Youjun Wang

5.1k total citations · 1 hit paper
136 papers, 3.7k citations indexed

About

Youjun Wang is a scholar working on Sensory Systems, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Youjun Wang has authored 136 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Sensory Systems, 46 papers in Molecular Biology and 38 papers in Cellular and Molecular Neuroscience. Recurrent topics in Youjun Wang's work include Ion Channels and Receptors (46 papers), Neurobiology and Insect Physiology Research (27 papers) and Phytochemicals and Antioxidant Activities (23 papers). Youjun Wang is often cited by papers focused on Ion Channels and Receptors (46 papers), Neurobiology and Insect Physiology Research (27 papers) and Phytochemicals and Antioxidant Activities (23 papers). Youjun Wang collaborates with scholars based in China, United States and Japan. Youjun Wang's co-authors include Donald L. Gill, Jonathan Soboloff, Xiaoxiang Deng, Yandong Zhou, Salvatore Mancarella, Eunan Hendron, Yubin Zhou, Guolin Ma, Xiang D. Tang and Robert M. Nwokonko and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Youjun Wang

122 papers receiving 3.6k citations

Hit Papers

CGI1746 targets σ1R to modulate ferroptosis through mitoc... 2024 2026 2025 2024 10 20 30 40

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Youjun Wang China 34 1.7k 1.5k 1.1k 594 417 136 3.7k
Bidhan C. Bandyopadhyay United States 26 1.3k 0.8× 945 0.6× 612 0.6× 254 0.4× 185 0.4× 87 2.5k
Bing Shen China 37 578 0.3× 1.5k 1.0× 316 0.3× 102 0.2× 80 0.2× 325 5.5k
Rory Curtis United States 34 675 0.4× 3.0k 2.0× 2.8k 2.5× 115 0.2× 138 0.3× 55 6.8k
Yusuke Mizuno Japan 25 346 0.2× 830 0.6× 204 0.2× 65 0.1× 92 0.2× 127 2.4k
Michael Poteser Austria 27 622 0.4× 741 0.5× 635 0.6× 96 0.2× 146 0.4× 53 1.9k
Trevor J. Shuttleworth United States 37 1.8k 1.1× 2.1k 1.4× 1.5k 1.4× 565 1.0× 162 0.4× 111 4.3k
Xianhua Wang China 33 242 0.1× 2.8k 1.9× 547 0.5× 30 0.1× 141 0.3× 80 4.2k
Larry E. Wagner United States 34 297 0.2× 1.3k 0.9× 316 0.3× 25 0.0× 71 0.2× 93 2.5k
Rudolf Schubert Germany 28 286 0.2× 1.6k 1.1× 539 0.5× 39 0.1× 278 0.7× 168 3.8k
Alan J. Williams United Kingdom 45 611 0.4× 6.3k 4.3× 1.7k 1.5× 21 0.0× 377 0.9× 158 7.7k

