Candida auris Pan-Drug-Resistant to Four Classes of Antifungal Agents

Simultaneous Emergence of Multidrug-Resistant <i>Candida auris</i> on 3 Continents Confirmed by Whole-Genome Sequencing and Epidemiological Analyses

Lockhart, S. R., Etienne, K. A., Vallabhaneni, S., Farooqi, J., Chowdhary, A., Govender, N. P., Colombo, A. L., Calvo, B., Cuomo, C. A., Desjardins, C. A., et al. (2017) · Clinical Infectious Diseases · doi:10.1093/cid/ciw691 · Cited by 1,662 · see citing works

<i>Candida auris</i> sp. nov., a novel ascomycetous yeast isolated from the external ear canal of an inpatient in a Japanese hospital

Satoh, K., Makimura, K., Hasumi, Y., Nishiyama, Y., Uchida, K., & Yamaguchi, H. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2008.00083.x · Cited by 1,381 · see citing works

A multicentre study of antifungal susceptibility patterns among 350 Candida auris isolates (2009–17) in India: role of the ERG11 and FKS1 genes in azole and echinocandin resistance

Chowdhary, A., Prakash, A., Sharma, C., Kordalewska, M., Kumar, A., Sarma, S., Tarai, B., Singh, A., Upadhyaya, G., Upadhyay, S., et al. (2018) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkx480 · Cited by 577 · see citing works

A <i>Candida auris</i> Outbreak and Its Control in an Intensive Care Setting

Eyre, D. W., Sheppard, A. E., Madder, H., Moir, I., Moroney, R., Quan, T. P., Griffiths, D., George, S., Butcher, L., Morgan, M., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1714373 · Cited by 517 · see citing works

Genomic insights into multidrug-resistance, mating and virulence in Candida auris and related emerging species

Muñoz, J. F., Gade, L., Chow, N. A., Loparev, V. N., Juieng, P., Berkow, E. L., Farrer, R. A., Litvintseva, A. P., & Cuomo, C. A. (2018) · Nature Communications · doi:10.1038/s41467-018-07779-6 · Cited by 458 · see citing works

First report of Candida auris in America: Clinical and microbiological aspects of 18 episodes of candidemia

Calvo, B., Melo, A. S. D. A., Mena, A. J. P., Hernandez, M., Francisco, E. C., Hagen, F., Meis, J. F. G. M., & Colombo, A. L. (2016) · Journal of Infection · doi:10.1016/j.jinf.2016.07.008 · Cited by 450 · see citing works

Candida auris candidaemia in Indian ICUs: analysis of risk factors

Rudramurthy, S. M., Chakrabarti, A., Paul, R. A., Sood, P., Kaur, H., Capoor, M. R., Kindo, A. J., Marak, R. S. K., Arora, A., Sardana, R., et al. (2017) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkx034 · Cited by 357 · see citing works

Multidrug-Resistant Candida auris Infections in Critically Ill Coronavirus Disease Patients, India, April–July 2020

Chowdhary, A., Tarai, B., Singh, A. K., & Sharma, A. (2020) · Emerging infectious diseases · doi:10.3201/eid2611.203504 · Cited by 328 · see citing works

Global epidemiology of emerging Candida auris

Rhodes, J., & Fisher, M. C. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.05.008 · Cited by 315 · see citing works

Investigation of the First Seven Reported Cases of <i>Candida auris,</i> a Globally Emerging Invasive, Multidrug-Resistant Fungus — United States, May 2013–August 2016

Vallabhaneni, S., Kallen, A., Tsay, S., Chow, N., Welsh, R., Kerins, J., Kemble, S. K., Pacilli, M., Black, S. R., Landon, E., et al. (2016) · MMWR. Morbidity and Mortality Weekly Report · doi:10.15585/mmwr.mm6544e1 · Cited by 302 · see citing works

Multiple introductions and subsequent transmission of multidrug-resistant Candida auris in the USA: a molecular epidemiological survey.

