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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:

The evolutionary trade‐offs in phage‐resistant Klebsiella pneumoniae entail cross‐phage sensitization and loss of multidrug resistance
Grażyna Majkowska-Skrobek, Paweł Markwitz, E. Sosnowska, et al.
Environmental Microbiology (2021) Vol. 23, Iss. 12, pp. 7723-7740
Closed Access | Times Cited: 64

Showing 1-25 of 64 citing articles:

Genetic determinants of host tropism in Klebsiella phages
Beatriz Beamud, Neris García‐González, Mar Gómez-Ortega, et al.
Cell Reports (2023) Vol. 42, Iss. 2, pp. 112048-112048
Open Access | Times Cited: 50
Evolutionary Dynamics between Phages and Bacteria as a Possible Approach for Designing Effective Phage Therapies against Antibiotic-Resistant Bacteria
Mahadi Hasan, Juhee Ahn
Antibiotics (2022) Vol. 11, Iss. 7, pp. 915-915
Open Access | Times Cited: 64
Translating bacteriophage-derived depolymerases into antibacterial therapeutics: Challenges and prospects
Honglan Wang, Yannan Liu, Changqing Bai, et al.
Acta Pharmaceutica Sinica B (2023) Vol. 14, Iss. 1, pp. 155-169
Open Access | Times Cited: 26
Characterization and comprehensive genome analysis of novel bacteriophage, vB_Kpn_ZCKp20p, with lytic and anti-biofilm potential against clinical multidrug-resistant Klebsiella pneumoniae
Bishoy Maher Zaki, Nada A. Fahmy, Ramy K. Aziz, et al.
Frontiers in Cellular and Infection Microbiology (2023) Vol. 13
Open Access | Times Cited: 25
Designing phage cocktails to combat the emergence of bacteriophage-resistant mutants in multidrug-resistant Klebsiella pneumoniae
Seongjun Yoo, Kang‐Mu Lee, Nayoung Kim, et al.
Microbiology Spectrum (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 24
Phage resistance formation and fitness costs of hypervirulent Klebsiella pneumoniae mediated by K2 capsule-specific phage and the corresponding mechanisms
Miran Tang, Zeyu Huang, Xiaodong Zhang, et al.
Frontiers in Microbiology (2023) Vol. 14
Open Access | Times Cited: 23
Enhanced Antibacterial Activity of Repurposed Mitomycin C and Imipenem in Combination with the Lytic Phage vB_KpnM-VAC13 against Clinical Isolates of Klebsiella pneumoniae
Olga Pacios, Laura Fernández-García, Inés Bleriot, et al.
Antimicrobial Agents and Chemotherapy (2021) Vol. 65, Iss. 9
Open Access | Times Cited: 42
Fitness Trade-Offs in Phage Cocktail-Resistant Salmonella enterica Serovar Enteritidis Results in Increased Antibiotic Susceptibility and Reduced Virulence
Dongyang Gao, Hongyue Ji, Linkang Wang, et al.
Microbiology Spectrum (2022) Vol. 10, Iss. 5
Open Access | Times Cited: 36
Epitopes in the capsular polysaccharide and the porin OmpK36 receptors are required for bacteriophage infection of Klebsiella pneumoniae
Rhys A. Dunstan, Rebecca S. Bamert, Kher Shing Tan, et al.
Cell Reports (2023) Vol. 42, Iss. 6, pp. 112551-112551
Open Access | Times Cited: 22
Competition between lysogenic and sensitive bacteria is determined by the fitness costs of the different emerging phage-resistance strategies
Olaya Rendueles, Jorge AM de Sousa, Eduardo P. C. Rocha
eLife (2023) Vol. 12
Open Access | Times Cited: 20
Phages against Noncapsulated Klebsiella pneumoniae: Broader Host range, Slower Resistance
Marta Lourenço, Lisa Osbelt, Virginie Passet, et al.
Microbiology Spectrum (2023) Vol. 11, Iss. 4
Open Access | Times Cited: 19
Virulence-associated factors as targets for phage infection
