Suzanne L. Tomchuck

2.5k total citations · 1 hit paper
20 papers, 1.9k citations indexed

About

Suzanne L. Tomchuck is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Suzanne L. Tomchuck has authored 20 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Immunology, 6 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Suzanne L. Tomchuck's work include Immune Cell Function and Interaction (5 papers), Erythrocyte Function and Pathophysiology (4 papers) and Mesenchymal stem cell research (3 papers). Suzanne L. Tomchuck is often cited by papers focused on Immune Cell Function and Interaction (5 papers), Erythrocyte Function and Pathophysiology (4 papers) and Mesenchymal stem cell research (3 papers). Suzanne L. Tomchuck collaborates with scholars based in United States, United Kingdom and Saudi Arabia. Suzanne L. Tomchuck's co-authors include Ruth S. Waterman, Aline M. Betancourt, Seth B. Coffelt, Kevin J. Zwezdaryk, Aline B. Scandurro, Elizabeth S. Danka, Heather L. LaMarca, Kerstin Höner zu Bentrup, Frank C. Marini and Jennifer L. Dembinski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Immunology and PLoS ONE.

In The Last Decade

Suzanne L. Tomchuck

20 papers receiving 1.9k citations

Hit Papers

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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.

A New Mesenchymal Stem Cell (MSC) Paradigm: Polarization into a Pro-Inflammatory MSC1 or an Immunosuppressive MSC2 Phenotype

2010 963 citations Ruth S. Waterman, Suzanne L. Tomchuck et al. PLoS ONE profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Suzanne L. Tomchuck	1.2k	562	536	440	384	20	1.9k
Aline M. Betancourt	1.2k 1.0×	532 0.9×	321 0.6×	328 0.7×	627 1.6×	21	1.9k
Karen English	2.6k 2.2×	963 1.7×	841 1.6×	455 1.0×	1.2k 3.1×	52	3.6k
Soufiane Ghannam	844 0.7×	355 0.6×	633 1.2×	236 0.5×	359 0.9×	11	1.7k
Olga DelaRosa	1.1k 0.9×	420 0.7×	966 1.8×	359 0.8×	478 1.2×	34	2.2k
Delin Zhu	1.4k 1.2×	872 1.6×	1.3k 2.3×	584 1.3×	291 0.8×	51	2.8k
Anna Corcione	1.3k 1.2×	620 1.1×	1.2k 2.3×	688 1.6×	493 1.3×	56	3.0k
Jacob Rachmilewitz	731 0.6×	812 1.4×	975 1.8×	297 0.7×	362 0.9×	56	2.4k
Juan José Montesinos	708 0.6×	454 0.8×	323 0.6×	278 0.6×	233 0.6×	73	1.5k
Roberta Angeli	1.4k 1.2×	597 1.1×	1.7k 3.2×	527 1.2×	643 1.7×	19	3.5k
Marek Honczarenko	682 0.6×	586 1.0×	1.0k 2.0×	720 1.6×	243 0.6×	31	2.2k

Countries citing papers authored by Suzanne L. Tomchuck

Since Specialization

Citations

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

Fields of papers citing papers by Suzanne L. Tomchuck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne L. Tomchuck

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne L. Tomchuck. A scholar is included among the top collaborators of Suzanne L. Tomchuck 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 Suzanne L. Tomchuck. Suzanne L. Tomchuck 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

Askew, David S., Vipin Kumar, Suzanne L. Tomchuck, et al.. (2025). Piezo1 deletion enhances cross-priming of CD8+ T cells by tumor-infiltrating CD11b+ dendritic cells. Journal for ImmunoTherapy of Cancer. 13(6). e011815–e011815. 1 indexed citations

Allan, Kevin, David Yan, Suzanne L. Tomchuck, et al.. (2024). Targeting the chromatin binding of exportin-1 disrupts NFAT and T cell activation. Nature Chemical Biology. 20(10). 1260–1271. 10 indexed citations

Choi, Sung Hee, Jay Myers, Byung‐Gyu Kim, et al.. (2024). Piezo1 restrains proinflammatory response but is essential in T-cell–mediated immunopathology. Journal of Leukocyte Biology. 117(3). 3 indexed citations

Tomchuck, Suzanne L., Jay Myers, Saada Eid, et al.. (2023). Functional tumor cell-intrinsic STING, not host STING, drives local and systemic antitumor immunity and therapy efficacy following cryoablation. Journal for ImmunoTherapy of Cancer. 11(8). e006608–e006608. 6 indexed citations

Myers, Jay, et al.. (2023). Piezo1 facilitates optimal T cell activation during tumor challenge. OncoImmunology. 12(1). 2281179–2281179. 12 indexed citations

