William E. LeSuer

743 total citations
17 papers, 527 citations indexed

About

William E. LeSuer is a scholar working on Surgery, Immunology and Physiology. According to data from OpenAlex, William E. LeSuer has authored 17 papers receiving a total of 527 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Surgery, 10 papers in Immunology and 9 papers in Physiology. Recurrent topics in William E. LeSuer's work include Eosinophilic Esophagitis (11 papers), IL-33, ST2, and ILC Pathways (9 papers) and Asthma and respiratory diseases (9 papers). William E. LeSuer is often cited by papers focused on Eosinophilic Esophagitis (11 papers), IL-33, ST2, and ILC Pathways (9 papers) and Asthma and respiratory diseases (9 papers). William E. LeSuer collaborates with scholars based in United States, Canada and China. William E. LeSuer's co-authors include Elizabeth A. Jacobsen, Alfred D. Doyle, Sergei I. Ochkur, Katie R. Zellner, Cheryl Protheroe, Dana Colbert, James J. Lee, Huijun Luo, Benjamin L. Wright and Paige Lacy and has published in prestigious journals such as American Journal of Respiratory and Critical Care Medicine, Diabetes and Journal of Allergy and Clinical Immunology.

In The Last Decade

William E. LeSuer

17 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William E. LeSuer United States 10 274 258 195 112 95 17 527
Kęstutis Malakauskas Lithuania 14 311 1.1× 181 0.7× 89 0.5× 30 0.3× 172 1.8× 52 460
Laura K. Johnston United States 6 216 0.8× 306 1.2× 176 0.9× 49 0.4× 29 0.3× 7 539
Ichiro Tojima Japan 14 366 1.3× 227 0.9× 179 0.9× 28 0.3× 86 0.9× 39 691
Jacqueline Cephus United States 9 224 0.8× 411 1.6× 245 1.3× 23 0.2× 61 0.6× 15 593
Tae Gi Uhm South Korea 8 169 0.6× 138 0.5× 52 0.3× 42 0.4× 67 0.7× 12 377
Emma Doran United Kingdom 9 352 1.3× 333 1.3× 92 0.5× 27 0.2× 129 1.4× 14 643
Ashraf Uzzaman United States 8 215 0.8× 154 0.6× 56 0.3× 95 0.8× 184 1.9× 9 521
Monica Boita Italy 15 175 0.6× 92 0.4× 95 0.5× 39 0.3× 145 1.5× 32 487
Cailong Fang United Kingdom 6 508 1.9× 403 1.6× 133 0.7× 60 0.5× 166 1.7× 7 735
Jane Gilbert United Kingdom 6 322 1.2× 68 0.3× 137 0.7× 67 0.6× 99 1.0× 9 501

Countries citing papers authored by William E. LeSuer

Since Specialization
Citations

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

Fields of papers citing papers by William E. LeSuer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William E. LeSuer

