonectria parasitica, enhances gene disruption efficiency. Current Genetics. 53(1). 59–66. 42 indexed citations
19.
Fan, Yunyan, et al.. (2007). Large-scale expressed sequence tag analysis for the chestnut blight fungus Cryphonectria parasitica. Fungal Genetics and Biology. 45(3). 319–327. 20 indexed citations
20.
Chen, Baoshan, et al.. (1994). cDNA-Derived Hypovirus RNA in Transformed Chestnut Blight Fungus Is Spliced and Trimmed of Vector Nucleotides. Virology. 202(1). 441–448. 16 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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