Candida auris : multi-omics signature of an emerging and multidrug-resistant pathogen

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

Huang, D. W., Sherman, B. T., & Lempicki, R. A. (2009) · Nature Protocols · doi:10.1038/nprot.2008.211 · Cited by 35,890 · see citing works

MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification

Cox, J., & Mann, M. (2008) · Nature Biotechnology · doi:10.1038/nbt.1511 · Cited by 14,855 · see citing works

Global quantification of mammalian gene expression control

Schwanhäusser, B., Busse, D., Li, N., Dittmar, G., Schuchhardt, J., Wolf, J., Chen, W., & Selbach, M. (2011) · Nature · doi:10.1038/nature10098 · Cited by 6,566 · cited 1× · see citing works

MZmine 2: Modular framework for processing, visualizing, and analyzing mass spectrometry-based molecular profile data

Pluskal, T., Castillo, S., Villar‐Briones, A., & Orešič, M. (2010) · BMC Bioinformatics · doi:10.1186/1471-2105-11-395 · Cited by 3,852 · see citing works

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

FiehnLib: Mass Spectral and Retention Index Libraries for Metabolomics Based on Quadrupole and Time-of-Flight Gas Chromatography/Mass Spectrometry

Kind, T., Wohlgemuth, G., Lee, D. Y., Lü, Y., Palazoglu, M., Shahbaz, S., & Fiehn, O. (2009) · Analytical Chemistry · doi:10.1021/ac9019522 · Cited by 1,485 · 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

First hospital outbreak of the globally emerging Candida auris in a European hospital

Schelenz, S., Hagen, F., Rhodes, J. L., Abdolrasouli, A., Chowdhary, A., Hall, A., Ryan, L., Shackleton, J., Trimlett, R., Meis, J. F., et al. (2016) · Antimicrobial Resistance &amp; Infection Control · doi:10.1186/s13756-016-0132-5 · Cited by 768 · see citing works

Candida auris: A rapidly emerging cause of hospital-acquired multidrug-resistant fungal infections globally

Chowdhary, A., Sharma, C., & Meis, J. F. (2017) · PLOS Pathogens · doi:10.1371/journal.ppat.1006290 · Cited by 750 · see citing works

A Recently Evolved Transcriptional Network Controls Biofilm Development in Candida albicans

Nobile, C. J., Fox, E. P., Nett, J. E., Sorrells, T. R., Mitrovich, Q. M., Hernday, A. D., Tuch, B. B., Andes, D. R., & Johnson, A. D. (2012) · Cell · doi:10.1016/j.cell.2011.10.048 · Cited by 711 · 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

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

RNA-Seq analysis in MeV

Howe, E., Sinha, R., Schlauch, D., & Quackenbush, J. F. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr490 · Cited by 514 · 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

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

MetaboliteDetector: Comprehensive Analysis Tool for Targeted and Nontargeted GC/MS Based Metabolome Analysis

Hiller, K., Hangebrauk, J., Jäger, C., Spura, J., Schreiber, K., & Schomburg, D. (2009) · Analytical Chemistry · doi:10.1021/ac802689c · Cited by 440 · 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

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

Multidrug-resistant endemic clonal strain of Candida auris in India

Chowdhary, A., Anil Kumar, V., Sharma, C., Prakash, A., Agarwal, K., Babu, R., Dinesh, K. R., Karim, S., Singh, S. K., Hagen, F., et al. (2014) · European Journal of Clinical Microbiology &amp; Infectious Diseases · doi:10.1007/s10096-013-2027-1 · Cited by 373 · see citing works

Candida Species Biofilms’ Antifungal Resistance

Silva, S. M., Rodrigues, C. F., Araújo, D., Rodrigues, M. E., & Henriques, M. (2017) · Journal of Fungi · doi:10.3390/jof3010008 · Cited by 308 · 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

<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

Migration to Apoptotic “Find-me” Signals Is Mediated via the Phagocyte Receptor G2A

Peter, C., Waibel, M., Radu, C. G., Yang, L. V., Witte, O. N., Schulze-Osthoff, K., Wesselborg, S., & Lauber, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m706586200 · Cited by 258 · 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

Cloning and Disruption of caPLB1, a Phospholipase B Gene Involved in the Pathogenicity of Candida albicans

Leidich, S. D., Ibrahim, A. S., Fu, Y., Koul, A., Jessup, C., Vitullo, J., Fonzi, W., Mirbod, F., Nakashima, S., Nozawa, Y., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.40.26078 · Cited by 241 · see citing works

MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses

Nakayasu, E. S., Nicora, C., Sims, A. M., Burnum-Johnson, K., Kim, Y., Kyle, J. E., Matzke, M. M., Shukla, A. K., Chu, R., Schepmoes, A., et al. (2016) · mSystems · doi:10.1128/msystems.00043-16 · Cited by 235 · 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

Can Multidrug-Resistant Candidaauris Be Reliably Identified in Clinical Microbiology Laboratories?

