Judith C. Gasson

8.9k total citations · 3 hit papers
78 papers, 7.4k citations indexed

About

Judith C. Gasson is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Judith C. Gasson has authored 78 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Immunology, 32 papers in Molecular Biology and 15 papers in Oncology. Recurrent topics in Judith C. Gasson's work include T-cell and Retrovirus Studies (14 papers), Immune Response and Inflammation (14 papers) and Acute Myeloid Leukemia Research (12 papers). Judith C. Gasson is often cited by papers focused on T-cell and Retrovirus Studies (14 papers), Immune Response and Inflammation (14 papers) and Acute Myeloid Leukemia Research (12 papers). Judith C. Gasson collaborates with scholars based in United States, Canada and Japan. Judith C. Gasson's co-authors include David W. Golde, Richard H. Weisbart, Steven C. Clark, H. Phillip Koeffler, Gordon Wong, Susan Kaufman, Irvin S. Y. Chen, Reinhold Munker, John F. DiPersio and Makio Ogawa and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Judith C. Gasson

78 papers receiving 7.1k citations

Hit Papers

Fate Tracing Reveals the ... 1986 2026 1999 2012 2008 1986 1987 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith C. Gasson United States 42 3.4k 2.6k 1.3k 1.2k 808 78 7.4k
Tetsuya Nosaka Japan 37 3.3k 1.0× 3.2k 1.2× 987 0.8× 2.4k 1.9× 513 0.6× 120 7.7k
Frank Köntgen Australia 25 5.0k 1.5× 3.7k 1.4× 563 0.4× 1.4k 1.1× 397 0.5× 28 9.2k
Ashley R. Dunn Australia 50 4.9k 1.4× 3.6k 1.4× 1.1k 0.9× 2.0k 1.6× 470 0.6× 101 10.0k
Mamoru Ito Japan 53 4.1k 1.2× 3.0k 1.1× 1.6k 1.2× 1.9k 1.6× 588 0.7× 220 10.0k
June Eisenman Canada 20 3.6k 1.0× 1.4k 0.5× 907 0.7× 1.0k 0.8× 483 0.6× 28 5.6k
Paul W. Kincade United States 59 5.4k 1.6× 3.0k 1.2× 2.0k 1.5× 1.2k 1.0× 544 0.7× 155 9.6k
Hans‐Jörg Bühring Germany 49 3.2k 0.9× 2.0k 0.8× 1.1k 0.9× 1.2k 1.0× 769 1.0× 144 7.4k
Donald E. Staunton United States 39 4.2k 1.2× 2.6k 1.0× 1.3k 1.0× 1.0k 0.8× 673 0.8× 67 9.2k
M P Beckmann United States 33 3.8k 1.1× 1.9k 0.7× 842 0.7× 1.7k 1.4× 515 0.6× 44 6.9k
David P. Gearing United States 44 3.5k 1.0× 3.6k 1.4× 664 0.5× 3.7k 3.1× 470 0.6× 65 8.2k

Countries citing papers authored by Judith C. Gasson

Since Specialization
Citations

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

Fields of papers citing papers by Judith C. Gasson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith C. Gasson. 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 Judith C. Gasson. The network helps show where Judith C. Gasson may publish in the future.

