Ashley F. George

1.2k total citations
24 papers, 583 citations indexed

About

Ashley F. George is a scholar working on Immunology, Virology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ashley F. George has authored 24 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Immunology, 5 papers in Virology and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ashley F. George's work include Reproductive System and Pregnancy (7 papers), HIV Research and Treatment (5 papers) and Immune Cell Function and Interaction (5 papers). Ashley F. George is often cited by papers focused on Reproductive System and Pregnancy (7 papers), HIV Research and Treatment (5 papers) and Immune Cell Function and Interaction (5 papers). Ashley F. George collaborates with scholars based in United States, Denmark and Canada. Ashley F. George's co-authors include Nadia R. Roan, Warner C. Greene, Xiaoyu Luo, Jason Neidleman, Linda C. Giudice, Matthew McGregor, Joshua Vasquez, Tongcui Ma, Trimble Spitzer and Guorui Xie and has published in prestigious journals such as The Journal of Immunology, Journal of Virology and Journal of Neurochemistry.

In The Last Decade

Ashley F. George

23 papers receiving 573 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ashley F. George United States 14 269 189 152 132 101 24 583
Roslyn M. Ray United States 13 119 0.4× 156 0.8× 34 0.2× 24 0.2× 253 2.5× 21 551
A. Beretta Italy 12 356 1.3× 49 0.3× 52 0.3× 54 0.4× 31 0.3× 22 612
Guorui Xie United States 10 133 0.5× 212 1.1× 21 0.1× 14 0.1× 74 0.7× 16 347
Prabagaran Esakky United States 12 48 0.2× 347 1.8× 84 0.6× 46 0.3× 114 1.1× 18 729
Chanel Avenant South Africa 13 188 0.7× 63 0.3× 46 0.3× 14 0.1× 88 0.9× 24 529
Sorour Khateri Iran 10 52 0.2× 43 0.2× 120 0.8× 110 0.8× 96 1.0× 22 422
Wensheng Fan China 16 122 0.5× 183 1.0× 177 1.2× 142 1.1× 119 1.2× 30 636
Stan A. Beyler United States 14 254 0.9× 29 0.2× 350 2.3× 144 1.1× 98 1.0× 23 737
Deirdre M. Logsdon United States 7 65 0.2× 128 0.7× 90 0.6× 71 0.5× 151 1.5× 25 440
Hong Cai United States 10 145 0.5× 48 0.3× 12 0.1× 52 0.4× 108 1.1× 21 331

Countries citing papers authored by Ashley F. George

Since Specialization
Citations

This map shows the geographic impact of Ashley F. George'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 Ashley F. George with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashley F. George more than expected).

Fields of papers citing papers by Ashley F. George

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ashley F. George. 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 Ashley F. George. The network helps show where Ashley F. George may publish in the future.

