Janet E. Lewis

599 total citations
22 papers, 476 citations indexed

About

Janet E. Lewis is a scholar working on Rheumatology, Immunology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Janet E. Lewis has authored 22 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Rheumatology, 6 papers in Immunology and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Janet E. Lewis's work include T-cell and B-cell Immunology (6 papers), Fibromyalgia and Chronic Fatigue Syndrome Research (5 papers) and Systemic Lupus Erythematosus Research (5 papers). Janet E. Lewis is often cited by papers focused on T-cell and B-cell Immunology (6 papers), Fibromyalgia and Chronic Fatigue Syndrome Research (5 papers) and Systemic Lupus Erythematosus Research (5 papers). Janet E. Lewis collaborates with scholars based in United States, Austria and Germany. Janet E. Lewis's co-authors include Shu Man Fu, Felicia Gaskin, Umesh S. Deshmukh, Carol C. Kannapell, Kenneth S. K. Tung, Samuel T. Waters, Gary W. Litman, Peter M. Kroisel, Yuko Ohta and Robert N. Haire and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Immunology and FEBS Letters.

In The Last Decade

Janet E. Lewis

21 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janet E. Lewis United States 11 233 142 110 100 56 22 476
T Uede Japan 14 182 0.8× 116 0.8× 91 0.8× 74 0.7× 86 1.5× 49 544
Leszek Noga Poland 14 111 0.5× 46 0.3× 129 1.2× 33 0.3× 37 0.7× 30 450
Geneviève Enault France 8 222 1.0× 121 0.9× 65 0.6× 37 0.4× 30 0.5× 10 397
Tianlu Li Spain 16 127 0.5× 59 0.4× 267 2.4× 65 0.7× 45 0.8× 26 534
Aidan Droogan United Kingdom 14 178 0.8× 83 0.6× 91 0.8× 126 1.3× 291 5.2× 21 535
Jacky Bismuth France 17 303 1.3× 52 0.4× 112 1.0× 36 0.4× 48 0.9× 18 1.1k
Sarah Fleischer Germany 11 237 1.0× 172 1.2× 63 0.6× 68 0.7× 20 0.4× 27 448
Csilla Rózsa Hungary 16 105 0.5× 72 0.5× 97 0.9× 61 0.6× 217 3.9× 32 535
Ivy Y. Choi Netherlands 12 179 0.8× 217 1.5× 158 1.4× 43 0.4× 20 0.4× 15 475
Inga Koneczny Austria 17 87 0.4× 116 0.8× 140 1.3× 54 0.5× 132 2.4× 27 952

Countries citing papers authored by Janet E. Lewis

Since Specialization
Citations

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

Fields of papers citing papers by Janet E. Lewis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janet E. Lewis. 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 Janet E. Lewis. The network helps show where Janet E. Lewis may publish in the future.

