Psychogenetic, genetic and epigenetic mechanisms in Candida auris: Role in drug resistance

Bacterial biofilms: from the Natural environment to infectious diseases

Hall‐Stoodley, L., Costerton, J. W., & Stoodley, P. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro821 · Cited by 7,133 · see citing works

Regulation of chromatin by histone modifications

Bannister, A. J., & Kouzarides, T. (2011) · Cell Research · doi:10.1038/cr.2011.22 · Cited by 6,012 · see citing works

The single-cell transcriptional landscape of mammalian organogenesis

Cao, J., Spielmann, M., Qiu, X., Huang, X., Ibrahim, D. M., Hill, A. J., Zhang, F., Mundlos, S., Christiansen, L., Steemers, F. J., et al. (2019) · Nature · doi:10.1038/s41586-019-0969-x · Cited by 4,490 · see citing works

The molecular hallmarks of epigenetic control

Allis, C. D., & Jenuwein, T. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.59 · Cited by 2,809 · 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

Mechanisms of action and regulation of ATP-dependent chromatin-remodelling complexes

Clapier, C. R., Iwasa, J., Cairns, B. R., & Peterson, C. L. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.26 · Cited by 1,305 · see citing works

Evolution of pathogenicity and sexual reproduction in eight Candida genomes

Butler, G., Rasmussen, M. D., Lin, M. F., Santos, M. A. S., Sakthikumar, S., Munro, C. A., Rheinbay, E., Grabherr, M., Forche, A., Reedy, J. L., et al. (2009) · Nature · doi:10.1038/nature08064 · Cited by 1,065 · see citing works

Candida auris: a Review of the Literature

Jeffery-Smith, A., Taori, S. K., Schelenz, S., Jeffery, K. J., Johnson, E. M., Borman, A. M., Candida auris Incident Management Team, Manuel, R. J., & Brown, C. S. (2017) · Clinical Microbiology Reviews · doi:10.1128/cmr.00029-17 · Cited by 610 · see citing works

Candida auris: Epidemiology, biology, antifungal resistance, and virulence

Du, H., Bing, J., Hu, T., Ennis, C. L., Nobile, C. J., & Huang, G. (2020) · PLOS Pathogens · doi:10.1371/journal.ppat.1008921 · Cited by 609 · see citing works

Chromatin remodelling: the industrial revolution of DNA around histones

Saha, A., Wittmeyer, J., & Cairns, B. R. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1945 · Cited by 590 · 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

The role of the surface environment in healthcare-associated infections

Weber, D. J., Anderson, D. J., & Rutala, W. A. (2013) · Current Opinion in Infectious Diseases · doi:10.1097/qco.0b013e3283630f04 · Cited by 568 · see citing works

First Three Reported Cases of Nosocomial Fungemia Caused by Candida auris

Lee, W. G., Shin, J. H., Uh, Y., Kang, M. G., Kim, S. H., Park, K. H., & Jang, H. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.00319-11 · Cited by 524 · see citing works

On the emergence of Candida auris: climate change, azoles, swamps, and birds

Casadevall, A., Kontoyiannis, D. P., & Robert, V. (2019) · mBio · doi:10.1128/mbio.01397-19 · Cited by 515 · see citing works

Survival, persistence, and isolation of the emerging multidrug-resistant pathogenic yeast Candida auris on a plastic health care surface.

Welsh, R. M., Bentz, M. L., Shams, A., Houston, H., Lyons, A., Rose, L. J., & Litvintseva, A. P. (2017) · Journal of Clinical Microbiology · doi:10.1128/jcm.00921-17 · Cited by 499 · see citing works

Tracing the evolutionary history and global expansion of <i>Candida auris</i> using population genomic analyses

Chow, N. A., Muñoz, J. F., Gade, L., Berkow, E., Li, X., Welsh, R. M., Forsberg, K., Lockhart, S. R., Adam, R., Alanio, A., et al. (2020) · doi:10.1101/2020.01.06.896548 · Cited by 463 · 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

