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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:

Imaging dynamic and selective low-complexity domain interactions that control gene transcription
Shasha Chong, Claire Dugast‐Darzacq, Zhe Liu, et al.
Science (2018) Vol. 361, Iss. 6400
Open Access | Times Cited: 911

Showing 1-25 of 911 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
Long-range enhancer–promoter contacts in gene expression control
Stefan Schoenfelder, Peter Fraser
Nature Reviews Genetics (2019) Vol. 20, Iss. 8, pp. 437-455
Closed Access | Times Cited: 949
Organization of Chromatin by Intrinsic and Regulated Phase Separation
Bryan A. Gibson, Lynda K. Doolittle, Maximilian W. G. Schneider, et al.
Cell (2019) Vol. 179, Iss. 2, pp. 470-484.e21
Open Access | Times Cited: 927
Liquid–Liquid Phase Separation in Disease
Simon Alberti, Dorothee Dormann
Annual Review of Genetics (2019) Vol. 53, Iss. 1, pp. 171-194
Open Access | Times Cited: 772
The molecular language of membraneless organelles
Edward Gomes, James Shorter
Journal of Biological Chemistry (2018) Vol. 294, Iss. 18, pp. 7115-7127
Open Access | Times Cited: 711
A framework for understanding the functions of biomolecular condensates across scales
Andrew S. Lyon, William B. Peeples, Michael K. Rosen
Nature Reviews Molecular Cell Biology (2020) Vol. 22, Iss. 3, pp. 215-235
Open Access | Times Cited: 686
Liquid Nuclear Condensates Mechanically Sense and Restructure the Genome
Yongdae Shin, Yi-Che Chang, Daniel S.W. Lee, et al.
Cell (2018) Vol. 175, Iss. 6, pp. 1481-1491.e13
Open Access | Times Cited: 637
Histone post-translational modifications — cause and consequence of genome function
Gonzalo Millán-Zambrano, Adam Burton, Andrew J. Bannister, et al.
Nature Reviews Genetics (2022) Vol. 23, Iss. 9, pp. 563-580
Closed Access | Times Cited: 625
Organization and regulation of gene transcription
Patrick Cramer
Nature (2019) Vol. 573, Iss. 7772, pp. 45-54
Closed Access | Times Cited: 621
Developmental enhancers and chromosome topology
Eileen E. M. Furlong, Michael Levine
Science (2018) Vol. 361, Iss. 6409, pp. 1341-1345
Open Access | Times Cited: 589
RNA polymerase II clustering through carboxy-terminal domain phase separation
Marc Boehning, Claire Dugast‐Darzacq, M. Ranković, et al.
Nature Structural & Molecular Biology (2018) Vol. 25, Iss. 9, pp. 833-840
Open Access | Times Cited: 567
The Self-Organizing Genome: Principles of Genome Architecture and Function
Tom Misteli
Cell (2020) Vol. 183, Iss. 1, pp. 28-45
Open Access | Times Cited: 558
Evaluating phase separation in live cells: diagnosis, caveats, and functional consequences
David T. McSwiggen, Mustafa Mir, Xavier Darzacq, et al.
Genes & Development (2019) Vol. 33, Iss. 23-24, pp. 1619-1634
Open Access | Times Cited: 543
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
Genome-Scale Imaging of the 3D Organization and Transcriptional Activity of Chromatin
Jun-Han Su, Pu Zheng, Seon Kinrot, et al.
Cell (2020) Vol. 182, Iss. 6, pp. 1641-1659.e26
Open Access | Times Cited: 476
Transcription factors and 3D genome conformation in cell-fate decisions
Ralph Stadhouders, Guillaume J. Filion, Thomas Graf
Nature (2019) Vol. 569, Iss. 7756, pp. 345-354
Closed Access | Times Cited: 471
Liquid–liquid phase separation in human health and diseases
Bin Wang, Lei Zhang, Tong Dai, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 460
Mapping Local and Global Liquid Phase Behavior in Living Cells Using Photo-Oligomerizable Seeds
Dan Bracha, Mackenzie T. Walls, Ming‐Tzo Wei, et al.
Cell (2018) Vol. 175, Iss. 6, pp. 1467-1480.e13
Open Access | Times Cited: 418
Enhancer Features that Drive Formation of Transcriptional Condensates
Krishna Shrinivas, Benjamin R. Sabari, Eliot L. Coffey, et al.
Molecular Cell (2019) Vol. 75, Iss. 3, pp. 549-561.e7
Open Access | Times Cited: 370
Biomolecular Condensates in the Nucleus
Benjamin R. Sabari, Alessandra Dall’Agnese, Richard A. Young
Trends in Biochemical Sciences (2020) Vol. 45, Iss. 11, pp. 961-977
Open Access | Times Cited: 362
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
Nuclear condensates of the Polycomb protein chromobox 2 (CBX2) assemble through phase separation
Roubina Tatavosian, Samantha Kent, Kyle Brown, et al.
Journal of Biological Chemistry (2018) Vol. 294, Iss. 5, pp. 1451-1463
Open Access | Times Cited: 313
Phase separation of Polycomb-repressive complex 1 is governed by a charged disordered region of CBX2
Aaron J. Plys, Christopher P. Davis, Jongmin Kim, et al.
Genes & Development (2019) Vol. 33, Iss. 13-14, pp. 799-813
Open Access | Times Cited: 312
Phase separation of ligand-activated enhancers licenses cooperative chromosomal enhancer assembly
Sreejith J. Nair, Yang Lu, Dario Meluzzi, et al.
Nature Structural & Molecular Biology (2019) Vol. 26, Iss. 3, pp. 193-203
Open Access | Times Cited: 308
Probing and engineering liquid-phase organelles
Dan Bracha, Mackenzie T. Walls, Clifford P. Brangwynne
Nature Biotechnology (2019) Vol. 37, Iss. 12, pp. 1435-1445
Closed Access | Times Cited: 303
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