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

All Works

17 of 17 papers shown
1.
Luo, Huijun, William E. LeSuer, Rish K. Pai, et al.. (2024). Tissue-specific inducible IL-33 expression elicits features of eosinophilic esophagitis. Journal of Allergy and Clinical Immunology. 154(6). 1545–1553.e2. 3 indexed citations
2.
LeSuer, William E., Melanie Kienzl, Sergei I. Ochkur, et al.. (2023). Eosinophils promote effector functions of lung group 2 innate lymphoid cells in allergic airway inflammation in mice. Journal of Allergy and Clinical Immunology. 152(2). 469–485.e10. 35 indexed citations
3.
LeSuer, William E., et al.. (2023). Food-Specific IgG4 Is Elevated Throughout the Upper Gastrointestinal Tract in Eosinophilic Esophagitis. Digestive Diseases and Sciences. 68(6). 2406–2413. 6 indexed citations
4.
Barshow, Suzanne, Shipra Garg, William E. LeSuer, et al.. (2022). Eosinophil Peroxidase Staining Enhances the Diagnostic Utility of the Cytosponge in Eosinophilic Esophagitis. Clinical and Translational Gastroenterology. 13(11). e00534–e00534. 5 indexed citations
5.
Doyle, Alfred D., Huijun Luo, William E. LeSuer, et al.. (2022). Detergent exposure induces epithelial barrier dysfunction and eosinophilic inflammation in the esophagus. Allergy. 78(1). 192–201. 58 indexed citations
6.
Li, Ting, William E. LeSuer, Panwen Wang, et al.. (2021). ω-3PUFA supplementation ameliorates adipose tissue inflammation and insulin-stimulated glucose disposal in subjects with obesity: a potential role for apolipoprotein E. International Journal of Obesity. 45(6). 1331–1341. 20 indexed citations
7.
LeSuer, William E., et al.. (2020). Assessment of Lung Eosinophils In Situ Using Immunohistological Staining. Methods in molecular biology. 2223. 237–266. 5 indexed citations
8.
Doyle, Alfred D., Manali Mukherjee, William E. LeSuer, et al.. (2019). Eosinophil-derived IL-13 promotes emphysema. European Respiratory Journal. 53(5). 1801291–1801291. 59 indexed citations
9.
Chojnacki, Andrew, Björn Petri, Gurpreet Kaur Aulakh, et al.. (2019). Intravital imaging allows real-time characterization of tissue resident eosinophils. Communications Biology. 2(1). 181–181. 32 indexed citations
10.
Jacobsen, Elizabeth A., William E. LeSuer, Sergei I. Ochkur, et al.. (2019). Eosinophils Induce Recruitment and Activation of ILC2s. Journal of Allergy and Clinical Immunology. 143(2). AB289–AB289. 5 indexed citations
11.
Li, Ting, William E. LeSuer, Xiaodong Zhang, et al.. (2019). 2006-P: The Role of Adipose Tissue-Resident Eosinophils in Adipocyte Metabolism and Whole-Body Energy Homeostasis. Diabetes. 68(Supplement_1). 1 indexed citations
12.
Doyle, Alfred D., Kelly P. Shim, Huijun Luo, et al.. (2019). Transgenic Expression of a Novel Secreted and Active Form of IL-33 Promotes Tissue Eosinophilia in a Mouse Model of Eosinophilic Esophagitis. Journal of Allergy and Clinical Immunology. 143(2). AB290–AB290. 2 indexed citations
13.
Jacobsen, Elizabeth A., Sergei I. Ochkur, Alfred D. Doyle, et al.. (2017). Lung Pathologies in a Chronic Inflammation Mouse Model Are Independent of Eosinophil Degranulation. American Journal of Respiratory and Critical Care Medicine. 195(10). 1321–1332. 30 indexed citations
14.
Ochkur, Sergei I., Alfred D. Doyle, Elizabeth A. Jacobsen, et al.. (2017). Frontline Science: Eosinophil-deficient MBP-1 and EPX double-knockout mice link pulmonary remodeling and airway dysfunction with type 2 inflammation. Journal of Leukocyte Biology. 102(3). 589–599. 13 indexed citations
15.
Jacobsen, Elizabeth A., Alfred D. Doyle, Dana Colbert, et al.. (2015). Differential activation of airway eosinophils inducesIL‐13‐mediated allergic Th2 pulmonary responses in mice. Allergy. 70(9). 1148–1159. 48 indexed citations
16.
Jacobsen, Elizabeth A., William E. LeSuer, Lian Willetts, et al.. (2013). Eosinophil activities modulate the immune/inflammatory character of allergic respiratory responses in mice. Allergy. 69(3). 315–327. 53 indexed citations
17.
Lee, James J., Elizabeth A. Jacobsen, Sergei I. Ochkur, et al.. (2012). Human versus mouse eosinophils: “That which we call an eosinophil, by any other name would stain as red”. Journal of Allergy and Clinical Immunology. 130(3). 572–584. 152 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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