Katherine A. Forbush

5.9k total citations · 1 hit paper
46 papers, 5.2k citations indexed

About

Katherine A. Forbush is a scholar working on Immunology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Katherine A. Forbush has authored 46 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Immunology, 17 papers in Molecular Biology and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Katherine A. Forbush's work include T-cell and B-cell Immunology (28 papers), Immune Cell Function and Interaction (20 papers) and Immunotherapy and Immune Responses (16 papers). Katherine A. Forbush is often cited by papers focused on T-cell and B-cell Immunology (28 papers), Immune Cell Function and Interaction (20 papers) and Immunotherapy and Immune Responses (16 papers). Katherine A. Forbush collaborates with scholars based in United States, Canada and France. Katherine A. Forbush's co-authors include Roger M. Perlmutter, Alexander Y. Rudensky, Kristin M. Abraham, Steven Z. Josefowicz, Ye Zheng, Ashutosh Chaudhry, Xiao Peng, Steven D. Levin, José Alberola‐Ila and M. Cooke and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Katherine A. Forbush

45 papers receiving 5.1k citations

Hit Papers

Role of conserved non-coding DNA elements in the Foxp3 ge... 2010 2026 2015 2020 2010 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katherine A. Forbush United States 33 3.7k 1.9k 1.2k 368 297 46 5.2k
José Alberola‐Ila United States 29 2.3k 0.6× 1.5k 0.8× 935 0.8× 274 0.7× 213 0.7× 59 3.6k
Nicolai S. C. van Oers United States 35 3.1k 0.8× 1.4k 0.8× 922 0.8× 249 0.7× 525 1.8× 81 4.4k
John G. Monroe United States 46 3.6k 1.0× 1.5k 0.8× 705 0.6× 509 1.4× 778 2.6× 126 5.3k
C H June United States 24 2.8k 0.8× 1.3k 0.7× 747 0.6× 212 0.6× 505 1.7× 33 4.0k
Takeshi Tsubata Japan 37 4.2k 1.1× 1.8k 1.0× 660 0.6× 327 0.9× 940 3.2× 126 5.7k
Ailsa G. Harpur Australia 20 1.9k 0.5× 1.6k 0.8× 2.6k 2.3× 453 1.2× 220 0.7× 30 4.1k
David L. Wiest United States 42 3.4k 0.9× 2.3k 1.2× 1.1k 1.0× 396 1.1× 202 0.7× 124 5.3k
Dominique Davidson Canada 37 2.3k 0.6× 1.6k 0.8× 870 0.8× 146 0.4× 281 0.9× 72 3.8k
Paul S. Changelian United States 27 1.6k 0.4× 1.7k 0.9× 1.5k 1.3× 284 0.8× 257 0.9× 39 4.4k
Satoru Senju Japan 38 2.7k 0.7× 3.1k 1.6× 1.8k 1.6× 451 1.2× 326 1.1× 101 5.8k

Countries citing papers authored by Katherine A. Forbush

Since Specialization
Citations

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

Fields of papers citing papers by Katherine A. Forbush

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katherine A. Forbush. 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 Katherine A. Forbush. The network helps show where Katherine A. Forbush may publish in the future.