Incidence, characteristics and outcome of ICU-acquired candidemia in India

Chakrabarti, A., Sood, P., Rudramurthy, S. M., Chen, S., Kaur, H., Capoor, M., Chhina, D., Rao, R., Eshwara, V. K., Xess, I., et al. (2015) · Intensive Care Medicine · doi:10.1007/s00134-014-3603-2 · Cited by 454 · 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

<i>Candida auris</i> : The recent emergence of a multidrug-resistant fungal pathogen

Forsberg, K., Woodworth, K., Walters, M., Berkow, E. L., Jackson, B., Chiller, T., & Vallabhaneni, S. (2019) · Medical Mycology · doi:10.1093/mmy/myy054 · Cited by 421 · see citing works

Biofilm-Forming Capability of Highly Virulent, Multidrug-Resistant <i>Candida auris</i>

Sherry, L., Ramage, G., Kean, R., Borman, A., Johnson, E. M., Richardson, M. D., & Rautemaa-Richardson, R. (2017) · Emerging Infectious Diseases · doi:10.3201/eid2302.161320 · Cited by 420 · see citing works

New Clonal Strain ofCandida auris, Delhi, India

Chowdhary, A., Sharma, C., Duggal, S., Agarwal, K., Prakash, A., Singh, P. K., Jain, S., Kathuria, S., Randhawa, H. S., Hagen, F., et al. (2013) · Emerging infectious diseases · doi:10.3201/eid1910.130393 · Cited by 418 · see citing works

The emerging pathogen Candida auris: growth phenotype, virulence factors, activity of antifungals, and effect of SCY-078, a novel glucan synthesis inhibitor, on growth morphology and biofilm formation

Larkin, E., Hager, C., Chandra, J., Mukherjee, P. K., Retuerto, M., Salem, I., Long, L., Isham, N., Kovanda, L., Borroto-Esoda, K., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02396-16 · Cited by 395 · see citing works

Introns: The Functional Benefits of Introns in Genomes

Jo, B.-S., & Choi, S. S. (2015) · Genomics & Informatics · doi:10.5808/gi.2015.13.4.112 · Cited by 357 · 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

Candida Infections and Therapeutic Strategies: Mechanisms of Action for Traditional and Alternative Agents

Santos, G. C. D. O., Vasconcelos, C. C., Lopes, A. J. O., Cartágenes, M. D. S. D. S., Filho, A. K. D. B., do Nascimento, F. R. F., Ramos, R. M., Pires, E. R. R. B., de Andrade, M. S., Rocha, F. M. G., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01351 · Cited by 357 · see citing works

Antisense RNA Stabilization Induces Transcriptional Gene Silencing via Histone Deacetylation in S. cerevisiae

Camblong, J., Iglesias, N., Fickentscher, C., Dieppois, G., & Stutz, F. (2007) · Cell · doi:10.1016/j.cell.2007.09.014 · Cited by 354 · see citing works

An outbreak due to <i>Candida auris</i> with prolonged colonisation and candidaemia in a tertiary care European hospital

Ruiz‐Gaitán, A., Moret, A. M., Tasias‐Pitarch, M., Aleixandre‐López, A. I., Martínez‐Morel, H., Calabuig, E., Salavert‐Lletí, M., Ramírez, P., López‐Hontangas, J. L., Hagen, F., et al. (2018) · Mycoses · doi:10.1111/myc.12781 · Cited by 343 · see citing works

Comparative Pathogenicity of United Kingdom Isolates of the Emerging Pathogen <i>Candida auris</i> and Other Key Pathogenic <i>Candida</i> Species

Borman, A. M., Szekely, A., & Johnson, E. M. (2016) · mSphere · doi:10.1128/msphere.00189-16 · Cited by 333 · see citing works

An isochromosome confers drug resistance <i>in vivo</i> by amplification of two genes, <i>ERG11</i> and <i>TAC1</i>

Selmecki, A., Gerami‐Nejad, M., Paulson, C., Forche, A., & Berman, J. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06176.x · Cited by 325 · 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