Mizusawa, M., Miller, H., Green, R., Lee, R. E., Jr., Durante, M., Perkins, R., Hewitt, C. M., Simner, P. J., Carroll, K. C., Hayden, R. T., et al. (2016) · Journal of Clinical Microbiology · doi:10.1128/jcm.02202-16 · Cited by 218 · see citing works

Overexpression or Deletion of Ergosterol Biosynthesis Genes Alters Doubling Time, Response to Stress Agents, and Drug Susceptibility in <i>Saccharomyces cerevisiae</i>

Bhattacharya, S., Esquivel, B. D., & White, T. C. (2018) · mBio · doi:10.1128/mbio.01291-18 · Cited by 210 · see citing works

Drug Susceptibilities of Yeast Cells Are Affected by Membrane Lipid Composition

Mukhopadhyay, K., Kohli, A., & Prasad, R. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.12.3695-3705.2002 · Cited by 202 · see citing works

VANTED v2: a framework for systems biology applications

Rohn, H., Junker, A., Hartmann, A., Grafahrend‐Belau, E., Treutler, H., Klapperstück, M., Czauderna, T., Klukas, C., & Schreiber, F. (2012) · BMC Systems Biology · doi:10.1186/1752-0509-6-139 · Cited by 192 · 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

Role of Extracellular Phospholipases and Mononuclear Phagocytes in Dissemination of Cryptococcosis in a Murine Model

Santangelo, R., Zoellner, H., Sorrell, T., Wilson, C., Donald, C., Djordjevic, J., Shounan, Y., & Wright, L. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2229-2239.2004 · Cited by 169 · see citing works

Evidence of genotypic diversity among Candida auris isolates by multilocus sequence typing, matrix-assisted laser desorption ionization time-of-flight mass spectrometry and amplified fragment length polymorphism

Prakash, A., Sharma, C., Singh, A. K., Singh, P. K., Kumar, A., Hagen, F., Govender, N. P., Colombo, A. L., Meis, J. F. G. M., & Chowdhary, A. (2015) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2015.10.022 · Cited by 167 · 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

Membrane Sphingolipid-Ergosterol Interactions Are Important Determinants of Multidrug Resistance in <i>Candida albicans</i>

Mukhopadhyay, K., Prasad, T., Saini, P., Pucadyil, T. J., Chattopadhyay, A., & Prasad, R. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.5.1778-1787.2004 · Cited by 163 · see citing works

Current perspective on emergence, diagnosis and drug resistance in Candida auris

Sarma, S., & Upadhyay, S. (2017) · Infection and Drug Resistance · doi:10.2147/idr.s116229 · Cited by 147 · see citing works

Cell wall integrity signalling in human pathogenic fungi: CWI signalling in pathogenic fungi

Dichtl, K., Samantaray, S., & Wagener, J. (2016) · Cellular Microbiology · doi:10.1111/cmi.12612 · Cited by 144 · 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

Matrix-assisted laser desorption ionization time-of-flight mass spectrometry for the rapid identification of yeasts causing bloodstream infections

Ghosh, A. K., Paul, S., Sood, P., Rudramurthy, S. M., Rajbanshi, A., Jillwin, T. J., & Chakrabarti, A. (2014) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2014.11.009 · Cited by 128 · 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

LIQUID: an-open source software for identifying lipids in LC-MS/MS-based lipidomics data

Kyle, J. E., Crowell, K. L., Casey, C., Fujimoto, G. M., Kim, S., Dautel, S. E., Smith, R. D., Payne, S., & Metz, T. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx046 · Cited by 119 · see citing works

Superoxide dismutases are involved in Candida albicans biofilm persistence against miconazole

Bink, A., Vandenbosch, D., Coenye, T., Nelis, H., Cammue, B. P. A., & Thevissen, K. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00280-11 · Cited by 119 · see citing works

<b><i>Candida albicans</i></b> biofilm formation is associated with increased anti‐oxidative capacities

Seneviratne, C. J., Wang, Y., Jin, L., Abiko, Y., & Samaranayake, L. P. (2008) · PROTEOMICS · doi:10.1002/pmic.200701097 · Cited by 104 · see citing works

Lipid Biosynthesis as an Antifungal Target

Pan, J., Hu, C., & Yu, J. (2018) · Journal of Fungi · doi:10.3390/jof4020050 · Cited by 99 · see citing works

The DNA Binding Protein Rfg1 Is a Repressor of Filamentation in Candida albicans

Khalaf, R. A., & Zitomer, R. S. (2001) · Genetics · doi:10.1093/genetics/157.4.1503 · Cited by 97 · see citing works

Antibody Binding Alters the Characteristics and Contents of Extracellular Vesicles Released by Histoplasma capsulatum

Baltazar, L. M., Nakayasu, E. S., Sobreira, T. J. P., Choi, H., Casadevall, A., Nimrichter, L., & Nosanchuk, J. D. (2016) · mSphere · doi:10.1128/msphere.00085-15 · Cited by 97 · see citing works

Protein–protein interactions among C-4 demethylation enzymes involved in yeast sterol biosynthesis

Mo, C., Valachovič, M., Randall, S. K., Nickels, J. T., & Bard, M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.112202799 · Cited by 81 · see citing works

Lipidomics reveals dramatic lipid compositional changes in the maturing postnatal lung

Dautel, S. E., Kyle, J. E., Clair, G., Sontag, R. L., Weitz, K., Shukla, A. K., Nguyen, S., Kim, Y., Zink, E., Luders, T., et al. (2017) · Scientific Reports · doi:10.1038/srep40555 · Cited by 78 · see citing works

Recent Insights into the Paradoxical Effect of Echinocandins

Wagener, J., & Loiko, V. (2017) · Journal of Fungi · doi:10.3390/jof4010005 · Cited by 73 · 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

Effects of fluconazole on<i>Candida glabrata</i>biofilms and its relationship with ABC transporter gene expression

Fonseca, E., Silva, S., Rodrigues, C. F., Alves, C. T., Azeredo, J., & Henriques, M. (2014) · Biofouling · doi:10.1080/08927014.2014.886108 · Cited by 56 · see citing works

Salmonella modulates metabolism during growth under conditions that induce expression of virulence genes

Kim, Y., Schmidt, B. J., Kidwai, A. S., Jones, M. B., Kaiser, B. L. D., Brewer, H. M., Mitchell, H. D., Palsson, B. Ø., McDermott, J., Heffron, F., et al. (2013) · Molecular BioSystems · doi:10.1039/c3mb25598k · Cited by 53 · see citing works

