Aimee Payne

8.1k total citations · 3 hit papers
100 papers, 4.5k citations indexed

About

Aimee Payne is a scholar working on Pathology and Forensic Medicine, Genetics and Rheumatology. According to data from OpenAlex, Aimee Payne has authored 100 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Pathology and Forensic Medicine, 40 papers in Genetics and 31 papers in Rheumatology. Recurrent topics in Aimee Payne's work include Autoimmune Bullous Skin Diseases (58 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (36 papers) and Urticaria and Related Conditions (28 papers). Aimee Payne is often cited by papers focused on Autoimmune Bullous Skin Diseases (58 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (36 papers) and Urticaria and Related Conditions (28 papers). Aimee Payne collaborates with scholars based in United States, Germany and Japan. Aimee Payne's co-authors include Christoph T. Ellebrecht, Xuming Mao, Lynn A. Cornelius, Jonathan D. Gitlin, Masayuki Amagai, John R. Stanley, Eun Jung Choi, Jun Yamagami, Edward J. Kelly and Michael C. Milone and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Aimee Payne

99 papers receiving 4.4k 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.

Reengineering chimeric antigen receptor T cells for targeted therapy of autoimmune disease

2016 512 citations Christoph T. Ellebrecht, Vijay Bhoj et al. Science profile →
Pemphigus

2017 327 citations Christoph T. Ellebrecht, Jun Yamagami et al. profile →
Precision targeting of autoantigen-specific B cells in muscle-specific tyrosine kinase myasthenia gravis with chimeric autoantibody receptor T cells

2023 107 citations Sangwook Oh, Xuming Mao et al. Nature Biotechnology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aimee Payne United States	35	2.0k	1.3k	1.3k	1.2k	867	100	4.5k
Jean‐Claude Bystryn United States	37	1.4k 0.7×	848 0.7×	887 0.7×	518 0.4×	1.3k 1.5×	122	3.6k
D Y Mason United Kingdom	36	1.4k 0.7×	739 0.6×	282 0.2×	1.4k 1.2×	1.5k 1.7×	72	5.5k
Shirou Fukuhara Japan	37	909 0.5×	627 0.5×	490 0.4×	943 0.8×	2.9k 3.4×	143	5.7k
Hideo Harigae Japan	35	444 0.2×	657 0.5×	732 0.6×	679 0.6×	1.1k 1.2×	316	4.7k
Annette Schmitt‐Graeff Germany	47	660 0.3×	1.4k 1.1×	580 0.5×	1.4k 1.2×	2.0k 2.3×	195	6.6k
Francisco Vega United States	44	2.6k 1.3×	974 0.7×	242 0.2×	2.2k 1.9×	1.1k 1.3×	266	6.2k
Claus-Werner Franzke Germany	27	548 0.3×	410 0.3×	503 0.4×	331 0.3×	532 0.6×	42	2.9k
Nicolás Ortonne France	37	1.4k 0.7×	329 0.3×	906 0.7×	702 0.6×	606 0.7×	203	4.8k
Richard Groves United Kingdom	37	773 0.4×	455 0.3×	681 0.5×	487 0.4×	1.6k 1.9×	99	4.3k
Naoyuki Tsuchiya Japan	42	450 0.2×	318 0.2×	1.7k 1.3×	471 0.4×	2.9k 3.3×	168	5.3k

Countries citing papers authored by Aimee Payne

Since Specialization

Citations

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

Fields of papers citing papers by Aimee Payne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aimee Payne

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

All Works

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20 of 20 papers shown

Wang, Baomei, Xuming Mao, Sílvio M. Vieira, et al.. (2025). Preclinical evaluation of antigen-specific B-cell depletion for phospholipase A2 receptor membranous nephropathy with chimeric autoantibody receptor T cells. Kidney International. 109(1). 89–100. 1 indexed citations

Pham, Minh, Abeer Obaid, Sangwook Oh, et al.. (2023). Individual myasthenia gravis autoantibody clones can efficiently mediate multiple mechanisms of pathology. Acta Neuropathologica. 146(2). 319–336. 19 indexed citations

Bratton, Benjamin P., Jaime G Lopez, Aimee Payne, et al.. (2023). Bacterial DNA on the skin surface overrepresents the viable skin microbiome. eLife. 12. 28 indexed citations

Oh, Sangwook, Xuming Mao, Sílvio M. Vieira, et al.. (2023). Precision targeting of autoantigen-specific B cells in muscle-specific tyrosine kinase myasthenia gravis with chimeric autoantibody receptor T cells. Nature Biotechnology. 41(9). 1229–1238. 107 indexed citations breakdown →