Candida auris : A systematic review and meta‐analysis of current updates on an emerging multidrug‐resistant pathogen

Sekyere, J. O. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.578 · Cited by 307 · see citing works

A ncRNA Modulates Histone Modification and mRNA Induction in the Yeast GAL Gene Cluster

Houseley, J. M., Rubbi, L., Grunstein, M. R., Tollervey, D. W., & Vogelauer, M. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.09.027 · Cited by 293 · see citing works

RNAi and Heterochromatin AssemblyPreprint

Martienssen, R. A., & Moazed, D. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a019323 · Cited by 281 · see citing works

The CUG codon is decodedin vivoas serine and not leucine inCandida albicans

Santos, M. A. S., & Tuite, M. F. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.9.1481 · Cited by 279 · 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

Investigation of the First Seven Reported Cases of Candida auris, 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. (2017) · American Journal of Transplantation · doi:10.1111/ajt.14121 · 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

Genomic epidemiology of the UK outbreak of the emerging human fungal pathogen <i>Candida auris</i>

Rhodes, J., Abdolrasouli, A., Farrer, R. A., Cuomo, C. A., Aanensen, D. M., Armstrong-James, D., Fisher, M. C., & Schelenz, S. (2018) · Emerging Microbes &amp; Infections · doi:10.1038/s41426-018-0045-x · Cited by 246 · see citing works

Controlling a possible outbreak of Candida auris infection: lessons learnt from multiple interventions

Biswal, M., Rudramurthy, S. M., Jain, N., Shankarnarayan, S. A., Sharma, D., Jain, K., Yaddanapudi, L. N., & Chakrabarti, A. (2017) · Journal of Hospital Infection · doi:10.1016/j.jhin.2017.09.009 · Cited by 224 · see citing works

Review on Antifungal Resistance Mechanisms in the Emerging Pathogen Candida auris

Chaabane, F., Graf, A., Jequier, L., & Coste, A. T. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02788 · Cited by 223 · 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

Transcriptome Assembly and Profiling of <i>Candida auris</i> Reveals Novel Insights into Biofilm-Mediated Resistance

Kean, R., Delaney, C., Sherry, L., Borman, A., Johnson, E. M., Richardson, M. D., Rautemaa-Richardson, R., Williams, C., & Ramage, G. (2018) · mSphere · doi:10.1128/msphere.00334-18 · Cited by 220 · see citing works

Multidrug-resistant Candida auris: ‘New kid on the block’ in hospital-associated infections?

Chowdhary, A., Voss, A., & Meis, J. F. (2016) · Journal of Hospital Infection · doi:10.1016/j.jhin.2016.08.004 · Cited by 214 · see citing works

Candida auris—the growing menace to global health

Lone, S. A., & Ahmad, A. (2019) · Mycoses · doi:10.1111/myc.12904 · Cited by 210 · see citing works

Candida auris and multidrug resistance: Defining the new normal

Lockhart, S. R. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103243 · Cited by 205 · see citing works

Whole genome sequencing of emerging multidrug resistant Candida auris isolates in India demonstrates low genetic variation

Sharma, C., Kumar, N., Pandey, R., Meis, J. F., & Chowdhary, A. (2016) · New Microbes and New Infections · doi:10.1016/j.nmni.2016.07.003 · Cited by 202 · see citing works

Community participation in biofilm matrix assembly and function

Mitchell, K. F., Zarnowski, R., Sanchez, H., Edward, J. A., Reinicke, E. L., Nett, J. E., Mitchell, A. P., & Andes, D. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421437112 · Cited by 183 · see citing works

Filamentation in <i>Candida auris</i> , an emerging fungal pathogen of humans: passage through the mammalian body induces a heritable phenotypic switch

Yue, H., Bing, J., Zheng, Q., Zhang, Y., Hu, T., Du, H., Wang, H., & Huang, G. (2018) · Emerging Microbes &amp; Infections · doi:10.1038/s41426-018-0187-x · Cited by 176 · see citing works