Cryptococcal Phospholipase B1 Is Required for Intracellular Proliferation and Control of Titan Cell Morphology during Macrophage Infection

Evans, R. J., Li, Z., Hughes, W. S., Djordjevic, J. T., Nielsen, K., & May, R. C. (2015) · Infection and Immunity · doi:10.1128/iai.03104-14 · Cited by 53 · see citing works

Identification and Functional Characterization of Rca1, a Transcription Factor Involved in both Antifungal Susceptibility and Host Response in Candida albicans

Vandeputte, P., Pradervand, S., Ischer, F., Coste, A. T., Ferrari, S., Harshman, K., & Sanglard, D. (2012) · Eukaryotic Cell · doi:10.1128/ec.00134-12 · Cited by 51 · see citing works

Lipid Mini-On: mining and ontology tool for enrichment analysis of lipidomic data

Clair, G., Akers, S. M., Stratton, K. G., Monroe, M. E., Tfaily, M., Ansong, C. K., & Kyle, J. E. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz250 · Cited by 48 · see citing works

Azole resistance inCandida albicansfrom animals: Highlights on efflux pump activity and gene overexpression

Rocha, M. F. G., Bandeira, S. P., de Alencar, L. P., Melo, L. M., Sales, J. A., Paiva, M. D. A. N., Teixeira, C. E. C., Castelo‐Branco, D. D. S. C. M., Pereira‐Neto, W. D. A., Cordeiro, R. D. A., et al. (2017) · Mycoses · doi:10.1111/myc.12611 · Cited by 45 · see citing works

Lipidomics and in Vitro Azole Resistance in Candida albicans

Singh, A., Mahto, K. K., & Prasad, R. (2013) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2012.0075 · Cited by 31 · see citing works

Mapping of functional domains and characterization of the transcription factor Cph1 that mediate morphogenesis in Candida albicans

Maiti, P., Ghorai, P., Ghosh, S., Kamthan, M., Tyagi, R. K., & Datta, A. (2015) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2015.08.004 · Cited by 22 · see citing works

Involvement of mitochondrial aerobic respiratory activity in efflux-mediated resistance of C. albicans to fluconazole

Guo, H., Xie, S. M., Shui-xiu, L. I., Song, Y. J., Zhong, X., & Zhang, H. (2017) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2017.04.004 · Cited by 22 · see citing works

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds

de-Souza-Silva, C. M., Guilhelmelli, F., Zamith‐Miranda, D., de Oliveira, M. A., Nosanchuk, J. D., Silva-Pereira, I., & Albuquerque, P. (2018) · Journal of Visualized Experiments · doi:10.3791/57127 · Cited by 16 · see citing works

Candida auris : An Overview of the Emerging Drug-Resistant Fungal Infection

Sanyaolu, A. O., Okorie, C., Marinkovic, A., Abbasi, A. F., Prakash, S., Mangat, J., Hosein, Z., Haider, N., & Chan, J. (2022) · Infection and Chemotherapy · doi:10.3947/ic.2022.0008 · Cited by 179 · see citing works

Combined Antifungal Resistance and Biofilm Tolerance: the Global Threat of Candida auris

Kean, R., & Ramage, G. (2019) · mSphere · doi:10.1128/msphere.00458-19 · Cited by 154 · see citing works

On the emergence, spread and resistance of Candida auris: host, pathogen and environmental tipping points

Chakrabarti, A., & Sood, P. (2021) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001318 · Cited by 132 · 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

Candidiasis and Other Emerging Yeasts

Sharma, M., & Chakrabarti, A. (2023) · Current Fungal Infection Reports · doi:10.1007/s12281-023-00455-3 · Cited by 105 · see citing works

Multiple Alternative Carbon Pathways Combine To Promote Candida albicans Stress Resistance, Immune Interactions, and Virulence

Williams, R. B., & Lorenz, M. C. (2020) · mBio · doi:10.1128/mbio.03070-19 · Cited by 87 · see citing works

Candida auris: A Decade of Understanding of an Enigmatic Pathogenic Yeast

Kean, R., Brown, J. L., Gülmez, D., Ware, A., & Ramage, G. (2020) · Journal of Fungi · doi:10.3390/jof6010030 · Cited by 86 · 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

Taxonomy of Pathogenic Yeasts Candida, Cryptococcus, Malassezia, and Trichosporon

Takashima, M., & Sugita, T. (2022) · Medical Mycology Journal · doi:10.3314/mmj.22.004 · Cited by 88 · see citing works

Comparative Molecular and Immunoregulatory Analysis of Extracellular Vesicles from Candida albicans and Candida auris

Zamith‐Miranda, D., Heyman, H. M., Couvillion, S., Cordero, R. J. B., Rodrigues, M. L., Nimrichter, L., Casadevall, A., Amatuzzi, R. F., Alves, L. R., Nakayasu, E. S., et al. (2021) · mSystems · doi:10.1128/msystems.00822-21 · Cited by 89 · see citing works

Drug Resistance and Novel Therapeutic Approaches in Invasive Candidiasis

Murphy, S. E., & Bicanic, T. A. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.759408 · Cited by 85 · see citing works

Functions of Sphingolipids in Pathogenesis During Host–Pathogen Interactions

Wang, J., Chen, Y., Li, Y.-K., Chen, D., He, J.-F., & Yao, N. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.701041 · Cited by 70 · see citing works

Fun(gi)omics: Advanced and Diverse Technologies to Explore Emerging Fungal Pathogens and Define Mechanisms of Antifungal Resistance

Ball, B., Langille, M. G. I., & Geddes‐McAlister, J. (2020) · mBio · doi:10.1128/mbio.01020-20 · Cited by 76 · see citing works

