OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Cryptococcus neoformans Dual GDP-Mannose Transporters and Their Role in Biology and Virulence
Zhuo A. Wang, Cara L. Griffith, Michael L. Skowyra, et al.
Eukaryotic Cell (2014) Vol. 13, Iss. 6, pp. 832-842
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Cryptococcus neoformans and Cryptococcus gattii, the Etiologic Agents of Cryptococcosis
Kyung J. Kwon‐Chung, James A. Fraser, Tamara L. Doering, et al.
Cold Spring Harbor Perspectives in Medicine (2014) Vol. 4, Iss. 7, pp. a019760-a019760
Open Access | Times Cited: 495

Targeted Genome Editing via CRISPR in the Pathogen Cryptococcus neoformans
Samantha D. M. Arras, Sheena M.H. Chua, Maha S.I. Wizrah, et al.
PLoS ONE (2016) Vol. 11, Iss. 10, pp. e0164322-e0164322
Open Access | Times Cited: 66

Unraveling synthesis of the cryptococcal cell wall and capsule
Zhuo A. Wang, Lucy X. Li, Tamara L. Doering
Glycobiology (2018) Vol. 28, Iss. 10, pp. 719-730
Open Access | Times Cited: 66

Peeling the onion: the outer layers of Cryptococcus neoformans
Daniel Paiva Agustinho, Liza Miller, Lucy X. Li, et al.
Memórias do Instituto Oswaldo Cruz (2018) Vol. 113, Iss. 7
Open Access | Times Cited: 56

Model-driven mapping of transcriptional networks reveals the circuitry and dynamics of virulence regulation
Ezekiel J. Maier, Brian C. Haynes, Stacey R. Gish, et al.
Genome Research (2015) Vol. 25, Iss. 5, pp. 690-700
Open Access | Times Cited: 54

Nutritional Requirements and Their Importance for Virulence of Pathogenic Cryptococcus Species
Rhys A. Watkins, Jason King, Simon A. Johnston
Microorganisms (2017) Vol. 5, Iss. 4, pp. 65-65
Open Access | Times Cited: 36

Cryptococcus neoformans Yap1 is required for normal fluconazole and oxidative stress resistance
Sanjoy Paul, Tamara L. Doering, W. Scott Moye‐Rowley
Fungal Genetics and Biology (2014) Vol. 74, pp. 1-9
Open Access | Times Cited: 35

Role of glucuronoxylomannan and steryl glucosides in protecting against cryptococcosis
Gabriel Soares Matos, Samyr Machado Querobino, Verônica S. Brauer, et al.
mBio (2025)
Open Access

Virulence factors released by extracellular vesicles from Cryptococcus neoformans
Wenhao Xiao, Keyuan Zhong, Bowei Jiang, et al.
Frontiers in Cellular and Infection Microbiology (2025) Vol. 15
Open Access

Xylose donor transport is critical for fungal virulence
Lucy X. Li, Carsten Rautengarten, Joshua L. Heazlewood, et al.
PLoS Pathogens (2018) Vol. 14, Iss. 1, pp. e1006765-e1006765
Open Access | Times Cited: 28

Ero1‐Pdi1 module‐catalysed dimerization of a nucleotide sugar transporter, FonNst2, regulates virulence of Fusarium oxysporum on watermelon
Yizhou Gao, Xiaohui Xiong, Hui Wang, et al.
Environmental Microbiology (2021) Vol. 24, Iss. 3, pp. 1200-1220
Closed Access | Times Cited: 21

UDP-Glucuronic Acid Transport Is Required for Virulence of Cryptococcus neoformans
Lucy X. Li, Carsten Rautengarten, Joshua L. Heazlewood, et al.
mBio (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 24

The GDP-mannose transporter gene (DoGMT) from Dendrobium officinale is critical for mannan biosynthesis in plant growth and development
Zhenming Yu, Chunmei He, Jaime A. Teixeira da Silva, et al.
Plant Science (2018) Vol. 277, pp. 43-54
Closed Access | Times Cited: 24

Cryptococcus neoformans UGT1encodes a UDP-Galactose/UDP-GalNAc transporter
Lucy X. Li, Angel Ashikov, Hong Liu, et al.
Glycobiology (2016) Vol. 27, Iss. 1, pp. 87-98
Open Access | Times Cited: 22

Virulence Factors as Targets for Anticryptococcal Therapy
Renata Azevedo, Juliana Rizzo, Márcio L. Rodrigues
Journal of Fungi (2016) Vol. 2, Iss. 4, pp. 29-29
Open Access | Times Cited: 20

Sac1 links phosphoinositide turnover to cryptococcal virulence
Elizabeth A. Gaylord, Hau Lam Choy, Guohua Chen, et al.
mBio (2024) Vol. 15, Iss. 8
Open Access | Times Cited: 2

Expansion of healthcare-associated hypervirulent KPC-2-producing Klebsiella pneumoniae ST11/KL64 beyond hospital settings
Fernanda Esposito, Brenda Cardoso, Fábio P. Sellera, et al.
One Health (2023) Vol. 17, pp. 100594-100594
Open Access | Times Cited: 6

Glycobiology of Human Fungal Pathogens: New Avenues for Drug Development
Danielle J. Lee, Holly O’Donnell, Françoise H. Routier, et al.
Cells (2019) Vol. 8, Iss. 11, pp. 1348-1348
Open Access | Times Cited: 16

Deletion of Aspergillus nidulans GDP-mannose transporters affects hyphal morphometry, cell wall architecture, spore surface character, cell adhesion, and biofilm formation
Ashraf A. Kadry, Amira M. El-Ganiny, Rasha Mosbah, et al.
Medical Mycology (2017) Vol. 56, Iss. 5, pp. 621-630
Open Access | Times Cited: 11

Sac1 links phosphoinositide turnover to cryptococcal virulence
Elizabeth A. Gaylord, Hau Lam Choy, Guohua Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1

Unbiased discovery of natural sequence variants that influence fungal virulence
Daniel Paiva Agustinho, Holly Leanne Brown, Guohua Chen, et al.
Cell Host & Microbe (2023) Vol. 31, Iss. 11, pp. 1910-1920.e5
Open Access | Times Cited: 3

Biology and Function of Exo-Polysaccharides from Human Fungal Pathogens
Krystal Y. Chung, Jessica C. S. Brown
Current Clinical Microbiology Reports (2020) Vol. 7, Iss. 1, pp. 1-11
Open Access | Times Cited: 7

RNAi machinery regulates nutrient metabolism and fluconazole resistance in the pathogenic fungusCryptococcus deneoformans
Xiaoyu Ma, Chenxi Li, Lan Ma, et al.
Medical Mycology (2022) Vol. 61, Iss. 2
Closed Access | Times Cited: 3

Cryptococcus neoformans in Association with Dermatophagoides pteronyssinus has Pro- (IL-6/STAT3 Overproduction) and Anti-inflammatory (CCL2/ERK1/2 Downregulation) Effects on Human Bronchial Epithelial Cells
Henrique Ismarsi de Souza, Aline Beatriz Mahler Pereira, Jhony Robison de Oliveira, et al.
Inflammation (2022) Vol. 45, Iss. 3, pp. 1269-1280
Closed Access | Times Cited: 1

Page 1 - Next Page

Scroll to top