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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:

Kinetics of viral load and antibody response in relation to COVID-19 severity
Yanqun Wang, Lu Zhang, Ling Sang, et al.
Journal of Clinical Investigation (2020) Vol. 130, Iss. 10, pp. 5235-5244
Open Access | Times Cited: 573

Showing 26-50 of 573 citing articles:

The relationship between COVID‐19 viral load and disease severity: A systematic review
Omid Dadras, Amir Masoud Afsahi, Zahra Pashaei, et al.
Immunity Inflammation and Disease (2021) Vol. 10, Iss. 3
Open Access | Times Cited: 144
Natural history of COVID-19 and therapeutic options
Philippe Gautret, Matthieu Million, Pierre‐André Jarrot, et al.
Expert Review of Clinical Immunology (2020) Vol. 16, Iss. 12, pp. 1159-1184
Closed Access | Times Cited: 143
Antibody Responses in COVID-19: A Review
Mateo Chvatal-Medina, Yorjagis Mendez-Cortina, Pablo Javier Patiño Grajales, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 137
Clinical Evaluation of BD Veritor SARS-CoV-2 Point-of-Care Test Performance Compared to PCR-Based Testing and versus the Sofia 2 SARS Antigen Point-of-Care Test
Stephen Young, Stephanie N. Taylor, Catherine L. Cammarata, et al.
Journal of Clinical Microbiology (2020) Vol. 59, Iss. 1
Open Access | Times Cited: 135
Understanding neutralising antibodies against SARS-CoV-2 and their implications in clinical practice
Natalie Yan‐Lin Pang, Alexander Shao‐Rong Pang, Vincent Chow, et al.
Military Medical Research (2021) Vol. 8, Iss. 1
Open Access | Times Cited: 132
Beyond neutralization: Fc-dependent antibody effector functions in SARS-CoV-2 infection
Ali Zhang, Hannah D. Stacey, Michael R. D’Agostino, et al.
Nature reviews. Immunology (2022) Vol. 23, Iss. 6, pp. 381-396
Open Access | Times Cited: 126
SARS-CoV-2 specific antibody and neutralization assays reveal the wide range of the humoral immune response to virus
Mikail Dogan, Lina Kozhaya, Lindsey Placek, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 125
Gut Microbiome Alterations in COVID-19
Tao Zuo, Xiaojian Wu, Weiping Wen, et al.
Genomics Proteomics & Bioinformatics (2021) Vol. 19, Iss. 5, pp. 679-688
Open Access | Times Cited: 115
COVID-19 convalescent plasma composition and immunological effects in severe patients
Yeny Acosta‐Ampudia, Diana M. Monsalve, Manuel Rojas, et al.
Journal of Autoimmunity (2021) Vol. 118, pp. 102598-102598
Open Access | Times Cited: 113
SARS-CoV-2 viremia is associated with distinct proteomic pathways and predicts COVID-19 outcomes
Yijia Li, Alexis M. Schneider, Arnav Mehta, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 13
Open Access | Times Cited: 110
A population-based analysis of the longevity of SARS-CoV-2 antibody seropositivity in the United States
David Alfego, Adam Sullivan, Brian Poirier, et al.
EClinicalMedicine (2021) Vol. 36, pp. 100902-100902
Open Access | Times Cited: 108
Impact of virus genetic variability and host immunity for the success of COVID-19 vaccines
Wagner Gouvêa dos Santos
Biomedicine & Pharmacotherapy (2021) Vol. 136, pp. 111272-111272
Open Access | Times Cited: 106
Performance evaluation of the Roche Elecsys Anti-SARS-CoV-2 S immunoassay
Elena Riester, Peter Findeisen, Johannes Kolja Hegel, et al.
Journal of Virological Methods (2021) Vol. 297, pp. 114271-114271
Open Access | Times Cited: 106
Longitudinal analysis of antibody dynamics in COVID-19 convalescents reveals neutralizing responses up to 16 months after infection
Yang Yang, Minghui Yang, Yun Peng, et al.
Nature Microbiology (2022) Vol. 7, Iss. 3, pp. 423-433
Open Access | Times Cited: 104
SARS-CoV-2 infection elicits a rapid neutralizing antibody response that correlates with disease severity
Benjamin Trinité, Ferran Tarrés-Freixas, Jordi Rodon, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 103
Robust SARS-CoV-2 infection in nasal turbinates after treatment with systemic neutralizing antibodies
Dongyan Zhou, Jasper Fuk‐Woo Chan, Biao Zhou, et al.
Cell Host & Microbe (2021) Vol. 29, Iss. 4, pp. 551-563.e5
Open Access | Times Cited: 102
SARS-CoV-2 S2–targeted vaccination elicits broadly neutralizing antibodies
Kevin W. Ng, Nikhil Faulkner, Katja Finsterbusch, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 655
Open Access | Times Cited: 84
A novel STING agonist-adjuvanted pan-sarbecovirus vaccine elicits potent and durable neutralizing antibody and T cell responses in mice, rabbits and NHPs
Zezhong Liu, Jie Zhou, Wei Xu, et al.
Cell Research (2022) Vol. 32, Iss. 3, pp. 269-287
Open Access | Times Cited: 71
The role of immune activation and antigen persistence in acute and long COVID
Skye Opsteen, Jacob K. Files, Tim Fram, et al.
Journal of Investigative Medicine (2023) Vol. 71, Iss. 5, pp. 545-562
Open Access | Times Cited: 40
Identification of a highly conserved neutralizing epitope within the RBD region of diverse SARS-CoV-2 variants
Yanqun Wang, An Yan, Deyong Song, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 15
Spike-specific circulating T follicular helper cell and cross-neutralizing antibody responses in COVID-19-convalescent individuals
Jian Zhang, Qian Wu, Ziyan Liu, et al.
Nature Microbiology (2020) Vol. 6, Iss. 1, pp. 51-58
Open Access | Times Cited: 134
Neutralizing Antibody Production in Asymptomatic and Mild COVID-19 Patients, in Comparison with Pneumonic COVID-19 Patients
Jae‐Hoon Ko, Eun‐Jeong Joo, Su‐Jin Park, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 7, pp. 2268-2268
Open Access | Times Cited: 128
Understanding viral shedding of severe acute respiratory coronavirus virus 2 (SARS-CoV-2): Review of current literature
Lauren Fontana, Angela Holly Villamagna, Monica Sikka, et al.
Infection Control and Hospital Epidemiology (2020) Vol. 42, Iss. 6, pp. 659-668
Open Access | Times Cited: 111
Comprehensive analysis of COVID-19 during pregnancy
Kathryn M. Moore, Mehul S. Suthar
Biochemical and Biophysical Research Communications (2020) Vol. 538, pp. 180-186
Open Access | Times Cited: 109
Loss of Anti–SARS-CoV-2 Antibodies in Mild Covid-19
Satoshi Kutsuna, Yusuke Asai, Akihiro Matsunaga
New England Journal of Medicine (2020) Vol. 383, Iss. 17, pp. 1694-1698
Closed Access | Times Cited: 102

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