Candida auris: An Overview of How to Screen, Detect, Test and Control This Emerging Pathogen

Fasciana, T., Cortegiani, A., Ippolito, M., Giarratano, A., Diquattro, O., Lipari, D., Graceffa, D., & Giammanco, A. (2020) · Antibiotics · doi:10.3390/antibiotics9110778 · Cited by 70 · see citing works

Analysis of Malassezia Lipidome Disclosed Differences Among the Species and Reveals Presence of Unusual Yeast Lipids

Ramírez, A. M. C., Amézquita, A., Cardona, J., Matiz-Céron, L., Andrade-Martínez, J. S., Triana, S., Mantilla, M. J., Restrepo, S., Barrios, A. F. G., & de Cock, H. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00338 · Cited by 66 · see citing works

Media matters! Alterations in the loading and release of Histoplasma capsulatum extracellular vesicles in response to different nutritional milieus

Cleare, L. G., Zamith‐Miranda, D., Heyman, H. M., Couvillion, S., Nimrichter, L., Rodrigues, M. L., Nakayasu, E. S., & Nosanchuk, J. D. (2020) · Cellular Microbiology · doi:10.1111/cmi.13217 · Cited by 65 · see citing works

Multidrug transporters of Candida species in clinical azole resistance

Prasad, R., Nair, R., & Banerjee, A. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103252 · Cited by 58 · see citing works

Polarization-sensitive stimulated Raman scattering imaging resolves amphotericin B orientation in Candida membrane

Dong, P., Zong, C., Dagher, Z., Hui, J., Li, J., Zhan, Y., Zhang, M., Mansour, M. K., & Cheng, J. (2021) · Science Advances · doi:10.1126/sciadv.abd5230 · Cited by 55 · see citing works

Candida auris: A Continuing Threat

Bhargava, A., Klamer, K., Sharma, M., Ortiz, D. A., & Saravolatz, L. I. I. (2025) · Microorganisms · doi:10.3390/microorganisms13030652 · Cited by 58 · see citing works

Phytogenic Fabrication of Ag–Fe Bimetallic Nanoparticles for Cell Cycle Arrest and Apoptosis Signaling Pathways in Candida auris by Generating Oxidative Stress

Kamli, M. R., Srivastava, V., Hajrah, N. H., Sabir, J. S. M., Ali, A., Malik, M. A., & Ahmad, A. (2021) · Antioxidants · doi:10.3390/antiox10020182 · Cited by 51 · see citing works

Caspofungin-resistance in <i>Candida auris</i> is cell wall-dependent phenotype and potential prevention by zinc oxide nanoparticles

Fayed, B., Jayakumar, M. N., & Soliman, S. S. M. (2021) · Medical Mycology · doi:10.1093/mmy/myab059 · Cited by 41 · see citing works

Metabolic profiling of Candida clinical isolates of different species and infection sources

Oliver, J. C., Laghi, L., Parolin, C., Foschi, C., Marangoni, A., Liberatore, A., Dias, A. L. T., Cricca, M., & Vitali, B. (2020) · Scientific Reports · doi:10.1038/s41598-020-73889-1 · Cited by 40 · see citing works

NO Candida auris: Nitric Oxide in Nanotherapeutics to Combat Emerging Fungal Pathogen Candida auris

Cleare, L. G., Li, K. L., Abuzeid, W. M., Nacharaju, P., Friedman, J. M., & Nosanchuk, J. D. (2020) · Journal of Fungi · doi:10.3390/jof6020085 · 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

High-Throughput Profiling of Candida auris Isolates Reveals Clade-Specific Metabolic Differences

Brandt, P., Mirhakkak, M. H., Wagner, L., Driesch, D., Möslinger, A., Fänder, P., Schäuble, S., Panagiotou, G., & Vylkova, S. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.00498-23 · Cited by 34 · see citing works

Candida auris:a fungus with identity crisis

Vila, T. V. M., Sultan, A. S., Montelongo‐Jauregui, D., & Jabra‐Rizk, M. A. (2020) · Pathogens and Disease · doi:10.1093/femspd/ftaa034 · Cited by 37 · see citing works

Advances in Fungal Peptide Vaccines

da Silva, L. B. R., Taborda, C. P., & Nosanchuk, J. D. (2020) · Journal of Fungi · doi:10.3390/jof6030119 · Cited by 34 · see citing works

Transcriptomics and Phenotyping Define Genetic Signatures Associated with Echinocandin Resistance in Candida auris

Jenull, S., Shivarathri, R., Tsymala, I., Penninger, P., Trinh, P.-C., Nogueira, F., Chauhan, M., Singh, A., Petryshyn, A., Stoiber, A., et al. (2022) · mBio · doi:10.1128/mbio.00799-22 · 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

Omics Approaches for Understanding Biogenesis, Composition and Functions of Fungal Extracellular Vesicles

Zamith‐Miranda, D., da Silva, R. P., Couvillion, S., Bredeweg, E., Burnet, M., Coelho, C., Camacho, E., Nimrichter, L., Puccia, R., de Almeida, I. C., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.648524 · Cited by 32 · see citing works

Sphingolipidomics of drug resistant Candida auris clinical isolates reveal distinct sphingolipid species signatures

Kumar, M., Singh, A., Kumari, S., Kumar, P., Wasi, M., Mondal, A. K., Rudramurthy, S. M., Chakrabarti, A., Gaur, N. A., Gow, N. A. R., et al. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158815 · Cited by 31 · see citing works

Development and characterization of an amphotericin B - loaded nanoemulsion applied to Candida auris biofilms control