Countries citing papers authored by Youjun Wang

Since Specialization
Citations

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

Fields of papers citing papers by Youjun Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Youjun Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Youjun Wang. A scholar is included among the top collaborators of Youjun Wang 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 Youjun Wang. Youjun Wang 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, Zili, Hong Zhou, Yuehan Wei, et al.. (2024). CGI1746 targets σ1R to modulate ferroptosis through mitochondria-associated membranes. Nature Chemical Biology. 20(6). 699–709. 49 indexed citations breakdown →
2.
Li, Weijia, Fengyan Pei, Jianzhong Zhang, et al.. (2024). Virulence gene polymorphisms in Shandong Helicobacter pylori strains and their relevance to gastric cancer. PLoS ONE. 19(9). e0309844–e0309844. 4 indexed citations
4.
Zhou, Yandong, Guolin Ma, Robert M. Nwokonko, et al.. (2023). An apical Phe-His pair defines the Orai1-coupling site and its occlusion within STIM1. Nature Communications. 14(1). 6921–6921. 4 indexed citations
5.
Li, Jia, et al.. (2023). Finding NEMO: The quest for next‐generation genetically encoded calcium indicators. Clinical and Translational Medicine. 13(10). e1428–e1428. 1 indexed citations
6.
Wang, Fang, Zhongrui Li, Youjun Wang, et al.. (2022). Mannan-Binding Lectin Regulates the Th17/Treg Axis Through JAK/STAT and TGF-β/SMAD Signaling Against Candida albicans Infection. SHILAP Revista de lepidopterología. 1 indexed citations
7.
Fan, Zhongxiong, Tong Ren, Youjun Wang, et al.. (2022). Aβ-responsive metformin-based supramolecular synergistic nanodrugs for Alzheimer's disease via enhancing microglial Aβ clearance. Biomaterials. 283. 121452–121452. 32 indexed citations
8.
Cheng, Pan, Juan Cheng, Jin Bao, et al.. (2021). Direct control of store-operated calcium channels by ultrafast laser. Cell Research. 31(7). 758–772. 12 indexed citations
9.
Wu, Wenping, Qingya Shen, Ruiling Zhang, et al.. (2020). The structure of the MICU 1‐ MICU 2 complex unveils the regulation of the mitochondrial calcium uniporter. The EMBO Journal. 39(19). e104285–e104285. 35 indexed citations
10.
Sun, Yu, et al.. (2019). Curcumin inhibits the proliferation and invasion of MG-63 cells through inactivation of the p-JAK2/p-STAT3 pathway. SHILAP Revista de lepidopterología. 4 indexed citations
11.
Zhou, Yandong, Robert M. Nwokonko, Xiangyu Cai, et al.. (2018). Cross-linking of Orai1 channels by STIM proteins. Proceedings of the National Academy of Sciences. 115(15). E3398–E3407. 50 indexed citations
12.
L, Li, Tengfei Zhang, Lu Xie, et al.. (2018). Potential therapeutic effects of Cordyceps cicadae and Paecilomyces cicadae on adenine-induced chronic renal failure in rats and their phytochemical analysis. SHILAP Revista de lepidopterología. 1 indexed citations
13.
Gudlur, Aparna, Ana Eliza Zeraik, Andrey A. Bobkov, et al.. (2018). Calcium sensing by the STIM1 ER-luminal domain. Nature Communications. 9(1). 4536–4536. 55 indexed citations
14.
Zhou, Lijuan, Tian Zhang, Jindou Liu, et al.. (2018). Digitoxin Suppresses Store Operated Calcium Entry by Modulating Phosphorylation and the Pore Region of Orai1. Current Molecular Medicine. 18(6). 392–399. 4 indexed citations
15.
Zhang, Bo, Weihong Hou, Hongyu Lin, et al.. (2017). Active and separate secretion of fiber and penton base during the early phase of Ad2 or Ad5 infection. Virology. 505. 172–180. 4 indexed citations
16.
Wang, Xizhuo, Youjun Wang, Yandong Zhou, et al.. (2014). Distinct Orai-Coupling Domains in Stim1 and Stim2 Define the Orai-Activating Site. Biophysical Journal. 106(2). 314a–314a. 3 indexed citations
17.
Wang, Youjun. (2012). Synthesis and investigation on stability of BN/EG nanofluids. Journal of Functional Biomaterials. 1 indexed citations
18.
Wang, Youjun, Xiaoxiang Deng, Salvatore Mancarella, et al.. (2010). The Calcium Store Sensor, STIM1, Reciprocally Controls Orai and Ca V 1.2 Channels. Science. 330(6000). 105–109. 284 indexed citations
19.
Deng, Xiaoxiang, Youjun Wang, Yandong Zhou, Jonathan Soboloff, & Donald L. Gill. (2009). STIM and Orai: Dynamic Intermembrane Coupling to Control Cellular Calcium Signals. Journal of Biological Chemistry. 284(34). 22501–22505. 99 indexed citations
20.
Wang, Youjun & Pla Uni. (2009). Gray correlation analysis method for scheme selection decision of camouflage screen design. Systems engineering and electronics.

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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