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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 drives aberrant chromatin looping and cancer development
Jeong Hyun Ahn, Eric S. Davis, Timothy A. Daugird, et al.
Nature (2021) Vol. 595, Iss. 7868, pp. 591-595
Open Access | Times Cited: 339

Showing 1-25 of 339 citing articles:

Long non-coding RNAs: definitions, functions, challenges and recommendations
John S. Mattick, Paulo Amaral, Piero Carninci, et al.
Nature Reviews Molecular Cell Biology (2023) Vol. 24, Iss. 6, pp. 430-447
Open Access | Times Cited: 1207
A conceptual framework for understanding phase separation and addressing open questions and challenges
Tanja Mittag, Rohit V. Pappu
Molecular Cell (2022) Vol. 82, Iss. 12, pp. 2201-2214
Open Access | Times Cited: 500
A guide to membraneless organelles and their various roles in gene regulation
Tetsuro Hirose, Kensuke Ninomiya, Shinichi Nakagawa, et al.
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 4, pp. 288-304
Closed Access | Times Cited: 297
Liquid–liquid phase separation drives cellular function and dysfunction in cancer
Sohum Mehta, Jin Zhang
Nature reviews. Cancer (2022) Vol. 22, Iss. 4, pp. 239-252
Open Access | Times Cited: 259
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: 236
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: 142
EZH2 noncanonically binds cMyc and p300 through a cryptic transactivation domain to mediate gene activation and promote oncogenesis
Jun Wang, Xufen Yu, Weida Gong, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 3, pp. 384-399
Open Access | Times Cited: 141
Phase Separation Mediates NUP98 Fusion Oncoprotein Leukemic Transformation
Bappaditya Chandra, Nicole L. Michmerhuizen, Hazheen K. Shirnekhi, et al.
Cancer Discovery (2021) Vol. 12, Iss. 4, pp. 1152-1169
Open Access | Times Cited: 114
MyoD is a 3D genome structure organizer for muscle cell identity
Ruiting Wang, Fengling Chen, Qian Chen, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 87
Improved predictions of phase behaviour of intrinsically disordered proteins by tuning the interaction range
Giulio Tesei, Kresten Lindorff‐Larsen
Open Research Europe (2023) Vol. 2, pp. 94-94
Open Access | Times Cited: 83
Nuclear transport proteins: structure, function, and disease relevance
Yang Yang, Lu Guo, Lin Chen, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 65
SARS-CoV-2 restructures host chromatin architecture
Ruoyu Wang, Joo‐Hyung Lee, Jieun Kim, et al.
Nature Microbiology (2023) Vol. 8, Iss. 4, pp. 679-694
Open Access | Times Cited: 63
Phase Separation in Biology and Disease; Current Perspectives and Open Questions
Steven Boeynaems, Shasha Chong, Jörg Gsponer, et al.
Journal of Molecular Biology (2023) Vol. 435, Iss. 5, pp. 167971-167971
Open Access | Times Cited: 53
Interaction modules that impart specificity to disordered protein
Kateřina Čermáková, H. Courtney Hodges
Trends in Biochemical Sciences (2023) Vol. 48, Iss. 5, pp. 477-490
Open Access | Times Cited: 51
Condensate interfacial forces reposition DNA loci and probe chromatin viscoelasticity
Amy R. Strom, Yoonji Kim, Hongbo Zhao, et al.
Cell (2024) Vol. 187, Iss. 19, pp. 5282-5297.e20
Open Access | Times Cited: 27
Transcriptional condensates: a blessing or a curse for gene regulation?
Martín Stortz, Diego M. Presman, Valeria Levi
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 26
Protein misfolding and amyloid nucleation through liquid–liquid phase separation
S. Mukherjee, Manisha Poudyal, K. Dave, et al.
Chemical Society Reviews (2024) Vol. 53, Iss. 10, pp. 4976-5013
Closed Access | Times Cited: 25
MYC phase separation selectively modulates the transcriptome
Junjiao Yang, Chan-I Chung, Jessica Koach, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 10, pp. 1567-1579
Closed Access | Times Cited: 18
The phenylalanine-and-glycine repeats of NUP98 oncofusions form condensates that selectively partition transcriptional coactivators
Jeong Hyun Ahn, Yiran Guo, Heankel Lyons, et al.
Molecular Cell (2025)
Closed Access | Times Cited: 4
Emerging regulatory mechanisms and functions of biomolecular condensates: implications for therapeutic targets
Soyoung Jeon, Yong‐Duck Chung, Jae‐Sung Lim, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 3
Pioneer factor GATA6 promotes colorectal cancer through 3D genome regulation
Huijue Lyu, X.-X. Chen, Yang Cheng, et al.
Science Advances (2025) Vol. 11, Iss. 6
Open Access | Times Cited: 3
Intrinsically disordered regions as facilitators of the transcription factor target search
Felix Jonas, Yoav Navon, Naama Barkai
Nature Reviews Genetics (2025)
Closed Access | Times Cited: 2
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
Loop-extrusion and polymer phase-separation can co-exist at the single-molecule level to shape chromatin folding
Mattia Conte, Ehsan Irani, Andrea M. Chiariello, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 70
Genetic variation associated with condensate dysregulation in disease
Salman F. Banani, Lena K. Afeyan, Susana Wilson Hawken, et al.
Developmental Cell (2022) Vol. 57, Iss. 14, pp. 1776-1788.e8
Open Access | Times Cited: 64
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