Marena, G. D., Ramos, M. A. D. S., Carvalho, G. C., de Lima, L. C., do Nascimento, A. L. C. S., Sábio, R. M., Rodero, C. F., Spósito, L., Bauab, T. M., & Chorilli, M. (2022) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2022.103566 · Cited by 30 · see citing works

Niclosamide-loaded nanoparticles disrupt Candida biofilms and protect mice from mucosal candidiasis

Sutar, Y. B., Nabeela, S., Singh, S., Alqarihi, A., Solis, N. V., Ghebremariam, T., Filler, S. G., Ibrahim, A. S., Date, A. A., & Uppuluri, P. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001762 · Cited by 30 · see citing works

Catch the wave: Metabolomic analyses in human pathogenic fungi

Brandt, P., Garbe, E., & Vylkova, S. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008757 · Cited by 29 · see citing works

Transcriptional and translational landscape of <i>Candida auris</i> in response to caspofungin

Zamith-Miranda, D., Amatuzzi, R. F., Munhoz da Rocha, I. F., Martins, S. T., Lucena, A. C. R., Vieira, A. Z., Trentin, G., Almeida, F., Rodrigues, M. L., Nakayasu, E. S., et al. (2021) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2021.09.007 · Cited by 29 · see citing works

A detailed lipidomic study of human pathogenic fungi Candida auris

Shahi, G., Kumar, M., Kumari, S., Rudramurthy, S. M., Chakrabarti, A., Gaur, N. A., Singh, A., & Prasad, R. (2020) · FEMS Yeast Research · doi:10.1093/femsyr/foaa045 · Cited by 29 · see citing works

Candida Infections: The Role of Saliva in Oral Health—A Narrative Review

Tamai, R., & Kiyoura, Y. (2025) · Microorganisms · doi:10.3390/microorganisms13040717 · Cited by 27 · see citing works

Melanization of Candida auris Is Associated with Alteration of Extracellular pH

Smith, D. F. Q., Mudrak, N. J., Zamith‐Miranda, D., Honorato, L., Nimrichter, L., Chrissian, C., Smith, B., Gerfen, G. J., Stark, R. E., Nosanchuk, J. D., et al. (2022) · Journal of Fungi · doi:10.3390/jof8101068 · Cited by 26 · see citing works

Insights into the Multi-Azole Resistance Profile in Candida haemulonii Species Complex

Silva, L. N., Ramos, L. S., de Oliveira, S. S. C., Magalhães, L. B., Squizani, E. D., Kmetzsch, L., Vainstein, M. H., Branquinha, M. H., & dos Santos, A. L. S. (2020) · Journal of Fungi · doi:10.3390/jof6040215 · Cited by 25 · see citing works

Similarities and Differences among Species Closely Related to Candida albicans: C. tropicalis, C. dubliniensis, and C. auris

Satała, D., Juszczak, M., Wronowska, E., Surowiec, M., Kulig, K., Kozik, A., Rąpała‐Kozik, M., & Karkowska‐Kuleta, J. (2022) · Cellular Microbiology · doi:10.1155/2022/2599136 · Cited by 26 · see citing works

Stepping out of the dark: how metabolomics shed light on fungal biology

Adejor, J., Tumukunde, E., Li, G., Alhaji, T. S., Wu, L., Jiang, Z., & Wang, S. (2025) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf028 · Cited by 23 · see citing works

Echinocandin Resistance in Aspergillus fumigatus Has Broad Implications for Membrane Lipid Perturbations That Influence Drug-Target Interactions

Satish, S., & Perlin, D. S. (2019) · Microbiology Insights · doi:10.1177/1178636119897034 · Cited by 23 · see citing works

Farnesol Boosts the Antifungal Effect of Fluconazole and Modulates Resistance in Candida auris through Regulation of the CDR1 and ERG11 Genes

Dekkerová, J., Černáková, L., Kendra, S., Borghi, E., Ottaviano, E., Willinger, B., & Bujdáková, H. (2022) · Journal of Fungi · doi:10.3390/jof8080783 · Cited by 23 · see citing works

Activities of nine antifungal agents against Candida auris biofilms

Chatzimoschou, A., Giampani, A., Meis, J. F. G. M., & Roilides, E. (2020) · Mycoses · doi:10.1111/myc.13223 · Cited by 21 · see citing works

Screening of the Pandemic Response Box Reveals an Association between Antifungal Effects of MMV1593537 and the Cell Wall of Cryptococcus neoformans , Cryptococcus deuterogattii , and Candida auris

de Oliveira, H. C., Castelli, R. F., Reis, F. C. G., Samby, K., Nosanchuk, J. D., Alves, L. R., & Rodrigues, M. L. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00601-22 · Cited by 21 · see citing works

Cellular and Extracellular Vesicle RNA Analysis in the Global Threat Fungus Candida auris

da Rocha, I. F. M., Martins, S. T., Amatuzzi, R. F., Zamith‐Miranda, D., Nosanchuk, J. D., Rodrigues, M. L., & Alves, L. R. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.01538-21 · Cited by 18 · see citing works

A Histoplasma capsulatum Lipid Metabolic Map Identifies Antifungal Targets

Zamith‐Miranda, D., Heyman, H. M., Burnet, M., Couvillion, S., Zheng, X., Munoz, N., Nelson, W. C., Kyle, J. E., Zink, E. M., Weitz, K. K., et al. (2021) · mBio · doi:10.1128/mbio.02972-21 · Cited by 20 · see citing works

Sphingolipid diversity in Candida auris: unraveling interclade and drug resistance fingerprints

Ali, B., Kumar, M., Kumar, P., Chauhan, A., Usmani, S. A., Rudramurthy, S. M., Meis, J. F. G. M., Chakrabarti, A., Singh, A., Gaur, N. A., et al. (2024) · FEMS Yeast Research · doi:10.1093/femsyr/foae008 · Cited by 17 · 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

