Shu‐Nong Bai

2.2k total citations
59 papers, 1.5k citations indexed

About

Shu‐Nong Bai is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Shu‐Nong Bai has authored 59 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Plant Science, 45 papers in Molecular Biology and 8 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Shu‐Nong Bai's work include Plant Molecular Biology Research (43 papers), Plant Reproductive Biology (34 papers) and Photosynthetic Processes and Mechanisms (15 papers). Shu‐Nong Bai is often cited by papers focused on Plant Molecular Biology Research (43 papers), Plant Reproductive Biology (34 papers) and Photosynthetic Processes and Mechanisms (15 papers). Shu‐Nong Bai collaborates with scholars based in China, United States and Sweden. Shu‐Nong Bai's co-authors include Zhihong Xu, Donghui Wang, Z. Renee Sung, Wenqian Chen, Yi‐Ben Peng, Yiqin Li, Lin‐Chen Li, Cui Liu, Sulan Bai and Haitao Gu and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Shu‐Nong Bai

58 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shu‐Nong Bai China 23 1.3k 1.1k 149 134 112 59 1.5k
Marian Bemer Netherlands 18 1.5k 1.2× 1.2k 1.1× 91 0.6× 84 0.6× 25 0.2× 28 1.7k
Veronica Gregis Italy 20 1.4k 1.1× 1.2k 1.1× 77 0.5× 105 0.8× 22 0.2× 32 1.5k
Mar Martín‐Trillo Spain 9 1.2k 0.9× 1.0k 0.9× 128 0.9× 51 0.4× 43 0.4× 10 1.3k
Eudald Illa-Berenguer United States 15 998 0.8× 609 0.6× 64 0.4× 240 1.8× 42 0.4× 19 1.1k
Ludovico Dreni Italy 16 1.3k 1.0× 1.0k 0.9× 150 1.0× 168 1.3× 18 0.2× 26 1.4k
Roderick W. Kumimoto United States 15 2.4k 1.9× 1.8k 1.6× 49 0.3× 160 1.2× 16 0.1× 17 2.6k
Yasufumi Daimon Japan 11 2.1k 1.7× 1.6k 1.5× 88 0.6× 186 1.4× 14 0.1× 12 2.2k
Takato Koba Japan 20 1.0k 0.8× 767 0.7× 369 2.5× 188 1.4× 30 0.3× 65 1.1k
Éric Lasserre France 13 1.0k 0.8× 707 0.6× 43 0.3× 85 0.6× 16 0.1× 16 1.2k
Diane Luth United States 12 766 0.6× 485 0.4× 44 0.3× 129 1.0× 16 0.1× 15 943

Countries citing papers authored by Shu‐Nong Bai

Since Specialization
Citations

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

Fields of papers citing papers by Shu‐Nong Bai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shu‐Nong Bai. 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 Shu‐Nong Bai. The network helps show where Shu‐Nong Bai may publish in the future.

