Shouhong Guang

2.6k total citations
57 papers, 1.7k citations indexed

About

Shouhong Guang is a scholar working on Molecular Biology, Aging and Plant Science. According to data from OpenAlex, Shouhong Guang has authored 57 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 23 papers in Aging and 8 papers in Plant Science. Recurrent topics in Shouhong Guang's work include CRISPR and Genetic Engineering (25 papers), RNA Research and Splicing (25 papers) and Genetics, Aging, and Longevity in Model Organisms (23 papers). Shouhong Guang is often cited by papers focused on CRISPR and Genetic Engineering (25 papers), RNA Research and Splicing (25 papers) and Genetics, Aging, and Longevity in Model Organisms (23 papers). Shouhong Guang collaborates with scholars based in China, United States and Rwanda. Shouhong Guang's co-authors include Scott Kennedy, Xuezhu Feng, Kirk B. Burkhart, Aaron F. Bochner, Derek M. Pavelec, Chengming Zhu, Xiangyang Chen, Jennifer Lachowiec, Nick Burton and Sandra Harding and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Shouhong Guang

54 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shouhong Guang China 19 1.5k 623 368 242 111 57 1.7k
Yanxia Bei United States 10 1.5k 1.0× 881 1.4× 287 0.8× 167 0.7× 95 0.9× 14 1.9k
Eva‐Maria Weick United States 8 1.2k 0.8× 375 0.6× 520 1.4× 201 0.8× 143 1.3× 9 1.4k
Sam Guoping Gu United States 18 1.2k 0.8× 633 1.0× 302 0.8× 236 1.0× 159 1.4× 24 1.5k
Qian Bian China 17 1.4k 0.9× 319 0.5× 329 0.9× 65 0.3× 257 2.3× 44 1.6k
Masaomi Kato United States 14 998 0.7× 299 0.5× 440 1.2× 595 2.5× 61 0.5× 14 1.5k
Shawn Ahmed United States 23 1.9k 1.3× 1.2k 1.9× 484 1.3× 127 0.5× 231 2.1× 43 2.4k
Carolyn M. Phillips United States 19 1.8k 1.2× 846 1.4× 423 1.1× 65 0.3× 234 2.1× 34 2.1k
Véronique Kalck Switzerland 19 2.1k 1.4× 280 0.4× 521 1.4× 59 0.2× 163 1.5× 23 2.3k
Allison L. Abbott United States 14 891 0.6× 425 0.7× 99 0.3× 726 3.0× 59 0.5× 19 1.4k
Christopher M. Hammell United States 15 932 0.6× 368 0.6× 105 0.3× 231 1.0× 47 0.4× 26 1.1k

Countries citing papers authored by Shouhong Guang

Since Specialization
Citations

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

Fields of papers citing papers by Shouhong Guang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shouhong Guang

