Genome plasticity in Candida albicans: A cutting-edge strategy for evolution, adaptation, and survival

The Gene Ontology Resource: 20 years and still GOing strong

The Gene Ontology Consortium (2019) · Nucleic Acids Research · doi:10.1093/nar/gky1055 · Cited by 4,747 · see citing works

Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem

Pfaller, M. A., & Diekema, D. J. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00029-06 · Cited by 4,174 · see citing works

Global and Multi-National Prevalence of Fungal Diseases-Estimate Precision

Bongomin, F., Gago, S., Oladele, R., & Denning, D. (2017) · Journal of Fungi · doi:10.3390/jof3040057 · Cited by 2,953 · see citing works

<i>Candida albicans</i> pathogenicity mechanisms

Mayer, F. L., Wilson, D., & Hube, B. (2013) · Virulence · doi:10.4161/viru.22913 · Cited by 1,848 · see citing works

INVITED REVIEW: What is a population? An empirical evaluation of some genetic methods for identifying the number of gene pools and their degree of connectivity

Waples, R. S., & Gaggiotti, O. E. (2006) · Molecular Ecology · doi:10.1111/j.1365-294x.2006.02890.x · Cited by 1,507 · see citing works

The Evolutionary Consequences of Polyploidy

Otto, S. P. (2007) · Cell · doi:10.1016/j.cell.2007.10.022 · Cited by 1,188 · see citing works

Candida species: current epidemiology, pathogenicity, biofilm formation, natural antifungal products and new therapeutic options

Sardi, J. C. O., Scorzoni, L., Bernardi, T., Fusco-Almeida, A. M., & Mendes Giannini, M. J. S. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.045054-0 · Cited by 1,184 · see citing works

Characterization of the oral fungal microbiome (mycobiome) in healthy individuals

Ghannoum, M. A., Jurevic, R. J., Mukherjee, P. K., Cui, F., Sikaroodi, M., Naqvi, A., & Gillevet, P. M. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000713 · Cited by 1,150 · 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

The gut mycobiome of the Human Microbiome Project healthy cohort

Nash, A. K., Auchtung, T. A., Wong, M. C., Smith, D. P., Gesell, J. R., Ross, M. C., Stewart, C. J., Metcalf, G., Muzny, D. M., Gibbs, R. A., et al. (2017) · Microbiome · doi:10.1186/s40168-017-0373-4 · Cited by 987 · see citing works

The diploid genome sequence of Candida albicans

Jones, T., Federspiel, N. A., Chibana, H., Dungan, J. M., Kalman, S., Magee, B. B., Newport, G., Thorstenson, Y. R., Agabian, N. M., Magee, P. T., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401648101 · Cited by 768 · see citing works

Aneuploidy and Isochromosome Formation in Drug-Resistant <i>Candida albicans</i>

Selmecki, A., Forche, A., & Berman, J. (2006) · Science · doi:10.1126/science.1128242 · Cited by 733 · see citing works

Global trends in the distribution of Candida species causing candidemia

Guinea, J. (2014) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12539 · Cited by 680 · see citing works

Ploidy Regulation of Gene Expression

Galitski, T., Saldanha, A. J., Styles, C. A., Lander, E. S., & Fink, G. R. (1999) · Science · doi:10.1126/science.285.5425.251 · Cited by 633 · see citing works

The Population Genetics of Clonal and Partially Clonal Diploids

Balloux, F., Lehmann, L., & Meeûs, T. D. (2003) · Genetics · doi:10.1093/genetics/164.4.1635 · Cited by 586 · see citing works

Aneuploidy confers quantitative proteome changes and phenotypic variation in budding yeast

Pavelka, N., Rancati, G., Zhu, J., Bradford, W. D., Saraf, A., Florens, L., Sanderson, B. W., Hattem, G. L., & Li, R. (2010) · Nature · doi:10.1038/nature09529 · Cited by 577 · see citing works

White-Opaque Switching in Candida albicans Is Controlled by Mating-Type Locus Homeodomain Proteins and Allows Efficient Mating

Miller, M. G., & Johnson, A. D. (2002) · Cell · doi:10.1016/s0092-8674(02)00837-1 · Cited by 569 · see citing works

Characteristic genome rearrangements in experimental evolution of <i>Saccharomyces</i> <i>cerevisiae</i>

Dunham, M. J., Badrane, H., Ferea, T., Adams, J., Brown, P. O., Rosenzweig, F., & Botstein, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242624799 · Cited by 564 · see citing works

The repertoire and dynamics of evolutionary adaptations to controlled nutrient-limited environments in yeast

Gresham, D., Desai, M. M., Tucker, C. M., Jenq, H. T., Pai, D. A., Ward, A., DeSevo, C. G., Botstein, D., & Dunham, M. J. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000303 · Cited by 482 · see citing works

Evidence for Mating of the "Asexual" Yeast Candida albicans in a Mammalian Host

Hull, C. M., Raisner, R. M., & Johnson, A. D. (2000) · Science · doi:10.1126/science.289.5477.307 · Cited by 464 · see citing works

Mechanism and Regulation of Meiotic Recombination InitiationPreprint

Lam, I., & Keeney, S. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016634 · Cited by 457 · see citing works

Induction of Mating in Candida albicans by Construction of MTL a and MTL α Strains

Magee, B. B., & Magee, P. T. (2000) · Science · doi:10.1126/science.289.5477.310 · Cited by 443 · see citing works

Sex speeds adaptation by altering the dynamics of molecular evolution

McDonald, M. J., Rice, D. P., & Desai, M. M. (2016) · Nature · doi:10.1038/nature17143 · Cited by 425 · see citing works

Precise estimates of mutation rate and spectrum in yeast

Zhu, Y. O., Siegal, M. L., Hall, D. W., & Petrov, D. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323011111 · Cited by 421 · see citing works

Aneuploidy: Cells Losing Their Balance

Torres, E. M., Williams, B. R., & Amon, A. (2008) · Genetics · doi:10.1534/genetics.108.090878 · Cited by 409 · see citing works

A Mutation in Tac1p, a Transcription Factor Regulating <i>CDR1</i> and <i>CDR2</i> , Is Coupled With Loss of Heterozygosity at Chromosome 5 to Mediate Antifungal Resistance in <i>Candida albicans</i>

Coste, A., Turner, V., Ischer, F., Morschhäuser, J., Forche, A., Selmecki, A., Berman, J., Bille, J., & Sanglard, D. (2006) · Genetics · doi:10.1534/genetics.105.054767 · Cited by 385 · see citing works

Role of the Hog1 Stress-activated Protein Kinase in the Global Transcriptional Response to Stress in the Fungal Pathogen<i>Candida albicans</i>

Enjalbert, B., Smith, D. A., Cornell, M. J., Alam, I., Nicholls, S., Brown, A. J. P., & Quinn, J. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-06-0501 · Cited by 381 · see citing works

Identification of a Mating Type-Like Locus in the Asexual Pathogenic Yeast Candida albicans

Hull, C. M., & Johnson, A. D. (1999) · Science · doi:10.1126/science.285.5431.1271 · Cited by 363 · see citing works

Genome-wide genetic analysis of polyploidy in yeast

Štorchová, Z., Breneman, A., Cande, J., Dunn, J. G., Burbank, K. S., O'Toole, E. T., & Pellman, D. S. (2006) · Nature · doi:10.1038/nature05178 · Cited by 360 · see citing works

The evolution of drug resistance in clinical isolates of Candida albicans.