Limited <i>ERG11</i> Mutations Identified in Isolates of Candida auris Directly Contribute to Reduced Azole Susceptibility

Healey, K. R., Kordalewska, M., Jiménez Ortigosa, C., Singh, A., Berrío, I., Chowdhary, A., & Perlin, D. S. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01427-18 · Cited by 165 · 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

Epigenetic regulation: A new frontier for biomedical engineers

Chen, Z., Li, S., Subramaniam, S., Shyy, J. Y.-J., & Chien, S. (2017) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071516-044720 · Cited by 163 · see citing works

The Key Role of DNA Methylation and Histone Acetylation in Epigenetics of Atherosclerosis

Lee, H., Oh, S., Ro, D. H., Yoo, H., & Kwon, Y. (2020) · Journal of Lipid and Atherosclerosis · doi:10.12997/jla.2020.9.3.419 · Cited by 158 · see citing works

The Quiet and Underappreciated Rise of Drug-Resistant Invasive Fungal Pathogens

Arastehfar, A., Lass-Flörl, C., Garcia-Rubio, R., Daneshnia, F., Ilkit, M., Boekhout, T., Gabaldon, T., & Perlin, D. S. (2020) · Journal of Fungi · doi:10.3390/jof6030138 · Cited by 145 · see citing works

Biofilm formation and genotyping ofCandida haemulonii, Candida pseudohaemulonii, and a proposed new species (Candida auris) isolates from Korea

Oh, B. J., Shin, J. H., Kim, M., Sung, H., Lee, K., Joo, M. Y., Shin, M., Suh, S., & Ryang, D. W. (2010) · Medical Mycology · doi:10.3109/13693786.2010.493563 · Cited by 143 · see citing works

Abrogation of Triazole Resistance upon Deletion of <i>CDR1</i> in a Clinical Isolate of <i>Candida auris</i>

Rybak, J. M., Doorley, L. A., Nishimoto, A. T., Barker, K. S., Palmer, G. E., & Rogers, P. D. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00057-19 · Cited by 141 · see citing works

Candida auris Clinical Isolates from South Korea: Identification, Antifungal Susceptibility, and Genotyping

Kwon, Y. J., Shin, J. H., Byun, S. A., Choi, M. J., Won, E. J., Lee, D., Lee, S. Y., Chun, S., Lee, J. H., Choi, H., et al. (2019) · Journal of Clinical Microbiology · doi:10.1128/jcm.01624-18 · Cited by 136 · see citing works

Isolates of the emerging pathogen Candida auris present in the UK have several geographic origins

Borman, A. M., Székely, A., & Johnson, E. M. (2016) · Medical Mycology · doi:10.1093/mmy/myw147 · Cited by 133 · see citing works

Candida Auris, An Agent of Hospital-Associated Outbreaks: Which Challenging Issues Do We Need to Have in Mind?

Sabino, R., Veríssimo, C., Pereira, Á. A., & Antunes, F. (2020) · Microorganisms · doi:10.3390/microorganisms8020181 · Cited by 133 · see citing works

Surface disinfection challenges for Candida auris: an in-vitro study

Kean, R., Sherry, L., Townsend, E. R., McKloud, E., Short, B., Akinbobola, A., Mackay, W. G., Williams, C., Jones, B., & Ramage, G. (2017) · Journal of Hospital Infection · doi:10.1016/j.jhin.2017.11.015 · Cited by 125 · see citing works

Comparative virulence of Candida auris with Candida haemulonii, Candida glabrata and Candida albicans in a murine model

Fakhim, H., Vaezi, A., Dannaoui, É., Chowdhary, A., Nasiry, D., Faeli, L., Meis, J. F. G. M., & Badali, H. (2018) · Mycoses · doi:10.1111/myc.12754 · Cited by 123 · see citing works

Ploidy Variation in Fungi: Polyploidy, Aneuploidy, and Genome Evolution

Todd, R. T., Forche, A., & Selmecki, A. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0051-2016 · Cited by 121 · see citing works

