David L. Wiest

8.7k total citations
124 papers, 5.3k citations indexed

About

David L. Wiest is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, David L. Wiest has authored 124 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Immunology, 53 papers in Molecular Biology and 33 papers in Oncology. Recurrent topics in David L. Wiest's work include Immune Cell Function and Interaction (77 papers), T-cell and B-cell Immunology (67 papers) and CAR-T cell therapy research (25 papers). David L. Wiest is often cited by papers focused on Immune Cell Function and Interaction (77 papers), T-cell and B-cell Immunology (67 papers) and CAR-T cell therapy research (25 papers). David L. Wiest collaborates with scholars based in United States, Canada and Japan. David L. Wiest's co-authors include Michele Rhodes, Juan Carlos Zúñiga‐Pflücker, Dietmar J. Kappes, Alfred Singer, Michael Carleton, Dario A.A. Vignali, Haiyan Liu, Juliette M. Lefebvre, Mariëlle C. Haks and Shawn P. Fahl and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

David L. Wiest

122 papers receiving 5.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David L. Wiest United States 42 3.4k 2.3k 1.1k 439 396 124 5.3k
Cynthia J. Guidos Canada 37 2.1k 0.6× 2.2k 1.0× 1.0k 0.9× 334 0.8× 439 1.1× 79 4.2k
Mayumi Naramura United States 29 1.8k 0.5× 1.8k 0.8× 971 0.9× 294 0.7× 406 1.0× 51 3.6k
Dragana Cado United States 36 3.8k 1.1× 3.4k 1.5× 1.2k 1.1× 292 0.7× 486 1.2× 49 6.4k
Katherine A. Forbush United States 33 3.7k 1.1× 1.9k 0.8× 1.2k 1.0× 168 0.4× 368 0.9× 46 5.2k
Heinz Jacobs Netherlands 38 2.4k 0.7× 2.5k 1.1× 1.2k 1.1× 168 0.4× 576 1.5× 98 4.9k
James Hagman United States 40 3.3k 1.0× 3.0k 1.3× 909 0.8× 192 0.4× 537 1.4× 81 6.3k
Ai Ishii Japan 11 1.4k 0.4× 2.3k 1.0× 606 0.5× 453 1.0× 371 0.9× 12 3.7k
Gary Rathbun United States 22 1.7k 0.5× 2.8k 1.2× 992 0.9× 487 1.1× 598 1.5× 38 4.3k
William G. Kerr United States 34 2.4k 0.7× 2.3k 1.0× 1.2k 1.1× 295 0.7× 335 0.8× 109 5.2k
Kathryn A. Hjerrild United States 12 2.0k 0.6× 1.8k 0.8× 653 0.6× 280 0.6× 261 0.7× 15 4.1k

Countries citing papers authored by David L. Wiest

Since Specialization
Citations

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

Fields of papers citing papers by David L. Wiest

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David L. Wiest. 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 David L. Wiest. The network helps show where David L. Wiest may publish in the future.