Choi, Sung Hee, et al.. (2022). Mechanosensory channel Piezo1 is essential in pathogenic T cell-mediated intestinal inflammation. The Journal of Immunology. 208(Supplement_1). 113.16–113.16. 4 indexed citations

Kreisman, Norman R., et al.. (2019). Preconditioning hippocampal slices with hypothermia promotes rapid tolerance to hypoxic depolarization and swelling: Mediation by erythropoietin. Brain Research. 1726. 146517–146517. 4 indexed citations

Pui, Ching‐Hon, Deqing Pei, Cheng Cheng, et al.. (2019). Treatment response and outcome of children with T-cell acute lymphoblastic leukemia expressing the gamma-delta T-cell receptor. OncoImmunology. 8(8). 1599637–1599637. 11 indexed citations

Guo, Xi-zhi J., et al.. (2016). Rapid cloning, expression, and functional characterization of paired αβ and γδ T-cell receptor chains from single-cell analysis. Molecular Therapy — Methods & Clinical Development. 3. 15054–15054. 37 indexed citations

10.

Tomchuck, Suzanne L., Wing Leung, & Mari Dallas. (2014). Enhanced Cytotoxic Function of Natural Killer and CD3+CD56+ Cells in Cord Blood after Culture. Biology of Blood and Marrow Transplantation. 21(1). 39–49. 19 indexed citations

11.

Tomchuck, Suzanne L., Wing Leung, & Mari Dallas. (2013). Isolation, Expansion & Function of Cord Blood Natural Killer Cells. Biology of Blood and Marrow Transplantation. 19(2). S208–S208. 1 indexed citations

12.

Tomchuck, Suzanne L., Wing Leung, & Mari Dallas. (2013). Isolation, expansion and function of cord blood natural killer cells. (P2226). The Journal of Immunology. 190(Supplement_1). 69.51–69.51. 1 indexed citations

13.

Tomchuck, Suzanne L., Elizabeth B. Norton, Robert F. Garry, et al.. (2012). Mesenchymal stem cells as a novel vaccine platform. Frontiers in Cellular and Infection Microbiology. 2. 140–140. 22 indexed citations

14.

Tomchuck, Suzanne L., et al.. (2012). Toll-Like Receptor 3 and Suppressor of Cytokine Signaling Proteins Regulate CXCR4 and CXCR7 Expression in Bone Marrow-Derived Human Multipotent Stromal Cells. PLoS ONE. 7(6). e39592–e39592. 13 indexed citations

15.

Waterman, Ruth S., et al.. (2010). A New Mesenchymal Stem Cell (MSC) Paradigm: Polarization into a Pro-Inflammatory MSC1 or an Immunosuppressive MSC2 Phenotype. PLoS ONE. 5(4). e10088–e10088. 963 indexed citations breakdown →

16.

Coffelt, Seth B., Suzanne L. Tomchuck, Kevin J. Zwezdaryk, Elizabeth S. Danka, & Aline B. Scandurro. (2009). Leucine Leucine-37 Uses Formyl Peptide Receptor–Like 1 to Activate Signal Transduction Pathways, Stimulate Oncogenic Gene Expression, and Enhance the Invasiveness of Ovarian Cancer Cells. Molecular Cancer Research. 7(6). 907–915. 69 indexed citations

17.

Coffelt, Seth B., Frank C. Marini, Kevin J. Zwezdaryk, et al.. (2009). The pro-inflammatory peptide LL-37 promotes ovarian tumor progression through recruitment of multipotent mesenchymal stromal cells. Proceedings of the National Academy of Sciences. 106(10). 3806–3811. 234 indexed citations

18.

Coffelt, Seth B., Ruth S. Waterman, Kerstin Höner zu Bentrup, et al.. (2007). Ovarian cancers overexpress the antimicrobial protein hCAP‐18 and its derivative LL‐37 increases ovarian cancer cell proliferation and invasion. International Journal of Cancer. 122(5). 1030–1039. 85 indexed citations

19.

Tomchuck, Suzanne L., Kevin J. Zwezdaryk, Seth B. Coffelt, et al.. (2007). Toll-Like Receptors on Human Mesenchymal Stem Cells Drive Their Migration and Immunomodulating Responses. Stem Cells. 26(1). 99–107. 368 indexed citations

20.

Elliott, Steven, Daniel E. Frigo, Lilia I. Melnik, et al.. (2006). AKT Regulation of Estrogen Receptor β Transcriptional Activity in Breast Cancer. Cancer Research. 66(17). 8373–8381. 31 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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