Hog1 regulates stress tolerance and virulence in the emerging fungal pathogen Candida auris

Day, A. M., McNiff, M. M., da Silva Dantas, A., Gow, N. A. R., & Quinn, J. (2018) · mSphere · doi:10.1128/msphere.00506-18 · Cited by 116 · see citing works

Candida auris: A Review of Recommendations for Detection and Control in Healthcare Settings

Caceres, D. H., Forsberg, K., Welsh, R. M., Sexton, D. J., Lockhart, S. R., Jackson, B. R., & Chiller, T. M. (2019) · Journal of Fungi · doi:10.3390/jof5040111 · Cited by 110 · see citing works

Gene Duplication Associated with Increased Fluconazole Tolerance in Candida auris cells of Advanced Generational Age

Bhattacharya, S., Holowka, T., Orner, E. P., & Fries, B. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-41513-6 · Cited by 104 · see citing works

Control of Candida auris in healthcare institutions: Outcome of an International Society for Antimicrobial Chemotherapy expert meeting

Kenters, N., Kiernan, M., Chowdhary, A., Denning, D. W., Pemán, J., Saris, K., Schelenz, S., Tartari, E., Widmer, A., Meis, J. F., et al. (2019) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2019.08.013 · Cited by 102 · see citing works

Multi-omics Signature of <i>Candida auris</i> , an Emerging and Multidrug-Resistant Pathogen

Zamith-Miranda, D., Heyman, H. M., Cleare, L. G., Couvillion, S. P., Clair, G. C., Bredeweg, E. L., Gacser, A., Nimrichter, L., Nakayasu, E. S., & Nosanchuk, J. D. (2019) · mSystems · doi:10.1128/msystems.00257-19 · Cited by 99 · see citing works

<i>Candida auris</i> : multi-omics signature of an emerging and multidrug-resistant pathogen

Zamith-Miranda, D., Heyman, H. M., Cleare, L. G., Couvillion, S., Clair, G., Bredeweg, E., Gacser, A., Nimrichter, L., Nakayasu, E. S., & Nosanchuk, J. D. (2019) · doi:10.1101/528232 · Cited by 99 · see citing works

Long non-coding RNA-mediated transcriptional interference of a permease gene confers drug tolerance in fission yeast

Ard, R., Tong, P., & Allshire, R. C. (2014) · Nature Communications · doi:10.1038/ncomms6576 · Cited by 98 · see citing works

Nine Things Genomics Can Tell Us About Candida auris

Chybowska, A. D., Childers, D. S., & Farrer, R. A. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00351 · Cited by 96 · see citing works

Itraconazole-resistant Candida auris with phospholipase, proteinase and hemolysin activity from a case of vulvovaginitis

Kumar, D., Banerjee, T., Pratap, C. B., & Tilak, R. (2015) · The Journal of Infection in Developing Countries · doi:10.3855/jidc.4582 · Cited by 90 · see citing works

ABC Transporter Genes Show Upregulated Expression in Drug-Resistant Clinical Isolates of Candida auris: A Genome-Wide Characterization of ATP-Binding Cassette (ABC) Transporter Genes

Wasi, M., Khandelwal, N. K., Moorhouse, A. J., Nair, R., Vishwakarma, P., Bravo Ruiz, G., Ross, Z. K., Lorenz, A., Rudramurthy, S. M., Chakrabarti, A., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01445 · Cited by 89 · see citing works

Candida auris exhibits resilient biofilm characteristics in vitro: implications for environmental persistence

Short, B., Brown, J., Delaney, C., Sherry, L., Williams, C., Ramage, G., & Kean, R. (2019) · Journal of Hospital Infection · doi:10.1016/j.jhin.2019.06.006 · Cited by 87 · see citing works

The comparative efficacy of antiseptics against Candida auris biofilms

Kean, R., McKloud, E., Townsend, E. M., Sherry, L., Delaney, C., Jones, B., Williams, C., & Ramage, G. (2018) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2018.05.007 · Cited by 86 · see citing works