Ford, C. B., Funt, J. M., Abbey, D., Issi, L., Guiducci, C., Martinez, D. A., Delorey, T., Li, B. Y., White, T. C., Cuomo, C., et al. (2015) · eLife · doi:10.7554/elife.00662 · Cited by 348 · see citing works

Completion of a parasexual cycle in Candida albicans by induced chromosome loss in tetraploid strains

Bennett, R. J., & Johnson, A. D. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg235 · Cited by 343 · see citing works

A Human-Curated Annotation of the Candida albicans Genome

Braun, B. R., van het Hoog, M., d'Enfert, C., Martchenko, M., Dungan, J., Kuo, A., Inglis, D. O., Uhl, M. A., Hogues, H., Berriman, M., et al. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010001 · Cited by 342 · see citing works

The Parasexual Cycle in Candida albicans Provides an Alternative Pathway to Meiosis for the Formation of Recombinant Strains

Forche, A., Alby, K., Schaefer, D., Johnson, A. D., Berman, J., & Bennett, R. J. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060110 · Cited by 338 · see citing works

Aneuploidy Underlies Rapid Adaptive Evolution of Yeast Cells Deprived of a Conserved Cytokinesis Motor

Rancati, G. I., Pavelka, N., Fleharty, B., Noll, A. C., Trimble, R., Walton, K., Perera, A. G., Staehling‐Hampton, K., Seidel, C. W., & Li, R. (2008) · Cell · doi:10.1016/j.cell.2008.09.039 · Cited by 335 · see citing works

Contrasting evolutionary genome dynamics between domesticated and wild yeasts

Yue, J., Li, J., Aigrain, L., Hallin, J., Persson, K. O., Oliver, K. L., Bergström, A., Coupland, P. G., Warringer, J., Lagomarsino, M. C., et al. (2017) · Nature Genetics · doi:10.1038/ng.3847 · Cited by 332 · 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

Genetic and phenotypic intra-species variation in <i>Candida albicans</i>

Hirakawa, M. P., Martinez, D. A., Sakthikumar, S., Anderson, M. Z., Berlin, A., Gujja, S., Zeng, Q., Zisson, E., Wang, J. M., Greenberg, J. M., et al. (2015) · Genome Research · doi:10.1101/gr.174623.114 · Cited by 320 · see citing works

Acquisition of Aneuploidy Provides Increased Fitness during the Evolution of Antifungal Drug Resistance

Selmecki, A. M., Dulmage, K., Cowen, L. E., Anderson, J. B., & Berman, J. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000705 · Cited by 319 · see citing works

The many costs of sex

Lehtonen, J., Jennions, M. D., & Kokko, H. (2011) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2011.09.016 · Cited by 312 · see citing works

Molecular Phylogenetics of Candida albicans

Odds, F. C., Bougnoux, M., Shaw, D. J., Bain, J. M., Davidson, A. D., Diogo, D., Jacobsen, M. D., Lecomte, M., Li, S.-Y., Tavanti, A., et al. (2007) · Eukaryotic Cell · doi:10.1128/ec.00041-07 · Cited by 306 · see citing works

Passage through the mammalian gut triggers a phenotypic switch that promotes Candida albicans commensalism

Pande, K., Chen, C., & Noble, S. M. (2013) · Nature Genetics · doi:10.1038/ng.2710 · Cited by 306 · see citing works

Bistable expression of WOR1 , a master regulator of white–opaque switching in Candida albicans

Huang, G., Wang, H., Chou, S., Nie, X., Chen, J., & Liu, H. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605270103 · Cited by 293 · see citing works

The ‘obligate diploid’ Candida albicans forms mating-competent haploids

Hickman, M. A., Zeng, G., Forche, A., Hirakawa, M. P., Abbey, D., Harrison, B. D., Wang, Y.-M., Su, C.-H., Bennett, R. J., Wang, Y., et al. (2013) · Nature · doi:10.1038/nature11865 · Cited by 284 · see citing works

Mutations in the multi‐drug resistance regulator <i>MRR1</i> , followed by loss of heterozygosity, are the main cause of <i>MDR1</i> overexpression in fluconazole‐resistant <i>Candida albicans</i> strains

Dunkel, N., Blaß, J., Rogers, P. D., & Morschhäuser, J. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06309.x · Cited by 278 · see citing works

Stress-induced Gene Expression inCandida albicans: Absence of a General Stress Response

Enjalbert, B., Nantel, A., & Whiteway, M. S. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-08-0546 · Cited by 277 · see citing works

Hsp90 stress potentiates rapid cellular adaptation through induction of aneuploidy

Chen, G., Bradford, W. D., Seidel, C. W., & Li, R. (2012) · Nature · doi:10.1038/nature10795 · Cited by 274 · see citing works

Characterization of the Vaginal Micro- and Mycobiome in Asymptomatic Reproductive-Age Estonian Women

Drell, T., Lillsaar, T., Tummeleht, L., Simm, J., Aaspõllu, A., Väin, E., Saarma, I., Salumets, A., Donders, G. G. G., & METSIS, M. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054379 · Cited by 262 · see citing works

Genomic Plasticity of the Human Fungal Pathogen Candida albicans

Selmecki, A., Forche, A., & Berman, J. (2010) · Eukaryotic Cell · doi:10.1128/ec.00060-10 · Cited by 247 · see citing works

Experimental evolution of a fungal pathogen into a gut symbiont

Tso, G. H. W., Reales‐Calderón, J. A., Tan, A. S. M., Sem, X., Le, G. T. T., Tan, T. G., Lai, G. C., Srinivasan, K. G., Yurieva, M., Liao, W. W. P., et al. (2018) · Science · doi:10.1126/science.aat0537 · Cited by 241 · see citing works

Candida albicans Morphogenesis Programs Control the Balance between Gut Commensalism and Invasive Infection

Witchley, J. N., Penumetcha, P., Abon, N. V., Woolford, C. A., Mitchell, A. P., & Noble, S. M. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.02.008 · Cited by 238 · see citing works

In Candida albicans, White-Opaque Switchers Are Homozygous for Mating Type

Lockhart, S. R., Pujol, C., Daniels, K. J., Miller, M. G., Johnson, A. D., Pfaller, M. A., & Soll, D. R. (2002) · Genetics · doi:10.1093/genetics/162.2.737 · Cited by 235 · see citing works

Stress Alters Rates and Types of Loss of Heterozygosity in Candida albicans

Forche, A., Abbey, D., Pisithkul, T., Weinzierl, M. A., Ringstrom, T., Bruck, D., Petersen, K., & Berman, J. (2011) · mBio · doi:10.1128/mbio.00129-11 · Cited by 234 · see citing works

Molecular markers reveal that population structure of the human pathogen Candida albicans exhibits both clonality and recombination.

Gräser, Y., Volovsek, M., Arrington, J., Schönian, G., Presber, W., Mitchell, T. G., & Vilgalys, R. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.22.12473 · Cited by 222 · see citing works

Homothallic and heterothallic mating in the opportunistic pathogen Candida albicans

Alby, K., Schaefer, D., & Bennett, R. J. (2009) · Nature · doi:10.1038/nature08252 · Cited by 218 · see citing works

The Flo8 Transcription Factor Is Essential for Hyphal Development and Virulence in Candida albicans

Cao, F., Lane, S., Raniga, P. P., Lü, Y., Zhou, Z., Ramon, K., Chen, J., & Liu, H. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-06-0502 · Cited by 207 · see citing works

Monosomy of a specific chromosome determines l -sorbose utilization: A novel regulatory mechanism in Candida albicans

Janbon, G., Sherman, F., & Rustchenko, E. P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.9.5150 · Cited by 202 · see citing works

Gene flow contributes to diversification of the major fungal pathogen Candida albicans

Ropars, J., Maufrais, C., Diogo, D., Marcet-Houben, M., Perin, A., Sertour, N., Mosca, K., Permal, E., Laval, G., Bouchier, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04787-4 · Cited by 197 · see citing works

CO2 Regulates White-to-Opaque Switching in Candida albicans

Huang, G., Srikantha, T., Sahni, N., Song, Y., & Soll, D. R. (2009) · Current Biology · doi:10.1016/j.cub.2009.01.018 · Cited by 180 · see citing works

Parent–progeny sequencing indicates higher mutation rates in heterozygotes

Yang, S., Wang, L., Huang, J. W., Zhang, X., Yuan, Y., Chen, J., Hurst, L. D., & Tian, D. (2015) · Nature · doi:10.1038/nature14649 · Cited by 179 · see citing works

Population Structure and Properties of Candida albicans , as Determined by Multilocus Sequence Typing

Tavanti, A., Davidson, A. D., Fordyce, M. J., Gow, N. A. R., Maiden, M. C. J., & Odds, F. C. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.11.5601-5613.2005 · Cited by 176 · see citing works

A Tetraploid Intermediate Precedes Aneuploid Formation in Yeasts Exposed to Fluconazole

Harrison, B. D., Hashemi, J., Bibi, M., Pulver, R., Bavli, D., Nahmias, Y., Wellington, M., Sapiro, G., & Berman, J. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001815 · Cited by 174 · see citing works

The Evolution of Sex Is Favoured During Adaptation to New Environments

Becks, L., & Agrawal, A. F. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001317 · Cited by 174 · see citing works

Cell biology of Candida albicans–host interactions

Dantas, A. D. S., Lee, K. K., Raziunaite, I., Schaefer, K., Wagener, J., Yadav, B., & Gow, N. A. R. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2016.08.006 · Cited by 170 · see citing works

Discovery of a “White-Gray-Opaque” Tristable Phenotypic Switching System in Candida albicans: Roles of Non-genetic Diversity in Host Adaptation

Li, T., Du, H., Guan, G., Dai, Y., Nobile, C. J., Liang, W., Cao, C., Zhang, Q., Zhong, J., & Huang, G. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001830 · Cited by 159 · see citing works

