Anna Gibbs

1.4k total citations · 1 hit paper
13 papers, 1.0k citations indexed

About

Anna Gibbs is a scholar working on Immunology, Virology and Epidemiology. According to data from OpenAlex, Anna Gibbs has authored 13 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 6 papers in Virology and 5 papers in Epidemiology. Recurrent topics in Anna Gibbs's work include T-cell and B-cell Immunology (7 papers), Immune Cell Function and Interaction (7 papers) and HIV Research and Treatment (6 papers). Anna Gibbs is often cited by papers focused on T-cell and B-cell Immunology (7 papers), Immune Cell Function and Interaction (7 papers) and HIV Research and Treatment (6 papers). Anna Gibbs collaborates with scholars based in Sweden, United States and Canada. Anna Gibbs's co-authors include Annelie Tjernlund, Andrea Introini, Kristina Broliden, Johan K. Sandberg, Edwin Leeansyah, Liv Eidsmo, Elisa Martini, Stanley Cheuk, Jakob Michaëlsson and Samuel C. C. Chiang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Immunity and The Journal of Immunology.

In The Last Decade

Anna Gibbs

13 papers receiving 997 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CD49a Expression Defines Tissue-Resident CD8 + T Cells Poised for Cytotoxic Function in Human Skin

2017 475 citations Stanley Cheuk, Heinrich Schlums et al. Immunity profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Gibbs Sweden	10	825	162	106	97	81	13	1.0k
S. R. Krieg Netherlands	12	577 0.7×	137 0.8×	87 0.8×	269 2.8×	39 0.5×	16	906
Norbert Kohrgruber Austria	10	610 0.7×	311 1.9×	159 1.5×	48 0.5×	15 0.2×	13	1.0k
Angela M. Wolbink Netherlands	13	383 0.5×	174 1.1×	62 0.6×	18 0.2×	23 0.3×	15	703
Fumiya Yamaide Japan	10	825 1.0×	78 0.5×	105 1.0×	77 0.8×	10 0.1×	23	1.1k
Giuliano Zuccati Italy	11	253 0.3×	131 0.8×	59 0.6×	91 0.9×	8 0.1×	31	502
John Browning United States	14	106 0.1×	96 0.6×	167 1.6×	238 2.5×	105 1.3×	76	698
Kerstin A. Stegmann United Kingdom	14	842 1.0×	299 1.8×	163 1.5×	15 0.2×	9 0.1×	17	1.1k
Sylvia L. Brice United States	16	114 0.1×	258 1.6×	79 0.7×	180 1.9×	41 0.5×	24	746
Renata Ferreira Magalhães Brazil	14	155 0.2×	145 0.9×	70 0.7×	201 2.1×	10 0.1×	51	488
Mihael Skerlev Croatia	15	103 0.1×	247 1.5×	43 0.4×	139 1.4×	59 0.7×	43	585

Countries citing papers authored by Anna Gibbs

Since Specialization

Citations

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

Fields of papers citing papers by Anna Gibbs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Gibbs. 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 Anna Gibbs. The network helps show where Anna Gibbs may publish in the future.

Co-authorship network of co-authors of Anna Gibbs

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Gibbs. A scholar is included among the top collaborators of Anna Gibbs 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 Anna Gibbs. Anna Gibbs is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Gibbs, Anna, Katie Healy, Christopher Sundling, et al.. (2022). Preserved Mucosal-Associated Invariant T Cells in the Cervical Mucosa of HIV-Infected Women with Dominant Expression of the TRAV1-2–TRAJ20 T Cell Receptor α-Chain. The Journal of Infectious Diseases. 226(8). 1428–1440. 6 indexed citations

Gibbs, Anna, Michał J. Sobkowiak, Johan K. Sandberg, & Annelie Tjernlund. (2019). In Situ Detection of MAIT Cells and MR1-Expressing Cells in Tissue Biopsies Utilizing Immunohistochemistry. Methods in molecular biology. 2098. 83–94. 1 indexed citations

Dias, Joana, Caroline Boulouis, Jean‐Baptiste Gorin, et al.. (2018). The CD4⁻CD8⁻MAIT cell subpopulation is a functionally distinct subset developmentally related to the main CD8⁺MAIT cell pool. Proceedings of the National Academy of Sciences. 115(49). E11513–E11522. 123 indexed citations

Sobkowiak, Michał J., Haleh Davanian, Robert Heymann, et al.. (2018). Tissue‐resident MAIT cell populations in human oral mucosa exhibit an activated profile and produce IL‐17. European Journal of Immunology. 49(1). 133–143. 89 indexed citations

Cheuk, Stanley, Heinrich Schlums, Irène Gallais Sérézal, et al.. (2017). CD49a Expression Defines Tissue-Resident CD8 + T Cells Poised for Cytotoxic Function in Human Skin. Immunity. 46(2). 287–300. 475 indexed citations breakdown →

Introini, Andrea, et al.. (2017). Seminal plasma induces inflammation and enhances HIV-1 replication in human cervical tissue explants. PLoS Pathogens. 13(5). e1006402–e1006402. 37 indexed citations

Gibbs, Anna, Marcus Buggert, Gabriella Edfeldt, et al.. (2017). Human Immunodeficiency Virus-Infected Women Have High Numbers of CD103−CD8+ T Cells Residing Close to the Basal Membrane of the Ectocervical Epithelium. The Journal of Infectious Diseases. 218(3). 453–465. 15 indexed citations

Eidsmo, Liv, Rajeev Kaul, Stanley Cheuk, et al.. (2017). HIV-infected women have high numbers of CD103-CD8+ T cells residing close to the basal membrane of the ectocervical epithelium.. 2 indexed citations

Paquin‐Proulx, Dominic, Anna Gibbs, Susanna M. Bächle, et al.. (2016). Innate Invariant NKT Cell Recognition of HIV-1–Infected Dendritic Cells Is an Early Detection Mechanism Targeted by Viral Immune Evasion. The Journal of Immunology. 197(5). 1843–1851. 17 indexed citations

10.

Gibbs, Anna, Edwin Leeansyah, Andrea Introini, et al.. (2016). MAIT cells reside in the female genital mucosa and are biased towards IL-17 and IL-22 production in response to bacterial stimulation. Mucosal Immunology. 10(1). 35–45. 171 indexed citations

11.

Ahlén, Gustaf, et al.. (2014). Long-term functional duration of immune responses to HCV NS3/4A induced by DNA vaccination. Gene Therapy. 21(8). 739–750. 13 indexed citations

12.

Gibbs, Anna, Taha Hirbod, Qingsheng Li, et al.. (2014). Presence of CD8+ T Cells in the Ectocervical Mucosa Correlates with Genital Viral Shedding in HIV-Infected Women despite a Low Prevalence of HIV RNA–Expressing Cells in the Tissue. The Journal of Immunology. 192(8). 3947–3957. 12 indexed citations

13.

Gibbs, Anna, et al.. (1992). Talc pneumoconiosis: A pathologic and mineralogic study. Human Pathology. 23(12). 1344–1354. 43 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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