Géza Erdös
About
Géza Erdös is a scholar working on Molecular Biology, Immunology and Pharmaceutical Science.
According to data from OpenAlex, Géza Erdös has authored 58 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 22 papers in Immunology and 12 papers in Pharmaceutical Science. Recurrent topics in Géza Erdös's work include Immunotherapy and Immune Responses (17 papers), Advancements in Transdermal Drug Delivery (12 papers) and Heat shock proteins research (10 papers). Géza Erdös is often cited by papers focused on Immunotherapy and Immune Responses (17 papers), Advancements in Transdermal Drug Delivery (12 papers) and Heat shock proteins research (10 papers). Géza Erdös collaborates with scholars based in United States, Hungary and Brazil. Géza Erdös's co-authors include Louis D. Falo, Adriana T. Larregina, Adrián E. Morelli, Simon C. Watkins, William J. Shufesky, О. Н. Ткачева, Donna B. Stolz, Sherrie J. Divito, Mara Sullivan and Gregory A. Gibson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.
In The Last Decade
Géza Erdös
57 papers receiving 3.5k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Géza Erdös United States | 28 | 1.8k | 882 | 806 | 508 | 432 | 58 | 3.5k | ||
| Robert C. Fuhlbrigge United States | 44 | 2.3k 1.2× | 5.1k 5.8× | 645 0.8× | 114 0.2× | 251 0.6× | 100 | 9.2k | ||
| Daniel Schmitt France | 37 | 1.1k 0.6× | 2.5k 2.8× | 159 0.2× | 88 0.2× | 156 0.4× | 175 | 5.2k | ||
| Christine T. N. Pham United States | 42 | 2.1k 1.1× | 2.4k 2.7× | 712 0.9× | 61 0.1× | 265 0.6× | 98 | 5.9k | ||
| Daniel N. Sauder Canada | 36 | 719 0.4× | 1.3k 1.5× | 180 0.2× | 72 0.1× | 186 0.4× | 78 | 3.8k | ||
| Wolfgang Kastenmüller Germany | 38 | 1.9k 1.1× | 4.6k 5.2× | 304 0.4× | 57 0.1× | 420 1.0× | 62 | 7.1k | ||
| Andreas Gebert Germany | 32 | 836 0.5× | 1.1k 1.2× | 72 0.1× | 173 0.3× | 177 0.4× | 86 | 3.3k | ||
| Daisuke Watanabe Japan | 30 | 1.4k 0.8× | 424 0.5× | 142 0.2× | 44 0.1× | 243 0.6× | 206 | 4.3k | ||
| Ben J. Glasgow United States | 40 | 1.2k 0.7× | 148 0.2× | 152 0.2× | 298 0.6× | 236 0.5× | 181 | 6.6k | ||
| Robert J. Debs United States | 34 | 3.4k 1.9× | 553 0.6× | 252 0.3× | 68 0.1× | 522 1.2× | 73 | 4.7k | ||
| Paul D. Rennert United States | 51 | 2.3k 1.3× | 6.9k 7.8× | 1.1k 1.4× | 47 0.1× | 883 2.0× | 84 | 10.6k |
Countries citing papers authored by Géza Erdös
Since
Specialization
Citations
This map shows the geographic impact of Géza Erdös'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 Géza Erdös with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Géza Erdös more than expected).
Fields of papers citing papers by Géza Erdös
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Géza Erdös. 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 Géza Erdös. The network helps show where Géza Erdös may publish in the future.
Co-authorship network of co-authors of Géza Erdös
This figure shows the co-authorship network connecting the top 25 collaborators of Géza Erdös. A scholar is included among the top collaborators of Géza Erdös 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 Géza Erdös. Géza Erdös is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Castanha, Priscila M. S., Kristine Cooper, Géza Erdös, et al.. (2025). Genetic ancestry shapes dengue virus infection in human skin explants. Proceedings of the National Academy of Sciences. 122(28). e2502793122–e2502793122.
2.
Zeng, Furong, Zhizhao Chen, William J. Shufesky, et al.. (2021). Graft-derived extracellular vesicles transported across subcapsular sinus macrophages elicit B cell alloimmunity after transplantation. Science Translational Medicine. 13(585).
3.
Korkmaz, Emrullah, Stephen C. Balmert, Tina L. Sumpter, et al.. (2021). Microarray patches enable the development of skin-targeted vaccines against COVID-19. Advanced Drug Delivery Reviews. 171. 164–186.
4.
