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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:

Friend or Foe: Interbacterial Competition in the Nasal Cavity
Britney L. Hardy, D. Scott Merrell
Journal of Bacteriology (2020) Vol. 203, Iss. 5
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Rothia from the Human Nose Inhibit Moraxella catarrhalis Colonization with a Secreted Peptidoglycan Endopeptidase
Reed M. Stubbendieck, Eishika Dissanayake, Peter M. Burnham, et al.
mBio (2023) Vol. 14, Iss. 2
Open Access | Times Cited: 19
Staphylococcus epidermidis bacteriocin A37 kills natural competitors with a unique mechanism of action
Jan-Samuel Puls, Benjamin Winnerling, Jeffrey J. Power, et al.
The ISME Journal (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 6
The Microbiota/Host Immune System Interaction in the Nose to Protect from COVID-19
Arianna Di Stadio, Claudio Costantini, Giorgia Renga, et al.
Life (2020) Vol. 10, Iss. 12, pp. 345-345
Open Access | Times Cited: 44
Compartmentalization of the host microbiome: how tumor microbiota shapes checkpoint immunotherapy outcome and offers therapeutic prospects
Maximilian Boesch, Lena Horvath, Florent Baty, et al.
Journal for ImmunoTherapy of Cancer (2022) Vol. 10, Iss. 11, pp. e005401-e005401
Open Access | Times Cited: 21
The human microbiome-derived antimicrobial lugdunin self-regulates its biosynthesis by a feed-forward mechanism
Leonie Reetz, Laura Schulze, Thales Kronenberger, et al.
mBio (2025)
Open Access
Staphylococcus hominis as a source of antimicrobial peptides: identification of a new peptide with potential antimicrobial properties using in silico approach
Mohammed Walid Chemao-Elfihri, Mohammed Hakmi, Hanane Abbou, et al.
Archives of Microbiology (2025) Vol. 207, Iss. 5
Closed Access
Association between short-term exposure to PM2.5 and nasal microbiota dysbiosis, inflammation and oxidative stress: A panel study of healthy young adults
Wenlong Li, Beibei Sun, Huijun Li, et al.
Ecotoxicology and Environmental Safety (2023) Vol. 262, pp. 115156-115156
Open Access | Times Cited: 10
Integrated large-scale metagenome assembly and multi-kingdom network analyses identify sex differences in the human nasal microbiome
Yanmei Ju, Zhe Zhang, Mingliang Liu, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 3
Alterations in the nasopharyngeal microbiota associated with active and latent tuberculosis
Yuan Huang, Jinhua Tang, Zheng Cai, et al.
Tuberculosis (2022) Vol. 136, pp. 102231-102231
Closed Access | Times Cited: 14
Nutritional Interactions between Bacterial Species Colonising the Human Nasal Cavity: Current Knowledge and Future Prospects
Lea Antje Adolf, Simon Heilbronner
Metabolites (2022) Vol. 12, Iss. 6, pp. 489-489
Open Access | Times Cited: 13
Temperature influences commensal-pathogen dynamics in a nasal epithelial cell co-culture model
Joshua T. Huffines, RaNashia L. Boone, Megan R. Kiedrowski
mSphere (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 2
The Facts and Family Secrets of Plasmids That Replicate via the Rolling-Circle Mechanism
M. Pilar Garcillán‐Barcia, Radosław Pluta, Fabián Lorenzo-Díaz, et al.
Microbiology and Molecular Biology Reviews (2021) Vol. 86, Iss. 1
Open Access | Times Cited: 16
Alterations in the nasopharyngeal microbiome associated with SARS-CoV-2 infection status and disease severity
Nick P. G. Gauthier, Kerstin Locher, Clayton MacDonald, et al.
PLoS ONE (2022) Vol. 17, Iss. 10, pp. e0275815-e0275815
Open Access | Times Cited: 12
Porcine Nasal Organoids as a model to study the interactions between the swine nasal microbiota and the host
Laura Bonillo-Lopez, Noelia Carmona-Vicente, Ferran Tarrés-Freixas, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Nasopharyngeal microbiome composition associated with Streptococcus pneumoniae colonization suggests a protective role of Corynebacterium in young children
Lei Xu, Joshua P. Earl, Michael E. Pichichero
PLoS ONE (2021) Vol. 16, Iss. 9, pp. e0257207-e0257207
Open Access | Times Cited: 15
The microbiome–nose–brain axis in health and disease
Françoise Lazarini, Emmanuel Roze, Annie Lannuzel, et al.
Trends in Neurosciences (2022) Vol. 45, Iss. 10, pp. 718-721
Open Access | Times Cited: 10
The Respiratory Commensal Bacterium Dolosigranulum pigrum 040417 Improves the Innate Immune Response to Streptococcus pneumoniae
Fernanda Raya Tonetti, Mikado Tomokiyo, Ramiro Ortiz Moyano, et al.
Microorganisms (2021) Vol. 9, Iss. 6, pp. 1324-1324
Open Access | Times Cited: 14
Nasal Microbiota Imbalance as a Contributory Link in the Emergence of COVID-19 Associated Mucormycosis
Rachna Singh, Anjna Kumari
ACS Infectious Diseases (2021) Vol. 7, Iss. 8, pp. 2211-2213
Open Access | Times Cited: 12
A High-Risk Profile for Invasive Fungal Infections Is Associated with Altered Nasal Microbiota and Niche Determinants
Claudio Costantini, Emilia Nunzi, Angelica Spolzino, et al.
Infection and Immunity (2022) Vol. 90, Iss. 4
Open Access | Times Cited: 8
Siderophore piracy enables the nasal commensalStaphylococcus lugdunensisto antagonize the pathogenStaphylococcus aureus
Ralf Rosenstein, Benjamin O. Torres Salazar, Claudia Sauer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Nasal microbiome dynamics: decoding the intricate nexus in the progression of respiratory and neurological diseases
Keerti Maheshwari, R. Gupta, Ruchika Sharma, et al.
Critical Reviews in Microbiology (2024), pp. 1-16
Closed Access | Times Cited: 1
The Staphylococcus aureus-antagonizing human nasal commensal Staphylococcus lugdunensis depends on siderophore piracy
Ralf Rosenstein, Benjamin O. Torres Salazar, Claudia Sauer, et al.
Microbiome (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 1
Nasal microbiota evolution within the congregate setting imposed by military training
Faith C. Blum, Jeannette M. Whitmire, Jason W. Bennett, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 6
The Role of Probiotics in Chronic Rhinosinusitis Treatment: An Update of the Current Literature
Maria Rita Bianco, Massimo Ralli, Domenico Michele Modica, et al.
Healthcare (2021) Vol. 9, Iss. 12, pp. 1715-1715
Open Access | Times Cited: 4
Microbiome in the nasopharynx: Insights into the impact of COVID-19 severity
David Galeana-Cadena, Gustavo Ramírez-Martínez, José Alberto Choreño-Parra, et al.
Heliyon (2024) Vol. 10, Iss. 10, pp. e31562-e31562
Open Access
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