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:

Nucleoporin 153 links nuclear pore complex to chromatin architecture by mediating CTCF and cohesin binding
Shinichi Kadota, Jianhong Ou, Yuming Shi, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 66

Showing 1-25 of 66 citing articles:

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

Nuclear pore complexes — a doorway to neural injury in neurodegeneration
Alyssa N. Coyne, Jeffrey D. Rothstein
Nature Reviews Neurology (2022) Vol. 18, Iss. 6, pp. 348-362
Open Access | Times Cited: 66

Nucleoporin93 limits Yap activity to prevent endothelial cell senescence
Tung Nguyen, Mihir K. Rao, Shaiva P. Dhyani, et al.
Aging Cell (2024) Vol. 23, Iss. 4
Open Access | Times Cited: 9

Nuclear pore dysfunction and disease: a complex opportunity
Charlotte M. Fare, Jeffrey D. Rothstein
Nucleus (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9

Biomolecular condensates: insights into early and late steps of the HIV-1 replication cycle
Francesca Di Nunzio, Vladimir N. Uversky, Andrew J. Mouland
Retrovirology (2023) Vol. 20, Iss. 1
Open Access | Times Cited: 21

Exportin-1 functions as an adaptor for transcription factor-mediated docking of chromatin at the nuclear pore complex.
Tiffany Ge, Donna Garvey Brickner, Kara Zehr, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 7

Regulation of 3D chromatin organization by CTCF
Jian‐Feng Xiang, Victor G. Corces
Current Opinion in Genetics & Development (2020) Vol. 67, pp. 33-40
Open Access | Times Cited: 49

The nuclear pore complex and the genome: organizing and regulatory principles
Pau Pascual‐García, Maya Capelson
Current Opinion in Genetics & Development (2021) Vol. 67, pp. 142-150
Open Access | Times Cited: 35

GBPL3 localizes to the nuclear pore complex and functionally connects the nuclear basket with the nucleoskeleton in plants
Yu Tang, Man Ip Ho, Byung‐Ho Kang, et al.
PLoS Biology (2022) Vol. 20, Iss. 10, pp. e3001831-e3001831
Open Access | Times Cited: 26

Nuclear pore complexes mediate subtelomeric gene silencing by regulating PCNA levels on chromatin
Sanjeev Kumar Choudhry, Maxwell L. Neal, Song Li, et al.
The Journal of Cell Biology (2023) Vol. 222, Iss. 9
Open Access | Times Cited: 16

A mechanistic insight into cancer progression mediated by Nucleoporins
Leila Jahangiri
Cancer Genetics (2024) Vol. 286-287, pp. 35-42
Open Access | Times Cited: 5

Factors that mold the nuclear landscape of HIV-1 integration
Gregory J. Bedwell, Alan Engelman
Nucleic Acids Research (2020) Vol. 49, Iss. 2, pp. 621-635
Open Access | Times Cited: 33

The Nuclear Pore Complex as a Transcription Regulator
Michael Chas Sumner, Jason H. Brickner
Cold Spring Harbor Perspectives in Biology (2021) Vol. 14, Iss. 1, pp. a039438-a039438
Open Access | Times Cited: 31

Interactions of Chromatin with the Nuclear Lamina and Nuclear Pore Complexes
Yuri Y. Shevelyov
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 21, pp. 15771-15771
Open Access | Times Cited: 11

Super-enhancer trapping by the nuclear pore via intrinsically disordered regions of proteins in squamous cell carcinoma cells
Masaharu Hazawa, Dini Kurnia Ikliptikawati, Yuki Iwashima, et al.
Cell chemical biology (2023) Vol. 31, Iss. 4, pp. 792-804.e7
Open Access | Times Cited: 11

Acute depletion of human core nucleoporin reveals direct roles in transcription control but dispensability for 3D genome organization
Xiaoyu Zhu, Chuangye Qi, Ruoyu Wang, et al.
Cell Reports (2022) Vol. 41, Iss. 5, pp. 111576-111576
Open Access | Times Cited: 17

Nuclear envelope components in vascular mechanotransduction: emerging roles in vascular health and disease
Tung Nguyen, Michael Winek, Mihir K. Rao, et al.
Nucleus (2025) Vol. 16, Iss. 1
Open Access

Novel Function of NUP153 in HNF4α Transcriptional Upregulation Contributes to Promoting HBV Replication
Qianqian Jiang, Zhou Zhao, Xinyu Du, et al.
Journal of Medical Virology (2025) Vol. 97, Iss. 3
Closed Access

Nuclear transport surveillance of p53 by nuclear pores in glioblastoma
Dini Kurnia Ikliptikawati, Nozomi Hirai, Kei Makiyama, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112882-112882
Open Access | Times Cited: 9

You are who your friends are—nuclear pore proteins as components of chromatin‐binding complexes
Maya Capelson
FEBS Letters (2023) Vol. 597, Iss. 22, pp. 2769-2781
Open Access | Times Cited: 9

PP2A and cancer epigenetics: a therapeutic opportunity waiting to happen
Samantha L. Tinsley, Brittany L. Allen-Petersen
NAR Cancer (2022) Vol. 4, Iss. 1
Open Access | Times Cited: 14

Nucleoporins facilitate ORC loading onto chromatin
Logan Richards, Christopher L. Lord, Mary Lauren Benton, et al.
Cell Reports (2022) Vol. 41, Iss. 6, pp. 111590-111590
Open Access | Times Cited: 13

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