Korkmaz, Emrullah, Stephen C. Balmert, Cara Donahue Carey, Géza Erdös, & Louis D. Falo. (2020). Emerging skin-targeted drug delivery strategies to engineer immunity: A focus on infectious diseases. Expert Opinion on Drug Delivery. 18(2). 151–167.
5.
Falo, Louis D., et al.. (2020). 052 Targeting keratinocytes to potentiate non-viral DNA skin immunization. Journal of Investigative Dermatology. 140(7). S6–S6.
6.
Epperly, Michael W., Peter Wipf, Renee Fisher, et al.. (2018). Evaluation of Different Formulations and Routes for the Delivery of the Ionizing Radiation Mitigator GS-Nitroxide (JP4-039). In Vivo. 32(5). 1009–1023.
7.
Balmert, Stephen C., et al.. (2017). In vivo induction of regulatory T cells promotes allergen tolerance and suppresses allergic contact dermatitis. Journal of Controlled Release. 261. 223–233.
8.
Erdös, Géza, Kate D. Ryman, Simon C. Watkins, et al.. (2017). Interplay between Keratinocytes and Myeloid Cells Drives Dengue Virus Spread in Human Skin. Journal of Investigative Dermatology. 138(3). 618–626.
9.
Liu, Quan, Darling Rojas-Canales, Sherrie J. Divito, et al.. (2016). Donor dendritic cell–derived exosomes promote allograft-targeting immune response. Journal of Clinical Investigation. 126(8). 2805–2820.
10.
Korkmaz, Emrullah, Emily E. Friedrich, Mohamed Ramadan, et al.. (2016). Tip-Loaded Dissolvable Microneedle Arrays Effectively Deliver Polymer-Conjugated Antibody Inhibitors of Tumor-Necrosis-Factor-Alpha Into Human Skin. Journal of Pharmaceutical Sciences. 105(11). 3453–3457.
11.
Erdös, Géza, Cara Donahue, Jiying Zhang, et al.. (2012). Dissolvable microneedle arrays deliver live adenovirus to the skin for genetic immunization. (58.16). The Journal of Immunology. 188(1_Supplement). 58.16–58.16.
12.
Kerschner, Joseph E., Géza Erdös, Fen Hu, et al.. (2010). Partial Characterization of Normal and Haemophilus Influenzae—Infected Mucosal Complementary DNA Libraries in Chinchilla Middle Ear Mucosa. Annals of Otology Rhinology & Laryngology. 119(4). 270–278.
13.
Erdös, Géza, et al.. (2009). Topical patch vaccines target antigen to cutaneous dendritic cells efficiently inducing potent cell mediated immune responses (132.19). The Journal of Immunology. 182(Supplement_1). 132.19–132.19.
14.
Janelsins, Brian, Alicia R. Mathers, О. Н. Ткачева, et al.. (2008). Proinflammatory tachykinins that signal through the neurokinin 1 receptor promote survival of dendritic cells and potent cellular immunity. Blood. 113(13). 3017–3026.
15.
Morelli, Adrián E., J. Peter Rubin, Géza Erdös, et al.. (2005). CD4+ T Cell Responses Elicited by Different Subsets of Human Skin Migratory Dendritic Cells. The Journal of Immunology. 175(12). 7905–7915.
16.
Stoodley, Paul, Sandeep Kathju, Fen Hu, et al.. (2005). Molecular and Imaging Techniques for Bacterial Biofilms in Joint Arthroplasty Infections. Clinical Orthopaedics and Related Research. &NA;(437). 31–40.
17.
Erdös, Géza, Sameera Sayeed, Fen Hu, et al.. (2003). Development and characterization of a pooled Haemophilus influenzae genomic library for the evaluation of gene expression changes associated with mucosal biofilm formation in otitis media. International Journal of Pediatric Otorhinolaryngology. 67(7). 749–755.
18.
Erdös, Géza, et al.. (1995). Heat‐Induced bFGF gene expression in the absence of heat shock element correlates with enhanced AP‐1 binding activity. Journal of Cellular Physiology. 164(2). 404–413.
19.
Lee, Yong J., Sandra Galoforo, Christine M. Berns, et al.. (1995). Effect of Ionizing Radiation on AP-1 Binding Activity and Basic Fibroblast Growth Factor Gene Expression in Drug-sensitive Human Breast Carcinoma MCF-7 and Multidrug-resistant MCF-7/ADR Cells. Journal of Biological Chemistry. 270(48). 28790–28796.
20.
Erdös, Géza, et al.. (1994). Effect of Isoquinolinesulfonamides on Heat Shock Gene Expression During Heating at 41°C in Human Carcinoma Cell Lines. Biochemical and Biophysical Research Communications. 199(2). 714–719.
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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