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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The protein complex crystallography beamline (BL19U1) at the Shanghai Synchrotron Radiation Facility
Weizhe Zhang, Jianchao Tang, Si-Sheng Wang, et al.
Nuclear Science and Techniques (2019) Vol. 30, Iss. 11
Closed Access | Times Cited: 167

Showing 26-50 of 167 citing articles:

An extended conformation of SARS-CoV-2 main protease reveals allosteric targets
Zengchao Sun, Lu Wang, Xiyang Li, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 15
Open Access | Times Cited: 28
Substrate Promiscuity, Crystal Structure, and Application of a Plant UDP-Glycosyltransferase UGT74AN3
Wei Huang, Xinlei Zhang, Junhao Li, et al.
ACS Catalysis (2023) Vol. 14, Iss. 1, pp. 475-488
Closed Access | Times Cited: 18
A seven-crystal spectrometer for high-energy resolution X-ray spectroscopy at Shanghai Synchrotron Radiation Facility
Bingbao Mei, Liang-Xin Wang, Songqi Gu, et al.
Nuclear Science and Techniques (2024) Vol. 35, Iss. 9
Closed Access | Times Cited: 7
Substrate binding and catalytic mechanism of the Se-glycosyltransferase SenB in the biosynthesis of selenoneine
Wei Huang, Jun Song, Tianxue Sun, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Structural insights into the catalytic selectivity of glycosyltransferase SgUGT94-289-3 towards mogrosides
Shengrong Cui, Shumeng Zhang, Ning Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
A Type I-F Anti-CRISPR Protein Inhibits the CRISPR-Cas Surveillance Complex by ADP-Ribosylation
Yiying Niu, Lingguang Yang, Teng Gao, et al.
Molecular Cell (2020) Vol. 80, Iss. 3, pp. 512-524.e5
Open Access | Times Cited: 47
Mechanism of forkhead transcription factors binding to a novel palindromic DNA site
Jun Li, Shuyan Dai, Xiaojuan Chen, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 6, pp. 3573-3583
Open Access | Times Cited: 35
NASP maintains histone H3–H4 homeostasis through two distinct H3 binding modes
Hongyu Bao, Massimo Carraro, Valentin Flury, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 9, pp. 5349-5368
Open Access | Times Cited: 25
Blockade of dual immune checkpoint inhibitory signals with a CD47/PD-L1 bispecific antibody for cancer treatment
Rongjuan Wang, Chang Zhang, Yuting Cao, et al.
Theranostics (2022) Vol. 13, Iss. 1, pp. 148-160
Open Access | Times Cited: 25
Anti-infective therapy using species-specific activators of Staphylococcus aureus ClpP
Bingyan Wei, Tao Zhang, Pengyu Wang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 24
Insights into the inhibition of type I-F CRISPR-Cas system by a multifunctional anti-CRISPR protein AcrIF24
Lingguang Yang, Laixing Zhang, Peipei Yin, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 23
Two natural compounds as potential inhibitors against the Helicobacter pylori and Acinetobacter baumannii IspD enzymes
Xiaoyu Chen, Huilin Zhao, Chuandong Wang, et al.
International Journal of Antimicrobial Agents (2024) Vol. 63, Iss. 5, pp. 107160-107160
Closed Access | Times Cited: 5
Discovery of Novel Nonpeptidic and Noncovalent Small Molecule 3CLpro Inhibitors as anti-SARS-CoV-2 Drug Candidate
Zhidong Jiang, Bo Feng, Lu Chen, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 15, pp. 12760-12783
Closed Access | Times Cited: 5
The structural basis of African swine fever virus pA104R binding to DNA and its inhibition by stilbene derivatives
Ruili Liu, Yeping Sun, Yan Chai, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 20, pp. 11000-11009
Open Access | Times Cited: 35
S19W, T27W, and N330Y mutations in ACE2 enhance SARS-CoV-2 S-RBD binding toward both wild-type and antibody-resistant viruses and its molecular basis
Fei Ye, Xi Lin, Zimin Chen, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 28
Structures of NPAS4-ARNT and NPAS4-ARNT2 heterodimers reveal new dimerization modalities in the bHLH-PAS transcription factor family
Xiangnan Sun, Linqian Jing, Fengwei Li, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 46
Open Access | Times Cited: 21
An open-like conformation of the sigma-1 receptor reveals its ligand entry pathway
Fu‐hui Meng, Yang Xiao, Yujia Ji, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 20
Molecular mechanism of S -adenosylmethionine sensing by SAMTOR in mTORC1 signaling
Xin Tang, Yifan Zhang, Guanchao Wang, et al.
Science Advances (2022) Vol. 8, Iss. 26
Open Access | Times Cited: 20
A unique hyperdynamic dimer interface permits small molecule perturbation of the melanoma oncoprotein MITF for melanoma therapy
Zaizhou Liu, Kaige Chen, Jun Dai, et al.
Cell Research (2023) Vol. 33, Iss. 1, pp. 55-70
Closed Access | Times Cited: 12
Deciphering the stereo-specific catalytic mechanisms of cis-epoxysuccinate hydrolases producing L(+)-tartaric acid
Sheng Dong, Jinsong Xuan, Yingang Feng, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 2, pp. 105635-105635
Open Access | Times Cited: 4
Insight into binding of endogenous neurosteroid ligands to the sigma-1 receptor
Chunting Fu, Yang Xiao, Xiaoming Zhou, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Ras S89D mutation induced allosteric changes that promoted its nucleotide exchange and signaling activation
Y Li, Wenxin Huang, Lu Guo, et al.
International Journal of Biological Macromolecules (2025) Vol. 294, pp. 139538-139538
Closed Access
Defining ortholog-specific UHRF1 inhibition by STELLA for cancer therapy
Wenjing Bai, Jinxin Xu, Wenbin Gu, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Structural analyses of Cryptosporidium parvum epitopes reveal a novel scheme of decapeptide binding to H-2Kb
Yongli Wang, Yankai Chang, Fangyuan Yin, et al.
Journal of Structural Biology (2025) Vol. 217, Iss. 1, pp. 108168-108168
Closed Access
Structures of two lyssavirus glycoproteins trapped in pre- and post-fusion states and the implications on the spatial-temporal conformational transition along with pH-decrease
Fanli Yang, Sheng Lin, Xin Yuan, et al.
PLoS Pathogens (2025) Vol. 21, Iss. 2, pp. e1012923-e1012923
Open Access

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