Biofilm formation by <i>Candida auris</i> isolated from colonising sites and candidemia cases

Singh, R., Kaur, M., Chakrabarti, A., Shankarnarayan, S. A., & Rudramurthy, S. M. (2019) · Mycoses · doi:10.1111/myc.12947 · Cited by 86 · see citing works

Experimental Evolution Identifies Adaptive Aneuploidy as a Mechanism of Fluconazole Resistance in Candida auris

Bing, J., Hu, T., Zheng, Q., Muñoz, J. F., Cuomo, C. A., & Huang, G. (2020) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01466-20 · Cited by 86 · see citing works

Histone Deacetylases and Their Inhibition in Candida Species

Garnaud, C., Champleboux, M., Maubon, D., Cornet, M., & Govin, J. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01238 · Cited by 85 · see citing works

What do we know about the biology of the emerging fungal pathogen of humans Candida auris?

Ruiz, G. B., & Lorenz, A. (2020) · Microbiological Research · doi:10.1016/j.micres.2020.126621 · Cited by 83 · see citing works

Epstein-Barr Virus BART Long Non-coding RNAs Function as Epigenetic Modulators in Nasopharyngeal Carcinoma

Verhoeven, R. J. A., Tong, S., Mok, B. W.-Y., Liu, J., He, S., Zong, J., Chen, Y., Tsao, S., Lung, M. L., & Chen, H. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01120 · Cited by 79 · see citing works

Viral Epigenetics

Milavetz, B. I., & Balakrishnan, L. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1804-1_30 · Cited by 78 · see citing works

First reported case of multidrug-resistant Candida auris in Canada

Schwartz, I. S., & Hammond, G. (2017) · Canada Communicable Disease Report · doi:10.14745/ccdr.v43i78a02 · Cited by 70 · see citing works

Clade II Candida auris possess genomic structural variations related to an ancestral strain

Sekizuka, T., Iguchi, S., Umeyama, T., Inamine, Y., Makimura, K., Kuroda, M., Miyazaki, Y., & Kikuchi, K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223433 · Cited by 60 · see citing works

Impact of <i>FKS1</i> Genotype on Echinocandin <i>In Vitro</i> Susceptibility in Candida auris and <i>In Vivo</i> Response in a Murine Model of Infection

Sharma, D., Paul, R. A., Rudramurthy, S. M., Kashyap, N., Bhattacharya, S., Soman, R., Shankarnarayan, S. A., Chavan, D., Singh, S., Das, P., et al. (2022) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01652-21 · Cited by 60 · see citing works

First report of Candida auris infections from Saudi Arabia

Abdalhamid, B. A., Almaghrabi, R. S., Althawadi, S., & Omrani, A. S. (2018) · Journal of Infection and Public Health · doi:10.1016/j.jiph.2018.05.010 · Cited by 56 · see citing works

A Zinc Cluster Transcription Factor Contributes to the Intrinsic Fluconazole Resistance of Candida auris

Mayr, E.-M., Ramı́rez-Zavala, B., Krüger, I., & Morschhäuser, J. (2020) · mSphere · doi:10.1128/msphere.00279-20 · Cited by 54 · see citing works

Roles of Candida albicans Mig1 and Mig2 in glucose repression, pathogenicity traits, and SNF1 essentiality

Lagree, K., Woolford, C. A., Huang, M. Y., May, G. E., McManus, C. J., Solis, N. V., Filler, S. G., & Mitchell, A. P. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008582 · Cited by 51 · see citing works

Candida auris: epidemiological situation, laboratory capacity and preparedness in the European Union and European Economic Area*, January 2018 to May 2019

Plachouras, D., Lötsch, F., Kohlenberg, A., Monnet, D. L., & the Candida auris survey collaborative group (2020) · Eurosurveillance · doi:10.2807/1560-7917.es.2020.25.12.2000240 · Cited by 48 · see citing works