Multilocus Sequence Typing Reveals Intrafamilial Transmission and Microevolutions of Candida albicans Isolates from the Human Digestive Tract

Bougnoux, M., Diogo, D., François, N., Sendid, B., Veirmeire, S., Colombel, J., Bouchier, C., Kruiningen, H. J. V., d’Enfert, C., & Poulain, D. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.44.5.1810-1820.2006 · Cited by 158 · see citing works

The genome-wide rate and spectrum of spontaneous mutations differ between haploid and diploid yeast

Sharp, N. P., Sandell, L., James, C. G., & Otto, S. P. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1801040115 · Cited by 157 · see citing works

Global analysis of mutations driving microevolution of a heterozygous diploid fungal pathogen

Ene, I. V., Farrer, R. A., Hirakawa, M. P., Agwamba, K., Cuomo, C. A., & Bennett, R. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1806002115 · Cited by 155 · see citing works

Evolution of Eukaryotic Microbial Pathogens via Covert Sexual Reproduction

Heitman, J. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.06.011 · Cited by 155 · see citing works

Unisexual and Heterosexual Meiotic Reproduction Generate Aneuploidy and Phenotypic Diversity De Novo in the Yeast Cryptococcus neoformans

Ni, M., Feretzaki, M., Li, W., Averette, A. F., Mieczkowski, P. A., Dietrich, F. S., & Heitman, J. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001653 · Cited by 155 · see citing works

Environmental Induction of White–Opaque Switching in Candida albicans

Ramı́rez-Zavala, B., Reuß, O., Park, Y.-N., Ohlsen, K., & Morschhäuser, J. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000089 · Cited by 154 · see citing works

DNA content, kinetic complexity, and the ploidy question in Candida albicans.

Riggsby, W. S., Torres-Bauzá, L. J., Wills, J. W., & Townes, T. M. (1982) · Molecular and Cellular Biology · doi:10.1128/mcb.2.7.853 · Cited by 152 · see citing works

Property Differences among the Four Major Candida albicans Strain Clades

MacCallum, D. M., Castillo, L., Nather, K., Munro, C. A., Brown, A. J. P., Gow, N. A. R., & Odds, F. C. (2009) · Eukaryotic Cell · doi:10.1128/ec.00387-08 · Cited by 150 · see citing works

Evolution in<i>Candida albicans</i>Populations During a Single Passage Through a Mouse Host

Forche, A., Magee, P. T., Selmecki, A., Berman, J., & May, G. (2009) · Genetics · doi:10.1534/genetics.109.103325 · Cited by 147 · see citing works

YMAP: a pipeline for visualization of copy number variation and loss of heterozygosity in eukaryotic pathogens

Abbey, D. A., Funt, J., Lurie-Weinberger, M. N., Thompson, D. A., Regev, A., Myers, C. L., & Berman, J. (2014) · Genome Medicine · doi:10.1186/s13073-014-0100-8 · Cited by 147 · see citing works

Gene Essentiality Is a Quantitative Property Linked to Cellular Evolvability

Liu, G., Yong, M. Y. J., Yurieva, M., Srinivasan, K. G., Liu, J., Lim, J. S. Y., Poidinger, M., Wright, G. D., Zolezzi, F., Choi, H., et al. (2015) · Cell · doi:10.1016/j.cell.2015.10.069 · Cited by 145 · see citing works

Development of Fluconazole Resistance in<i>Candida albicans</i>Causing Disseminated Infection in a Patient Undergoing Marrow Transplantation

Marr, K. A., White, T. C., van Burik, J. H., & Bowden, R. A. (1997) · Clinical Infectious Diseases · doi:10.1086/515553 · Cited by 145 · see citing works

Mechanism of Candida pathogenesis: Revisiting the vital drivers

Mba, I. E., & Nweze, E. I. (2020) · European Journal of Clinical Microbiology &amp; Infectious Diseases · doi:10.1007/s10096-020-03912-w · Cited by 143 · see citing works

Msn2- and Msn4-Like Transcription Factors Play No Obvious Roles in the Stress Responses of the Fungal Pathogen Candida albicans

Nicholls, S., Straffon, M. J., Enjalbert, B., Nantel, A., Macaskill, S., Whiteway, M. S., & Brown, A. J. P. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1111-1123.2004 · Cited by 140 · see citing works

Expandable and reversible copy number amplification drives rapid adaptation to antifungal drugs

Todd, R. T., & Selmecki, A. (2020) · eLife · doi:10.7554/elife.58349 · Cited by 138 · see citing works

Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness

Tye, B., Commins, N., Ryazanova, L. V., Wühr, M., Springer, M., Pincus, D., & Churchman, L. S. (2019) · eLife · doi:10.7554/elife.43002 · Cited by 134 · see citing works

The intraspecies diversity of C. albicans triggers qualitatively and temporally distinct host responses that determine the balance between commensalism and pathogenicity

Schönherr, F. A., Sparber, F., Kirchner, F. R., Guiducci, E., Trautwein-Weidner, K., Gladiator, A., Sertour, N., Hetzel, U., Le, G. T. T., Pavelka, N., et al. (2017) · Mucosal Immunology · doi:10.1038/mi.2017.2 · Cited by 133 · see citing works

Variations of Candida albicans electrophoretic karyotypes

Rustchenko-Bulgac, E. P. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.20.6586-6596.1991 · Cited by 132 · see citing works

Ploidy and the Causes of Genomic Evolution

Gerstein, A. C., & Otto, S. P. (2009) · Journal of Heredity · doi:10.1093/jhered/esp057 · Cited by 131 · see citing works

Dosage compensation can buffer copy-number variation in wild yeast

Hose, J., Yong, C. M., Sardi, M. I., Wang, Z., Newton, M. A., & Gasch, A. P. (2015) · eLife · doi:10.7554/elife.05462 · Cited by 131 · see citing works

White-Opaque Switching in Natural MTLa/α Isolates of Candida albicans: Evolutionary Implications for Roles in Host Adaptation, Pathogenesis, and Sex

Xie, J., Li, T., Nobile, C. J., Tong, Y., Guan, G., Sun, Y., Cao, C., Hernday, A. D., Johnson, A. D., Zhang, L., et al. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001525 · Cited by 128 · see citing works

Assembly of a phased diploid Candida albicansgenome facilitates allele-specific measurements and provides a simple model for repeat and indel structure

Muzzey, D., Schwartz, K., Weissman, J. S., & Sherlock, G. (2013) · Genome biology · doi:10.1186/gb-2013-14-9-r97 · Cited by 123 · see citing works

Environmental change drives accelerated adaptation through stimulated copy number variation

Hull, R. M., Cruz, C., Jack, C. V., & Houseley, J. M. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2001333 · Cited by 123 · see citing works

Variation in Candida albicans EFG1 Expression Enables Host-Dependent Changes in Colonizing Fungal Populations

Pierce, J. V., & Kumamoto, C. A. (2012) · mBio · doi:10.1128/mbio.00117-12 · Cited by 122 · see citing works

Single-cell copy number variant detection reveals the dynamics and diversity of adaptation

Lauer, S. L., Avecilla, G., Spealman, P., Sethia, G., Brandt, N. J., Levy, S. F., & Gresham, D. (2018) · PLoS Biology · doi:10.1371/journal.pbio.3000069 · Cited by 121 · 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

Sex and Virulence of Human Pathogenic Fungi

Nielsen, K., & Heitman, J. (2007) · Advances in genetics · doi:10.1016/s0065-2660(06)57004-x · Cited by 119 · see citing works

Stress-Induced Phenotypic Switching in Candida albicans

Alby, K., & Bennett, R. J. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-01-0040 · Cited by 119 · see citing works

Rapid Mechanisms for Generating Genome Diversity: Whole Ploidy Shifts, Aneuploidy, and Loss of Heterozygosity

Bennett, R. J., Forche, A., & Berman, J. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019604 · Cited by 118 · see citing works

The development of fluconazole resistance in Candida albicans – an example of microevolution of a fungal pathogen

Morschhäuser, J. (2016) · Journal of Microbiology · doi:10.1007/s12275-016-5628-4 · Cited by 118 · see citing works

Genome plasticity in Candida albicans is driven by long repeat sequences

Todd, R. T., Wikoff, T. D., Forche, A., & Selmecki, A. (2019) · eLife · doi:10.7554/elife.45954 · Cited by 118 · see citing works

Chromosome instability in Candida albicans

Rustchenko, E. P. (2006) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2006.00150.x · Cited by 117 · see citing works

Control of Transcription by Cell Size

Wu, C., Rolfe, A., Gifford, D. K., & Fink, G. R. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000523 · Cited by 117 · see citing works

Evidence from comparative genomics for a complete sexual cycle in the 'asexual' pathogenic yeast Candida glabrata

Wong, S., Fares, M. A., Zimmermann, W., Butler, G., & Wolfe, K. H. (2003) · Genome biology · doi:10.1186/gb-2003-4-2-r10 · Cited by 113 · see citing works

Parasexual Ploidy Reduction Drives Population Heterogeneity Through Random and Transient Aneuploidy in <i>Candida albicans</i>

Hickman, M. A., Paulson, C., Dudley, A., & Berman, J. (2015) · Genetics · doi:10.1534/genetics.115.178020 · Cited by 113 · see citing works

Chromosomal alterations of Candida albicans are associated with the gain and loss of assimilating functions

Rustchenko, E. P., Howard, D. H., & Sherman, F. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.11.3231-3241.1994 · Cited by 111 · see citing works

Aneuploidy in yeast: Segregation error or adaptation mechanism?