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

Rabaan, A. A., Eljaaly, K., Alfouzan, W. A., Mutair, A. A., Alhumaid, S., Alfaraj, A. H., Aldawood, Y., Alsaleh, A. A., Albayat, H., Azmi, R. A., et al. (2023) · Journal of Infection and Public Health · doi:10.1016/j.jiph.2022.12.012 · Cited by 14 · see citing works

Two Cases of the Emerging Candida auris in a university hospital from Saudi Arabia

AlJindan, R. Y., & AlEraky, D. M. (2020) · Saudi Journal of Medicine and Medical Sciences · doi:10.4103/sjmms.sjmms_449_19 · Cited by 12 · see citing works

Identification of four compounds from the Pharmakon library with antifungal activity against Candida auris and species of Cryptococcus

de Oliveira, H. C., Castelli, R. F., Alves, L. R., Nosanchuk, J. D., Salama, E. A., Seleem, M. N., & Rodrigues, M. L. (2022) · Medical Mycology · doi:10.1093/mmy/myac033 · Cited by 12 · see citing works

The sphingolipid inhibitor myriocin increases Candida auris susceptibility to amphotericin B

Stieber, H., Junghanns, L., Wilhelm, H., Batliner, M., Aldejohann, A. M., Kurzai, O., & Martin, R. (2024) · Mycoses · doi:10.1111/myc.13723 · Cited by 11 · see citing works

Impairing the interaction between Erg11 and cytochrome P450 reductase Ncp1 enhances azoles’ antifungal activities

Li, W., Whiteway, M., Hang, S., Yu, J., Lu, H., & Jiang, Y. (2025) · Nature Communications · doi:10.1038/s41467-025-62131-z · Cited by 13 · see citing works

Highly Reactive Group I Introns Ubiquitous in Pathogenic Fungi

Liu, T., & Pyle, A. M. (2024) · Journal of Molecular Biology · doi:10.1016/j.jmb.2024.168513 · Cited by 10 · see citing works

A comprehensive analysis of the effect of quorum-sensing molecule 3-oxo-C12-homoserine lactone on Candida auris and Candida albicans

Kovács, F., Jakab, Á., Balla, N., Tóth, Z., Balázsi, D., Forgács, L., Harmath, A., Bozó, A., Ragyák, Á. Z., Majoros, L., et al. (2025) · Biofilm · doi:10.1016/j.bioflm.2025.100259 · Cited by 8 · see citing works

Effects of antifungal agents on the fungal proteome: informing on mechanisms of sensitivity and resistance

Owens, R. A., & Doyle, S. (2021) · Expert Review of Proteomics · doi:10.1080/14789450.2021.1912601 · Cited by 8 · see citing works

The adaptive response to alternative carbon sources in the pathogen Candida albicans involves a remodeling of thiol- and glutathione-dependent redox status

Bayot, J., Martin, C., Chevreux, G., Camadro, J., & Auchère, F. (2023) · Biochemical Journal · doi:10.1042/bcj20220505 · Cited by 8 · see citing works

AFM evaluation of a humanized recombinant antibody affecting C. auris cell wall and stability

Vanzolini, T., Mambro, T. D., Magnani, M., & Menotta, M. (2023) · RSC Advances · doi:10.1039/d2ra07217c · Cited by 8 · see citing works

Comparative molecular and immunoregulatory analysis of extracellular vesicles from Candida albicans and Candida aurisPreprint

Zamith‐Miranda, D., Heyman, H. M., Couvillion, S., Cordero, R. J. B., Rodrigues, M. L., Nimrichter, L., Casadevall, A., Amatuzzi, R. F., Alves, L. R., Nakayasu, E. S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.04.368472 · Cited by 8 · see citing works

A Comprehensive Analysis of the Lipidomic Signatures in Rhizopus delemar

Ali, B., Chauhan, A., Kumar, M., Kumar, P., Carolus, H., Romero, C. L., Vergauwen, R., Singh, A., Banerjee, A., Prakash, A., et al. (2024) · Journal of Fungi · doi:10.3390/jof10110760 · Cited by 7 · see citing works

Acquired Triazole Resistance Alters Pathogenicity-Associated Features in Candida auris in an Isolate-Dependent Manner

Bohner, F., Papp, C., Takács, T., Varga, M., Szekeres, A., Nosanchuk, J. D., Vágvölgyi, C., Tóth, R., & Gácser, A. (2023) · Journal of Fungi · doi:10.3390/jof9121148 · Cited by 7 · see citing works

Emerging evidence for a multitude of mechanisms and factors that determine amphotericin B resistance in pathogenic fungi

Chauhan, A., Gow, N. A. R., & Prasad, R. (2026) · The Cell Surface · doi:10.1016/j.tcsw.2026.100168 · Cited by 6 · see citing works

Pathogen-Host Interaction Repertoire at Proteome and Posttranslational Modification Levels During Fungal Infections

Li, Y., Li, H., Sun, T., & Ding, C. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.774340 · Cited by 6 · see citing works

Deciphering cargo contents in extracellular vesicles of Candida haemulonii var. vulnera

Oliveira, B., Bitencourt, T. A., dos Santos, P. W. D. S., Pagano, A. D., Pessoni, A. M., Rezende, C. P., Piraine, R. E. A., Masson, A. P., Faça, V. M., Campos, V. F., et al. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.04.014 · Cited by 5 · see citing works

Mass Spectrometry-based Proteomics of Eukaryotes

Geddes‐McAlister, J., Rizakos, T., & Muselius, B. (2023) · Royal Society of Chemistry eBooks · doi:10.1039/bk9781837670338-00215 · Cited by 5 · see citing works