Genomic epidemiology of Candida auris in a general hospital in Shenyang, China: a three-year surveillance study

Tian, S., Bing, J., Chu, Y., Chen, J., Cheng, S., Wang, Q., Zhang, J., Ma, X., Zhou, B., Liu, L., et al. (2021) · Emerging Microbes & Infections · doi:10.1080/22221751.2021.1934557 · Cited by 47 · see citing works

Genetic Analysis of NDT80 Family Transcription Factors in Candida albicans Using New CRISPR-Cas9 Approaches

Min, K., Biermann, A. R., Hogan, D. A., & Konopka, J. B. (2018) · mSphere · doi:10.1128/msphere.00545-18 · Cited by 46 · see citing works

Effect of body surface decolonisation on bacteriuria and candiduria in intensive care units: an analysis of a cluster-randomised trial

Huang, S. S., Septimus, E. J., Hayden, M. K., et al. (2015) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(15)00238-8 · Cited by 43 · see citing works

Novel <i>FKS1</i> and <i>FKS2</i> modifications in a high-level echinocandin resistant clinical isolate of <i>Candida glabrata</i>

Hou, X., Healey, K. R., Shor, E., Kordalewska, M., Ortigosa, C. J., Paderu, P., Xiao, M., Wang, H., Zhao, Y., Lin, L.-Y., et al. (2019) · Emerging Microbes &amp; Infections · doi:10.1080/22221751.2019.1684209 · Cited by 43 · see citing works

New Clox Systems for Rapid and Efficient Gene Disruption in Candida albicans

Shahana, S., Childers, D. S., Ballou, E. R., Bohovych, I., Odds, F. C., Gow, N. A. R., & Brown, A. J. P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100390 · Cited by 42 · see citing works

Fungal KATs/KDACs: A New Highway to Better Antifungal Drugs?

Kuchler, K., Jenull, S., Shivarathri, R., & Chauhan, N. (2016) · PLOS Pathogens · doi:10.1371/journal.ppat.1005938 · Cited by 40 · see citing works

Rapid Assessment and Containment of Candida auris Transmission in Postacute Care Settings—Orange County, California, 2019

Karmarkar, E. N., O'Donnell, K. M., Prestel, C., Forsberg, K., Gade, L., Jain, S., Schan, D. K., Chow, N. A., McDermott, D., Rossow, J. A., et al. (2021) · Annals of Internal Medicine · doi:10.7326/m21-2013 · Cited by 40 · see citing works

Analysis of Fungal Genomes Reveals Commonalities of Intron Gain or Loss and Functions in Intron-Poor Species

Lim, C. S., Weinstein, B. N., Roy, S. W., & Brown, C. M. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab094 · Cited by 37 · see citing works

The evolutionary advantage of heritable phenotypic heterogeneity

Carja, O., & Plotkin, J. B. (2017) · Scientific Reports · doi:10.1038/s41598-017-05214-2 · Cited by 36 · see citing works

Photodynamic Therapy Is Effective Against Candida auris Biofilms

Bapat, P. S., & Nobile, C. J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.713092 · Cited by 36 · see citing works

An Overview on Identification and Regulatory Mechanisms of Long Non-coding RNAs in Fungi

Li, J., Liu, X., Yin, Z., Hú, Z., & Zhang, K. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.638617 · Cited by 34 · see citing works

Rapid Worldwide Emergence of Pathogenic Fungi

Rhodes, J. L. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.06.009 · Cited by 32 · see citing works

Candida auris in Singapore: Genomic epidemiology, antifungal drug resistance, and identification using the updated 8.01 VITEKⓇ2 system

Tan, Y. E., Teo, J. Q.-M., Rahman, N. B. A., Ng, O. T., Marimuthu, K., Tan, A. L., Koh, T. H., & Ong, R. T. (2019) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2019.09.016 · Cited by 32 · see citing works

