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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:

Forward and reverse genetic dissection of morphogenesis identifies filament-competent Candida auris strains
Darian J. Santana, Teresa R. O’Meara
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 58

Showing 1-25 of 58 citing articles:

Candida auris Genetics and Emergence
Anuradha Chowdhary, Kusum Jain, Neeraj Chauhan
Annual Review of Microbiology (2023) Vol. 77, Iss. 1, pp. 583-602
Open Access | Times Cited: 67
A Candida auris –specific adhesin, Scf1 , governs surface association, colonization, and virulence
Darian J. Santana, Juliet A. E. Anku, Guolei Zhao, et al.
Science (2023) Vol. 381, Iss. 6665, pp. 1461-1467
Open Access | Times Cited: 52
An Overlooked and Underrated Endemic Mycosis—Talaromycosis and the Pathogenic Fungus Talaromyces marneffei
Fang Wang, Runhua Han, Shi Chen
Clinical Microbiology Reviews (2023) Vol. 36, Iss. 1
Open Access | Times Cited: 47
Clinical isolates of Candida auris with enhanced adherence and biofilm formation due to genomic amplification of ALS4
Jian Bing, Zhangyue Guan, Tianhong Zheng, et al.
PLoS Pathogens (2023) Vol. 19, Iss. 3, pp. e1011239-e1011239
Open Access | Times Cited: 43
Rapid evolution of an adaptive multicellular morphology of Candida auris during systemic infection
Jian Bing, Zhangyue Guan, Tianhong Zheng, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 26
The many faces of Candida auris: Phenotypic and strain variation in an emerging pathogen
Darian J. Santana, Guolei Zhao, Teresa R. O’Meara
PLoS Pathogens (2024) Vol. 20, Iss. 3, pp. e1012011-e1012011
Open Access | Times Cited: 23
Candida auris undergoes adhesin-dependent and -independent cellular aggregation
Chloe Pelletier, Sophie Shaw, Sakinah Alsayegh, et al.
PLoS Pathogens (2024) Vol. 20, Iss. 3, pp. e1012076-e1012076
Open Access | Times Cited: 19
One population, multiple lifestyles: Commensalism and pathogenesis in the human mycobiome
Diana M. Proctor, Rebecca A. Drummond, Michail S. Lionakis, et al.
Cell Host & Microbe (2023) Vol. 31, Iss. 4, pp. 539-553
Open Access | Times Cited: 39
Candida auris uses metabolic strategies to escape and kill macrophages while avoiding robust activation of the NLRP3 inflammasome response
Harshini Weerasinghe, Claudia Simm, Tirta M. Djajawi, et al.
Cell Reports (2023) Vol. 42, Iss. 5, pp. 112522-112522
Open Access | Times Cited: 23
Mechanisms of pathogenicity for the emerging fungus Candida auris
Mark V. Horton, Ashley M. Holt, Jeniel E. Nett
PLoS Pathogens (2023) Vol. 19, Iss. 12, pp. e1011843-e1011843
Open Access | Times Cited: 19
Skin and hard surface disinfection against Candida auris – What we know today
Soraya Omardien, Peter J. Teska
Frontiers in Medicine (2024) Vol. 11
Open Access | Times Cited: 8
Collateral sensitivity counteracts the evolution of antifungal drug resistance in Candida auris
Hans Carolus, Dimitrios Sofras, Giorgio Boccarella, et al.
Nature Microbiology (2024) Vol. 9, Iss. 11, pp. 2954-2969
Closed Access | Times Cited: 7
Strain and temperature dependent aggregation of Candida auris is attenuated by inhibition of surface amyloid proteins
Dhara Malavia, Rhys A. Farrer, Mark H. T. Stappers, et al.
The Cell Surface (2023) Vol. 10, pp. 100110-100110
Open Access | Times Cited: 16
Gut fungal mycobiome: A significant factor of tumor occurrence and development
Fan Li, Yunhuan Gao, Wenyue Cheng, et al.
Cancer Letters (2023) Vol. 569, pp. 216302-216302
Open Access | Times Cited: 14
Advanced genetic techniques in fungal pathogen research
Robbi L. Ross, Felipe H. Santiago‐Tirado
mSphere (2024) Vol. 9, Iss. 4
Open Access | Times Cited: 5
Yeast and filamentous Candida auris stimulate distinct immune responses in the skin
Garrett Bryak, Abigail Cox, Michail S. Lionakis, et al.
mSphere (2024) Vol. 9, Iss. 7
Open Access | Times Cited: 5
Candida auris —macrophage cellular interactions and transcriptional response
Pedro Miramón, Andrew W. Pountain, Michael Lorenz
Infection and Immunity (2023) Vol. 91, Iss. 11
Open Access | Times Cited: 12
Comprehensive Overview of Candida auris: An Emerging Multidrug-Resistant Fungal Pathogen
Ji-Seok Kim, Hyunjin Cha, Yong‐Sun Bahn
Journal of Microbiology and Biotechnology (2024) Vol. 34, Iss. 7, pp. 1365-1375
Open Access | Times Cited: 4
A comparative evaluation of CRISPR-Cas9 allele editing systems in Candida auris: challenging research in a challenging bug
Hans Carolus, Dimitrios Sofras, Ana Subotić, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Genomics insights of candidiasis: mechanisms of pathogenicity and drug resistance
Xin Huang, Qin Dong, Qi Zhou, et al.
Frontiers in Microbiology (2025) Vol. 16
Open Access
Biofilm-Associated Candidiasis: Pathogenesis, Prevalence, Challenges and Therapeutic Options
Valerie Amann, Ann‐Kathrin Kissmann, Carolina Firacative, et al.
Pharmaceuticals (2025) Vol. 18, Iss. 4, pp. 460-460
Open Access
Gene dosage of PDR16 modulates azole susceptibility in Candida auris
Trinh Phan-Canh, Tamires A. Bitencourt, Karl Kuchler
Microbiology Spectrum (2025)
Open Access
Signaling pathways governing the pathobiological features and antifungal drug resistance of Candida auris
Hyunjin Cha, Doyeon Won, Yong‐Sun Bahn
mBio (2025)
Open Access
Dry Surface Biofilm Formation by Candida auris Facilitates Persistence and Tolerance to Sodium Hypochlorite
Alicia Ware, William Johnston, Christopher Delaney, et al.
Apmis (2025) Vol. 133, Iss. 4
Open Access
Candida aurisskin colonization is mediated by Als4112 and interactions with host extracellular matrix proteins
Guolei Zhao, Jingwen Lyu, Natalia A. Veniaminova, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
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