Bratton, Benjamin P., Jaime G Lopez, Aimee Payne, et al.. (2023). Bacterial DNA on the skin surface overrepresents the viable skin microbiome. eLife. 12. 1 indexed citations

Pham, Minh, Sangwook Oh, Aimee Payne, et al.. (2023). Clinicoserological insights into patients with immune checkpoint inhibitor‐induced myasthenia gravis. Annals of Clinical and Translational Neurology. 10(5). 825–831. 11 indexed citations

Spindler, Volker, Brenda Gerull, Kathleen J. Green, et al.. (2023). Meeting report – Desmosome dysfunction and disease: Alpine desmosome disease meeting. Journal of Cell Science. 136(1). 15 indexed citations

Maseda, Damián, Sílvio M. Vieira, & Aimee Payne. (2023). T cell and bacterial microbiota interaction at intestinal and skin epithelial interfaces. PubMed. 2(1). kyad024–kyad024. 4 indexed citations

France, Katherine, Luiz Alcino Gueiros, Remberto Marcelo Argandoña Valdez, et al.. (2022). World Workshop on Oral Medicine VII : Oral adverse effects to biologic agents in patients with inflammatory disorders. A scoping review. Journal of Oral Pathology and Medicine. 52(1). 1–8. 3 indexed citations

10.

Fichtner, Miriam L., Kenneth B. Hoehn, Marina Mané-Damas, et al.. (2022). Reemergence of pathogenic, autoantibody-producing B cell clones in myasthenia gravis following B cell depletion therapy. Acta Neuropathologica Communications. 10(1). 154–154. 26 indexed citations

11.

Zhao, Wenling, Xuming Mao, Aimee Payne, et al.. (2020). Detection of underlying dementia in bullous pemphigoid patients using cognitive evaluation tests: a multicenter case-control study. Annals of Translational Medicine. 8(21). 1397–1397. 7 indexed citations

12.

Pearson, David R., Munir Tarazi, Rebecca G. Gaffney, et al.. (2018). 515 Assessing the quality of quality of life measurement tools in autoimmune blistering disease. Journal of Investigative Dermatology. 138(5). S88–S88. 1 indexed citations

13.

Leibman, Rachel S., Max W. Richardson, Christoph T. Ellebrecht, et al.. (2017). Supraphysiologic control over HIV-1 replication mediated by CD8 T cells expressing a re-engineered CD4-based chimeric antigen receptor. PLoS Pathogens. 13(10). e1006613–e1006613. 94 indexed citations

14.

Ellebrecht, Christoph T., Vijay Bhoj, Arben Nace, et al.. (2016). Reengineering chimeric antigen receptor T cells for targeted therapy of autoimmune disease. Science. 353(6295). 179–184. 512 indexed citations breakdown →

15.

Cho, Michael Jeffrey, Christoph T. Ellebrecht, Christoph M. Hammers, et al.. (2016). Determinants of VH1-46 Cross-Reactivity to Pemphigus Vulgaris Autoantigen Desmoglein 3 and Rotavirus Antigen VP6. The Journal of Immunology. 197(4). 1065–1073. 20 indexed citations

16.

Cho, Michael Jeffrey, Christoph T. Ellebrecht, & Aimee Payne. (2014). The dual nature of interleukin-10 in pemphigus vulgaris. Cytokine. 73(2). 335–341. 24 indexed citations

17.

Lunardon, Luisa, Kathleen J. Propert, Nicole Fett, et al.. (2012). Adjuvant Rituximab Therapy of Pemphigus. Archives of Dermatology. 148(9). 1031–6. 83 indexed citations

18.

Mao, Xuming, Arielle R. Nagler, Eun Jung Choi, et al.. (2010). Autoimmunity to Desmocollin 3 in Pemphigus Vulgaris. American Journal Of Pathology. 177(6). 2724–2730. 63 indexed citations

19.

Yamagami, Jun, Stephen Kacir, Ken Ishii, et al.. (2009). Antibodies to the Desmoglein 1 Precursor Proprotein but Not to the Mature Cell Surface Protein Cloned from Individuals without Pemphigus. The Journal of Immunology. 183(9). 5615–5621. 25 indexed citations

20.

Goyal, Rakesh K., et al.. (1999). Ajuba, a Novel LIM Protein, Interacts with Grb2, Augments Mitogen-Activated Protein Kinase Activity in Fibroblasts, and Promotes Meiotic Maturation of Xenopus Oocytes in a Grb2- and Ras-Dependent Manner. Molecular and Cellular Biology. 19(6). 4379–4389. 85 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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