Alessandra Gonçalves de Melo, Carlee Morency, Sylvain Moineau
Current Opinion in Microbiology (2024) Vol. 79, pp. 102471-102471
Open Access | Times Cited: 6
Digital phagograms: predicting phage infectivity through a multilayer machine learning approach
Cédric Lood, Dimitri Boeckaerts, Michiel Stock, et al.
Current Opinion in Virology (2021) Vol. 52, pp. 174-181
Closed Access | Times Cited: 34
Recent advances in phage defense systems and potential overcoming strategies
Xiaoming Yuan, Zhichao Huang, Zhenjun Zhu, et al.
Biotechnology Advances (2023) Vol. 65, pp. 108152-108152
Closed Access | Times Cited: 14
Bacteriophage-resistant carbapenem-resistant Klebsiella pneumoniae shows reduced antibiotic resistance and virulence
Qiao Chen, Feiyang Zhang, Jiawei Bai, et al.
International Journal of Antimicrobial Agents (2024) Vol. 64, Iss. 2, pp. 107221-107221
Closed Access | Times Cited: 5
Emerging Phage Resistance in Pseudomonas aeruginosa PAO1 Is Accompanied by an Enhanced Heterogeneity and Reduced Virulence
Paweł Markwitz, Tomasz Olszak, Grzegorz Guła, et al.
Viruses (2021) Vol. 13, Iss. 7, pp. 1332-1332
Open Access | Times Cited: 32
Phage Selective Pressure Reduces Virulence of Hypervirulent Klebsiella pneumoniae Through Mutation of the wzc Gene
Lingjie Song, Xianggui Yang, Jinwei Huang, et al.
Frontiers in Microbiology (2021) Vol. 12
Open Access | Times Cited: 31
Shopping for phages? Unpacking design rules for therapeutic phage cocktails
Cédric Lood, Pieter‐Jan Haas, Vera van Noort, et al.
Current Opinion in Virology (2021) Vol. 52, pp. 236-243
Closed Access | Times Cited: 28
Exploiting phage-derived carbohydrate depolymerases for combating infectious diseases
Hugo Oliveira, Zuzanna Drulis‐Kawa, Joana Azeredo
Trends in Microbiology (2022) Vol. 30, Iss. 8, pp. 707-709
Closed Access | Times Cited: 21
Klebsiella phage KP34gp57 capsular depolymerase structure and function: from a serendipitous finding to the design of active mini-enzymes against K. pneumoniae
Barbara Maciejewska, Flavia Squeglia, Agnieszka Łątka, et al.
mBio (2023) Vol. 14, Iss. 5
Open Access | Times Cited: 12
Isolation, Characterization, Genome Analysis and Host Resistance Development of Two Novel Lastavirus Phages Active against Pandrug-Resistant Klebsiella pneumoniae
Mina Obradović, Milka Malešević, Mariagrazia Di Luca, et al.
Viruses (2023) Vol. 15, Iss. 3, pp. 628-628
Open Access | Times Cited: 11
Phage therapy of antibiotic-resistant strains of Klebsiella pneumoniae, opportunities and challenges from the past to the future
Mehrdad Mohammadi, Mahmood Saffari, Seyed Davar Siadat
Folia Microbiologica (2023) Vol. 68, Iss. 3, pp. 357-368
Closed Access | Times Cited: 11
Phage treatment of Pseudomonas aeruginosa yields a phage-resistant population with different susceptibility to innate immune responses and mild effects on metabolic profiles
Tomasz Olszak, Daria Augustyniak, Inmaculada García‐Romero, et al.
Microbiological Research (2024) Vol. 282, pp. 127609-127609
Closed Access | Times Cited: 4
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: 4
Phages adapt to recognize an O-antigen polysaccharide site by mutating the ‘backup’ tail protein ORF59, enabling reinfection of phage-resistant Klebsiella pneumoniae
Ping Li, Wenjie Ma, Jun Cheng, et al.
Emerging Microbes & Infections (2025)
Open Access
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