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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:

SUMOylation-Mediated Regulation of Cell Cycle Progression and Cancer
Karolin Eifler, Alfred C.O. Vertegaal
Trends in Biochemical Sciences (2015) Vol. 40, Iss. 12, pp. 779-793
Open Access | Times Cited: 258

Showing 1-25 of 258 citing articles:

Quantitative Proteomics of the Cancer Cell Line Encyclopedia
David P. Nusinow, John Szpyt, Mahmoud Ghandi, et al.
Cell (2020) Vol. 180, Iss. 2, pp. 387-402.e16
Open Access | Times Cited: 818
A comprehensive compilation of SUMO proteomics
Ivo A. Hendriks, Alfred C.O. Vertegaal
Nature Reviews Molecular Cell Biology (2016) Vol. 17, Iss. 9, pp. 581-595
Closed Access | Times Cited: 442
SUMO and the robustness of cancer
Jacob-S. Seeler, Anne Dejean
Nature reviews. Cancer (2017) Vol. 17, Iss. 3, pp. 184-197
Closed Access | Times Cited: 363
Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation
Ivo A. Hendriks, David Lyon, Clifford Young, et al.
Nature Structural & Molecular Biology (2017) Vol. 24, Iss. 3, pp. 325-336
Closed Access | Times Cited: 332
The Cilium: Cellular Antenna and Central Processing Unit
Jarema Malicki, Colin A. Johnson
Trends in Cell Biology (2016) Vol. 27, Iss. 2, pp. 126-140
Open Access | Times Cited: 327
The post-translational modification, SUMOylation, and cancer (Review)
Zhi‐Jian Han, Yan-Hu Feng, Bao-Hong Gu, et al.
International Journal of Oncology (2018)
Open Access | Times Cited: 292
SUMO conjugation – a mechanistic view
Andrea Pichler, Chronis Fatouros, Heekyoung Lee, et al.
BioMolecular Concepts (2017) Vol. 8, Iss. 1, pp. 13-36
Open Access | Times Cited: 226
Signalling mechanisms and cellular functions of SUMO
Alfred C.O. Vertegaal
Nature Reviews Molecular Cell Biology (2022) Vol. 23, Iss. 11, pp. 715-731
Closed Access | Times Cited: 209
Probing the roles of SUMOylation in cancer cell biology by using a selective SAE inhibitor
Xingyue He, Jessica Riceberg, Teresa A. Soucy, et al.
Nature Chemical Biology (2017) Vol. 13, Iss. 11, pp. 1164-1171
Closed Access | Times Cited: 201
Site-specific characterization of endogenous SUMOylation across species and organs
Ivo A. Hendriks, David Lyon, Dan Su, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 185
Sumoylation on its 25th anniversary: mechanisms, pathology, and emerging concepts
Arda Celen, Umut Şahin
FEBS Journal (2020) Vol. 287, Iss. 15, pp. 3110-3140
Open Access | Times Cited: 182
Cytosolic DNA sensing by cGAS: regulation, function, and human diseases
Le Yu, Pengda Liu
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 152
SUMO1 modification of methyltransferase-like 3 promotes tumor progression via regulating Snail mRNA homeostasis in hepatocellular carcinoma
Hongfa Xu, Hao Wang, Wei Zhao, et al.
Theranostics (2020) Vol. 10, Iss. 13, pp. 5671-5686
Open Access | Times Cited: 142
SUMOylation promotes extracellular vesicle–mediated transmission of lncRNA ELNAT1 and lymph node metastasis in bladder cancer
Changhao Chen, Hanhao Zheng, Yuming Luo, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 8
Open Access | Times Cited: 107
Targeting pancreatic cancer by TAK-981: a SUMOylation inhibitor that activates the immune system and blocks cancer cell cycle progression in a preclinical model
Sumit Kumar, Mark J.A. Schoonderwoerd, Jessie S. Kroonen, et al.
Gut (2022) Vol. 71, Iss. 11, pp. 2266-2283
Open Access | Times Cited: 75
Current understanding of the cGAS-STING signaling pathway: Structure, regulatory mechanisms, and related diseases
Jing Pan, Chen-Jie Fei, Yang Hu, et al.
动物学研究 (2023) Vol. 44, Iss. 1, pp. 183-218
Open Access | Times Cited: 51
Mitochondrial quality control in human health and disease
Bohao Liu, Chen-Zhen Xu, Yi Liu, et al.
Military Medical Research (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 30
The regulations of telomerase reverse transcriptase (TERT) in cancer
Mingdi Liu, Yuning Zhang, Yong‐Ping Jian, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 28
Comprehensive Overview of Bottom-Up Proteomics Using Mass Spectrometry
Yuming Jiang, Rex Devasahayam Arokia Balaya, Dina Schuster, et al.
ACS Measurement Science Au (2024) Vol. 4, Iss. 4, pp. 338-417
Open Access | Times Cited: 25
TRIM28-mediated nucleocapsid protein SUMOylation enhances SARS-CoV-2 virulence
Jiang Ren, Shuai Wang, Zhi Zong, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 19
A SUMO-ubiquitin relay recruits proteasomes to chromosome axes to regulate meiotic recombination
H. B. D. Prasada Rao, Huanyu Qiao, Shubhang K. Bhatt, et al.
Science (2017) Vol. 355, Iss. 6323, pp. 403-407
Open Access | Times Cited: 165
Chlorogenic acid effectively treats cancers through induction of cancer cell differentiation
Shuai Huang, Lulu Wang, Nina Xue, et al.
Theranostics (2019) Vol. 9, Iss. 23, pp. 6745-6763
Open Access | Times Cited: 140
DiSUMO-LIKE Interacts with RNA-Binding Proteins and Affects Cell-Cycle Progression during Maize Embryogenesis
Junyi Chen, Kamila Kalinowska, Benedikt Müller, et al.
Current Biology (2018) Vol. 28, Iss. 10, pp. 1548-1560.e5
Open Access | Times Cited: 111
Impaired albumin function: a novel potential indicator for liver function damage?
Lejia Sun, Huanhuan Yin, Meixi Liu, et al.
Annals of Medicine (2019) Vol. 51, Iss. 7-8, pp. 333-344
Open Access | Times Cited: 101
Targeting SUMO Signaling to Wrestle Cancer
Jessie S. Kroonen, Alfred C.O. Vertegaal
Trends in cancer (2020) Vol. 7, Iss. 6, pp. 496-510
Open Access | Times Cited: 86
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