Gilchrist, C., & Stelkens, R. B. (2019) · Yeast · doi:10.1002/yea.3427 · Cited by 110 · see citing works

Homozygosity at the <i>MTL</i> locus in clinical strains of <i>Candida albicans</i>: karyotypic rearrangements and tetraploid formation^†

Legrand, M., Lephart, P., Forche, A., Mueller, F. C., Walsh, T., Magee, P. T., & Magee, B. B. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04068.x · Cited by 110 · see citing works

The Role of Copper Homeostasis at the Host-Pathogen Axis: From Bacteria to Fungi

Li, C., Li, Y., & Ding, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20010175 · Cited by 107 · see citing works

Heterozygosity of genes on the sex chromosome regulates Candida albicans virulence

Wu, W., Lockhart, S. R., Pujol, C., Srikantha, T., & Soll, D. R. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05759.x · Cited by 104 · see citing works

Aneuploidy Enables Cross-Adaptation to Unrelated Drugs

Yang, F., Teoh, F., Tan, A. S. M., Cao, Y., Pavelka, N., & Berman, J. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz104 · Cited by 101 · see citing works

Ploidy determination of Canadida albicans

Olaiya, A. F., & Sogin, S. J. (1979) · Journal of Bacteriology · doi:10.1128/jb.140.3.1043-1049.1979 · Cited by 98 · see citing works

Candida africana sp. nov., a new human pathogen or a variant of Candida albicans?

Tietz, H., Hopp, M., Schmalreck, A., Sterry, W., & Czaika, V. A. (2001) · Mycoses · doi:10.1046/j.1439-0507.2001.00707.x · Cited by 96 · see citing works

Ancient Evolutionary Trade-Offs between Yeast Ploidy States

Zörgö, E., Chwiałkowska, K., Gjuvsland, A. B., Garré, E., Sunnerhagen, P., Liti, G., Blomberg, A., Omholt, S. W., & Warringer, J. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003388 · Cited by 95 · see citing works

Infrequent Genetic Exchange and Recombination in the Mitochondrial Genome of Candida albicans

Anderson, J. B., Wickens, C., Khan, M., Cowen, L. E., Federspiel, N. A., Jones, T., & Kohn, L. M. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.3.865-872.2001 · Cited by 95 · see citing works

The yeast form of the fungus Candida albicans promotes persistence in the gut of gnotobiotic mice

Böhm, L., Torsin, S., Tint, S. H., Eckstein, M., Ludwig, T., & Pérez, J. C. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006699 · Cited by 95 · see citing works

The Early days of yeast genetics

Hall, M., & Linder, P. (1993) · Choice Reviews Online · doi:10.5860/choice.31-6029 · Cited by 95 · see citing works

Rapid Phenotypic and Genotypic Diversification After Exposure to the Oral Host Niche in <i>Candida albicans</i>

Forche, A., Cromie, G., Gerstein, A. C., Solis, N. V., Pisithkul, T., Srifa, W., Jeffery, E., Abbey, D., Filler, S. G., Dudley, A. M., et al. (2018) · Genetics · doi:10.1534/genetics.118.301019 · Cited by 94 · see citing works

The Fitness Consequences of Aneuploidy Are Driven by Condition-Dependent Gene Effects

Sunshine, A. B., Payen, C., Ong, G. T., Liachko, I., Tan, K. M., & Dunham, M. J. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002155 · Cited by 93 · see citing works

The stepwise acquisition of fluconazole resistance mutations causes a gradual loss of fitness in <i><scp>C</scp>andida albicans</i>

Sasse, C., Dunkel, N., Schäfer, T., Schneider, S., Dierolf, F., Ohlsen, K., & Morschhäuser, J. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08210.x · Cited by 93 · see citing works

Ca3 Fingerprinting of Candida albicans Isolates from Human Immunodeficiency Virus-Positive and Healthy Individuals Reveals a New Clade in South Africa

Blignaut, E., Pujol, C., Lockhart, S. R., Joly, S., & Soll, D. R. (2002) · Journal of Clinical Microbiology · doi:10.1128/jcm.40.3.826-836.2002 · Cited by 92 · see citing works

Global Analysis of the Fungal Microbiome in Cystic Fibrosis Patients Reveals Loss of Function of the Transcriptional Repressor Nrg1 as a Mechanism of Pathogen Adaptation

Kim, S. H., Clark, S. T., Surendra, A., Copeland, J. K., Wang, P. W., Ammar, R., Collins, C., Tullis, D. E., Nislow, C., Hwang, D. M., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005308 · Cited by 90 · see citing works

Hemizygosity Enables a Mutational Transition Governing Fungal Virulence and Commensalism

Liang, S.-H., Anderson, M. Z., Hirakawa, M. P., Wang, J. M., Frazer, C., Alaalm, L., Thomson, G. J., Ene, I. V., & Bennett, R. J. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.01.005 · Cited by 87 · see citing works

Aneuploidy underlies a multicellular phenotypic switch

Tan, Z., Hays, M., Cromie, G. A., Jeffery, E. W., Scott, A. C., Ahyong, V., Sirr, A., Skupin, A., & Dudley, A. M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301047110 · Cited by 84 · see citing works

Normal Adaptation of Candida albicans to the Murine Gastrointestinal Tract Requires Efg1p-Dependent Regulation of Metabolic and Host Defense Genes

Pierce, J. V., Dignard, D., Whiteway, M. S., & Kumamoto, C. A. (2012) · Eukaryotic Cell · doi:10.1128/ec.00236-12 · Cited by 84 · see citing works

Chromosome 1 trisomy compromises the virulence of Candida albicans

Chen, X., Magee, B. B., Dawson, D., Magee, P. T., & Kumamoto, C. A. (2004) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03852.x · Cited by 83 · see citing works

The parasexual lifestyle of Candida albicans

Bennett, R. J. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.06.017 · Cited by 82 · see citing works

Spontaneous Changes in Ploidy Are Common in Yeast

Harari, Y., Ram, Y., Rappoport, N., Hadany, L., & Kupiec, M. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.062 · Cited by 81 · see citing works

Tolerance to Caspofungin in Candida albicans Is Associated with at Least Three Distinctive Mechanisms That Govern Expression of <i>FKS</i> Genes and Cell Wall Remodeling

Yang, F., Zhang, L., Wakabayashi, H., Myers, J., Jiang, Y., Cao, Y., Jimenez-Ortigosa, C., Perlin, D. S., & Rustchenko, E. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00071-17 · Cited by 81 · see citing works

Candida albicansclades

Soll, D. R., & Pujol, C. (2003) · FEMS Immunology & Medical Microbiology · doi:10.1016/s0928-8244(03)00242-6 · Cited by 80 · see citing works

Ploidy plasticity: a rapid and reversible strategy for adaptation to stress

Berman, J. G. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fow020 · Cited by 80 · see citing works

Genetic Structure of Typical and Atypical Populations of Candida albicans from Africa

Forche, A., Schönian, G., Gräser, Y., Vilgalys, R. J., & Mitchell, T. G. (1999) · Fungal Genetics and Biology · doi:10.1006/fgbi.1999.1164 · Cited by 78 · see citing works

Mitotic recombination in Candida albicans: Recessive lethal alleles linked to a gene required for methionine biosynthesis

Whelan, W. L., & Soll, D. R. (1982) · Molecular and General Genetics MGG · doi:10.1007/bf00332632 · Cited by 77 · see citing works

Does stress induce (para)sex? Implications for Candida albicans evolution

Berman, J. G., & Hadany, L. (2012) · Trends in Genetics · doi:10.1016/j.tig.2012.01.004 · Cited by 76 · see citing works

Phenotypic Switching and Mating Type Switching of <i>Candida glabrata</i> at Sites ofColonization

Brockert, P. J., Lachke, S. A., Srikantha, T., Pujol, C., Galask, R., & Soll, D. R. (2003) · Infection and Immunity · doi:10.1128/iai.71.12.7109-7118.2003 · Cited by 75 · see citing works

