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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:

The molecular virology of coronaviruses
Ella Hartenian, Divya Nandakumar, Azra Lari, et al.
Journal of Biological Chemistry (2020) Vol. 295, Iss. 37, pp. 12910-12934
Open Access | Times Cited: 514

Showing 1-25 of 514 citing articles:

Structures and functions of coronavirus replication–transcription complexes and their relevance for SARS-CoV-2 drug design
Brandon Malone, Nadya Urakova, Eric J. Snijder, et al.
Nature Reviews Molecular Cell Biology (2021) Vol. 23, Iss. 1, pp. 21-39
Open Access | Times Cited: 389
ORF3a of the COVID-19 virus SARS-CoV-2 blocks HOPS complex-mediated assembly of the SNARE complex required for autolysosome formation
Guangyan Miao, Hongyu Zhao, Yan Li, et al.
Developmental Cell (2020) Vol. 56, Iss. 4, pp. 427-442.e5
Open Access | Times Cited: 309
TMPRSS2 expression dictates the entry route used by SARS‐CoV‐2 to infect host cells
Jana Koch, Zina M. Uckeley, Patricio Doldan, et al.
The EMBO Journal (2021) Vol. 40, Iss. 16
Open Access | Times Cited: 292
SARS-CoV-2: from its discovery to genome structure, transcription, and replication
Ayslan Castro Brant, Wei Tian, Vladimır Majerčiak, et al.
Cell & Bioscience (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 222
Innate immune sensing of coronavirus and viral evasion strategies
Yusuke Kasuga, Baohui Zhu, Kyoung‐Jin Jang, et al.
Experimental & Molecular Medicine (2021) Vol. 53, Iss. 5, pp. 723-736
Open Access | Times Cited: 186
Main protease mutants of SARS-CoV-2 variants remain susceptible to nirmatrelvir
Sven Ullrich, Kasuni B. Ekanayake, Gottfried Otting, et al.
Bioorganic & Medicinal Chemistry Letters (2022) Vol. 62, pp. 128629-128629
Open Access | Times Cited: 182
Dynamic competition between SARS-CoV-2 NSP1 and mRNA on the human ribosome inhibits translation initiation
Christopher P. Lapointe, Rosslyn Grosely, Alex G. Johnson, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 6
Open Access | Times Cited: 173
ORF3a of SARS-CoV-2 promotes lysosomal exocytosis-mediated viral egress
Di Chen, Qiaoxia Zheng, Long Sun, et al.
Developmental Cell (2021) Vol. 56, Iss. 23, pp. 3250-3263.e5
Open Access | Times Cited: 156
The role of NSP6 in the biogenesis of the SARS-CoV-2 replication organelle
Simona Ricciardi, Andrea Maria Guarino, Laura Giaquinto, et al.
Nature (2022) Vol. 606, Iss. 7915, pp. 761-768
Open Access | Times Cited: 146
The viral protein NSP1 acts as a ribosome gatekeeper for shutting down host translation and fostering SARS-CoV-2 translation
Antonin Tidu, Aurélie Janvier, Laure Schaeffer, et al.
RNA (2020) Vol. 27, Iss. 3, pp. 253-264
Open Access | Times Cited: 143
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules
Matteo Stravalaci, Isabel Pagani, Elvezia Maria Paraboschi, et al.
Nature Immunology (2022) Vol. 23, Iss. 2, pp. 275-286
Open Access | Times Cited: 135
SARS-CoV-2 hijacks folate and one-carbon metabolism for viral replication
Yuchen Zhang, Rui Guo, Sharon H. Kim, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 127
A critical review on SARS-CoV-2 infectivity in water and wastewater. What do we know?
Alexandre Giacobbo, Marco Antônio Siqueira Rodrigues, Jane Zoppas Ferreira, et al.
The Science of The Total Environment (2021) Vol. 774, pp. 145721-145721
Open Access | Times Cited: 119
Crystal structure of SARS-CoV-2 nsp10 bound to nsp14-ExoN domain reveals an exoribonuclease with both structural and functional integrity
Sheng Lin, Hua Chen, Zimin Chen, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 9, pp. 5382-5392
Open Access | Times Cited: 113
Two Years into the COVID-19 Pandemic: Lessons Learned
Severino Jefferson Ribeiro da Silva, Jéssica Catarine Frutuoso do Nascimento, Renata Pessôa Germano Mendes, et al.
ACS Infectious Diseases (2022) Vol. 8, Iss. 9, pp. 1758-1814
Open Access | Times Cited: 111
Genome-wide bidirectional CRISPR screens identify mucins as host factors modulating SARS-CoV-2 infection
Scott B. Biering, Sylvia A. Sarnik, Eleanor Wang, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1078-1089
Open Access | Times Cited: 102
Targeting stem-loop 1 of the SARS-CoV-2 5′ UTR to suppress viral translation and Nsp1 evasion
Setu M. Vora, Pietro Fontana, Tianyang Mao, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 9
Open Access | Times Cited: 93
Mutations in SARS-CoV-2: Insights on structure, variants, vaccines, and biomedical interventions
Ahmed I. Abulsoud, Hussein M. El‐Husseiny, Ahmed A. El-Husseiny, et al.
Biomedicine & Pharmacotherapy (2022) Vol. 157, pp. 113977-113977
Open Access | Times Cited: 90
A dual mechanism of action of AT-527 against SARS-CoV-2 polymerase
Ashleigh Shannon, Véronique Fattorini, Bhawna Sama, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 86
The Remarkable Evolutionary Plasticity of Coronaviruses by Mutation and Recombination: Insights for the COVID-19 Pandemic and the Future Evolutionary Paths of SARS-CoV-2
Grigoris D. Amoutzias, Marios Nikolaidis, Eleni Tryfonopoulou, et al.
Viruses (2022) Vol. 14, Iss. 1, pp. 78-78
Open Access | Times Cited: 82
SARS-CoV-2 and the Host Cell: A Tale of Interactions
Massimo Pizzato, Chiara Baraldi, Giulia Boscato Sopetto, et al.
Frontiers in Virology (2022) Vol. 1
Open Access | Times Cited: 72
The SARS-CoV-2 accessory protein Orf3a is not an ion channel, but does interact with trafficking proteins
Alexandria N. Miller, Patrick R. Houlihan, Ella Matamala, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 48
ACE2-dependent and -independent SARS-CoV-2 entries dictate viral replication and inflammatory response during infection
Tianhao Duan, Changsheng Xing, Junjun Chu, et al.
Nature Cell Biology (2024) Vol. 26, Iss. 4, pp. 628-644
Closed Access | Times Cited: 21
Interstitial macrophages are a focus of viral takeover and inflammation in COVID-19 initiation in human lung
Ting-Hsuan Wu, Kyle J. Travaglini, Arjun Rustagi, et al.
The Journal of Experimental Medicine (2024) Vol. 221, Iss. 6
Open Access | Times Cited: 18
Immune Response to Respiratory Viral Infections
Antonella Gambadauro, Francesca Galletta, Alessandra Li Pomi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 11, pp. 6178-6178
Open Access | Times Cited: 18
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