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:

Systematic discovery of pseudomonad genetic factors involved in sensitivity to tailocins
Sean Carim, Ashley L. Azadeh, Alexey E. Kazakov, et al.
The ISME Journal (2021) Vol. 15, Iss. 8, pp. 2289-2305
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

Phage Paride can kill dormant, antibiotic-tolerant cells of Pseudomonas aeruginosa by direct lytic replication
Enea Maffei, Anne-Kathrin Woischnig, Marco Burkolter, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 30

Mining of Thousands of Prokaryotic Genomes Reveals High Abundance of Prophages with a Strictly Narrow Host Range
Gamaliel López-Leal, Laura Carolina Camelo-Valera, Juan Manuel Hurtado-Ramírez, et al.
mSystems (2022) Vol. 7, Iss. 4
Open Access | Times Cited: 42

A phage tail–like bacteriocin suppresses competitors in metapopulations of pathogenic bacteria
Talia Backman, Sergio M. Latorre, Efthymia Symeonidi, et al.
Science (2024) Vol. 384, Iss. 6701
Closed Access | Times Cited: 12

R-pyocins as targeted antimicrobials against Pseudomonas aeruginosa
Madeline Mei, Iris Estrada, Stephen P. Diggle, et al.
npj Antimicrobials and Resistance (2025) Vol. 3, Iss. 1
Open Access | Times Cited: 1

To kill or to be killed: pangenome analysis of Escherichia coli strains reveals a tailocin specific for pandemic ST131
Erwin Tantoso, Birgit Eisenhaber, Miles Kirsch, et al.
BMC Biology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 34

The genetic basis of phage susceptibility, cross-resistance and host-range in Salmonella
Benjamin A. Adler, Alexey E. Kazakov, Crystal Zhong, et al.
Microbiology (2021) Vol. 167, Iss. 12
Open Access | Times Cited: 35

A lipopolysaccharide‐dependent phage infects a pseudomonad phytopathogen and can evolve to evade phage resistance
Suzanne L. Warring, Lucía M. Malone, Jay Jayaraman, et al.
Environmental Microbiology (2022) Vol. 24, Iss. 10, pp. 4834-4852
Open Access | Times Cited: 27

A Phage Foundry Framework to Systematically Develop Viral Countermeasures to Combat Antibiotic-Resistant Bacterial Pathogens
Vivek K. Mutalik, Adam P. Arkin
iScience (2022) Vol. 25, Iss. 4, pp. 104121-104121
Open Access | Times Cited: 25

Pivotal role of O-antigenic polysaccharide display in the sensitivity against phage tail-like particles in environmental Pseudomonas kin competition
Clara Margot Heiman, M. Maurhofer, Sandra Calderon, et al.
The ISME Journal (2022) Vol. 16, Iss. 7, pp. 1683-1693
Open Access | Times Cited: 25

Evolutionary and ecological role of extracellular contractile injection systems: from threat to weapon
Clara Margot Heiman, Jordan Vacheron, Christoph Keel
Frontiers in Microbiology (2023) Vol. 14
Open Access | Times Cited: 15

The expanding universe of contractile injection systems in bacteria
Lin Lin
Current Opinion in Microbiology (2024) Vol. 79, pp. 102465-102465
Open Access | Times Cited: 5

Tradeoffs and constraints on the evolution of tailocins
Talia Backman, Hernán A. Burbano, Talia L. Karasov
Trends in Microbiology (2024) Vol. 32, Iss. 11, pp. 1084-1095
Open Access | Times Cited: 5

Solvent-Producing Clostridia Revisited
David Jones, Frederik Schulz, Simon Roux, et al.
Microorganisms (2023) Vol. 11, Iss. 9, pp. 2253-2253
Open Access | Times Cited: 11

Microbes and metabolites of a plant-parasite interaction: Deciphering the ecology of Tetrastigma host choice in the world’s largest parasitic flower, Rafflesia
Jeanmaire Molina, Roche C. de Guzman, Rinat R. Abzalimov, et al.
Current Plant Biology (2025) Vol. 42, pp. 100456-100456
Open Access

«The world of phage tail-like bacteriocins: State of the art and biotechnological perspectives»
Clara Ibarguren, Inés Bleriot, Lucia Blasco, et al.
Microbiological Research (2025) Vol. 295, pp. 128121-128121
Open Access

Tailocin‐Mediated Interactions Among Soft Rot Pectobacteriaceae
Marcin Borowicz, Dorota M. Krzyżanowska, M Sobolewska, et al.
Molecular Ecology (2025)
Open Access

Intraspecific bacterial competition mediated by rapidly diversifying tailocin and prophage loci
Sarah Kauffman, Ryan Musumba Awori, Emmanuel C. Allwell, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Variation at the common polysaccharide antigen locus drives lipopolysaccharide diversity within the Pseudomonas syringae species complex
Jay Jayaraman, William T. Jones, Dawn Harvey, et al.
Environmental Microbiology (2020) Vol. 22, Iss. 12, pp. 5356-5372
Open Access | Times Cited: 23

Genomic Correlates of Tailocin Sensitivity inPseudomonas syringae
David A. Baltrus, Savannah Weaver, Laura Krings, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 8

Phage-tail-like bacteriocins as a biomedical platform to counter anti-microbial resistant pathogens
Rahul Bhattacharjee, Aditya Nandi, Adrija Sinha, et al.
Biomedicine & Pharmacotherapy (2022) Vol. 155, pp. 113720-113720
Open Access | Times Cited: 11

Multiparametric Sensing of Outer Membrane Vesicle-Derived Supported Lipid Bilayers Demonstrates the Specificity of Bacteriophage Interactions
Karan Bali, Reece McCoy, Zixuan Lu, et al.
ACS Biomaterials Science & Engineering (2023) Vol. 9, Iss. 6, pp. 3632-3642
Open Access | Times Cited: 6

A weaponized phage suppresses competitors in historical and modern metapopulations of pathogenic bacteria
Talia Backman, Sergio M. Latorre, Efthymia Symeonidi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5

High prevalence of lipopolysaccharide mutants and R2-pyocin susceptible variants in Pseudomonas aeruginosa populations sourced from cystic fibrosis lung infections
Madeline Mei, Preston Pheng, Detriana Kurzeja-Edwards, et al.
Microbiology Spectrum (2023) Vol. 11, Iss. 6
Open Access | Times Cited: 5

Pantailocins: phage-derived bacteriocins from Pantoea ananatis and Pantoea stewartii subsp. indologenes
Shaun P. Stice, Hsiao-Hsuan Jan, Hsiao-Chun Chen, et al.
Applied and Environmental Microbiology (2023) Vol. 89, Iss. 12
Open Access | Times Cited: 5

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