Variance of ploidy in Candida albicans

Suzuki, T., Nishibayashi, S., Kuroiwa, T., Kanbe, T., & Tanaka, K. (1982) · Journal of Bacteriology · doi:10.1128/jb.152.2.893-896.1982 · Cited by 74 · see citing works

A combinational theory for maintenance of sex

Hörandl, E. (2009) · Heredity · doi:10.1038/hdy.2009.85 · Cited by 74 · see citing works

Ploidy variation as an adaptive mechanism in human pathogenic fungi

Morrow, C. A., & Fraser, J. A. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.01.008 · Cited by 72 · see citing works

DNA translocations contribute to chromosome length polymorphisms in Candida albicans

Thrash-Bingham, C., & Gorman, J. A. (1992) · Current Genetics · doi:10.1007/bf00351467 · Cited by 69 · see citing works

Population genomics of the pathogenic yeast Candida tropicalis identifies hybrid isolates in environmental samples

O’Brien, C. E., Oliveira-Pacheco, J., Cinnéide, E. Ó., Haase, M. A. B., Hittinger, C. T., Rogers, T. R., Zaragoza, Ó., Bond, U., & Butler, G. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009138 · Cited by 68 · see citing works

Genetic Diversity among Korean Candida albicans Bloodstream Isolates: Assessment by Multilocus Sequence Typing and Restriction Endonuclease Analysis of Genomic DNA by Use of BssHII

Shin, J. H., Bougnoux, M., d’Enfert, C., Kim, S. H., Moon, C.-J., Joo, M. Y., Lee, K., Kim, M., Lee, H. S., Shin, M., et al. (2011) · Journal of Clinical Microbiology · doi:10.1128/jcm.02153-10 · Cited by 68 · see citing works

Genomic evidence for a hybrid origin of the yeast opportunistic pathogen Candida albicans

Mixão, V., & Gabaldón, T. (2020) · BMC Biology · doi:10.1186/s12915-020-00776-6 · Cited by 67 · see citing works

Mating is rare within as well as between clades of the human pathogen Candida albicans

Bougnoux, M., Pujol, C., Diogo, D., Bouchier, C., Soll, D. R., & d’Enfert, C. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2007.10.008 · Cited by 66 · see citing works

Appearance and Properties of l-Sorbose-Utilizing Mutants of Candida albicans Obtained on a Selective Plate

Janbon, G., Sherman, F., & Rustchenko, E. P. (1999) · Genetics · doi:10.1093/genetics/153.2.653 · Cited by 64 · see citing works

High-Resolution SNP/CGH Microarrays Reveal the Accumulation of Loss of Heterozygosity in Commonly UsedCandida albicansStrains

Abbey, D., Hickman, M. A., Gresham, D., & Berman, J. G. (2011) · G3 Genes Genomes Genetics · doi:10.1534/g3.111.000885 · Cited by 64 · see citing works

Ploidy dynamics and evolvability in fungi

Wertheimer, N. B., Stone, N. R. H., & Berman, J. G. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0461 · Cited by 63 · see citing works

Chromosome 5 Monosomy of Candida albicans Controls Susceptibility to Various Toxic Agents, Including Major Antifungals

Yang, F., Kravets, A., Bethlendy, G., Welle, S., & Rustchenko, E. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00516-13 · Cited by 60 · see citing works

The Genome of the Human Pathogen Candida albicans Is Shaped by Mutation and Cryptic Sexual Recombination

Wang, J. M., Bennett, R. J., & Anderson, M. Z. (2018) · mBio · doi:10.1128/mbio.01205-18 · Cited by 59 · see citing works

Metabolism‐induced oxidative stress and DNA damage selectively trigger genome instability in polyploid fungal cells

Thomson, G. J., Hernon, C., Austriaco, N. P. G., Shapiro, R. S., Belenky, P. A., & Bennett, R. J. (2019) · The EMBO Journal · doi:10.15252/embj.2019101597 · Cited by 59 · see citing works

Host versus in vitro signals and intrastrain allelic differences in the expression of a Candida albicans virulence gene

Staib, P., Kretschmar, M., Nichterlein, T., Hof, H., & Morschhäuser, J. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.02967.x · Cited by 58 · see citing works

Genetic Analysis Using an Isogenic Mating Pair of Aspergillus fumigatus Identifies Azole Resistance Genes and Lack of MAT Locus’s Role in Virulence

Losada, L. C., Sugui, J. A., Eckhaus, M., Chang, Y. C., Mounaud, S. H., Abigail, F., Joardar, V., Pakala, S., Pakala, S. M., Venepally, P., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004834 · Cited by 58 · see citing works

Parasexuality and Ploidy Change in Candida tropicalis

Seervai, R. N. H., Jones, S. K., Hirakawa, M. P., Porman, A. M., & Bennett, R. J. (2013) · Eukaryotic Cell · doi:10.1128/ec.00128-13 · Cited by 57 · see citing works

Fitness benefits of loss of heterozygosity in Saccharomyces hybridsPreprint

Lancaster, S. M., Payen, C., Heil, C. S., & Dunham, M. J. (2019) · Genome Research · doi:10.1101/gr.245605.118 · Cited by 57 · see citing works

A ‘parameiosis’ drives depolyploidization and homologous recombination in Candida albicans

Anderson, M. Z., Thomson, G. J., Hirakawa, M. P., & Bennett, R. J. (2019) · Nature Communications · doi:10.1038/s41467-019-12376-2 · Cited by 57 · see citing works

Homologous recombination in Candida albicans : role of CaRad52p in DNA repair, integration of linear DNA fragments and telomere length

Ciudad, T., Andaluz, E., Steinberg‐Neifach, O., Lue, N. F., Gow, N. A. R., Calderone, R., & Larriba, G. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04197.x · Cited by 56 · see citing works

Interspecies pheromone signaling promotes biofilm formation and same-sex mating in Candida albicans

Alby, K., & Bennett, R. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017234108 · Cited by 56 · see citing works

A chromosome 4 trisomy contributes to increased fluconazole resistance in a clinical isolate of Candida albicans

Anderson, M. Z., Saha, A., Haseeb, A., & Bennett, R. J. (2017) · Microbiology · doi:10.1099/mic.0.000478 · Cited by 53 · see citing works

Comparison of classical multi-locus sequence typing software for next-generation sequencing data

Page, A. J., Alikhan, N.-F., Carleton, H. A., Seemann, T., Keane, J. A., & Katz, L. S. (2017) · Microbial Genomics · doi:10.1099/mgen.0.000124 · Cited by 53 · see citing works

Microevolution of the pathogenic yeasts Candida albicans and Candida glabrata during antifungal therapy and host infection

Pais, P., Galocha, M., Viana, R., Cavalheiro, M., Pereira, D., & Teixeira, M. C. (2019) · Microbial Cell · doi:10.15698/mic2019.03.670 · Cited by 52 · see citing works

Within-Host Genomic Diversity of Candida albicans in Healthy Carriers

Sitterlé, E., Maufrais, C., Sertour, N., Palayret, M., d’Enfert, C., & Bougnoux, M.-E. (2019) · Scientific Reports · doi:10.1038/s41598-019-38768-4 · Cited by 51 · see citing works

Effects of Ploidy and Mating Type on Virulence of Candida albicans

Ibrahim, A. S., Magee, B. B., Sheppard, D. C., Yang, M., Kauffman, S., Becker, J., Edwards, J. E., & Magee, P. T. (2005) · Infection and Immunity · doi:10.1128/iai.73.11.7366-7374.2005 · Cited by 48 · see citing works

Candida albicans repetitive elements display epigenetic diversity and plasticity

Freire-Benéitez, V., Price, R. J., Tarrant, D., Berman, J. G., & Buscaino, A. (2016) · Scientific Reports · doi:10.1038/srep22989 · Cited by 47 · see citing works

Selection of Candida albicans trisomy during oropharyngeal infection results in a commensal-like phenotype

Forche, A., Solis, N., Swidergall, M., Thomas, R. W., Guyer, A., Beach, A., Cromie, G., Le, G. T., Lowell, E., Pavelka, N., et al. (2019) · bioRxiv · doi:10.1371/journal.pgen.1008137 · Cited by 47 · see citing works

Parasex Generates Phenotypic Diversity <i>de Novo</i> and Impacts Drug Resistance and Virulence in <i>Candida albicans</i>

Hirakawa, M. P., Chyou, D. E., Huang, D., Slan, A. R., & Bennett, R. J. (2017) · Genetics · doi:10.1534/genetics.117.300295 · Cited by 47 · see citing works