Co-authorship network of co-authors of Judith C. Gasson

This figure shows the co-authorship network connecting the top 25 collaborators of Judith C. Gasson. A scholar is included among the top collaborators of Judith C. Gasson 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 Judith C. Gasson. Judith C. Gasson 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.
Zhu, Min, Romaine E. Saxton, Lillian Ramos, et al.. (2011). Neutralizing Monoclonal Antibody to Periostin Inhibits Ovarian Tumor Growth and Metastasis. Molecular Cancer Therapeutics. 10(8). 1500–1508. 64 indexed citations
2.
Lynch, Maureen, Judith C. Gasson, & Helicia Paz. (2011). Modified ES / OP9 Co-Culture Protocol Provides Enhanced Characterization of Hematopoietic Progeny. Journal of Visualized Experiments. 9 indexed citations
3.
Lynch, Maureen, Judith C. Gasson, & Helicia Paz. (2011). Modified ES / OP9 Co-Culture Protocol Provides Enhanced Characterization of Hematopoietic Progeny. Journal of Visualized Experiments. 3 indexed citations
4.
Zovein, Ann C., Kirsten A. Turlo, Maureen Lynch, et al.. (2010). Vascular remodeling of the vitelline artery initiates extravascular emergence of hematopoietic clusters. Blood. 116(18). 3435–3444. 68 indexed citations
5.
Rubin, Ethel, Xinyan Wu, Tao Zhu, et al.. (2007). A Role for the HOXB7 Homeodomain Protein in DNA Repair. Cancer Research. 67(4). 1527–1535. 75 indexed citations
6.
Carlson, Anne B., et al.. (2005). Expression of c-Fes Protein Isoforms Correlates with Differentiation in Myeloid Leukemias. DNA and Cell Biology. 24(5). 311–316. 7 indexed citations
7.
Carlson, Anne B., Karen E. Yates, Dennis J. Slamon, & Judith C. Gasson. (2005). Spatial and Temporal Changes in the Subcellular Localization of the Nuclear Protein–Tyrosine Kinase, c-Fes. DNA and Cell Biology. 24(4). 225–234. 3 indexed citations
8.
Gasson, Judith C.. (2005). Why cancer centers matter. Cancer Biology & Therapy. 4(4). 499–501. 1 indexed citations
9.
Lynch, Maureen, et al.. (2001). Identification of Novel Functional Regions Important for the Activity of HOXB7 in Mammalian Cells. The Journal of Immunology. 166(8). 5058–5067. 39 indexed citations
10.
Villa, Natividad, Liberty Walker, C.E. Lindsell, et al.. (2001). Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels. Mechanisms of Development. 108(1-2). 161–164. 326 indexed citations
11.
Walker, Liberty, et al.. (2000). Notch Signaling Enhances Survival and Alters Differentiation of 32D Myeloblasts. The Journal of Immunology. 165(8). 4428–4436. 43 indexed citations
12.
Fraser, John K., et al.. (1994). Characterization of a Cell-Type-Restricted Negative Regulatory Activity of the Human Granulocyte-Macrophage Colony-Stimulating Factor Gene. Molecular and Cellular Biology. 14(3). 2213–2221. 4 indexed citations
13.
Economou, James S., Kristina Rhoades, Richard Essner, et al.. (1989). Genetic analysis of the human tumor necrosis factor alpha/cachectin promoter region in a macrophage cell line.. The Journal of Experimental Medicine. 170(1). 321–326. 109 indexed citations
14.
Nimer, Stephen D., et al.. (1989). Multiple mechanisms control the expression of granulocyte-macrophage colony-stimulating factor by human fibroblasts.. The Journal of Immunology. 143(7). 2374–2377. 35 indexed citations
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Benveniste, Etty N., et al.. (1988). Response of human glioblastoma cells to recombinant interleukin-2. Journal of Neuroimmunology. 17(4). 301–314. 19 indexed citations
18.
Baldwin, Gayle Cocita, Judith C. Gasson, Jacob Fleischmann, et al.. (1988). Granulocyte-macrophage colony-stimulating factor enhances neutrophil function in acquired immunodeficiency syndrome patients.. Proceedings of the National Academy of Sciences. 85(8). 2763–2766. 155 indexed citations
19.
Owen, W F, Marc E. Rothenberg, David S. Silberstein, et al.. (1987). Regulation of human eosinophil viability, density, and function by granulocyte/macrophage colony-stimulating factor in the presence of 3T3 fibroblasts.. The Journal of Experimental Medicine. 166(1). 129–141. 336 indexed citations breakdown →
20.
Benveniste, Etty, J E Merrill, Susan Kaufman, David W. Golde, & Judith C. Gasson. (1985). Purification and characterization of a human T-lymphocyte-derived glial growth-promoting factor.. Proceedings of the National Academy of Sciences. 82(11). 3930–3934. 34 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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