This figure shows the co-authorship network connecting the top 25 collaborators of Shouhong Guang. A scholar is included among the top collaborators of Shouhong Guang 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 Shouhong Guang. Shouhong Guang 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.
Zhou, Peng, Y.F. Jia, Tianyu Zhang, et al.. (2025). Red Light-Activated Reversible Inhibition of Protein Functions by Assembled Trap. ACS Synthetic Biology. 14(5). 1437–1450.
2.
Li, Kun, Xuezhu Feng, Ke Wang, et al.. (2025). TurboID-based proximity labeling identifies novel germline proteins that maintain E granule integrity and small RNA homeostasis in C. elegans. Science China Life Sciences. 68(12). 3466–3485. 1 indexed citations
3.
Kuang, Yan, Jiewei Cheng, Tongtong Huang, et al.. (2025). The H3K27me3 reader UAD-2 recruits a TAF-12-containing transcription machinery to initiate piRNA expression within heterochromatic clusters. Nature Communications. 16(1). 10538–10538.
4.
Zhu, Chengming, Panpan Xu, Jianing Gao, et al.. (2025). piRNA gene density and SUMOylation organize piRNA transcriptional condensate formation. Nature Structural & Molecular Biology. 32(8). 1503–1516. 1 indexed citations
5.
Wang, Ke, et al.. (2025). Nucleolar Proteomics Revealed the Regulation of RNA Exosome Localization by MTR4. Molecular & Cellular Proteomics. 24(8). 101031–101031.
6.
Zhou, Xiaotian, Chenming Zeng, Ting Xu, et al.. (2024). Nucleolar stress induces nucleolar stress body formation via the NOSR-1/NUMR-1 axis in Caenorhabditis elegans. Nature Communications. 15(1). 7256–7256. 1 indexed citations
7.
Feng, Xuezhu & Shouhong Guang. (2024). Functions and applications of RNA interference and small regulatory RNAs. Acta Biochimica et Biophysica Sinica. 57(1). 119–130. 2 indexed citations
8.
Chen, Xiangyang, Ke Wang, Chengming Zhu, et al.. (2024). Germ granule compartments coordinate specialized small RNA production. Nature Communications. 15(1). 5799–5799. 15 indexed citations
9.
Liu, Ling, Peng Liu, Shouhong Guang, et al.. (2024). The absence of the ribosomal protein Rpl2702 elicits the MAPK-mTOR signaling to modulate mitochondrial morphology and functions. Redox Biology. 73. 103174–103174. 5 indexed citations
10.
Belly, Henry De, Bingying Wang, Andrew Wong, et al.. (2024). Early-life stress triggers long-lasting organismal resilience and longevity via tetraspanin. Science Advances. 10(4). eadj3880–eadj3880. 8 indexed citations
11.
Huang, Xiaona, Xuezhu Feng, Ke Wang, et al.. (2024). Compartmentalized localization of perinuclear proteins within germ granules in C. elegans. Developmental Cell. 60(8). 1251–1270.e3. 7 indexed citations
12.
Wang, Bingying, et al.. (2023). Acquired stress resilience through bacteria‐to‐nematode interdomain horizontal gene transfer. The EMBO Journal. 42(24). e114835–e114835. 4 indexed citations
13.
Zhu, Zhiwen, Wenhao Zhang, Yuling Chen, et al.. (2023). Global histone H2B degradation regulates insulin/ IGF signaling‐mediated nutrient stress. The EMBO Journal. 42(19). e113328–e113328. 8 indexed citations
14.
Huang, Meng, et al.. (2022). H3K9me1/2 methylation limits the lifespan of daf-2 mutants in C. elegans. eLife. 11. 14 indexed citations
15.
Zeng, Chenming, Shanhui Liao, Zhongliang Zhu, et al.. (2021). Molecular basis for PICS-mediated piRNA biogenesis and cell division. Nature Communications. 12(1). 5595–5595. 8 indexed citations
16.
Zeng, Chenming, Chenchun Weng, Yonghong Yan, et al.. (2019). Functional Proteomics Identifies a PICS Complex Required for piRNA Maturation and Chromosome Segregation. Cell Reports. 27(12). 3561–3572.e3. 24 indexed citations
17.
Weng, Chenchun, Joanna Kosałka-Węgiel, Przemysław Stempor, et al.. (2018). The USTC co-opts an ancient machinery to drive piRNA transcription in C. elegans. Genes & Development. 33(1-2). 90–102. 31 indexed citations
18.
Mao, Hui, Chengming Zhu, Dandan Zong, et al.. (2015). The Nrde Pathway Mediates Small-RNA-Directed Histone H3 Lysine 27 Trimethylation in Caenorhabditis elegans. Current Biology. 25(18). 2398–2403. 89 indexed citations
19.
Burkhart, Kirk B., Shouhong Guang, Bethany A. Buckley, et al.. (2011). A Pre-mRNA–Associating Factor Links Endogenous siRNAs to Chromatin Regulation. PLoS Genetics. 7(8). e1002249–e1002249. 110 indexed citations
20.
Guang, Shouhong, Aaron F. Bochner, Derek M. Pavelec, et al.. (2008). An Argonaute Transports siRNAs from the Cytoplasm to the Nucleus. Science. 321(5888). 537–541. 263 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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