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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 ecological roles of bacterial chemotaxis
Johannes M. Keegstra, Francesco Carrara, Roman Stocker
Nature Reviews Microbiology (2022) Vol. 20, Iss. 8, pp. 491-504
Open Access | Times Cited: 188

Showing 1-25 of 188 citing articles:

Successional action of Bacteroidota and Firmicutes in decomposing straw polymers in a paddy soil
Jun-Jie Huang, Kailin Gao, Yang Lü, et al.
Environmental Microbiome (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 59
Spatial structure, chemotaxis and quorum sensing shape bacterial biomass accumulation in complex porous media
David Scheidweiler, Ankur Bordoloi, Wenqiao Jiao, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 22
Molecular Insights into Plant–Microbe Interactions: A Comprehensive Review of Key Mechanisms
César J. Chiquito-Contreras, Thuluz Meza‐Menchaca, Oswaldo Guzmán-López, et al.
Frontiers in Bioscience-Elite (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 18
Growth of microbes in competitive lifestyles promotes increased ARGs in soil microbiota: insights based on genetic traits
Zishu Liu, Xiangwu Yao, Cheng‐Yi Chen, et al.
Microbiome (2025) Vol. 13, Iss. 1
Open Access | Times Cited: 4
A Simple Three-Dimensional Microfluidic Platform for Studying Chemotaxis and Cell Sorting
Xiaobo Li, Yanqing Song, Andrew Glidle, et al.
Lab on a Chip (2025)
Open Access | Times Cited: 2
An atlas of metabolites driving chemotaxis in prokaryotes
Maéva Brunet, Shady A. Amin, Iurii Bodachivskyi, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Chemotaxis and autoinducer-2 signalling mediate colonization and contribute to co-existence of Escherichia coli strains in the murine gut
Leanid Laganenka, Jae Wook Lee, Lukas Malfertheiner, et al.
Nature Microbiology (2023) Vol. 8, Iss. 2, pp. 204-217
Closed Access | Times Cited: 32
Cell‐Based Micro/Nano‐Robots for Biomedical Applications: A Review
Bo Chen, Hongyan Sun, Jiaying Zhang, et al.
Small (2023) Vol. 20, Iss. 1
Closed Access | Times Cited: 25
Swimming towards each other: the role of chemotaxis in bacterial interactions
Justin R. Seymour, Douglas R. Brumley, Roman Stocker, et al.
Trends in Microbiology (2024) Vol. 32, Iss. 7, pp. 640-649
Closed Access | Times Cited: 13
Ecological relevance of flagellar motility in soil bacterial communities
Josep Ramoneda, Kunkun Fan, Jane Lucas, et al.
The ISME Journal (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 11
Coordinated regulation of chemotaxis and resistance to copper by CsoR in Pseudomonas putida
Meina He, Yongxin Tao, Kexin Mu, et al.
(2025)
Open Access | Times Cited: 1
Cyanobacteria and Chloroflexota cooperate to structure light-responsive biofilms
Freddy Bunbury, Carlos Rivas, Victoria Calatrava, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 5
Open Access | Times Cited: 1
Specificities of Chemosensory Receptors in the Human Gut Microbiota
Wenhao Xu, Ekaterina Jalomo-Khayrova, Vadim M. Gumerov, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Physics of swimming and its fitness cost determine strategies of bacterial investment in flagellar motility
Irina Lisevich, Rémy Colin, Hao Yuan Yang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Disentangling the feedback loops driving spatial patterning in microbial communities
A. D. Henderson, Alessia Del Panta, Olga T. Schubert, et al.
npj Biofilms and Microbiomes (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
Bacterial chemotaxis in human diseases
Bibi Zhou, Christine M. Szymanski, Arden Baylink
Trends in Microbiology (2022) Vol. 31, Iss. 5, pp. 453-467
Open Access | Times Cited: 38
Sphingomonas Relies on Chemotaxis to Degrade Polycyclic Aromatic Hydrocarbons and Maintain Dominance in Coking Sites
Meng Zhou, Zishu Liu, Jiaqi Wang, et al.
Microorganisms (2022) Vol. 10, Iss. 6, pp. 1109-1109
Open Access | Times Cited: 36
Collective behavior and nongenetic inheritance allow bacterial populations to adapt to changing environments
Henry H. Mattingly, Thierry Emonet
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 26
Open Access | Times Cited: 29
Accessing nutrients as the primary benefit arising from chemotaxis
Miguel A. Matilla, J.A. Gavira, Tino Krell
Current Opinion in Microbiology (2023) Vol. 75, pp. 102358-102358
Open Access | Times Cited: 22
Strong chemotaxis by marine bacteria towards polysaccharides is enhanced by the abundant organosulfur compound DMSP
Estelle E. Clerc, Jean‐Baptiste Raina, Johannes M. Keegstra, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 21
Tradeoffs of microbial life history strategies drive the turnover of microbial-derived organic carbon in coastal saline soils
Qi Ning, Lin Chen, Fang Li, et al.
Frontiers in Microbiology (2023) Vol. 14
Open Access | Times Cited: 18
Adaptation strategies and functional transitions of microbial community in pyrene-contaminated soils promoted by lead with Pseudomonas veronii and its extracellular polymeric substances
Zijun Ni, Zongqiang Gong, Lei Song, et al.
Chemosphere (2024) Vol. 351, pp. 141139-141139
Closed Access | Times Cited: 8
Enhancing carbon fixation and suppressing bacterial chemotaxis through carbon matrix nano-selenium to mitigate emissions of antibiotic resistance genes and virulence factors from chicken manure
Weikun Guan, Lizhi Li, Cheng Zhang, et al.
Chemical Engineering Journal (2024) Vol. 483, pp. 149076-149076
Closed Access | Times Cited: 8
Microbes in porous environments: from active interactions to emergent feedback
Chenyu Jin, Anupam Sengupta
Biophysical Reviews (2024) Vol. 16, Iss. 2, pp. 173-188
Open Access | Times Cited: 8
Micro-biophysical interactions at bacterium-mineral interfaces determine potassium dissolution
Miao Han, Xiaoyan Zhu, Chujin Ruan, et al.
Environmental Technology & Innovation (2024) Vol. 33, pp. 103524-103524
Open Access | Times Cited: 6
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