Interactions of the emerging fungus Candida auris with Acanthamoeba castellanii reveal phenotypic changes with direct implications on the response to stress and virulence

Valente, M. R., Alcântara, L. M., Cintra, D. S., Mendoza, S. R., Medeiros, E. G., Gomes, K. X., Honorato, L., Almeida, M. D. A., Vieira, C. B., Nosanchuk, J. D., et al. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.01746-24 · Cited by 5 · see citing works

Potential Influence of Antifungal-drug Resistant Pathogens in Patients with Cholangiocarcinoma and the Application of Nanoparticle Mechanisms as Novel Antifungal and Anticancer Agents

Achilonu, C. C., Ramatla, T. A., Maleke, M., Kumar, P., Igbalajobi, O. A., & Noel, C. B. (2025) · Current Clinical Microbiology Reports · doi:10.1007/s40588-024-00239-4 · Cited by 5 · see citing works

Dual function of <i>Candida auris</i> mannosyltransferase, MNT5, in biofilm community protection from antifungal therapy and the host

Zarnowski, R., Horton, M. V., Johnson, C. J., Vang, P. C., Uram, J., Fernando, L. D. P., Vlach, J., Heiss, C., Azadi, P., Nett, J. E., et al. (2025) · mBio · doi:10.1128/mbio.00346-25 · Cited by 5 · see citing works

Genomic landscape of the DHA1 family in Candida auris and mapping substrate repertoire of CauMdr1

Khatoon, R., Sharma, S., Vishwakarma, P., Saini, A., Aggarwal, P., Lynn, A. M., Prakash, A., Prasad, R., & Banerjee, A. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-12189-2 · Cited by 5 · see citing works

Comprehensive characterization of extracellular vesicles produced by environmental (Neff) and clinical (T4) strains of Acanthamoeba castellanii

Medeiros, E. G., Valente, M. R., Honorato, L., Ferreira, M. D. S., Mendoza, S. R., Gonçalves, D. D. S., Alcântara, L. M., Gomes, K. X., Pinto, M. R., Nakayasu, E. S., et al. (2024) · mSystems · doi:10.1128/msystems.01226-23 · Cited by 5 · see citing works

Candida auris Antifungal Resistance, Virulence and Susceptibility to a Novel Nitric Oxide-Releasing Microparticle and Its Correlations to Clade Identification

Valdez, A. F., Bohner, F., Goldman, J. P., Jaquiery, A. B., do Amaral, E. V. C., Corrêa-Junior, D., Draganski, A. R., Nimrichter, L., Nosanchuk, J. D., & Zamith‐Miranda, D. (2025) · Microbiology Research · doi:10.3390/microbiolres16010015 · Cited by 4 · see citing works

Managing Candida auris in dialysis units: challenges, strategies, and future directions

Zoi, V., Skoulatou, M., Vassilikopoulos, T., & Vovlianou, S. (2025) · International Urology and Nephrology · doi:10.1007/s11255-025-04600-4 · Cited by 4 · see citing works

Interconnected worlds: a comprehensive review of fungal defenses, antimicrobial resistance, and their evolutionary dynamics

Sui, Y., Nizamani, M. M., Tarafder, E., Zhang, H.-L., Zhang, Q., Acharya, K., Sarkar, J., Muhae‐Ud‐Din, G., & Wang, Y. (2026) · IMA Fungus · doi:10.3897/imafungus.17.171995 · Cited by 4 · see citing works

Antibiofilm activity of truncated Staphylococcus aureus phenol soluble modulin α2 (SaΔ1Δ2PSMα2) against Candida auris in vitro and in an animal model of catheter-associated infection

Kumari, A., Sharma, A., Kumari, L., Pawar, S. V., & Singh, R. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.106943 · Cited by 3 · see citing works

Revisiting threats associated with neglected and emerging fungal pathogens in sub-Saharan Africa

Akinola, S. A., Adeyemo, R. O., Bale, M. I., Eilu, E., Afodun, A. M., Akinola, R. A. A., Binuyo, M. O., Odoma, S., Suleiman, I. E., Adegboyega, T. T., et al. (2024) · Discover Public Health · doi:10.1186/s12982-024-00318-3 · Cited by 3 · see citing works

Guaiazulene and aureusidin inhibit metabolic adaptability and virulence in Candida albicans by targeting the glyoxylate cycle under alternative carbon conditions

Shastry, R. P., Ghate, S. D., Rao, R. S. P., Giri, J. P., Mallik, S., & Zhao, Z. (2024) · Green Chemistry Letters and Reviews · doi:10.1080/17518253.2024.2438073 · Cited by 3 · see citing works

Antifungal efficacy of pyrolysis-derived bio-oil aqueous phases from Tropical plant biomass against Candida auris

Cintra, D. S., Alcântara, L. M., Nardy, K. A., Valente, M. R., de Oliveira, P. C. O., Peixoto, B. S., Veloso, M. C. D. C., Romeiro, G. A., Zamith‐Miranda, D., Nosanchuk, J. D., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-17626-6 · Cited by 3 · see citing works

Omics and Multiomics-Based Diagnostics for Invasive Candidiasis: Toward Precision Medicine

Pitarch, A., Arribas, V., & Gil, C. (2025) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2025.101463 · Cited by 2 · see citing works

Fungal Sphingolipids: Biosynthesis Pathways, Structural Features and Biological Functions

Xue, Z., Wang, L., & Du, C. (2026) · Journal of Fungi · doi:10.3390/jof12020113 · Cited by 2 · see citing works

2-ethyl-1-hexanol: a promising molecule against priority fungal pathogens

Marcomini, E. K., Rezende, P. S. T., Gomes, J., Leite, C. R., de Oliveira, K. M. P., Pomini, A. M., Svidzinski, T. I. E., & Negri, M. (2025) · Journal of Applied Microbiology · doi:10.1093/jambio/lxaf165 · Cited by 1 · see citing works