Mechanisms of genome evolution in Candida albicans

Ene, I. V., Bennett, R. J., & Anderson, M. Z. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.05.001 · Cited by 46 · see citing works

Phenotypic screening, transcriptional profiling, and comparative genomic analysis of an invasive and non-invasive strain of Candida albicans

Thewes, S., Moran, G. P., Magee, B. B., Schaller, M., Sullivan, D. J., & Hube, B. (2008) · BMC Microbiology · doi:10.1186/1471-2180-8-187 · Cited by 44 · see citing works

Genotyping Candida albicans from Candida Leukoplakia and Non-Candida Leukoplakia Shows No Enrichment of Multilocus Sequence Typing Clades but Enrichment of ABC Genotype C in Candida Leukoplakia

Abdulrahim, M. H., McManus, B. A., Flint, S. R., & Coleman, D. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073738 · Cited by 44 · see citing works

Ploidy tug-of-war: Evolutionary and genetic environments influence the rate of ploidy drive in a human fungal pathogen

Gerstein, A. C., Lim, H., Berman, J. G., & Hickman, M. A. (2017) · Evolution · doi:10.1111/evo.13205 · Cited by 43 · see citing works

The Yeast Mating-Type Switching Mechanism: A Memoir

Klar, A. J. S. (2010) · Genetics · doi:10.1534/genetics.110.122531 · Cited by 42 · see citing works

A study of the DNA damage checkpoint in C andida albicans: uncoupling of the functions of Rad 53 in DNA repair, cell cycle regulation and genotoxic stress‐induced polarized growth

Loll‐Krippleber, R., d’Enfert, C., Feri, A., Diogo, D., Perin, A., Marcet‐Houben, M., Bougnoux, M., & Legrand, M. (2013) · Molecular Microbiology · doi:10.1111/mmi.12471 · Cited by 42 · see citing works

Candida albicans Genetic Background Influences Mean and Heterogeneity of Drug Responses and Genome Stability during Evolution in Fluconazole

Gerstein, A. C., & Berman, J. G. (2020) · mSphere · doi:10.1128/msphere.00480-20 · Cited by 42 · see citing works

Species Distribution, Antifungal Susceptibility, and Molecular Epidemiology of Candida Species Causing Candidemia in a Tertiary Care Hospital in Bangkok, Thailand

Boonsilp, S., Homkaew, A., Phumisantiphong, U., Nutalai, D., & Wongsuk, T. (2021) · Journal of Fungi · doi:10.3390/jof7070577 · Cited by 42 · see citing works

Evolution of Fluconazole-Resistant Candida albicans Strains by Drug-Induced Mating Competence and Parasexual Recombination

Popp, C., Ramı́rez-Zavala, B., Schwanfelder, S., Krüger, I., & Morschhäuser, J. (2019) · mBio · doi:10.1128/mbio.02740-18 · Cited by 41 · see citing works

Drug Resistance Is Not Directly Affected by Mating Type Locus Zygosity in Candida albicans

Pujol, C., Messer, S. A., Pfaller, M. A., & Soll, D. R. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.4.1207-1212.2003 · Cited by 40 · see citing works

Disentangling the Benefits of Sex

Roze, D. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001321 · Cited by 38 · see citing works

The Three Clades of the Telomere-Associated TLO Gene Family of Candida albicans Have Different Splicing, Localization, and Expression Features

Anderson, M. Z., Baller, J. A., Dulmage, K., Wigen, L., & Berman, J. G. (2012) · Eukaryotic Cell · doi:10.1128/ec.00230-12 · Cited by 38 · see citing works

Mitotic Recombination and Adaptive Genomic Changes in Human Pathogenic Fungi

Gusa, A., & Jinks-Robertson, S. (2019) · Genes · doi:10.3390/genes10110901 · Cited by 38 · see citing works

THE EFFECTS OF SEX AND MUTATION RATE ON ADAPTATION IN TEST TUBES AND TO MOUSE HOSTS BY SACCHAROMYCES CEREVISIAE

Grimberg, B. T., & Zeyl, C. (2005) · Evolution · doi:10.1111/j.0014-3820.2005.tb01001.x · Cited by 37 · see citing works

Analysis of Repair Mechanisms following an Induced Double-Strand Break Uncovers Recessive Deleterious Alleles in the Candida albicans Diploid Genome

Feri, A., Loll‐Krippleber, R., Commère, P., Maufrais, C., Sertour, N., Schwartz, K., Sherlock, G., Bougnoux, M., d’Enfert, C., & Legrand, M. (2016) · mBio · doi:10.1128/mbio.01109-16 · Cited by 37 · see citing works

Effect of the Major Repeat Sequence on Mitotic Recombination in Candida albicans

Lephart, P., & Magee, P. T. (2006) · Genetics · doi:10.1534/genetics.106.063271 · Cited by 36 · see citing works

Nonsex Genes in the Mating Type Locus of Candida albicans Play Roles in a/α Biofilm Formation, Including Impermeability and Fluconazole Resistance

Srikantha, T., Daniels, K. J., Pujol, C., Sahni, N., Song, Y., & Soll, D. R. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002476 · Cited by 36 · see citing works

Real-Time Evolution of a Subtelomeric Gene Family in Candida albicans

Anderson, M. Z., Wigen, L., Burrack, L. S., & Berman, J. G. (2015) · Genetics · doi:10.1534/genetics.115.177451 · Cited by 35 · see citing works

Functional diversification accompanies gene family expansion of MED2 homologs in Candida albicans

Dunn, M. J., Kinney, G. M., Washington, P. M., Berman, J. G., & Anderson, M. Z. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007326 · Cited by 34 · see citing works

Candida africana vulvovaginitis: Prevalence and geographical distribution

Fakhim, H., Vaezi, A., Javidnia, J., Nasri, E., Mahdi, D., Diba, K., & Badali, H. (2020) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2020.100966 · Cited by 33 · see citing works

The Impact of Gene Dosage and Heterozygosity on the Diploid Pathobiont Candida albicans

Liang, S.-H., & Bennett, R. J. (2019) · Journal of Fungi · doi:10.3390/jof6010010 · Cited by 32 · see citing works

Genomic clustering within functionally related gene families in Ascomycota fungi

Hagee, D., Hardan, A. A., Botero, J., & Arnone, J. T. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.10.020 · Cited by 32 · see citing works

PAP1 [poly(A) polymerase 1] homozygosity and hyperadenylation are major determinants of increased mRNA stability of CDR1 in azole-resistant clinical isolates of Candida albicans

Manoharlal, R., Gorantala, J., Sharma, M., Sanglard, D., & Prasad, R. (2009) · Microbiology · doi:10.1099/mic.0.035154-0 · Cited by 30 · see citing works

Rad52 function prevents chromosome loss and truncation in Candida albicans

Andaluz, E., Bellido, A., Gómez‐Raja, J., Selmecki, A. M., Bouchonville, K. J., Calderone, R., Berman, J. G., & Larriba, G. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07532.x · Cited by 29 · see citing works

Efficient mating-type switching in Candida glabrata induces cell death

Boisnard, S., Zhou Li, Y., Arnaise, S., Sequeira, G., Raffoux, X., Enache-Angoulvant, A., Bolotin-Fukuhara, M., & Fairhead, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140990 · Cited by 29 · see citing works

Selective Advantages of a Parasexual Cycle for the YeastCandida albicans

Zhang, N., Magee, B. B., Magee, P. T., Holland, B. R., Rodrigues, E., Holmes, A. R., Cannon, R. D., & Schmid, J. (2015) · Genetics · doi:10.1534/genetics.115.177170 · Cited by 28 · see citing works

Chromosome 5 of Human Pathogen Candida albicans Carries Multiple Genes for Negative Control of Caspofungin and Anidulafungin Susceptibility

Suwunnakorn, S., Wakabayashi, H., & Rustchenko, E. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01888-16 · Cited by 28 · see citing works

Particular Candida albicans Strains in the Digestive Tract of Dyspeptic Patients, Identified by Multilocus Sequence Typing

Gong, Y., Zheng, J.-L., Jin, B., Zhuo, D., Huang, Z.-Q., Qi, H., Zhang, W., Duan, W., Fu, J.-T., Chui-jie, W., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035311 · Cited by 27 · see citing works

Correction: N-Acetylglucosamine Induces White to Opaque Switching, a Mating Prerequisite in Candida albicans

Huang, G., Yi, S. S., Sahni, N., Daniels, K. J., Srikantha, T., & Soll, D. R. (2010) · PLoS Pathogens · doi:10.1371/annotation/ed4d1473-cf80-4e85-ad9d-7a390be260f6 · Cited by 27 · see citing works

The role of aneuploidy in the emergence of echinocandin resistance in human fungal pathogen Candida albicans