Co-authorship network of co-authors of Ashley F. George

This figure shows the co-authorship network connecting the top 25 collaborators of Ashley F. George. A scholar is included among the top collaborators of Ashley F. George 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 Ashley F. George. Ashley F. George 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.
George, Ashley F., Jason Neidleman, Xiaoyu Luo, et al.. (2025). Anatomical, subset, and HIV-dependent expression of viral sensors and restriction factors. Cell Reports. 44(1). 115202–115202. 2 indexed citations
2.
Vallvé-Juanico, Júlia, Ashley F. George, Sushmita Sen, et al.. (2022). Deep immunophenotyping reveals endometriosis is marked by dysregulation of the mononuclear phagocytic system in endometrium and peripheral blood. BMC Medicine. 20(1). 31 indexed citations
3.
Ma, Tongcui, Matthew McGregor, Leila B. Giron, et al.. (2022). Single-cell glycomics analysis by CyTOF-Lec reveals glycan features defining cells differentially susceptible to HIV. eLife. 11. 18 indexed citations
4.
George, Ashley F., Matthew McGregor, David Gingrich, et al.. (2022). Female Genital Fibroblasts Diminish the In Vitro Efficacy of PrEP against HIV. Viruses. 14(8). 1723–1723.
5.
George, Ashley F., Xiaoyu Luo, Jason Neidleman, et al.. (2022). Deep Phenotypic Analysis of Blood and Lymphoid T and NK Cells From HIV+ Controllers and ART-Suppressed Individuals. Frontiers in Immunology. 13. 803417–803417. 10 indexed citations
6.
Neidleman, Jason, Xiaoyu Luo, Ashley F. George, et al.. (2021). Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19. Cell Reports. 36(3). 109414–109414. 58 indexed citations
7.
Ma, Tongcui, Heeju Ryu, Matthew McGregor, et al.. (2021). Protracted yet Coordinated Differentiation of Long-Lived SARS-CoV-2-Specific CD8+ T Cells during Convalescence. The Journal of Immunology. 207(5). 1344–1356. 9 indexed citations
8.
Adeniji, Opeyemi S., Leticia Kuri-Cervantes, Chenfei Yu, et al.. (2021). Siglec-9 defines and restrains a natural killer subpopulation highly cytotoxic to HIV-infected cells. PLoS Pathogens. 17(11). e1010034–e1010034. 14 indexed citations
9.
Ma, Tongcui, Xiaoyu Luo, Ashley F. George, et al.. (2020). HIV efficiently infects T cells from the endometrium and remodels them to promote systemic viral spread. eLife. 9. 28 indexed citations
10.
Neidleman, Jason, Xiaoyu Luo, Julie Frouard, et al.. (2020). SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential. Cell Reports Medicine. 1(6). 100081–100081. 126 indexed citations
12.
George, Ashley F., et al.. (2018). Effects of colostrum, feeding method and oral IGF1 on porcine uterine development. Reproduction. 155(3). 259–271. 8 indexed citations
13.
George, Ashley F., Nripesh Prasad, Brittney N. Keel, et al.. (2018). Neonatal lactocrine deficiency affects the adult porcine endometrial transcriptome at pregnancy day 13†. Biology of Reproduction. 100(1). 71–85. 4 indexed citations
14.
Bartol, Frank F., et al.. (2017). PHYSIOLOGY AND ENDOCRINOLOGY SYMPOSIUM: Postnatal reproductive development and the lactocrine hypothesis12. Journal of Animal Science. 95(5). 2200–2210. 13 indexed citations
15.
Bagnell, Carol A., et al.. (2017). Maternal lactocrine programming of porcine reproductive tract development. Molecular Reproduction and Development. 84(9). 957–968. 14 indexed citations
16.
Bartol, Frank F., Carol A. Bagnell, & Ashley F. George. (2016). 1163 Postnatal reproductive development and the lactocrine hypothesis.. Journal of Animal Science. 94(supplement5). 558–558. 3 indexed citations
17.
Barragan, Fatima, Juan C. Irwin, Shaina Balayan, et al.. (2016). Human Endometrial Fibroblasts Derived from Mesenchymal Progenitors Inherit Progesterone Resistance and Acquire an Inflammatory Phenotype in the Endometrial Niche in Endometriosis1. Biology of Reproduction. 94(5). 118–118. 112 indexed citations
18.
Fan, Jing, et al.. (2010). N‐Methyl‐d‐aspartate receptor subunit‐ and neuronal‐type dependence of excitotoxic signaling through post‐synaptic density 95. Journal of Neurochemistry. 115(4). 1045–1056. 25 indexed citations
19.
Martini, Luigi G., et al.. (1999). Solubility parameter and oral absorption. European Journal of Pharmaceutics and Biopharmaceutics. 48(3). 259–263. 25 indexed citations
20.
Applegarth, Derek A., et al.. (1977). Plasma arginine esterase activity in cystic fibrosis of the pancreas. Clinica Chimica Acta. 74(1). 71–75. 12 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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