Chow, N. A., Gade, L., Tsay, S. V., Forsberg, K., Greenko, J. A., Southwick, K. L., Barrett, P. M., Kerins, J. L., Lockhart, S. R., Chiller, T. M., et al. (2018) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(18)30597-8 · Cited by 289 · see citing works

<i>Candida auris</i> in Healthcare Facilities, New York, USA, 2013–2017

Adams, E., Quinn, M., Tsay, S., Poirot, E., Chaturvedi, S., Southwick, K., Greenko, J., Fernandez, R., Kallen, A., Vallabhaneni, S., et al. (2018) · Emerging Infectious Diseases · doi:10.3201/eid2410.180649 · Cited by 284 · see citing works

Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris

Chatterjee, S., Alampalli, S. V., Nageshan, R. K., Chettiar, S. T., Joshi, S., & Tatu, U. S. (2015) · BMC Genomics · doi:10.1186/s12864-015-1863-z · Cited by 247 · see citing works

Understanding Echinocandin Resistance in the Emerging Pathogen Candida auris

Kordalewska, M., Lee, A., Park, S., Berrio, I., Chowdhary, A., Zhao, Y., & Perlin, D. S. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00238-18 · Cited by 247 · see citing works

Candida auris Isolates Resistant to Three Classes of Antifungal Medications — New York, 2019

Ostrowsky, B. E., Greenko, J. A., Adams, E. H., Quinn, M., O’Brien, B., Chaturvedi, V. P., Berkow, E. L., Vallabhaneni, S., Forsberg, K., Chaturvedi, S., et al. (2020) · MMWR Morbidity and Mortality Weekly Report · doi:10.15585/mmwr.mm6901a2 · Cited by 247 · see citing works

Comparison of Etest, chequerboard dilution and time-kill studies for the detection of synergy or antagonism between antifungal agents tested against Candida species

Lewis, R. E. (2002) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/49.2.345 · Cited by 226 · see citing works

Molecular Epidemiology of <i>Candida auris</i> in Colombia Reveals a Highly Related, Countrywide Colonization With Regional Patterns in Amphotericin B Resistance

Escandón, P., Chow, N. A., Caceres, D. H., Gade, L., Berkow, E. L., Armstrong, P., Rivera, S., Misas, E., Duarte, C., Moulton-Meissner, H., et al. (2019) · Clinical Infectious Diseases · doi:10.1093/cid/ciy411 · Cited by 222 · see citing works

<i>In Vitro</i> Activity of E1210, a Novel Antifungal, against Clinically Important Yeasts and Molds

Miyazaki, M., Horii, T., Hata, K., Watanabe, N.-A., Nakamoto, K., Tanaka, K., Shirotori, S., Murai, N., Inoue, S., Matsukura, M., et al. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00291-11 · Cited by 200 · see citing works

Integrated genomic, epidemiologic investigation of Candida auris skin colonization in a skilled nursing facility

Proctor, D. M., Dangana, T., Sexton, D. J., Fukuda, C., Yelin, R. D., Stanley, M., Bell, P. B., Baskaran, S., Deming, C., Chen, Q., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01383-w · Cited by 198 · see citing works

Development and Validation of a Real-Time PCR Assay for Rapid Detection of Candida auris from Surveillance Samples

Leach, L., Zhu, Y., & Chaturvedi, S. (2017) · Journal of Clinical Microbiology · doi:10.1128/jcm.01223-17 · Cited by 170 · see citing works

Laboratory Analysis of an Outbreak of Candida auris in New York from 2016 to 2018: Impact and Lessons Learned

Zhu, Y., O’Brien, B., Leach, L., Clark, A., Bates, M., Adams, E. H., Ostrowsky, B. E., Quinn, M., Dufort, E. M., Southwick, K. L., et al. (2019) · Journal of Clinical Microbiology · doi:10.1128/jcm.01503-19 · Cited by 166 · see citing works

On the Origins of a Species: What Might Explain the Rise of Candida auris?

