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:

Microbial Arsenal of Antiviral Defenses. Part II
Artem Isaev, Olga Musharova, Konstantin Severinov
Biochemistry (Moscow) (2021) Vol. 86, Iss. 4, pp. 449-470
Open Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

Antibiotics and Bacterial Resistance—A Short Story of an Endless Arms Race
Aleksandra Baran, Aleksandra Kwiatkowska, Leszek Potocki
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 6, pp. 5777-5777
Open Access | Times Cited: 119

PADLOC: a web server for the identification of antiviral defence systems in microbial genomes
Leighton Payne, Sean Meaden, Mario Rodríguez Mestre, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. W1, pp. W541-W550
Open Access | Times Cited: 112

CRISPR–Cas9: A History of Its Discovery and Ethical Considerations of Its Use in Genome Editing
Irina Gostimskaya
Biochemistry (Moscow) (2022) Vol. 87, Iss. 8, pp. 777-788
Open Access | Times Cited: 98

Bacteriophage therapy for drug-resistant Staphylococcus aureus infections
Kaixin Liu, Chao Wang, Xudong Zhou, et al.
Frontiers in Cellular and Infection Microbiology (2024) Vol. 14
Open Access | Times Cited: 19

A short prokaryotic Argonaute activates membrane effector to confer antiviral defense
Zhifeng Zeng, Yu Chen, Rafael Pinilla‐Redondo, et al.
Cell Host & Microbe (2022) Vol. 30, Iss. 7, pp. 930-943.e6
Open Access | Times Cited: 60

Type III CRISPR-Cas provides resistance against nucleus-forming jumbo phages via abortive infection
David Mayo-Muñoz, Leah Smith, Carmela Garcia‐Doval, et al.
Molecular Cell (2022) Vol. 82, Iss. 23, pp. 4471-4486.e9
Open Access | Times Cited: 42

Anti-phage defence through inhibition of virion assembly
Pramalkumar H. Patel, Véronique L. Taylor, Chi Zhang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13

Biosynthesis and function of 7-deazaguanine derivatives in bacteria and phages
Valérie de Crécy‐Lagard, Geoffrey Hutinet, José D. D. Cediel-Becerra, et al.
Microbiology and Molecular Biology Reviews (2024) Vol. 88, Iss. 1
Open Access | Times Cited: 11

Reversible bacteriophage resistance by shedding the bacterial cell wall
Véronique Ongenae, Adam Sidi Mabrouk, Marjolein E. Crooijmans, et al.
Open Biology (2022) Vol. 12, Iss. 6
Open Access | Times Cited: 34

A Bacterial Dynamin-Like Protein Confers a Novel Phage Resistance Strategy on the Population Level in Bacillus subtilis
Lijun Guo, Laura Sattler, Samia Shafqat, et al.
mBio (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 31

Molecular basis of foreign DNA recognition by BREX anti-phage immunity system
Alena Drobiazko, Myfanwy C. Adams, Mikhail Skutel, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Recent advancements in bacterial anti-phage strategies and the underlying mechanisms altering susceptibility to antibiotics
Hao Zou, Xiaoyi Huang, W. Xiao, et al.
Microbiological Research (2025) Vol. 295, pp. 128107-128107
Closed Access

UG/Abi: a highly diverse family of prokaryotic reverse transcriptases associated with defense functions
Mario Rodríguez Mestre, Linyi Gao, Shiraz A. Shah, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 11, pp. 6084-6101
Open Access | Times Cited: 26

The abortive infection functions of CRISPR-Cas and Argonaute
Yu Chen, Zhifeng Zeng, Qunxin She, et al.
Trends in Microbiology (2022) Vol. 31, Iss. 4, pp. 405-418
Closed Access | Times Cited: 20

The novel anti-phage system Shield co-opts an RmuC domain to mediate phage defense across Pseudomonas species
Elliot Macdonald, Rosanna C. T. Wright, James P. R. Connolly, et al.
PLoS Genetics (2023) Vol. 19, Iss. 6, pp. e1010784-e1010784
Open Access | Times Cited: 12

The book of Lambda does not tell us that naturally occurring lysogens of Escherichia coli are likely to be resistant as well as immune
Brandon A. Berryhill, Rodrigo García, Ingrid C. McCall, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 11
Open Access | Times Cited: 11

A game of resistance: War between bacteria and phages and how phage cocktails can be the solution
Pedro Costa, Carla Pereira, Jesús L. Romalde, et al.
Virology (2024) Vol. 599, pp. 110209-110209
Open Access | Times Cited: 3

Cell wall deficiency as an escape mechanism from phage infection
Véronique Ongenae, Ariane Briegel, Dennis Claessen
Open Biology (2021) Vol. 11, Iss. 9
Open Access | Times Cited: 17

Reassembling a cannon in the DNA defense arsenal: Genetics of StySA, a BREX phage exclusion system in Salmonella lab strains
Julie Zaworski, Oyut Dagva, Julius Brandt, et al.
PLoS Genetics (2022) Vol. 18, Iss. 4, pp. e1009943-e1009943
Open Access | Times Cited: 11

RB49-like Bacteriophages Recognize O Antigens as One of the Alternative Primary Receptors
Alexandr D. Efimov, Alla K. Golomidova, Eugene E. Kulikov, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 19, pp. 11329-11329
Open Access | Times Cited: 11

Tailed Lytic Bacteriophages of Soft Rot Pectobacteriaceae
Konstantin A. Miroshnikov, Peter V. Evseev, Anna A. Lukianova, et al.
Microorganisms (2021) Vol. 9, Iss. 9, pp. 1819-1819
Open Access | Times Cited: 13

Four additional natural 7-deazaguanine derivatives in phages and how to make them
Cui Liang, Seetharamsing Balamkundu, Chuan‐Fa Liu, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 17, pp. 9214-9226
Open Access | Times Cited: 5

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