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.

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Showing 1-25 of 49 citing articles:

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: 139

Interaction between host G3BP and viral nucleocapsid protein regulates SARS-CoV-2 replication and pathogenicity
Zemin Yang, Bryan A. Johnson, Victoria Meliopoulos, et al.
Cell Reports (2024) Vol. 43, Iss. 3, pp. 113965-113965
Open Access | Times Cited: 22

SND1 binds SARS-CoV-2 negative-sense RNA and promotes viral RNA synthesis through NSP9
Nora Schmidt, Sabina Ganskih, Yuanjie Wei, et al.
Cell (2023) Vol. 186, Iss. 22, pp. 4834-4850.e23
Open Access | Times Cited: 25

G3BP1-dependent condensation of translationally inactive viral RNAs antagonizes infection
James M. Burke, Oshani C. Ratnayake, J. Monty Watkins, et al.
Science Advances (2024) Vol. 10, Iss. 5
Open Access | Times Cited: 7

Sensitive visualization of SARS-CoV-2 RNA with CoronaFISH
Elena Rensen, Stefano Pietropaoli, Florian Mueller, et al.
Life Science Alliance (2022) Vol. 5, Iss. 4, pp. e202101124-e202101124
Open Access | Times Cited: 29

Viable SARS-CoV-2 Omicron sub-variants isolated from autopsy tissues
Santiago Maffia‐Bizzozero, Cintia Cevallos, Federico Remes Lenicov, et al.
Frontiers in Microbiology (2023) Vol. 14
Open Access | Times Cited: 15

Nanoscale cellular organization of viral RNA and proteins in SARS-CoV-2 replication organelles
Leonid Andronov, Mengting Han, Yan‐Yu Zhu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5

The transcriptional and translational landscape of HCoV-OC43 infection
Stefan Bresson, Emanuela Sani, Alicja Armatowska, et al.
PLoS Pathogens (2025) Vol. 21, Iss. 1, pp. e1012831-e1012831
Open Access

Beyond droplet deposition: Virus transport and deposition modeling in respiratory tract influenced by ambient environment and exhalation activities
Danting Luo, Zhiwen Luo, Xiaohong Zheng, et al.
Building and Environment (2024) Vol. 255, pp. 111406-111406
Closed Access | Times Cited: 4

A C57BL/6 Mouse Model of SARS-CoV-2 Infection Recapitulates Age- and Sex-Based Differences in Human COVID-19 Disease and Recovery
Michael A. Davis, Kathleen Voss, Julie Turnbull, et al.
Vaccines (2022) Vol. 11, Iss. 1, pp. 47-47
Open Access | Times Cited: 18

Identification of the viral and cellular microRNA interactomes during SARS-CoV-2 infection
Nicolas Fossat, Emma A. Lundsgaard, Rui Costa, et al.
Cell Reports (2023) Vol. 42, Iss. 4, pp. 112282-112282
Open Access | Times Cited: 11

The multiple roles of nsp6 in the molecular pathogenesis of SARS-CoV-2
Cody J. Bills, Xuping Xie, Pei‐Yong Shi
Antiviral Research (2023) Vol. 213, pp. 105590-105590
Open Access | Times Cited: 11

Visualization of Early RNA Replication Kinetics of SARS-CoV-2 by Using Single Molecule RNA-FISH Combined with Immunofluorescence
Rajiv Pathak, Carolina Eliscovich, Ignacio Mena, et al.
Viruses (2024) Vol. 16, Iss. 2, pp. 262-262
Open Access | Times Cited: 3

Alphavirus infection triggers selective cytoplasmic translocation of nuclear RBPs with moonlighting antiviral roles
Wael Kamel, Vincenzo Ruscica, Azman Embarc‐Buh, et al.
Molecular Cell (2024) Vol. 84, Iss. 24, pp. 4896-4911.e7
Open Access | Times Cited: 3

Machine learning for cross-scale microscopy of viruses
Anthony Petkidis, Vardan Andriasyan, Urs F. Greber
Cell Reports Methods (2023) Vol. 3, Iss. 9, pp. 100557-100557
Open Access | Times Cited: 9

An ACAT inhibitor suppresses SARS-CoV-2 replication and boosts antiviral T cell activity
Peter A. C. Wing, Nathalie Schmidt, Rory Peters, et al.
PLoS Pathogens (2023) Vol. 19, Iss. 5, pp. e1011323-e1011323
Open Access | Times Cited: 8

Exploring the expanding universe of host-virus interactions mediated by viral RNA
Alfredo Castelló, Lucı́a Álvarez, Wael Kamel, et al.
Molecular Cell (2024) Vol. 84, Iss. 19, pp. 3706-3721
Open Access | Times Cited: 2

Nonproductive exposure of PBMCs to SARS‐CoV ‐2 induces cell‐intrinsic innate immune responses
Julia Kazmierski, Kirstin Friedmann, Dylan Postmus, et al.
Molecular Systems Biology (2022) Vol. 18, Iss. 8
Open Access | Times Cited: 13

XNAzymes targeting the SARS-CoV-2 genome inhibit viral infection
Pehuén Pereyra Gerber, Maria J. Donde, Nicholas J. Matheson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 11

Towards Understanding Long COVID: SARS-CoV-2 Strikes the Host Cell Nucleus
Laura Lafon-Hughes
Pathogens (2023) Vol. 12, Iss. 6, pp. 806-806
Open Access | Times Cited: 5

Diminished antiviral innate immune gene expression in the placenta following a maternal SARS-CoV-2 infection
Brahm Coler, Tsung-Yen Wu, Lindsey Carlson, et al.
American Journal of Obstetrics and Gynecology (2022) Vol. 228, Iss. 4, pp. 463.e1-463.e20
Open Access | Times Cited: 9

SARS‐CoV‐2, periodontal pathogens, and host factors: The trinity of oral post‐acute sequelae of COVID‐19
Joel Schwartz, Kristelle J. Capistrano, Joseph L. Gluck, et al.
Reviews in Medical Virology (2024) Vol. 34, Iss. 3
Open Access | Times Cited: 1

XRN1 supplies free nucleotides to feed alphavirus replication
Vincenzo Ruscica, Louisa Iselin, Ryan M. Hull, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1

Membrane architects: how positive-strand RNA viruses restructure the cell
Christopher J. Neufeldt, Mirko Cortese
Journal of General Virology (2022) Vol. 103, Iss. 8
Closed Access | Times Cited: 8

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