Co-authorship network of co-authors of Katherine A. Forbush

This figure shows the co-authorship network connecting the top 25 collaborators of Katherine A. Forbush. A scholar is included among the top collaborators of Katherine A. Forbush 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 Katherine A. Forbush. Katherine A. Forbush 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.
Forbush, Katherine A., et al.. (2025). The evolution of AKAPs and emergence of PKA isotype selective anchoring determinants. Journal of Biological Chemistry. 301(5). 108480–108480. 1 indexed citations
2.
Forbush, Katherine A., Oscar Vivas, Cassandra J. Wong, et al.. (2025). Long AKAP18 isoforms anchor ubiquitin specific proteinases and coordinate calcium reuptake at the sarcoplasmic reticulum. Journal of Biological Chemistry. 301(7). 110317–110317.
3.
Omar, Mitchell H., Dominic P. Byrne, Kyung‐Soon Lee, et al.. (2022). Mislocalization of protein kinase A drives pathology in Cushing’s syndrome. Cell Reports. 40(2). 111073–111073. 26 indexed citations
4.
Nystoriak, Matthew A., Madeline Nieves‐Cintrón, Tommaso Patriarchi, et al.. (2017). Ser 1928 phosphorylation by PKA stimulates the L-type Ca 2+ channel Ca V 1.2 and vasoconstriction during acute hyperglycemia and diabetes. Science Signaling. 10(463). 85 indexed citations
5.
Bautista, Jhoanne L., Chan‐Wang Jerry Lio, Stephanie K. Lathrop, et al.. (2009). Intraclonal competition limits the fate determination of regulatory T cells in the thymus. Nature Immunology. 10(6). 610–617. 192 indexed citations
6.
Honey, Karen, Katherine A. Forbush, Peter E. Jensen, & Alexander Y. Rudensky. (2004). Effect of Decreasing the Affinity of the Class II-Associated Invariant Chain Peptide on the MHC Class II Peptide Repertoire in the Presence or Absence of H-2M. The Journal of Immunology. 172(7). 4142–4150. 14 indexed citations
7.
He, You-Wen, Congjun Li, Jun Zhang, et al.. (2003). The extracellular matrix protein mindin is a pattern-recognition molecule for microbial pathogens. Nature Immunology. 5(1). 88–97. 138 indexed citations
8.
Kirchner, Jacqueline, Katherine A. Forbush, & Michael J. Bevan. (2001). Identification and Characterization of Thymus LIM Protein: Targeted Disruption Reduces Thymus Cellularity. Molecular and Cellular Biology. 21(24). 8592–8604. 28 indexed citations
9.
Trobridge, Patty, Katherine A. Forbush, & Steven D. Levin. (2001). Positive and Negative Selection of Thymocytes Depends on Lck Interaction with the CD4 and CD8 Coreceptors. The Journal of Immunology. 166(2). 809–818. 32 indexed citations
10.
Sohn, Sue J., et al.. (2001). Activated p56 lck Directs Maturation of Both CD4 and CD8 Single-Positive Thymocytes. The Journal of Immunology. 166(4). 2209–2217. 31 indexed citations
11.
Wong, Phillip, Gregory M. Barton, Katherine A. Forbush, & Alexander Y. Rudensky. (2001). Dynamic Tuning of T Cell Reactivity by Self-Peptide–Major Histocompatibility Complex Ligands. The Journal of Experimental Medicine. 193(10). 1179–1188. 96 indexed citations
12.
He, You-Wen, Courtney Beers, Michael Deftos, et al.. (2000). Down-Regulation of the Orphan Nuclear Receptor RORγt Is Essential for T Lymphocyte Maturation. The Journal of Immunology. 164(11). 5668–5674. 59 indexed citations
13.
Deftos, Michael, Eugene Huang, Ethan W. Ojala, Katherine A. Forbush, & Michael J. Bevan. (2000). Notch1 Signaling Promotes the Maturation of CD4 and CD8 SP Thymocytes. Immunity. 13(1). 73–84. 286 indexed citations
14.
Sohn, Sue J., Katherine A. Forbush, Nhan Nguyen, et al.. (1998). Requirement for Jak3 in Mature T Cells: Its Role in Regulation of T Cell Homeostasis. The Journal of Immunology. 160(5). 2130–2138. 33 indexed citations
15.
Wildin, Robert S., et al.. (1995). Functional dissection of the murine lck distal promoter. The Journal of Immunology. 155(3). 1286–1295. 56 indexed citations
16.
Levin, Steven D., Kristin M. Abraham, Sarah Anderson, Katherine A. Forbush, & Roger M. Perlmutter. (1993). The protein tyrosine kinase p56lck regulates thymocyte development independently of its interaction with CD4 and CD8 coreceptors [corrected]. The Journal of Experimental Medicine. 178(1). 245–255. 30 indexed citations
17.
Levin, Steven D., Sarah Anderson, Katherine A. Forbush, & Roger M. Perlmutter. (1993). A dominant-negative transgene defines a role for p56lck in thymopoiesis.. The EMBO Journal. 12(4). 1671–1680. 276 indexed citations
18.
Oers, Nicolai S. C. van, Alex M. Garvin, Craig B. Davis, et al.. (1992). Disruption of CD8‐dependent negative and positive selection of thymocytes is correlated with a decreased association between CD8 and the protein tyrosine kinase, p56lck. European Journal of Immunology. 22(3). 735–743. 55 indexed citations
19.
Abraham, Kristin M., Steven D. Levin, Jamey D. Marth, Katherine A. Forbush, & Roger M. Perlmutter. (1991). Delayed thymocyte development induced by augmented expression of p56lck.. The Journal of Experimental Medicine. 173(6). 1421–1432. 108 indexed citations
20.
Wildin, Robert S., Alex M. Garvin, Shashi Singh Pawar, et al.. (1991). Developmental regulation of lck gene expression in T lymphocytes.. The Journal of Experimental Medicine. 173(2). 383–393. 108 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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