Co-authorship network of co-authors of Janet E. Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Janet E. Lewis. A scholar is included among the top collaborators of Janet E. Lewis 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 Janet E. Lewis. Janet E. Lewis 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.
Kandasamy, A., et al.. (2025). Identification of immunogenic KIF5B-RET fusion neopeptides driving immune stimulation in tumor specific CD8+ T cells. Frontiers in Immunology. 16. 1635810–1635810.
2.
Lewis, Janet E., et al.. (2024). The Role of Vimentin Peptide Citrullination in the Structure and Dynamics of HLA-DRB1 Rheumatoid Arthritis Risk-Associated Alleles. International Journal of Molecular Sciences. 26(1). 34–34. 1 indexed citations
3.
Anderson, Joel G., et al.. (2014). Effects of Cranial Electrical Stimulation on Activity in Regions of the Basal Ganglia in Individuals with Fibromyalgia. The Journal of Alternative and Complementary Medicine. 20(3). 206–207. 2 indexed citations
4.
Sharma, Aditya, Shailendra Singh, & Janet E. Lewis. (2014). Diagnostic Approach in Patients With Suspected Vasculitis. Techniques in vascular and interventional radiology. 17(4). 226–233. 3 indexed citations
5.
Goehler, Lisa E., Michael M. Scott, Ronald P. Gaykema, et al.. (2014). 18. Stress, pain and monocytes in fibromyalgia. Brain Behavior and Immunity. 40. e6–e6. 1 indexed citations
6.
Coquery, Christine M., William Loo, Kenneth S. K. Tung, et al.. (2014). BAFF Regulates Follicular Helper T Cells and Affects Their Accumulation and Interferon‐γ Production in Autoimmunity. Arthritis & Rheumatology. 67(3). 773–784. 49 indexed citations
7.
8.
Lewis, Janet E., Shu Man Fu, & Felicia Gaskin. (2013). Autoimmunity, end organ damage, and the origin of autoantibodies and autoreactive T cells in systemic lupus erythematosus.. PubMed. 15(81). 85–92. 26 indexed citations
9.
Taylor, Ann Gill, et al.. (2011). Cranial Electrical Stimulation Improves Symptoms and Functional Status in Individuals with Fibromyalgia. Pain Management Nursing. 14(4). 327–335. 24 indexed citations
10.
Boothman, David A., Heather L. Burrows, Chin-Rang Yang, et al.. (2009). Damage-Sensing mechanisms in human cells after ionizing radiation. Stem Cells. 15(S1). 27–42. 5 indexed citations
11.
Setiady, Yulius Y., Sally Agersborg, Eileen T. Samy, Janet E. Lewis, & Kenneth S. K. Tung. (2005). Neonatal Autoimmune Disease: Influence of CD4+CD25+Regulatory T Cells. International Reviews of Immunology. 24(3-4). 227–245. 7 indexed citations
12.
Deshmukh, Umesh S., Felicia Gaskin, Janet E. Lewis, Carol C. Kannapell, & Shu Man Fu. (2003). Mechanisms of Autoantibody Diversification to SLE‐Related Autoantigens. Annals of the New York Academy of Sciences. 987(1). 91–98. 44 indexed citations
13.
Fu, Shu Man, Juan González del Castillo, Umesh S. Deshmukh, et al.. (2003). Autoantibodies and glomerulonephritis in systemic lupus erythematosus. Lupus. 12(3). 175–180. 5 indexed citations
14.
Deshmukh, Umesh S., Janet E. Lewis, Felicia Gaskin, et al.. (2000). Ro60 Peptides Induce Antibodies to Similar Epitopes Shared Among Lupus-Related Autoantigens. The Journal of Immunology. 164(12). 6655–6661. 38 indexed citations
15.
Deshmukh, Umesh S., Janet E. Lewis, Felicia Gaskin, et al.. (1999). Immune Responses to Ro60 and Its Peptides in Mice. I.  The Nature of the Immunogen and Endogenous Autoantigen Determine the Specificities of the Induced Autoantibodies. The Journal of Experimental Medicine. 189(3). 531–540. 71 indexed citations
16.
Edwards, T. Bradley, Janet E. Lewis, & Carlos A. Guanche. (1997). Patellar Tendon and Tibial Tubercle Reconstruction Using Quadriceps Tendon With Patellar Bone Plug Autograft. Journal of Orthopaedic Trauma. 11(4). 304–307. 3 indexed citations
17.
Meyers, Mark, Maria Theodosiou, Samir Acharya, et al.. (1997). Cell cycle regulation of the human DNA mismatch repair genes hMSH2, hMLH1, and hPMS2.. PubMed. 57(2). 206–8. 52 indexed citations
18.
Haire, Robert N., Yuko Ohta, Janet E. Lewis, et al.. (1994). TXK, a novel human tyrosine kinase expressed in T cells shares sequence identity with Tec family kinases and maps to 4p12. Human Molecular Genetics. 3(6). 897–901. 74 indexed citations
19.
Lewis, Janet E. & C. William Birky. (1984). Homoplasmic yeast cells contain no selectable “hidden” mitochondrial alleles. Current Genetics. 8(1). 81–84. 2 indexed citations
20.
Lewis, Janet E., et al.. (1974). The interpretation of temporomandibular joint radiographs.. PubMed. 48(45). 1905–12. 7 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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