Jackson, B. R., Chow, N. A., Forsberg, K., Litvintseva, A. P., Lockhart, S. R., Welsh, R. M., Vallabhaneni, S., & Chiller, T. M. (2019) · Journal of Fungi · doi:10.3390/jof5030058 · Cited by 165 · see citing works

Molecular Mechanisms of Primary Resistance to Flucytosine in <i>Candida albicans</i>

Hope, W. W., Tabernero, L., Denning, D. W., & Anderson, M. J. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.11.4377-4386.2004 · Cited by 160 · see citing works

Epidemiologic Shift in Candidemia Driven by <i>Candida auris</i>, South Africa, 2016–20171

van Schalkwyk, E., Mpembe, R. S., Thomas, J., Shuping, L., Ismail, H., Lowman, W., Karstaedt, A. S., Chibabhai, V., Wadula, J., Avenant, T., et al. (2019) · Emerging Infectious Diseases · doi:10.3201/eid2509.190040 · Cited by 137 · see citing works

Factors Associated With <i>Candida auris</i> Colonization and Transmission in Skilled Nursing Facilities With Ventilator Units, New York, 2016–2018

Rossow, J., Ostrowsky, B., Adams, E., Greenko, J., McDonald, R., Vallabhaneni, S., Forsberg, K., Perez, S., Lucas, T., Alroy, K. A., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciaa1462 · Cited by 125 · see citing works

In vivo emergence of high-level resistance during treatment reveals the first identified mechanism of amphotericin B resistance in Candida auris

Rybak, J. M., Barker, K. S., Muñoz, J. F., Parker, J. E., Ahmad, S., Mokaddas, E., Abdullah, A., Elhagracy, R. S., Kelly, S. L., Cuomo, C. A., et al. (2022) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2021.11.024 · Cited by 120 · see citing works

Facultative Sterol Uptake in an Ergosterol-Deficient Clinical Isolate of Candida glabrata Harboring a Missense Mutation in <i>ERG11</i> and Exhibiting Cross-Resistance to Azoles and Amphotericin B

Hull, C. M., Parker, J. E., Bader, O., Weig, M., Gross, U., Warrilow, A. G. S., Kelly, D. E., & Kelly, S. L. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.06253-11 · Cited by 113 · see citing works

<i>Notes from the Field:</i> Transmission of Pan-Resistant and Echinocandin-Resistant <i>Candida auris</i> in Health Care Facilities ― Texas and the District of Columbia, January–April 2021

Lyman, M., Forsberg, K., Reuben, J., Dang, T., Free, R., Seagle, E. E., Sexton, D. J., Soda, E., Jones, H., Hawkins, D., et al. (2021) · MMWR. Morbidity and Mortality Weekly Report · doi:10.15585/mmwr.mm7029a2 · Cited by 104 · see citing works

In Vitro Activity of a Novel Glucan Synthase Inhibitor, SCY-078, against Clinical Isolates of Candida auris

Berkow, E. L., Angulo, D. A., & Lockhart, S. R. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00435-17 · Cited by 103 · see citing works

Hospital-Associated Multicenter Outbreak of Emerging Fungus Candida auris, Colombia, 2016

Armstrong, P. A., Rivera, S. M., Escandón, P., Caceres, D. H., Chow, N. A., Stuckey, M. J., Díaz, J., Gomez, A., Vélez, N., Espinosa-Bode, A., et al. (2019) · Emerging infectious diseases · doi:10.3201/eid2507.180491 · Cited by 93 · see citing works

Ibrexafungerp: A Novel Oral Triterpenoid Antifungal in Development for the Treatment of Candida auris Infections

Ghannoum, M. A., Arendrup, M. C., Chaturvedi, V. P., Lockhart, S. R., McCormick, T. S., Chaturvedi, S., Berkow, E. L., Juneja, D., Tarai, B., Azie, N. E., et al. (2020) · Antibiotics · doi:10.3390/antibiotics9090539 · Cited by 92 · see citing works

Candidemia caused by amphotericin B and Fluconazole resistant Candida auris

Sarma, S., Kumar, N., Sharma, S., Govil, D., Ali, T., Mehta, Y. B., & Rattan, A. (2013) · Indian Journal of Medical Microbiology · doi:10.4103/0255-0857.108746 · Cited by 91 · see citing works

Donor-Derived Transmission of Candida auris During Lung Transplantation

Azar, M. M., Turbett, S. E., Fishman, J. A., & Pierce, V. (2017) · Clinical Infectious Diseases · doi:10.1093/cid/cix460 · Cited by 89 · see citing works

