Yuhua Shang

2.4k total citations · 1 hit paper
19 papers, 1.9k citations indexed

About

Yuhua Shang is a scholar working on Cellular and Molecular Neuroscience, Endocrine and Autonomic Systems and Genetics. According to data from OpenAlex, Yuhua Shang has authored 19 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 9 papers in Endocrine and Autonomic Systems and 5 papers in Genetics. Recurrent topics in Yuhua Shang's work include Circadian rhythm and melatonin (9 papers), Neurobiology and Insect Physiology Research (9 papers) and Light effects on plants (3 papers). Yuhua Shang is often cited by papers focused on Circadian rhythm and melatonin (9 papers), Neurobiology and Insect Physiology Research (9 papers) and Light effects on plants (3 papers). Yuhua Shang collaborates with scholars based in United States, China and South Korea. Yuhua Shang's co-authors include Michael Rosbash, Leslie C. Griffith, Martin A. Gorovsky, Marc Pypaert, Lucas Sjulson, Gero Miesenböck, Adam Claridge‐Chang, Bing Li, Robert A. Mooney and Joseph J. Senn and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Yuhua Shang

18 papers receiving 1.8k citations

Hit Papers

PDF Cells Are a GABA-Responsive Wake-Promoting Component ... 2008 2026 2014 2020 2008 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuhua Shang United States 14 1.1k 817 456 448 258 19 1.9k
Xiangzhong Zheng United States 21 1.1k 0.9× 1.4k 1.7× 380 0.8× 301 0.7× 625 2.4× 28 2.1k
Herman Wijnen United States 15 463 0.4× 648 0.8× 658 1.4× 245 0.5× 537 2.1× 25 1.6k
Erik C. Johnson United States 19 1.3k 1.2× 470 0.6× 365 0.8× 380 0.8× 148 0.6× 30 1.7k
Brian Y. Chung United States 14 775 0.7× 694 0.8× 205 0.4× 258 0.6× 257 1.0× 21 1.3k
Junjiro Horiuchi Japan 22 700 0.6× 170 0.2× 824 1.8× 235 0.5× 131 0.5× 34 1.5k
Robert Kreber United States 14 821 0.7× 257 0.3× 1.2k 2.6× 331 0.7× 289 1.1× 19 2.1k
Elisabeth Chélot France 13 986 0.9× 1.2k 1.5× 180 0.4× 150 0.3× 608 2.4× 16 1.4k
Seogang Hyun South Korea 21 699 0.6× 298 0.4× 600 1.3× 253 0.6× 201 0.8× 37 1.6k
Katharine C. Abruzzi United States 22 700 0.6× 838 1.0× 959 2.1× 159 0.4× 474 1.8× 32 1.9k

Countries citing papers authored by Yuhua Shang

Since Specialization
Citations

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

Fields of papers citing papers by Yuhua Shang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuhua Shang

