Gordon D. Brown

45.0k total citations · 16 hit papers
218 papers, 32.1k citations indexed

About

Gordon D. Brown is a scholar working on Infectious Diseases, Immunology and Epidemiology. According to data from OpenAlex, Gordon D. Brown has authored 218 papers receiving a total of 32.1k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Infectious Diseases, 100 papers in Immunology and 96 papers in Epidemiology. Recurrent topics in Gordon D. Brown's work include Antifungal resistance and susceptibility (97 papers), Fungal Infections and Studies (78 papers) and Immune Cell Function and Interaction (37 papers). Gordon D. Brown is often cited by papers focused on Antifungal resistance and susceptibility (97 papers), Fungal Infections and Studies (78 papers) and Immune Cell Function and Interaction (37 papers). Gordon D. Brown collaborates with scholars based in United Kingdom, South Africa and United States. Gordon D. Brown's co-authors include Siamon Gordon, Janet A. Willment, Neil A. R. Gow, Mihai G. Netea, Philip R. Taylor, David L. Williams, Stuart M. Levitz, David W. Denning, Theodore C. White and Luisa Martı́nez-Pomares and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Gordon D. Brown

214 papers receiving 31.6k citations

Hit Papers

Hidden Killers: Human Fun... 2001 2026 2009 2017 2012 2001 2005 2003 2007 1000 2.0k 3.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Gordon D. Brown 13.5k 12.4k 10.4k 8.2k 4.7k 218 32.1k
Luigina Romani 10.3k 0.8× 10.8k 0.9× 8.7k 0.8× 6.0k 0.7× 1.1k 0.2× 370 25.6k
David M. Underhill 13.3k 1.0× 4.7k 0.4× 5.0k 0.5× 8.7k 1.1× 1.4k 0.3× 117 25.7k
Victor Nizet 11.4k 0.8× 8.5k 0.7× 6.6k 0.6× 15.3k 1.9× 891 0.2× 564 43.2k
Herbert W. Virgin 10.5k 0.8× 10.4k 0.8× 16.0k 1.5× 12.7k 1.5× 1.1k 0.2× 258 38.7k
Neil A. R. Gow 2.9k 0.2× 19.0k 1.5× 13.5k 1.3× 10.9k 1.3× 7.5k 1.6× 360 31.5k
Vojo Deretić 6.6k 0.5× 6.0k 0.5× 16.3k 1.6× 15.0k 1.8× 1.3k 0.3× 241 33.0k
Jean‐Paul Latgé 2.5k 0.2× 13.5k 1.1× 8.5k 0.8× 9.4k 1.1× 9.2k 2.0× 370 27.2k
David L. Williams 6.6k 0.5× 3.2k 0.3× 3.4k 0.3× 5.1k 0.6× 3.2k 0.7× 356 19.4k
Naoki Yamamoto 12.9k 1.0× 5.5k 0.4× 5.1k 0.5× 9.9k 1.2× 943 0.2× 741 30.6k
Bernhard Hube 1.8k 0.1× 14.9k 1.2× 10.3k 1.0× 6.2k 0.7× 2.1k 0.4× 301 21.3k

Countries citing papers authored by Gordon D. Brown

Since Specialization
Citations

This map shows the geographic impact of Gordon D. Brown's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gordon D. Brown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gordon D. Brown more than expected).

Fields of papers citing papers by Gordon D. Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gordon D. Brown. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gordon D. Brown. The network helps show where Gordon D. Brown may publish in the future.