Co-authorship network of co-authors of Shu‐Nong Bai

This figure shows the co-authorship network connecting the top 25 collaborators of Shu‐Nong Bai. A scholar is included among the top collaborators of Shu‐Nong Bai 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 Shu‐Nong Bai. Shu‐Nong Bai 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.
Bai, Shu‐Nong. (2024). Two-way induction: how germ cells are differentiated in plants. Discover Plants.. 1(1). 1 indexed citations
2.
Liu, Na, et al.. (2023). Rice tapetum differentiation is sensitive to downregulation of OsUCH3, a ubiquitin C‐terminal hydrolase. Plant Biotechnology Journal. 21(7). 1314–1316.
3.
Zheng, Yafeng, Wenqian Chen, Guilan Li, et al.. (2021). Auxin guides germ-cell specification in Arabidopsis anthers. Proceedings of the National Academy of Sciences. 118(22). 31 indexed citations
4.
Zhang, Huimin, Shuai Li, Li Yang, et al.. (2020). Gain-of-function of the 1-aminocyclopropane-1-carboxylate synthase geneACS1Ginduces female flower development in cucumber gynoecy. The Plant Cell. 33(2). 306–321. 43 indexed citations
5.
Chen, Wenqian, et al.. (2019). Histone Deacetylase HDA19 Affects Root Cortical Cell Fate by Interacting with SCARECROW. PLANT PHYSIOLOGY. 180(1). 276–288. 20 indexed citations
6.
Bai, Shu‐Nong. (2019). Plant Morphogenesis 123: a renaissance in modern botany?. Science China Life Sciences. 62(4). 453–466. 6 indexed citations
7.
Wang, Donghui, Wei Song, Shaowei Wei, et al.. (2018). Characterization of the Ubiquitin C-Terminal Hydrolase and Ubiquitin-Specific Protease Families in Rice (Oryza sativa). Frontiers in Plant Science. 9. 1636–1636. 24 indexed citations
8.
Zhao, Feng, Yafeng Zheng, Ting Zeng, et al.. (2017). Phosphorylation of SPOROCYTELESS/NOZZLE by the MPK3/6 Kinase Is Required for Anther Development. PLANT PHYSIOLOGY. 173(4). 2265–2277. 59 indexed citations
9.
Fang, Yuhan, Xia Li, Shu‐Nong Bai, & Guang‐Yuan Rao. (2017). Sugar Treatments Can Induce AcLEAFY COTYLEDON1 Expression and Trigger the Accumulation of Storage Products during Prothallus Development of Adiantum capillus-veneris. Frontiers in Plant Science. 8. 541–541. 3 indexed citations
10.
Chen, Wenqian, Dongxu Li, Feng Zhao, Zhihong Xu, & Shu‐Nong Bai. (2015). One additional histone deacetylase and 2 histone acetyltransferases are involved in cellular patterning of Arabidopsis root epidermis. Plant Signaling & Behavior. 11(2). e1131373–e1131373. 10 indexed citations
11.
Bai, Shu‐Nong. (2015). The concept of the sexual reproduction cycle and its evolutionary significance. Frontiers in Plant Science. 6. 11–11. 32 indexed citations
12.
Li, Feng, Jinjing Sun, Donghui Wang, et al.. (2014). The B-Box Family Gene STO (BBX24) in Arabidopsis thaliana Regulates Flowering Time in Different Pathways. PLoS ONE. 9(2). e87544–e87544. 62 indexed citations
13.
Sun, Jinjing, Xia Li, Guang‐Yuan Rao, et al.. (2010). Why is ethylene involved in selective promotion of female flower development in cucumber?. Plant Signaling & Behavior. 5(8). 1052–1056. 24 indexed citations
14.
Huang, Moli, Sulan Bai, Xizeng Mao, et al.. (2006). Molecular analysis of early rice stamen development using organ-specific gene expression profiling. Plant Molecular Biology. 61(6). 845–861. 27 indexed citations
15.
Xu, Cheng‐Ran, Cui Liu, Yilan Wang, et al.. (2005). Histone acetylation affects expression of cellular patterning genes in the Arabidopsis root epidermis. Proceedings of the National Academy of Sciences. 102(40). 14469–14474. 128 indexed citations
16.
Hao, Yu‐Jin, Donghui Wang, Yi‐Ben Peng, et al.. (2003). DNA damage in the early primordial anther is closely correlated with stamen arrest in the female flower of cucumber ( Cucumis sativus L.). Planta. 217(6). 888–895. 63 indexed citations
17.
Xu, Zhihong & Shu‐Nong Bai. (2002). Impact of biotechnology on agriculture in China. Trends in Plant Science. 7(8). 374–375. 4 indexed citations
18.
Bai, Shu‐Nong, et al.. (2000). The exgenous hormonal control of the development of regenerated flower buds in Hyacinthus orientalis. Zhiwu xuebao. 42(10). 996–1002. 3 indexed citations
19.
Zhang, Xiansheng, et al.. (2000). Molecular cloning and expression analysis ofHAG1 in the floral organs ofHyacinthus orientalis L. Science in China Series C Life Sciences. 43(4). 395–401. 2 indexed citations
20.
Bai, Shu‐Nong, et al.. (1999). Induction of Continuous Tepal Differentiation from in Vitro Regenerated Flower Buds of Hyacinthus orientalis. Journal of Integrative Plant Biology. 41(9). 8 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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