Shenghai Chang

3.3k total citations
33 papers, 1.1k citations indexed

About

Shenghai Chang is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Shenghai Chang has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in Shenghai Chang's work include Bacterial Genetics and Biotechnology (8 papers), Ion channel regulation and function (7 papers) and Antibiotic Resistance in Bacteria (6 papers). Shenghai Chang is often cited by papers focused on Bacterial Genetics and Biotechnology (8 papers), Ion channel regulation and function (7 papers) and Antibiotic Resistance in Bacteria (6 papers). Shenghai Chang collaborates with scholars based in China, United States and Japan. Shenghai Chang's co-authors include Xing Zhang, Hangjun Wu, Tingyun Kuang, Wenda Wang, Jian‐Ren Shen, Guangye Han, C. Xu, Jiangtao Guo, Zihui Huang and Sheng Ye and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Shenghai Chang

31 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shenghai Chang China 20 736 225 216 91 89 33 1.1k
Christoph von Ballmoos Switzerland 30 2.0k 2.7× 285 1.3× 206 1.0× 75 0.8× 161 1.8× 69 2.6k
Alexander V. Bogachev Russia 25 1.1k 1.6× 239 1.1× 188 0.9× 150 1.6× 91 1.0× 70 1.6k
Goragot Wisedchaisri United States 16 767 1.0× 176 0.8× 187 0.9× 50 0.5× 71 0.8× 23 1.2k
Peilong Lu China 17 1.4k 1.9× 130 0.6× 193 0.9× 73 0.8× 22 0.2× 32 2.1k
Angela Corcelli Italy 28 1.3k 1.7× 268 1.2× 103 0.5× 280 3.1× 41 0.5× 90 1.9k
Claudio Anselmi Italy 23 1.4k 1.9× 108 0.5× 120 0.6× 53 0.6× 108 1.2× 62 2.0k
Christophe Wirth Germany 13 1.0k 1.4× 77 0.3× 163 0.8× 42 0.5× 32 0.4× 25 1.3k
Norimichi Nomura Japan 26 1.6k 2.1× 324 1.4× 162 0.8× 163 1.8× 49 0.6× 61 2.3k
Jonathan T. S. Hopper United Kingdom 23 1.6k 2.1× 101 0.4× 166 0.8× 97 1.1× 46 0.5× 37 2.2k
Albert Konijnenberg Belgium 23 845 1.1× 64 0.3× 157 0.7× 98 1.1× 72 0.8× 37 1.7k

