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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:

Nuclear pores dilate and constrict in cellulo
Christian E. Zimmerli, Matteo Allegretti, Vasileios Rantos, et al.
Science (2021) Vol. 374, Iss. 6573
Open Access | Times Cited: 249

Showing 1-25 of 249 citing articles:

Cone-shaped HIV-1 capsids are transported through intact nuclear pores
Vojtěch Žíla, Erica Margiotta, Beata Turoňová, et al.
Cell (2021) Vol. 184, Iss. 4, pp. 1032-1046.e18
Open Access | Times Cited: 277
Mechanics and functional consequences of nuclear deformations
Yohalie Kalukula, Andrew D. Stephens, Jan Lammerding, et al.
Nature Reviews Molecular Cell Biology (2022) Vol. 23, Iss. 9, pp. 583-602
Open Access | Times Cited: 270
AI-based structure prediction empowers integrative structural analysis of human nuclear pores
Shyamal Mosalaganti, Agnieszka Obarska-Kosińska, Marc Siggel, et al.
Science (2022) Vol. 376, Iss. 6598
Closed Access | Times Cited: 239
Comprehensive structure and functional adaptations of the yeast nuclear pore complex
Christopher W. Akey, Digvijay Singh, Christna Ouch, et al.
Cell (2022) Vol. 185, Iss. 2, pp. 361-378.e25
Open Access | Times Cited: 145
Mechanical regulation of chromatin and transcription
Sirio Dupont, Sara A. Wickström
Nature Reviews Genetics (2022) Vol. 23, Iss. 10, pp. 624-643
Closed Access | Times Cited: 143
Mechanical force application to the nucleus regulates nucleocytoplasmic transport
Ion Andreu, Ignasi Granero-Moya, Nimesh R. Chahare, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 6, pp. 896-905
Open Access | Times Cited: 113
Convolutional networks for supervised mining of molecular patterns within cellular context
Irene de Teresa, Sara K. Goetz, Alexander Mattausch, et al.
Nature Methods (2023) Vol. 20, Iss. 2, pp. 284-294
Open Access | Times Cited: 88
Architecture of the linker-scaffold in the nuclear pore
Stefan Petrovic, Dipanjan Samanta, Thibaud Perriches, et al.
Science (2022) Vol. 376, Iss. 6598
Open Access | Times Cited: 83
Bringing Structure to Cell Biology with Cryo-Electron Tomography
Lindsey N. Young, Elizabeth Villa
Annual Review of Biophysics (2023) Vol. 52, Iss. 1, pp. 573-595
Open Access | Times Cited: 79
Cardiac fibroblasts and mechanosensation in heart development, health and disease
Maurizio Pesce, Georg N. Duda, Giancarlo Forte, et al.
Nature Reviews Cardiology (2022) Vol. 20, Iss. 5, pp. 309-324
Closed Access | Times Cited: 74
Visualizing the disordered nuclear transport machinery in situ
Miao Yu, Maziar Heidari, Sofya Mikhaleva, et al.
Nature (2023) Vol. 617, Iss. 7959, pp. 162-169
Open Access | Times Cited: 74
In situ structural analysis reveals membrane shape transitions during autophagosome formation
Anna Bieber, Cristina Capitanio, Philipp S. Erdmann, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 39
Open Access | Times Cited: 70
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: 62
SARS-CoV-2 nsp3 and nsp4 are minimal constituents of a pore spanning replication organelle
Liv Zimmermann, Xiaohan Zhao, Jana Makroczyová, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 48
CombFold: predicting structures of large protein assemblies using a combinatorial assembly algorithm and AlphaFold2
Ben Shor, Dina Schneidman‐Duhovny
Nature Methods (2024) Vol. 21, Iss. 3, pp. 477-487
Open Access | Times Cited: 41
High-confidence 3D template matching for cryo-electron tomography
Sergio Cruz-León, Tomáš Majtner, Patrick C. Hoffmann, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 33
The molecular architecture of the nuclear basket
Digvijay Singh, Neelesh Soni, Joshua Hutchings, et al.
Cell (2024) Vol. 187, Iss. 19, pp. 5267-5281.e13
Open Access | Times Cited: 24
HIV-1 capsid shape, orientation, and entropic elasticity regulate translocation into the nuclear pore complex
Arpa Hudait, Gregory A. Voth
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 4
Open Access | Times Cited: 22
Understanding the cell: Future views of structural biology
Martin Beck, Roberto Covino, Inga Hänelt, et al.
Cell (2024) Vol. 187, Iss. 3, pp. 545-562
Open Access | Times Cited: 21
Passage of the HIV capsid cracks the nuclear pore
Jan Philipp Kreysing, Maziar Heidari, Vojtěch Žíla, et al.
Cell (2025)
Open Access | Times Cited: 8
Nuclear Capsid Uncoating and Reverse Transcription of HIV-1
Thorsten G. Müller, Vojtěch Žíla, Bárbara Müller, et al.
Annual Review of Virology (2022) Vol. 9, Iss. 1, pp. 261-284
Open Access | Times Cited: 68
Recent advances and current trends in cryo-electron microscopy
Margherita Guaita, Scott C. Watters, Sarah Loerch
Current Opinion in Structural Biology (2022) Vol. 77, pp. 102484-102484
Open Access | Times Cited: 60
The Nuclear Pore Complex: Birth, Life, and Death of a Cellular Behemoth
Elisa Dultz, Matthias Wojtynek, Ohad Medalia, et al.
Cells (2022) Vol. 11, Iss. 9, pp. 1456-1456
Open Access | Times Cited: 44
Intracellular localization of the proteasome in response to stress conditions
Cordula Enenkel, Ryu Won Kang, Florian Wilfling, et al.
Journal of Biological Chemistry (2022) Vol. 298, Iss. 7, pp. 102083-102083
Open Access | Times Cited: 43
Can’t handle the stress? Mechanobiology and disease
Noam Zuela-Sopilniak, Jan Lammerding
Trends in Molecular Medicine (2022) Vol. 28, Iss. 9, pp. 710-725
Open Access | Times Cited: 42
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