Sah, S. K., Hayes, J. J., & Rustchenko, E. (2021) · PLOS Pathogens · doi:10.1371/journal.ppat.1009564 · Cited by 26 · see citing works

Molecular mechanism of azoles resistant Candida albicans in a patient with chronic mucocutaneous candidiasis

Zhang, M.-R., Zhao, F., Wang, S., Lv, S., Mou, Y., Yao, C.-L., Zhou, Y., & Li, F.-Q. (2020) · BMC Infectious Diseases · doi:10.1186/s12879-020-4856-8 · Cited by 26 · see citing works

The Magnitude of Candida albicans Stress-Induced Genome Instability Results from an Interaction Between Ploidy and Antifungal Drugs

Avramovska, O., & Hickman, M. A. (2019) · G3 Genes Genomes Genetics · doi:10.1534/g3.119.400752 · Cited by 25 · see citing works

Genomic and Phenotypic Variation in Morphogenetic Networks of Two Candida albicans Isolates Subtends Their Different Pathogenic Potential

Cavalieri, D., Paola, M. D., Rizzetto, L., Tocci, N., Filippo, C. D., Lionetti, P., Ardizzoni, A., Colombari, B., Paulone, S., Gut, I. G., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01997 · Cited by 25 · see citing works

Comparison of Candida albicans strain types among isolates from three countries

Takakura, S., Ichiyama, S., Bain, J. M., Davidson, A. D., Jacobsen, M. D., Shaw, D. J., Gow, N. A. R., & Odds, F. C. (2008) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2007.11.002 · Cited by 24 · see citing works

Environment-induced same-sex mating in the yeast Candida albicans through the Hsf1–Hsp90 pathway

Guan, G., Li, T., Yue, H., Liang, W., Gong, J., Bing, J., Zheng, Q., Veri, A. O., Fan, S., Robbins, N., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.2006966 · Cited by 24 · see citing works

Synchronization of stochastic expressions drives the clustering of functionally related genes

Xu, H., Liu, J., Liu, Z., Li, Y., Jin, Y., & Zhang, J. (2019) · Science Advances · doi:10.1126/sciadv.aax6525 · Cited by 24 · see citing works

Modulation of the Fungal-Host Interaction by the Intra-Species Diversity of C. albicans

Braunsdorf, C., & LeibundGut‐Landmann, S. (2018) · Pathogens · doi:10.3390/pathogens7010011 · Cited by 23 · see citing works

The Mechanisms of Mating in Pathogenic Fungi—A Plastic Trait

Usher, J. (2019) · Genes · doi:10.3390/genes10100831 · Cited by 23 · see citing works

Chromatin Profiling of the Repetitive and Nonrepetitive Genomes of the Human Fungal Pathogen Candida albicans

Price, R. J., Weindling, E., Berman, J. G., & Buscaino, A. (2019) · mBio · doi:10.1128/mbio.01376-19 · Cited by 22 · see citing works

Host-Induced Genome Instability Rapidly Generates Phenotypic Variation across Candida albicans Strains and Ploidy States

Smith, A. C., & Hickman, M. A. (2020) · mSphere · doi:10.1128/msphere.00433-20 · Cited by 22 · see citing works

A Predominance of Clade 17 Candida albicans Isolated From Hemocultures in a Tertiary Care Hospital in Thailand

Pham, L. T. T., Pharkjaksu, S., Chongtrakool, P., Suwannakarn, K., & Ngamskulrungroj, P. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01194 · Cited by 21 · see citing works

Functionally Related Genes Cluster into Genomic Regions That Coordinate Transcription at a Distance in Saccharomyces cerevisiae

Cera, A., Holganza, M. K., Hardan, A. A., Gamarra, I., Eldabagh, R. S., Deschaine, M., Elkamhawy, S., Sisso, E. M., Foley, J. J., & Arnone, J. T. (2019) · mSphere · doi:10.1128/msphere.00063-19 · Cited by 20 · see citing works

The rapid emergence of antifungal-resistant human-pathogenic fungi

Lockhart, S. R., Chowdhary, A., & Gold, J. A. W. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-023-00960-9 · Cited by 315 · see citing works

Candida albicans and Candida glabrata : global priority pathogens

Katsipoulaki, M., Stappers, M. H. T., Malavia, D., Brunke, S., Hube, B., & Gow, N. A. R. (2024) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00021-23 · Cited by 174 · see citing works

Metal Nanoparticles to Combat Candida albicans Infections: An Update

do Carmo, P. H. F., Garcia, M. T., Figueiredo-Godoi, L. M. A., Lage, A. C. P., da Silva, N. S., & Junqueira, J. C. (2023) · Microorganisms · doi:10.3390/microorganisms11010138 · Cited by 87 · see citing works

The Candida Genome Database: annotation and visualization updates

Lew-Smith, J., Binkley, J., & Sherlock, G. J. (2025) · Genetics · doi:10.1093/genetics/iyaf001 · Cited by 37 · see citing works

Loss of Heterozygosity Spectrum Depends on Ploidy Level in Natural Yeast Populations

Dutta, A., Dutreux, F., & Schacherer, J. (2022) · Molecular Biology and Evolution · doi:10.1093/molbev/msac214 · Cited by 27 · see citing works

The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi

Boyce, K. J. (2023) · Microorganisms · doi:10.3390/microorganisms11112757 · Cited by 25 · see citing works

The evil companion of OSCC : Candida albicans

Yang, Z., Zhang, S., Ji, N., Li, J., & Chen, Q. (2023) · Oral Diseases · doi:10.1111/odi.14700 · Cited by 23 · see citing works

Understanding the clinical and environmental drivers of antifungal resistance in the One Health context

Williams, C. C., Gregory, J., & Usher, J. (2024) · Microbiology · doi:10.1099/mic.0.001512 · Cited by 22 · see citing works

Genomics insights of candidiasis: mechanisms of pathogenicity and drug resistance

Huang, X., Dong, Q., Zhou, Q., Fang, S., Xu, Y., Hu, L., Chen, J., Li, X. Y., Qin, H., Mu, D., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1531543 · Cited by 20 · see citing works

Antifungal, anti-biofilm, and anti-hyphal properties of N-substituted phthalimide derivatives against Candida species

Shaik, S., Lee, J.-H., Kim, Y., & Lee, J. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1414618 · Cited by 17 · see citing works

Research advances and public health strategies in China on WHO priority fungal pathogens

Wang, Y., Han, L., Gong, J., Liu, L., Miao, B., & Xu, J. (2025) · Mycology&#58 An International Journal on Fungal Biology · doi:10.1080/21501203.2025.2561612 · Cited by 13 · see citing works

Advances in fungal vaccine development: Progress in the face of emerging challenges

Moses, M., Huang, X., Xue, X., & Chen, C. (2025) · iScience · doi:10.1016/j.isci.2025.114091 · Cited by 13 · see citing works

Adaptation to an amoeba host drives selection of virulence-associated traits and genetic variation in saprotrophic Candida albicans

Amsri, A., Pruksaphon, K., Thammasit, P., Nosanchuk, J. D., & Youngchim, S. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1367656 · Cited by 12 · see citing works

Candida albicans : Insights into the Biology and Experimental Innovations of a Commonly Isolated Human Fungal Pathogen

Sahoo, B., Goyal, R., Dutta, S., Joshi, P., & Sanyal, K. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5c00079 · Cited by 12 · see citing works

Antimicrobial, anti-biofouling, antioxidant, and biocompatible fabrics with high durability via green growth of trimetallic nanoparticles

Sahin, G. D., Şahin, F., Barlas, F. B., Önses, M. S., & Acar, S. (2024) · Materials Today Communications · doi:10.1016/j.mtcomm.2024.110807 · Cited by 9 · see citing works

Cultivable Microbiome Approach Applied to Cervical Cancer Exploration

Mulato-Briones, I. B., Rodríguez-Ildefonso, I. O., Jiménez-Tenorio, J. A., Cauich-Sánchez, P. I., Méndez-Tovar, M. D. S., Aparicio‐Ozores, G., Bautista-Hernández, M. Y., González-Parra, J. F., Cruz-Hernández, J., López-Romero, R., et al. (2024) · Cancers · doi:10.3390/cancers16020314 · Cited by 11 · see citing works

Distinct properties of human pathogenic Candida species revealed by systematic comparative phenotypic screening of clinical isolates

Beyer, R., Zangl, I., Seidl, B., Pap, I.-J., Lackner, M., Strauss, J., Willinger, B., & Schüller, C. (2025) · mSystems · doi:10.1128/msystems.00786-25 · Cited by 7 · see citing works

Is There a Relationship Between Mating and Pathogenesis in Two Human Fungal Pathogens, Candida albicans and Candida glabrata?