Countries citing papers authored by Shenghai Chang

Since Specialization
Citations

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

Fields of papers citing papers by Shenghai Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shenghai Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Shenghai Chang. A scholar is included among the top collaborators of Shenghai Chang 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 Shenghai Chang. Shenghai Chang 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.
Zhao, Fangyuan, Xin Wang, Zhibo Zhang, et al.. (2025). Deciphering the molecular mechanism of the bacterial division motor TolQRA. Cell Discovery. 11(1). 87–87.
2.
Du, Mei, Ning Liu, Shenghai Chang, et al.. (2025). Molecular basis of β-arrestin coupling to the metabotropic glutamate receptor mGlu3. Nature Chemical Biology. 21(8). 1262–1269. 2 indexed citations
3.
Huang, Haomin, Chen Wang, Shenghai Chang, et al.. (2025). Structure and catalytic mechanism of exogenous fatty acid recycling by AasS, a versatile acyl-ACP synthetase. Nature Structural & Molecular Biology. 32(5). 802–817. 3 indexed citations
4.
Wen, Qiao, Yujiao Chen, Shenghai Chang, et al.. (2024). Deciphering the molecular basis of lipoprotein recognition and transport by LolCDE. Signal Transduction and Targeted Therapy. 9(1). 354–354. 3 indexed citations
5.
Hu, Meiqin, Yong Wang, Ximing Xu, et al.. (2024). Structural basis for sugar perception by Drosophila gustatory receptors. Science. 383(6685). eadj2609–eadj2609. 28 indexed citations
6.
Chang, Shenghai, Qinghua Luo, Chun Chan, et al.. (2023). Structural basis of BAM-mediated outer membrane β-barrel protein assembly. Nature. 617(7959). 185–193. 38 indexed citations
7.
Xu, Lingyi, Ziwei Zheng, Shenghai Chang, et al.. (2023). Structures of the human Wilson disease copper transporter ATP7B. Cell Reports. 42(5). 112417–112417. 34 indexed citations
8.
Li, Yang, Yue Ren, Shenghai Chang, et al.. (2023). Molecular basis of Mg2+ permeation through the human mitochondrial Mrs2 channel. Nature Communications. 14(1). 4713–4713. 13 indexed citations
9.
Ren, Yue, Yang Li, Yaojie Wang, et al.. (2022). Cryo-EM structure of the heptameric calcium homeostasis modulator 1 channel. Journal of Biological Chemistry. 298(5). 101838–101838. 11 indexed citations
10.
Chen, Xiaozhe, Yue Ren, Yangfei Xing, et al.. (2021). Structural basis for activation and allosteric modulation of full-length calcium-sensing receptor. Science Advances. 7(23). 40 indexed citations
11.
Tang, Xiaodi, Shenghai Chang, Ke Zhang, et al.. (2021). Structural basis for bacterial lipoprotein relocation by the transporter LolCDE. Nature Structural & Molecular Biology. 28(4). 347–355. 47 indexed citations
12.
Shen, Liangliang, Wenda Wang, Chen Wang, et al.. (2021). Architecture of the chloroplast PSI–NDH supercomplex in Hordeum vulgare. Nature. 601(7894). 649–654. 53 indexed citations
13.
Ling, Shenglong, Pan Shi, Sanling Liu, et al.. (2021). Structural mechanism of cooperative activation of the human calcium-sensing receptor by Ca2+ ions and L-tryptophan. Cell Research. 31(4). 383–394. 61 indexed citations
14.
Zhang, Bo, Lizhen Xu, Ningning Li, et al.. (2020). Cooperative transport mechanism of human monocarboxylate transporter 2. Nature Communications. 11(1). 2429–2429. 48 indexed citations
15.
Sun, Demeng, Sanling Liu, Siyu Li, et al.. (2020). Structural insights into human acid-sensing ion channel 1a inhibition by snake toxin mambalgin1. eLife. 9. 40 indexed citations
16.
Chen, Jing‐Hua, Hangjun Wu, C. Xu, et al.. (2020). Architecture of the photosynthetic complex from a green sulfur bacterium. Science. 370(6519). 71 indexed citations
17.
Xie, Yuan, Shenghai Chang, Cheng Zhao, et al.. (2020). Structures and an activation mechanism of human potassium-chloride cotransporters. Science Advances. 6(50). 46 indexed citations
18.
Tang, Xiaodi, Shenghai Chang, Qiao Wen, et al.. (2020). Structural insights into outer membrane asymmetry maintenance in Gram-negative bacteria by MlaFEDB. Nature Structural & Molecular Biology. 28(1). 81–91. 63 indexed citations
19.
Liu, Si, Shenghai Chang, Lingyi Xu, et al.. (2019). Cryo-EM structures of the human cation-chloride cotransporter KCC1. Science. 366(6464). 505–508. 60 indexed citations
20.
Zhang, Jinbao, Shenghai Chang, Pan Xu, et al.. (2018). Structural Basis of the Proton Sensitivity of Human GluN1-GluN2A NMDA Receptors. Cell Reports. 25(13). 3582–3590.e4. 48 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Christoph von Ballmoos Breakdown of academic impact, for papers by Alexander V. Bogachev Breakdown of academic impact, for papers by Goragot Wisedchaisri Breakdown of academic impact, for papers by Peilong Lu Breakdown of academic impact, for papers by Angela Corcelli Breakdown of academic impact, for papers by Claudio Anselmi Breakdown of academic impact, for papers by Christophe Wirth Breakdown of academic impact, for papers by Norimichi Nomura Breakdown of academic impact, for papers by Jonathan T. S. Hopper Breakdown of academic impact, for papers by Albert Konijnenberg
Rankless by CCL
2026