This figure shows the co-authorship network connecting the top 25 collaborators of Yuhua Shang. A scholar is included among the top collaborators of Yuhua Shang 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 Yuhua Shang. Yuhua Shang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Yin, Ling, et al.. (2025). Revolution of AAV in Drug Discovery: From Delivery System to Clinical Application. Journal of Medical Virology. 97(6). e70447–e70447. 2 indexed citations
2.
Hu, Jing, Mengyao Liu, Meng Guo, et al.. (2025). A potent protective bispecific nanobody targeting Herpes simplex virus gD reveals vulnerable epitope for neutralizing. Nature Communications. 16(1). 4196–4196. 3 indexed citations
4.
Liu, Muziying, Dan Zhao, Guilai Liu, et al.. (2025). FcRn-guided antigen trafficking enhances cancer vaccine efficacy. Cancer Immunology Immunotherapy. 74(2). 54–54. 1 indexed citations
5.
Lü, Junchang, Yoshitsugu Kobayashi, Li Xu, et al.. (2015). A New Oviraptorid Dinosaur (Dinosauria: Oviraptorosauria) from the Late Cretaceous of Southern China and Its Paleobiogeographical Implications. Scientific Reports. 5(1). 11490–11490. 34 indexed citations
6.
Shang, Yuhua, Nathan C. Donelson, Christopher G. Vecsey, et al.. (2013). Short Neuropeptide F Is a Sleep-Promoting Inhibitory Modulator. Neuron. 80(1). 171–183. 105 indexed citations
7.
Choi, Charles, Guan Cao, Yuhua Shang, et al.. (2012). Autoreceptor Control of Peptide/Neurotransmitter Corelease from PDF Neurons Determines Allocation of Circadian Activity in Drosophila. Cell Reports. 2(2). 332–344. 72 indexed citations
8.
Shang, Yuhua, Paula Haynes, Nicolás Pírez, et al.. (2011). Imaging analysis of clock neurons reveals light buffers the wake-promoting effect of dopamine. Nature Neuroscience. 14(7). 889–895. 83 indexed citations
9.
10.
Kula-Eversole, Elżbieta, Emi Nagoshi, Yuhua Shang, et al.. (2010). Surprising gene expression patterns within and between PDF-containing circadian neurons in Drosophila. Proceedings of the National Academy of Sciences. 107(30). 13497–13502. 138 indexed citations
11.
Parisky, Katherine M., José L. Agosto, Stefan R. Pulver, et al.. (2009). PDF Cells Are a GABA-Responsive Wake-Promoting Component of the Drosophila Sleep Circuit. Neuron. 61(1). 152–152. 9 indexed citations
12.
Parisky, Katherine M., José L. Agosto, Stefan R. Pulver, et al.. (2008). PDF Cells Are a GABA-Responsive Wake-Promoting Component of the Drosophila Sleep Circuit. Neuron. 60(4). 672–682. 304 indexed citations breakdown →
13.
Shang, Yuhua, Leslie C. Griffith, & Michael Rosbash. (2008). Light-arousal and circadian photoreception circuits intersect at the large PDF cells of the Drosophila brain. Proceedings of the National Academy of Sciences. 105(50). 19587–19594. 205 indexed citations
14.
Shang, Yuhua, Adam Claridge‐Chang, Lucas Sjulson, Marc Pypaert, & Gero Miesenböck. (2007). Excitatory Local Circuits and Their Implications for Olfactory Processing in the Fly Antennal Lobe. Cell. 128(3). 601–612. 266 indexed citations
15.
Rosbash, Michael, Sebastián Kadener, Jérôme S. Menet, et al.. (2007). Transcriptional Feedback and Definition of the Circadian Pacemaker inDrosophilaand Animals. Cold Spring Harbor Symposia on Quantitative Biology. 72(1). 75–83. 39 indexed citations
16.
Shang, Yuhua, Che-Chia Tsao, & Martin A. Gorovsky. (2005). Mutational analyses reveal a novel function of the nucleotide-binding domain of γ-tubulin in the regulation of basal body biogenesis. The Journal of Cell Biology. 171(6). 1035–1044. 30 indexed citations
17.
Shang, Yuhua, Bing Li, & Martin A. Gorovsky. (2002). Tetrahymena thermophila contains a conventional γ-tubulin that is differentially required for the maintenance of different microtubule-organizing centers. The Journal of Cell Biology. 158(7). 1195–1206. 100 indexed citations
18.
Shang, Yuhua, Xiaoyuan Song, Josephine Bowen, et al.. (2002). A robust inducible-repressible promoter greatly facilitates gene knockouts, conditional expression, and overexpression of homologous and heterologous genes in Tetrahymena thermophila. Proceedings of the National Academy of Sciences. 99(6). 3734–3739. 192 indexed citations
19.
Mooney, Robert A., Joseph J. Senn, Scott J. Cameron, et al.. (2001). Suppressors of Cytokine Signaling-1 and -6 Associate with and Inhibit the Insulin Receptor. Journal of Biological Chemistry. 276(28). 25889–25893. 221 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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