Bedekovic, T., & Usher, J. (2023) · Current Clinical Microbiology Reports · doi:10.1007/s40588-023-00192-8 · Cited by 6 · see citing works

The Potential Antifungal Activity of the Developed Palladium Nanoparticles

Bi, S., Srivastava, R., & Ahmed, T. (2024) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/3053 · Cited by 7 · see citing works

Candida albicans Potassium Transporters

Ruiz-Castilla, F. J., Ruiz-Pérez, F., Ramos‐Moreno, L., & Ramos, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094884 · Cited by 7 · see citing works

Transcriptional Response of Candida albicans to Nanostructured Surfaces Provides Insight into Cellular Rupture and Antifungal Drug Sensitization

Chivukula, L. G., & LaJeunesse, D. (2023) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.3c00938 · Cited by 7 · 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

The combinatorial action of hyphal growth and candidalysin is critical for promoting Candida albicans oropharyngeal infection

Paulin, O. K. A., Tsavou, A., Priest, E. L., Griffiths, J. S., Lortal, L., Kempf, A., Chow, E. W. L., Pang, L. M., Wickramasinghe, D. N., Lyon, C. M., et al. (2025) · mBio · doi:10.1128/mbio.03304-25 · Cited by 7 · see citing works

Genetic and Epigenetic Mechanisms Underlying Reversible Adaptive Responses in Fungi

Dan, L., Liu, S., Qiang, Z., Ye, X., & Zhang, J. (2026) · Journal of Fungi · doi:10.3390/jof12050309 · Cited by 6 · see citing works

Bibliometric analysis and thematic review of Candida pathogenesis: Fundamental omics to applications as potential antifungal drugs and vaccines

Lim, S. J., Noor, N. D. M., Sabri, S., Ali, M. S. M., Salleh, A. B., & Oslan, S. N. (2023) · Medical Mycology · doi:10.1093/mmy/myad126 · Cited by 6 · see citing works

Computational frameworks for zoonotic disease control in Society 5.0: opportunities, challenges and future research directions

Bag, A. K., & Sengupta, D. (2024) · AI & Society · doi:10.1007/s00146-024-01992-2 · Cited by 6 · see citing works

Genetic modification of Candida maltosa, a non-pathogenic CTG species, reveals EFG1 function

Chávez-Tinoco, M., García-Ortega, L. F., & Mancera, E. (2024) · Microbiology · doi:10.1099/mic.0.001447 · Cited by 5 · see citing works

Fungal plasticity drives adaptation and survival across pathogenic and free-living contexts

Gebreyesus, T. G. (2026) · Discover Life · doi:10.1007/s11084-026-09731-x · Cited by 4 · see citing works

Anti-fungal peptides: an emerging category with enthralling therapeutic prospects in the treatment of candidiasis

Prusty, J. S., Kumar, A., & Kumar, A. (2024) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2024.2418125 · Cited by 5 · see citing works

Amino acid substitutions in specific proteins correlate with farnesol unresponsiveness in Candida albicans

Mohammadi, S., Leduc, A., Charette, S. J., Barbeau, J., & Vincent, A. T. (2023) · BMC Genomics · doi:10.1186/s12864-023-09174-y · Cited by 3 · see citing works

Selection of ethanol tolerant strains of Candida albicans by repeated ethanol exposure results in strains with reduced susceptibility to fluconazole

Day, A. W., & Kumamoto, C. A. (2024) · PLoS ONE · doi:10.1371/journal.pone.0298724 · Cited by 3 · see citing works

Metallic and lipid nanoparticles against multidrug resistant Candida : advances and translational hurdles

Dalabehera, M., Subudhi, R. N., Boateng, J. S., Choonara, Y. E., Chaudhari, S., Chellappan, D. K., Kanojia, N., Mnqiwu, K., Singh, T. G., & Negi, P. (2025) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2025.2556014 · Cited by 3 · see citing works

Exploration of New Plant-Based Nanoparticles with Potential Antifungal Activity and their Mode of Action

Kaur, H., & Wadhwa, K. (2024) · Springer eBooks · doi:10.1007/978-981-97-5165-5_12 · Cited by 2 · see citing works

Biofilm Formation in Candida Species

Elibe, M. I., & Innocent, N. E. (2024) · Springer eBooks · doi:10.1007/978-981-97-4909-6_9 · Cited by 2 · see citing works

Global population genetics and evolutionary dynamics of Candida albicans

Dalmieda, J., & Xu, J. (2026) · Canadian Journal of Microbiology · doi:10.1139/cjm-2025-0248 · Cited by 2 · see citing works

Emerging antifungal resistance: an updated review on current scenario, pathogens involved and tackling strategies

Mitra, S. (2026) · Future Microbiology · doi:10.1080/17460913.2026.2671628 · Cited by 1 · see citing works

Genome-wide mapping of replication stress response factors reveals the management of polycistronic transcription, replication initiation, and responses to replication stress in Leishmania

Black, J. A., Virgílio, S., Bastos, M. S. E., Silva, G. L. A., Damasceno, J. D., Crouch, K., Lapsley, C. T., McCulloch, R., & Tosi, L. R. O. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag754 · Cited by 1 · see citing works

First comparative proteomic and in vitro behavioral study of Echinococcus granulosus metacestodes in Felis catus

Maglioco, A., Miana, V. V., Valacco, P., Agüero, F. A., Gertiser, M. L., Ávila, H. G., Venturi, M. S. B., Jensen, O., Valdez, A., González, E. A. P., et al. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1546420 · Cited by 1 · see citing works

Loss of heterozygosity spectrum varies with ploidy levels in natural yeast populationsPreprint

Dutta, A., Dutreux, F., & Schacherer, J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.23.493037 · Cited by 1 · see citing works

The Potential Antifungal Activity of the Developed Palladium NanoparticlesPreprint

l, H. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5101909

Strong Bottlenecks Constrain Adaptive Coevolution in a Host–Parasite Metapopulation

Angst, P., Haag, C. R., Ben‐Ami, F., Fields, P. D., & Ebert, D. (2025) · Molecular Ecology · doi:10.1111/mec.70047

Azole Antifungals Under Pressure: Therapeutic Challenges and Multifaceted Resistance Mechanisms

dos Santos, A. L. S., Ramos, L. S., de Mello, T. P., Viganor, L., Nonato, N. M. B. D. M., Pinheiro, R. E. E., & Branquinha, M. H. (2025) · Current Medicinal Chemistry · doi:10.2174/0109298673413219250826055238

Additional file 1 of Amino acid substitutions in specific proteins correlate with farnesol unresponsiveness in Candida albicans

Mohammadi, S., Leduc, A., Charette, S. J., Barbeau, J., & Vincent, A. T. (2023) · Figshare · doi:10.6084/m9.figshare.22608494

Influence of porphyrin cationic charges on photoinactivation of Candida albicans morphotypes

Alvarez, M. G., Cordero, P. V., González, J. M., Pérez, M. E., & Durantini, E. N. (2025) · Photochemical & Photobiological Sciences · doi:10.1007/s43630-025-00835-3

Etude structurale du remodeleur de la chromatine RSC chez Candida albicans

Dupeyron, R. (2023) · theses.fr (ABES) · doi:10.70675/5f7d1879zcfb3z42d7z91e1z9a2a37a29c1f

Comparative genomics of Candida albicans isolates from Bogotá, Colombia: Phylogenetic insights and resistance-related mutations

Patiño, L. H., Muñoz, M. A. M., Ramírez, A. L., Jiménez-A, M. J., Ceballos-Garzón, A., Parra‐Giraldo, C. M., & Ramírez, J. D. (2026) · Acta Tropica · doi:10.1016/j.actatropica.2026.108235

P335 Genome plasticity in Candida albicans : acutting-edge strategy for evolution, adaptation, and survival

Mba, I. E., & Nweze, E. I. (2022) · Medical Mycology · doi:10.1093/mmy/myac072.p335

Mechanisms of genome evolution in Candida albicans

Ene, I. V., Bennett, R. J., & Anderson, M. Z. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.05.001 · Cited by 46 · see citing works

Genomic Plasticity of the Human Fungal Pathogen Candida albicans

Selmecki, A., Forche, A., & Berman, J. (2010) · Eukaryotic Cell · doi:10.1128/ec.00060-10 · Cited by 247 · see citing works

The Impact of Gene Dosage and Heterozygosity on the Diploid Pathobiont Candida albicans

Liang, S.-H., & Bennett, R. J. (2019) · Journal of Fungi · doi:10.3390/jof6010010 · Cited by 32 · see citing works

Genomic variation in C. albicans.

Wickes, B. L., & Petter, R. (1996) · PubMed · Cited by 11 · see citing works