SCY-078 is fungicidal against Candida species in time-kill studies

Scorneaux, B., Angulo, D., Borroto-Esoda, K., Ghannoum, M., Peel, M., & Wring, S. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01961-16 · Cited by 88 · see citing works

Molecular Mechanism of Flucytosine Resistance in Candida lusitaniae : Contribution of the FCY2 , FCY1 , and FUR1 Genes to 5-Fluorouracil and Fluconazole Cross-Resistance

Papon, N., Noël, T., Florent, M., Gibot‐Leclerc, S., Jean, D., Chastin, C., Villard, J.-F., & Chapeland‐Leclerc, F. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00824-06 · Cited by 86 · see citing works

Mutational Analysis of Flucytosine Resistance in Candida glabrata

Edlind, T. D., & Katiyar, S. K. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00605-10 · Cited by 84 · see citing works

<i>In Vitro</i> Antifungal Resistance of Candida auris Isolates from Bloodstream Infections, South Africa

Maphanga, T. G., Naicker, S. D., Kwenda, S., Muñoz, J. F., van Schalkwyk, E., Wadula, J., Nana, T., Ismail, A., Coetzee, J., Govind, C., et al. (2021) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00517-21 · Cited by 78 · see citing works

Antifungal Resistance Trends of Candida auris Clinical Isolates in New York and New Jersey from 2016 to 2020

Kilburn, S., Innes, G. K., Quinn, M., Southwick, K. L., Ostrowsky, B. E., Greenko, J. A., Lutterloh, E. C., Greeley, R. D., Magleby, R., Chaturvedi, V. P., et al. (2022) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02242-21 · Cited by 67 · see citing works

In Vitro Antifungal Combination of Flucytosine with Amphotericin B, Voriconazole, or Micafungin against Candida auris Shows No Antagonism

Bidaud, A.-L., Botterel, F., Chowdhary, A., & Dannaoui, É. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01393-19 · Cited by 64 · see citing works

Retrospective analysis of the clinical characteristics of Candida auris infection worldwide from 2009 to 2020

Hu, S., Zhu, F., Jiang, W., Wang, Y., Quan, Y., Zhang, G., Gu, F., & Yang, Y. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.658329 · Cited by 64 · see citing works

In Vitro Evaluation of Antifungal Drug Combinations against Multidrug-Resistant Candida auris Isolates from New York Outbreak

O’Brien, B., Chaturvedi, S., & Chaturvedi, V. P. (2020) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02195-19 · Cited by 63 · see citing works

Pan-resistant Candida auris: New York subcluster susceptible to antifungal combinations

O'Brien, B., Liang, J., Chaturvedi, S., Jacobs, J. L., & Chaturvedi, V. (2020) · The Lancet Microbe · doi:10.1016/s2666-5247(20)30090-2 · Cited by 60 · see citing works

So Many Diagnostic Tests, So Little Time: Review and Preview of Candida auris Testing in Clinical and Public Health Laboratories

Dennis, E. K., Chaturvedi, S., & Chaturvedi, V. P. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.757835 · Cited by 51 · see citing works

Nonsense and Missense Mutations in FCY2 and FCY1 Genes Are Responsible for Flucytosine Resistance and Flucytosine-Fluconazole Cross-Resistance in Clinical Isolates of Candida lusitaniae

Florent, M., Noël, T., Ruprich‐Robert, G., Silva, B. D., Fitton‐Ouhabi, V., Chastin, C., Papon, N., & Chapeland‐Leclerc, F. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00880-08 · Cited by 50 · see citing works

Multilaboratory Testing of Two-Drug Combinations of Antifungals againstCandida albicans,Candida glabrata, andCandida parapsilosis

Chaturvedi, V. P., Ramani, R., Andes, D. R., Diekema, D. J., Pfaller, M. A., Ghannoum, M. A., Knapp, C. C., Lockhart, S. R., Ostrosky‐Zeichner, L., Walsh, T. J., et al. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01510-09 · Cited by 46 · see citing works

MARDy: Mycology Antifungal Resistance Database

Nash, A., Sewell, T. R., Farrer, R. A., Abdolrasouli, A., Shelton, J., Fisher, M. C., & Rhodes, J. L. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty321 · Cited by 45 · see citing works

