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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:

Phase separation and DAXX redistribution contribute to LANA nuclear body and KSHV genome dynamics during latency and reactivation
Olga Vladimirova, Alessandra De Leo, Zhong Deng, et al.
PLoS Pathogens (2021) Vol. 17, Iss. 1, pp. e1009231-e1009231
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Modulating biomolecular condensates: a novel approach to drug discovery
Diana M. Mitrea, Matthäus Mittasch, Beatriz Ferreira Gomes, et al.
Nature Reviews Drug Discovery (2022) Vol. 21, Iss. 11, pp. 841-862
Open Access | Times Cited: 239
Deciphering the role of liquid-liquid phase separation in sarcoma: Implications for pathogenesis and treatment
Zehao Cheng, Hua Wang, Y M Zhang, et al.
Cancer Letters (2025) Vol. 616, pp. 217585-217585
Closed Access | Times Cited: 2
Deconstructing virus condensation
Nora López, Gabriela Camporeale, Mariano Salgueiro, et al.
PLoS Pathogens (2021) Vol. 17, Iss. 10, pp. e1009926-e1009926
Open Access | Times Cited: 62
Human cytomegalovirus forms phase-separated compartments at viral genomes to facilitate viral replication
Enrico Caragliano, Stefano Bonazza, Giada Frascaroli, et al.
Cell Reports (2022) Vol. 38, Iss. 10, pp. 110469-110469
Open Access | Times Cited: 42
Liquid-liquid Phase Separation in Viral Function
Xiaoyue Zhang, Run Zheng, Zhengshuo Li, et al.
Journal of Molecular Biology (2023) Vol. 435, Iss. 16, pp. 167955-167955
Open Access | Times Cited: 29
Kaposi’s sarcoma-associated herpesvirus terminal repeat regulates inducible lytic gene promoters
Yoshihiro Izumiya, Adhraa Algalil, Jonna Magdallene Espera, et al.
Journal of Virology (2024) Vol. 98, Iss. 2
Open Access | Times Cited: 15
Kaposi’s sarcoma-associated herpesvirus (KSHV) LANA prevents KSHV episomes from degradation
K Nakajima, Tomoki Inagaki, Jonna Magdallene Espera, et al.
Journal of Virology (2024) Vol. 98, Iss. 2
Open Access | Times Cited: 9
Phase separation in Cancer: From the Impacts and Mechanisms to Treatment potentials
Peng Qiu, Shiming Tan, Longzheng Xia, et al.
International Journal of Biological Sciences (2022) Vol. 18, Iss. 13, pp. 5103-5122
Open Access | Times Cited: 34
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: 18
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: 15
Histone chaperone HIRA, promyelocytic leukemia protein, and p62/SQSTM1 coordinate to regulate inflammation during cell senescence
Nirmalya Dasgupta, Xue Lei, Christina Huan Shi, et al.
Molecular Cell (2024) Vol. 84, Iss. 17, pp. 3271-3287.e8
Closed Access | Times Cited: 5
Molecular mechanisms and cellular functions of liquid-liquid phase separation during antiviral immune responses
Shuai Yang, Weishan Shen, Jiajia Hu, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 13
Biomolecular phase separation in stress granule assembly and virus infection
Yi Liu, Zhiying Yao, Guiwei Lian, et al.
Acta Biochimica et Biophysica Sinica (2023) Vol. 55, Iss. 7, pp. 1099-1118
Open Access | Times Cited: 13
Biomolecular Condensates as Novel Antiviral Targets
Erik Martin, Christiane Iserman, Balaji Olety, et al.
Journal of Molecular Biology (2023) Vol. 436, Iss. 4, pp. 168380-168380
Open Access | Times Cited: 10
Unidirectional recruitment between MeCP2 and KSHV-encoded LANA revealed by CRISPR/Cas9 recruitment assay
Ido Lavi, Supriya Bhattacharya, Ankita Awase, et al.
PLoS Pathogens (2025) Vol. 21, Iss. 3, pp. e1012972-e1012972
Open Access
LANA-Dependent Transcription-Replication Conflicts and R-Loops at the Terminal Repeats (TR) Correlate with KSHV Episome Maintenance
Atif H. Asghar, Olga Vladimirova, Asher Sobotka, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Daxx and HIRA go viral – How chromatin remodeling complexes affect DNA virus infection
Julia Mai, Mehdi Nazari, Thomas Stamminger, et al.
Tumour Virus Research (2025), pp. 200317-200317
Open Access
Studies on Gene Enhancer with KSHV mini-chromatin
Tomoki Inagaki, Ashish Kumar, Kang-Hsin Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Viral oncogenesis in cancer: from mechanisms to therapeutics
Qing Xiao, Yi Liu, Tingting Li, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access
Herpesvirus Replication Compartments: Dynamic Biomolecular Condensates?
Enrico Caragliano, Wolfram Brune, Jens B. Bosse
Viruses (2022) Vol. 14, Iss. 5, pp. 960-960
Open Access | Times Cited: 16
HOP/STIP1 is required for KSHV lytic replication
Elisa Kirigin, Lorraine Matandirotya, Jamie-Lee Ruck, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Biomolecular condensates with liquid properties formed during viral infections
Damien Glon, Benjamin Léonardon, Ariane Guillemot, et al.
Microbes and Infection (2024) Vol. 26, Iss. 8, pp. 105402-105402
Open Access | Times Cited: 3
Elevated iNOS and 3′-nitrotyrosine in Kaposi's Sarcoma tumors and mouse model
Olga Vladimirova, Samantha S. Soldan, Chenhe Su, et al.
Tumour Virus Research (2023) Vol. 15, pp. 200259-200259
Open Access | Times Cited: 8
Kaposi sarcoma-associated herpesvirus latency-associated nuclear antigen: more than a key mediator of viral persistence
Thomas F. Schulz, Anika Freise, Saskia C. Stein
Current Opinion in Virology (2023) Vol. 61, pp. 101336-101336
Open Access | Times Cited: 8
ICP22-defined condensates mediate RNAPII deubiquitylation by UL36 and promote HSV-1 transcription
Hansong Qi, Mengqiu Yin, Feng Xiong, et al.
Cell Reports (2024) Vol. 43, Iss. 10, pp. 114792-114792
Open Access | Times Cited: 2
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