Transcriptome Signatures Predict Phenotypic Variations of Candida auris

Jenull, S., Tscherner, M., Kashko, N., Shivarathri, R., Stoiber, A., Chauhan, M., Petryshyn, A., Chauhan, N., & Kuchler, K. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.662563 · Cited by 32 · see citing works

The interaction of fungi with the environment orchestrated by RNAi

Villalobos‐Escobedo, J. M., Herrera‐Estrella, A., & Carreras-Villaseñor, N. (2016) · Mycologia · doi:10.3852/15-246 · Cited by 31 · see citing works

Importation, Mitigation, and Genomic Epidemiology of Candida auris at a Large Teaching Hospital

Lesho, E. P., Bronstein, M. Z., McGann, P., Stam, J. A., Kwak, Y. I., Maybank, R. A., McNamara, J., Callahan, M., Campbell, J., Hinkle, M. K., et al. (2017) · Infection Control and Hospital Epidemiology · doi:10.1017/ice.2017.231 · Cited by 29 · see citing works

Candida auris, what do paediatricians need to know?

Warris, A. (2018) · Archives of Disease in Childhood · doi:10.1136/archdischild-2017-313960 · Cited by 26 · see citing works

Contribution of Clinically Derived Mutations in the Gene Encoding the Zinc Cluster Transcription Factor Mrr2 to Fluconazole Antifungal Resistance and CDR1 Expression in Candida albicans

Nishimoto, A. T., Zhang, Q., Hazlett, B. T., Morschhäuser, J., & Rogers, P. D. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00078-19 · Cited by 24 · see citing works

Inhibiting Fungal Echinocandin Resistance by Small-Molecule Disruption of Geranylgeranyltransferase Type I Activity

Sun, Q., Xiong, K., Yuan, Y., Yu, J., Yang, L., Shen, C., Su, C., & Lü, Y. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02046-19 · Cited by 14 · see citing works

Infection Control Measures against Candidaauris in Healthcare Facilities

Alfouzan, W. A., Dhar, R., Alabbad, J., & Rabaan, A. A. (2022) · Processes · doi:10.3390/pr10081625 · Cited by 10 · see citing works

Statins as Antifungal Agents: A Review on Drug Repurposing and Nanotechnology-Driven Delivery Strategies

e Silva, D. M., de Souza Lacerda, L., de Souza Andrioli, A., Braz, W. R., Campos, L. M., de Paiva, M. R. B., Pittella, F., Fabri, R. L., & Tavares, G. D. (2025) · Fundamental &amp; Clinical Pharmacology · doi:10.1111/fcp.70046 · Cited by 7 · see citing works

On Fruits and Fungi: A Risk of Antifungal Usage in Food Storage and Distribution in Driving Drug Resistance in Candida auris

Yadav, V., & Heitman, J. (2022) · mBio · doi:10.1128/mbio.00739-22 · Cited by 17 · see citing works

Identification and Elimination of Antifungal Tolerance in Candida auris

Rasouli Koohi, S., Shankarnarayan, S. A., Galon, C. M., & Charlebois, D. A. (2023) · Biomedicines · doi:10.3390/biomedicines11030898 · Cited by 20 · see citing works

Multi-omics Signature of <i>Candida auris</i> , an Emerging and Multidrug-Resistant Pathogen

Zamith-Miranda, D., Heyman, H. M., Cleare, L. G., Couvillion, S. P., Clair, G. C., Bredeweg, E. L., Gacser, A., Nimrichter, L., Nakayasu, E. S., & Nosanchuk, J. D. (2019) · mSystems · doi:10.1128/msystems.00257-19 · Cited by 99 · see citing works

Identification and Elimination of Antifungal Tolerance in Candida aurisPreprint

Koohi, S. R., Shankarnarayan, S. A., Galon, C. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.22.521687 · Cited by 1 · see citing works

Antifungal Drugs Work Together to Treat Germs Causing Fungal Infections

Pfaller, M. A., Messer, S. A., Deshpande, L. M., et al. (2021) · Future Microbiology · doi:10.2217/fmb-2021-0086 · Cited by 1 · see citing works