Candida auris outbreak involving liver transplant recipients in a surgical intensive care unit

Theodoropoulos, N. M., Bolstorff, B., Bozorgzadeh, A., Brandeburg, C., Cumming, M., Daly, J. S., Ellison, R. T., Forsberg, K., Gade, L., Gibson, L. L., et al. (2020) · American Journal of Transplantation · doi:10.1111/ajt.16144 · Cited by 41 · see citing works

Trichoderma polysporum selectively inhibits white-nose syndrome fungal pathogen Pseudogymnoascus destructans amidst soil microbes

Singh, A., Lasek‐Nesselquist, E., Chaturvedi, V. P., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0512-6 · Cited by 37 · see citing works

Pan-resistant Candida auris isolates from the outbreak in New York are susceptible to ibrexafungerp (a glucan synthase inhibitor)

Zhu, Y. C., Barat, S., Borroto–Esoda, K., Angulo, D., Chaturvedi, S., & Chaturvedi, V. P. (2020) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2020.105922 · Cited by 36 · see citing works

Flucytosine-Fluconazole Cross-Resistance in Purine-Cytosine Permease-Deficient Candida lusitaniae Clinical Isolates: Indirect Evidence of a Fluconazole Uptake Transporter

Noël, T., François, F., Paumard, P., Chastin, C., Brèthes, D., & Villard, J.-F. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.4.1275-1284.2003 · Cited by 34 · see citing works

Expression profiling of the response of Saccharomyces cerevisiae to 5-fluorocytosine using a DNA microarray

Zhang, L., Zhang, Y., Zhou, Y., Zhao, Y., Zhou, Y., & Cheng, J. (2002) · International Journal of Antimicrobial Agents · doi:10.1016/s0924-8579(02)00201-7 · Cited by 27 · see citing works

Case–Case Comparison of Candida auris Versus Other Candida Species Bloodstream Infections: Results of an Outbreak Investigation in Colombia

Caceres, D. H., Rivera, S. M., Armstrong, P. A., Escandón, P., Chow, N. A., Ovalle, M. V., Díaz, J., Derado, G., Salcedo, S., Berrío, I., et al. (2020) · Mycopathologia · doi:10.1007/s11046-020-00478-1 · Cited by 27 · see citing works

Acquired flucytosine resistance during combination therapy with caspofungin and flucytosine for Candida glabrata cystitis

Charlier, C., El Sissy, C., Bachelier-Bassi, S., Scemla, A., Quesne, G., Sitterlé, E., Legendre, C., Lortholary, O., & Bougnoux, M.-E. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02265-15 · Cited by 26 · see citing works

Reverse Transcription-Quantitative Real-Time PCR (RT-qPCR) Assay for the Rapid Enumeration of Live Candida auris Cells from the Health Care Environment

Freitas, B. L., Leach, L., Chaturvedi, V., & Chaturvedi, S. (2021) · Journal of Clinical Microbiology · doi:10.1128/jcm.00779-21 · Cited by 22 · see citing works

Detection of Candida auris Antifungal Drug Resistance Markers Directly from Clinical Skin Swabs

Kordalewska, M., Lee, A., Zhao, Y., & Perlin, D. S. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01754-19 · Cited by 19 · see citing works

In vitro Etest synergy of doripenem with amikacin, colistin, and levofloxacin against Pseudomonas aeruginosa with defined carbapenem resistance mechanisms as determined by the Etest method

He, W. W., Kaniga, K., Lynch, A. S., et al. (2012) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2012.08.014 · Cited by 18 · see citing works

Sentinel Case of Candida auris in the Western United States Following Prolonged Occult Colonization in a Returned Traveler from India

Woodworth, M. H., Dynerman, D., Crawford, E. D., Doernberg, S. B., Ramírez-Àvila, L., Serpa, P. H., Nichols, A. D., Li, L. M., Lyden, A., Tato, C. M., et al. (2019) · Microbial Drug Resistance · doi:10.1089/mdr.2018.0408 · Cited by 17 · see citing works

Multilaboratory Testing of Antifungal Drug Combinations against Candida Species and Aspergillus fumigatus: Utility of 100 Percent Inhibition as the Endpoint