Co-authorship network of co-authors of David L. Wiest

This figure shows the co-authorship network connecting the top 25 collaborators of David L. Wiest. A scholar is included among the top collaborators of David L. Wiest 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 David L. Wiest. David L. Wiest 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.
Martı́nez, Esteban, Daniela Di Marcantonio, Jeffrey A. Magee, et al.. (2024). Disruption of polyunsaturated fatty acid biosynthesis drives STING-dependent acute myeloid leukemia cell maturation and death. Journal of Biological Chemistry. 300(5). 107214–107214. 4 indexed citations
2.
Lee, Sang-Yun, Susan A. Shinton, Mitchell I. Parker, et al.. (2024). E proteins control the development of NKγδT cells through their invariant T cell receptor. Nature Communications. 15(1). 5078–5078. 2 indexed citations
3.
He, Shan, Tien D. Bui, Yuanyuan Tian, et al.. (2023). Tissue-infiltrating alloreactive T cells require Id3 to deflect PD-1–mediated immune suppression during GVHD. Blood. 143(2). 166–177. 6 indexed citations
4.
Kappes, Dietmar J. & David L. Wiest. (2023). Doubling down to make killer T cells. Nature Immunology. 24(9). 1407–1408.
5.
Zhang, Baojun, et al.. (2018). Id3 Restricts γδ NKT Cell Expansion by Controlling Egr2 and c-Myc Activity. The Journal of Immunology. 201(5). 1452–1459. 11 indexed citations
6.
Fahl, Shawn P., Edward L.Y. Chen, Payam Zarin, et al.. (2017). HEB is required for the specification of fetal IL-17-producing γδ T cells. Nature Communications. 8(1). 2004–2004. 43 indexed citations
7.
Rao, Shuyun, Kathy Q. Cai, Jason Stadanlick, et al.. (2016). Ribosomal Protein Rpl22 Controls the Dissemination of T-cell Lymphoma. Cancer Research. 76(11). 3387–3396. 28 indexed citations
8.
Zhang, Yong & David L. Wiest. (2015). Using the Zebrafish Model to Study T Cell Development. Methods in molecular biology. 1323. 273–292. 12 indexed citations
9.
Xia, Mingcan, et al.. (2010). Differential Roles of IL-2–Inducible T Cell Kinase-Mediated TCR Signals in Tissue-Specific Localization and Maintenance of Skin Intraepithelial T Cells. The Journal of Immunology. 184(12). 6807–6814. 20 indexed citations
10.
Zhang, Yong, Xiaoli Sun, Jennifer Rhodes, & David L. Wiest. (2010). Identification and characterization of zebrafish Rpl22 and its role in T cell development in vivo (36.66). The Journal of Immunology. 184(Supplement_1). 36.66–36.66. 1 indexed citations
11.
Xu, Mai, Archna Sharma, David L. Wiest, & Jyoti Misra Sen. (2009). Pre-TCR-Induced β-Catenin Facilitates Traversal through β-Selection. The Journal of Immunology. 182(2). 751–758. 24 indexed citations
12.
Xu, Mai, Archna Sharma, M. Zulfiquer Hossain, David L. Wiest, & Jyoti Misra Sen. (2009). Sustained Expression of Pre-TCR Induced β-Catenin in Post-β-Selection Thymocytes Blocks T Cell Development. The Journal of Immunology. 182(2). 759–765. 17 indexed citations
13.
Tan, Yinfei, Deborah A. Altomare, Jinfei Xu, et al.. (2008). A Novel Recurrent Chromosomal Inversion Implicates the Homeobox Gene Dlx5 in T-Cell Lymphomas from Lck-Akt2 Transgenic Mice. Cancer Research. 68(5). 1296–1302. 29 indexed citations
14.
Gururajan, Murali, Alan J. Simmons, Trivikram Dasu, et al.. (2008). Early Growth Response Genes Regulate B Cell Development, Proliferation, and Immune Response. The Journal of Immunology. 181(7). 4590–4602. 49 indexed citations
15.
Koltsova, Ekaterina K., Maria Ciofani, Robert Benezra, et al.. (2007). Early Growth Response 1 and NF-ATc1 Act in Concert to Promote Thymocyte Development beyond the β-Selection Checkpoint. The Journal of Immunology. 179(7). 4694–4703. 22 indexed citations
16.
Mao, Changchuin, Esmerina Tili, Marei Dose, et al.. (2007). Unequal Contribution of Akt Isoforms in the Double-Negative to Double-Positive Thymocyte Transition. The Journal of Immunology. 178(9). 5443–5453. 85 indexed citations
17.
Haks, Mariëlle C., Stanley M. Belkowski, Maria Ciofani, et al.. (2003). Low Activation Threshold As a Mechanism for Ligand-Independent Signaling in Pre-T Cells. The Journal of Immunology. 170(6). 2853–2861. 53 indexed citations
18.
Carleton, Michael, Mariëlle C. Haks, Allan R. Jones, et al.. (2002). Early Growth Response Transcription Factors Are Required for Development of CD4−CD8− Thymocytes to the CD4+CD8+ Stage. The Journal of Immunology. 168(4). 1649–1658. 80 indexed citations
19.
Trop, Sébastien, Michele Rhodes, David L. Wiest, Patrice Hugo, & Juan Carlos Zúñiga‐Pflücker. (2000). Competitive Displacement of pTα by TCR-α During TCR Assembly Prevents Surface Coexpression of Pre-TCR and αβ TCR. The Journal of Immunology. 165(10). 5566–5572. 38 indexed citations
20.
Wiest, David L., Kelly P. Kearse, Elizabeth W. Shores, & Alfred Singer. (1994). Developmentally regulated expression of CD3 components independent of clonotypic T cell antigen receptor complexes on immature thymocytes.. The Journal of Experimental Medicine. 180(4). 1375–1382. 55 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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