Co-authorship network of co-authors of Gordon D. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Gordon D. Brown. A scholar is included among the top collaborators of Gordon D. Brown based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gordon D. Brown. Gordon D. Brown is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Liddle, Corin, Emma Camacho, Elizabeth R. Ballou, et al.. (2024). Cryptococcus neoforman s rapidly invades the murine brain by sequential breaching of airway and endothelial tissues barriers, followed by engulfment by microglia. mBio. 15(4). e0307823–e0307823. 13 indexed citations
2.
Reedy, Jennifer L., Rebecca Ward, Christopher Reardon, et al.. (2024). Fungal melanin suppresses airway epithelial chemokine secretion through blockade of calcium fluxing. Nature Communications. 15(1). 5817–5817. 5 indexed citations
3.
Roselletti, Elena, Eva Pericolini, Alexandre Nore, et al.. (2023). Zinc prevents vaginal candidiasis by inhibiting expression of an inflammatory fungal protein. Science Translational Medicine. 15(725). eadi3363–eadi3363. 30 indexed citations
4.
Willment, Janet A., et al.. (2022). C‐type lectin receptors in antifungal immunity: Current knowledge and future developments. Parasite Immunology. 45(2). e12951–e12951. 18 indexed citations
5.
Sephton-Clark, Poppy, Diana Tamayo, Xin Zhou, et al.. (2022). A bacterial endosymbiont of the fungus Rhizopus microsporus drives phagocyte evasion and opportunistic virulence. Current Biology. 32(5). 1115–1130.e6. 28 indexed citations
6.
Bain, Judith M., Delma S. Childers, K. MacKenzie, et al.. (2021). Immune cells fold and damage fungal hyphae. Proceedings of the National Academy of Sciences. 118(15). 35 indexed citations
7.
Wong, Sarah Sze Wah, Vishukumar Aimanianda, Catherine Simenel, et al.. (2021). Complement-Mediated Differential Immune Response of Human Macrophages to Sporothrix Species Through Interaction With Their Cell Wall Peptidorhamnomannans. Frontiers in Immunology. 12. 749074–749074. 14 indexed citations
8.
Baldassarre, Massimiliano, Ivy M. Dambuza, Delyth M. Reid, et al.. (2021). The Rab32/BLOC-3–dependent pathway mediates host defense against different pathogens in human macrophages. Science Advances. 7(3). 25 indexed citations
9.
Valsecchi, Isabel, Emmanuel Stephen‐Victor, Sarah Sze Wah Wong, et al.. (2020). The Role of RodA-Conserved Cysteine Residues in the Aspergillus fumigatus Conidial Surface Organization. Journal of Fungi. 6(3). 151–151. 10 indexed citations
10.
Dambuza, Ivy M., Patawee Asamaphan, Mark H. T. Stappers, et al.. (2019). The pattern recognition receptors dectin-2, mincle, and FcRγ impact the dynamics of phagocytosis of Candida, Saccharomyces, Malassezia, and Mucor species. PLoS ONE. 14(8). e0220867–e0220867. 26 indexed citations
11.
Pradhan, Arnab, Gabriela M. Avelar, Judith M. Bain, et al.. (2018). Hypoxia Promotes Immune Evasion by Triggering β-Glucan Masking on the Candida albicans Cell Surface via Mitochondrial and cAMP-Protein Kinase A Signaling. mBio. 9(6). 94 indexed citations
12.
Lim, Jenson, Christopher J. Coates, Paula I. Seoane, et al.. (2018). Characterizing the Mechanisms of Nonopsonic Uptake of Cryptococci by Macrophages. The Journal of Immunology. 200(10). 3539–3546. 28 indexed citations
13.
Dambuza, Ivy M., Thomas A. Drake, Xin Zhou, et al.. (2018). The Cryptococcus neoformans Titan cell is an inducible and regulated morphotype underlying pathogenesis. PLoS Pathogens. 14(5). e1006978–e1006978. 117 indexed citations
14.
Loures, Flávio V., Eliseu Frank de Araújo, Cláudia Feriotti, et al.. (2014). Dectin-1 Induces M1 Macrophages and Prominent Expansion of CD8+IL-17+ Cells in Pulmonary Paracoccidioidomycosis. The Journal of Infectious Diseases. 210(5). 762–773. 67 indexed citations
15.
Iliev, Iliyan D., Vincent Funari, Kent D. Taylor, et al.. (2012). Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis. Science. 336(6086). 1314–1317. 827 indexed citations breakdown →
16.
Suram, Saritha, Philip R. Taylor, Marcela Rosas, et al.. (2010). Pathways Regulating Cytosolic Phospholipase A2 Activation and Eicosanoid Production in Macrophages by Candida albicans. Journal of Biological Chemistry. 285(40). 30676–30685. 47 indexed citations
17.
Groß, Olaf, Christoph Hölscher, Else Marie Agger, et al.. (2009). Adjuvanticity of a synthetic cord factor analogue for subunit Mycobacterium tuberculosis vaccination requires FcRγ–Syk–Card9–dependent innate immune activation. The Journal of Experimental Medicine. 206(1). 89–97. 258 indexed citations
18.
Suram, Saritha, Gordon D. Brown, Moumita Ghosh, et al.. (2006). Regulation of Cytosolic Phospholipase A2 Activation and Cyclooxygenase 2 Expression in Macrophages by the β-Glucan Receptor. Journal of Biological Chemistry. 281(9). 5506–5514. 104 indexed citations
19.
Graham, Lisa M., S. Vicky Tsoni, Janet A. Willment, et al.. (2006). Soluble Dectin-1 as a tool to detect β-glucans. Journal of Immunological Methods. 314(1-2). 164–169. 100 indexed citations
20.
Palma, Angelina S., Ten Feizi, Yi-Bing Zhang, et al.. (2005). Ligands for the β-Glucan Receptor, Dectin-1, Assigned Using “Designer” Microarrays of Oligosaccharide Probes (Neoglycolipids) Generated from Glucan Polysaccharides. Journal of Biological Chemistry. 281(9). 5771–5779. 290 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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