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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:

Regulation of liquid–liquid phase separation with focus on post-translational modifications
Yun-Yi Luo, Jun Wu, Yanmei Li
Chemical Communications (2021) Vol. 57, Iss. 98, pp. 13275-13287
Closed Access | Times Cited: 79

Showing 1-25 of 79 citing articles:

Liquid–liquid phase separation in tumor biology
Xuhui Tong, Rong Tang, Jin Xu, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 122
Post-translational modifications in liquid-liquid phase separation: a comprehensive review
Jingxian Li, Mengdi Zhang, Weirui Ma, et al.
Molecular Biomedicine (2022) Vol. 3, Iss. 1
Open Access | Times Cited: 85
Effects of pH alterations on stress- and aging-induced protein phase separation
Xuejiao Jin, Min Zhou, Shuxin Chen, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 7
Open Access | Times Cited: 39
The evolution of post-translational modifications
David Bradley
Current Opinion in Genetics & Development (2022) Vol. 76, pp. 101956-101956
Closed Access | Times Cited: 37
Targeting Biomolecular Condensation and Protein Aggregation against Cancer
Jerson L. Silva, Débora Foguel, Vı́tor F. Ferreira, et al.
Chemical Reviews (2023) Vol. 123, Iss. 14, pp. 9094-9138
Closed Access | Times Cited: 31
Linear ubiquitination induces NEMO phase separation to activate NF-κB signaling
Simran Goel, Rosario Oliva, Sadasivam Jeganathan�, et al.
Life Science Alliance (2023) Vol. 6, Iss. 4, pp. e202201607-e202201607
Open Access | Times Cited: 23
Theoretical and Data-Driven Approaches for Biomolecular Condensates
Kadi L. Saar, Daoyuan Qian, Lydia L. Good, et al.
Chemical Reviews (2023) Vol. 123, Iss. 14, pp. 8988-9009
Open Access | Times Cited: 22
Intrinsic factors behind long COVID: IV. Hypothetical roles of the SARS‐CoV‐2 nucleocapsid protein and its liquid–liquid phase separation
Ahmed Eltayeb, Faisal Al‐Sarraj, Mona G. Alharbi, et al.
Journal of Cellular Biochemistry (2024) Vol. 125, Iss. 3
Closed Access | Times Cited: 6
Biphasic modulation of tau liquid–liquid phase separation by polyphenols
Hariharan Moorthy, Nimsha Kamala, Madhu Ramesh, et al.
Chemical Communications (2024) Vol. 60, Iss. 32, pp. 4334-4337
Closed Access | Times Cited: 6
C9ORF72 poly-PR induces TDP-43 nuclear condensation via NEAT1 and is modulated by HSP70 activity
Diksha Agnihotri, Chi-Chang Lee, Po-Chao Lu, et al.
Cell Reports (2025) Vol. 44, Iss. 1, pp. 115173-115173
Closed Access
PRMT1-methylated MSX1 phase separates to control palate development
Meng Li, Yucheng Jiang, Jiawen You, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Lessons from proteomics and phosphoproteomics on axon growth and regeneration
Michihiro Igarashi
Elsevier eBooks (2025), pp. 225-231
Closed Access
Functional Biomaterials Derived from Protein Liquid–Liquid Phase Separation and Liquid‐to‐Solid Transition
Tianchen Li, Dea Prianka Ayu Ilhamsyah, Benjamin C.U. Tai, et al.
Advanced Materials (2025)
Open Access
Dishevelled phase separation promotes Wnt signalosome assembly and destruction complex disassembly
Kexin Kang, Qiaoni Shi, Xu Wang, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 12
Open Access | Times Cited: 34
CPSF6 regulates alternative polyadenylation and proliferation of cancer cells through phase separation
Susu Liu, Runze Wu, Liutao Chen, et al.
Cell Reports (2023) Vol. 42, Iss. 10, pp. 113197-113197
Open Access | Times Cited: 19
Phase separations in oncogenesis, tumor progressions and metastasis: a glance from hallmarks of cancer
Lewei Zheng, Cuicui Liu, Ke‐Da Yu
Journal of Hematology & Oncology (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 17
Liquid–liquid phase separation in plants: Advances and perspectives from model species to crops
Qianwen Liu, Wenxuan Liu, Yiding Niu, et al.
Plant Communications (2023) Vol. 5, Iss. 1, pp. 100663-100663
Open Access | Times Cited: 15
Phase separation in cancer at a glance
Qingqing Xie, Jiejuan Cheng, Wuxuan Mei, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 14
Lopinavir enhances anoikis by remodeling autophagy in a circRNA-dependent manner
Yaran Wu, Yang Chen, Xiaojing Yan, et al.
Autophagy (2024) Vol. 20, Iss. 7, pp. 1651-1672
Closed Access | Times Cited: 5
Exploring the frontier of plant phase separation: Current insights and future prospects
Panting Fan, Jingjing Zhang, Lefei Gao, et al.
New Crops (2024) Vol. 1, pp. 100026-100026
Open Access | Times Cited: 4
Regulation of Biomolecular Condensates by Poly(ADP-ribose)
Kevin Rhine, Hana M. Odeh, James Shorter, et al.
Chemical Reviews (2023) Vol. 123, Iss. 14, pp. 9065-9093
Closed Access | Times Cited: 13
Exogenous Pregnane X Receptor Does Not Undergo Liquid-liquid Phase Separation in Nucleus under Cell-based In Vitro Conditions
Pengfei Zhao, Yue Gao, Yanying Zhou, et al.
Drug Metabolism and Disposition (2024) Vol. 52, Iss. 11, pp. 1161-1169
Open Access | Times Cited: 4
Coarse-Grained Modeling of Liquid–Liquid Phase Separation in Cells: Challenges and Opportunities
Shaokang Shi, Zhao Li, Zhong‐Yuan Lu
The Journal of Physical Chemistry Letters (2024) Vol. 15, Iss. 28, pp. 7280-7287
Closed Access | Times Cited: 4
Biomolecular condensates – extant relics or evolving microcompartments?
Vijayaraghavan Rangachari
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 10
Melatonin: Regulation of Prion Protein Phase Separation in Cancer Multidrug Resistance
Doris Loh, Russel J. Reíter
Molecules (2022) Vol. 27, Iss. 3, pp. 705-705
Open Access | Times Cited: 16
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