Ren, P., Luo, M., Lin, S., Ghannoum, M. A., Isham, N. C., Diekema, D. J., Pfaller, M. A., Messer, S. A., Lockhart, S. R., Iqbal, N. J., et al. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.04545-14 · Cited by 7 · see citing works

Increasing number of cases and outbreaks caused by Candida auris in the EU/EEA, 2020 to 2021

Kohlenberg, A., Monnet, D. L., Plachouras, D., & Candida auris survey collaborative group (2022) · Eurosurveillance · doi:10.2807/1560-7917.es.2022.27.46.2200846 · Cited by 108 · see citing works

Ergosterol Biosynthesis and Regulation Impact the Antifungal Resistance and Virulence of Candida spp

Eliaš, D., Tóth Hervay, N., & Gbelská, Y. (2024) · Stresses · doi:10.3390/stresses4040041 · Cited by 63 · see citing works

Native human and mouse skin infection models to study Candida auris-host interactions

Seiser, S., Arzani, H., Ayub, T., Phan-Canh, T., Staud, C., Worda, C., Kuchler, K., & Elbe-Bürger, A. (2024) · Microbes and Infection · doi:10.1016/j.micinf.2023.105234 · Cited by 29 · see citing works

Lansoprazole interferes with fungal respiration and acts synergistically with amphotericin B against multidrug-resistant <i>Candida auris</i>

Salama, E. A., Elgammal, Y., Wijeratne, A., Lanman, N. A., Utturkar, S. M., Farhangian, A., Li, J., Meunier, B., Hazbun, T. R., & Seleem, M. N. (2024) · Emerging Microbes &amp; Infections · doi:10.1080/22221751.2024.2322649 · Cited by 16 · see citing works

Insight into the Mechanisms and Clinical Relevance of Antifungal Heteroresistance

Su, Y., Li, Y., Yi, Q., Xu, Y., Sun, T., & Li, Y. (2025) · Journal of Fungi · doi:10.3390/jof11020143 · Cited by 18 · see citing works

Exploring synergy between azole antifungal drugs and statins for <i>Candida auris</i>

Halliday, C., Kim, H. Y., Tay, E., Chen, S. C. A., & Alffenaar, J.-W. (2023) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkad303 · Cited by 14 · see citing works

Tn-seq screens in <i>Candida glabrata</i> treated with echinocandins and ibrexafungerp reveal pathways of antifungal resistance and cross-resistance

Nickels, T. J., & Cunningham, K. W. (2025) · mSphere · doi:10.1128/msphere.00270-25 · Cited by 8 · see citing works

Rapid Detection of <i>ERG11</i> -Associated Azole Resistance and <i>FKS</i> -Associated Echinocandin Resistance in Candida auris

Hou, X., Lee, A., Jiménez-Ortigosa, C., Kordalewska, M., Perlin, D. S., & Zhao, Y. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01811-18 · Cited by 66 · see citing works

Development and Validation of TaqMan Chemistry Probe-Based Rapid Assay for the Detection of Echinocandin-Resistance in Candida auris

Zhu, Y., Hager, K. M., Manjari, S. R., Banavali, N. K., Chaturvedi, V. P., & Chaturvedi, S. (2023) · Journal of Clinical Microbiology · doi:10.1128/jcm.01767-22 · Cited by 15 · see citing works

Activity of CD101, a long-acting echinocandin, against clinical isolates of Candida auris

Berkow, E. L., & Lockhart, S. R. (2018) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2017.10.021 · Cited by 110 · see citing works

Echinocandins as Biotechnological Tools for Treating Candida auris Infections

Cândido, E. D. S., Affonseca, F., Cardoso, M. H. E. S., & Franco, O. L. (2020) · Journal of Fungi · doi:10.3390/jof6030185 · Cited by 22 · see citing works

Echinocandin Resistance in Candida auris Occurs in the Murine Gastrointestinal Tract Due to FKS1 Mutations

Hirayama, T., Miyazaki, T., Sumiyoshi, M., Yuya, I. T. O., Ashizawa, N., Takeda, K., Iwanaga, N., Takazono, T., Yamamoto, K., Izumikawa, K., et al. (2023) · Institutional Repositories DataBase (IRDB) · doi:10.1128/aac.01243-22