Candida auris: a multidimensional focus on its identification, epidemiology, pathogenesis, and therapeutic options

Negi, P., Verma, N., Rishi, P., Multani, K., Sharma, M., Kumari, S., & Raj, K. (2026) · Archives of Microbiology · doi:10.1007/s00203-026-04864-z · Cited by 1 · see citing works

Unraveling clade-specific differences in Candida auris: evolution, adaptation, and pathogenicity

Sharma, P., Bari, V. K., & Pasrija, R. (2026) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-026-05569-3 · Cited by 1 · see citing works

A Culture Supernatant from an Actinomycete sp. Affects Biofilm Formation and Virulence Expression of Candida auris

Yamane, K., Niki, M., Tsubouchi, T., Watanabe, T., Asai, K., Oinuma, K.-I., Sakiyama, A., Saren, C., Matsumoto, Y., Makimura, K., et al. (2023) · Medical Mycology Journal · doi:10.3314/mmj.22-00026 · Cited by 1 · see citing works

Genomic Innovation and Virulence Evolution in the Emerging Human Fungal Pathogen Candida auris

Gifford, H., Rhodes, J. L., Wilson, D., & Farrer, R. A. (2024) · The mycota · doi:10.1007/978-3-031-75666-5_10 · Cited by 2 · see citing works

Genomic landscape of the DHA1 family in the newly emerged pathogen Candida auris and mapping substrate repertoire of the prominent member Cau Mdr1Preprint

Khatoon, R., Sharma, S., Vishwakarma, P., Saini, A., Aggarwal, P., Lynn, A. M., Prakash, A., Prasad, R., & Banerjee, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.09.483563

Faculty Opinions recommendation of Multiple Alternative Carbon Pathways Combine To Promote Candida albicans Stress Resistance, Immune Interactions, and Virulence.

Hube, B., & Brunke, S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737216998.793573821

Niclosamide loaded Eudragit EPO nanoparticles show enhanced Candida biofilm penetration, trigger biofilm detachment and protect from mucosal candidiasisPreprint

Sutar, Y. B., Nabeela, S., Singh, S., Alqarihi, A., Solis, N. V., Ghebremariam, T., Filler, S. G., Ibrahim, A. S., Date, A. A., & Uppuluri, P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.02.494588

Identificação de metabólitos secundários presentes em vesículas extracelulares de Candida albicans durante estresse oxidativo

Trentin, G. (2022) · doi:10.11606/d.17.2022.tde-20062022-161952

Identificação fenotípica e proteômica da micobiota oral de cães sensibilidade a antifúngicos e virulência

Bonci, M. M. (2022) · doi:10.11606/t.23.2022.tde-31012023-095553

Identification and classification of microorganisms based on their fatty acid profiles

Huỳnh, T. (2023) · doi:10.14232/phd.11336

Geoenvironmental variables as causal cofactors of diseases of unknown etiology

Davies, T. C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-818748-7.00013-7

Tüm Yönleriyle Candida Auris

Erganiş, S., Şahin, E. A., Öztürk, A., Yıldız, P. A., Şahin, C., Top, Ö. Ö., & Tunçcan, Ö. G. (2024) · Akademisyen Kitabevi eBooks · doi:10.37609/akya.3202

Yeast Lipids: Emerging Key Players in Antifungal Resistance and Pathogenesis

Ali, B., Laitthma, D. T., Singh, A. K., & Prasad, R. (2025) · Current Clinical Microbiology Reports · doi:10.1007/s40588-025-00261-0

Comprehensive Insights into Sugar Transporters of Candidozyma auris and Their Roles in Antifungal Resistance

Kumar, P., Kumar, M., Saini, A., Mohamad, S. O., Ali, B., Esquivel, B. D., Banerjee, A., White, T. C., Gaur, N. A., Shah, A. H., et al. (2026) · Journal of Fungi · doi:10.3390/jof12020094

Fatty Acid Profiling Identification Method of Emerging Fungal Pathogen Candidozyma auris (Formally Candida auris)

Huỳnh, T., Bohner, F., Turbat, A., Sipos, G., Gácser, A., Vágvölgyi, C., Papp, T., Varga, M., & Szekeres, A. (2026) · Journal of Fungi · doi:10.3390/jof12020130

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Ramos‐Pardo, A., Quindós, G., Eraso, E., Sevillano, E., & Kaberdin, V. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.14.718400

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Liu, L. L., Niu, T., Zhang, T., Tan, D., Duan, X., & Li, X. (2026) · Microbiological Research · doi:10.1016/j.micres.2026.128542

Comparative Transcriptomic and Lipidomic Analysis of Amphotericin B-Susceptible and Resistant Clinical Isolates of Malassezia spp

Marín, J. C. G., Tabares-Villa, F. A., Zuluaga‐Vélez, A., Rojas-Estévez, P., Cala, M. P., Celis-Ramírez, A. M., & Arias, J. C. (2026) · ACS Omega · doi:10.1021/acsomega.6c09344

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

Newly Emerging Candida Specie: Should Clinicians and Mycologist be Concerned?

Ashcroft, O. F., Kumurya, A. S., Mohammed, K., Iduh, M. U., Yusuf, A. A., Bunza, N. M., & Nataala, S. U. (2019) · Asian Journal of Research in Infectious Diseases · doi:10.9734/ajrid/2019/v2i430109

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

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Brandt, P., Mirhakkak, M. H., Wagner, L., Driesch, D., Möslinger, A., Fänder, P., Schäuble, S., Panagiotou, G., & Vylkova, S. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.00498-23 · Cited by 34 · see citing works