Janet Jackman

2.5k total citations
15 papers, 1.3k citations indexed

About

Janet Jackman is a scholar working on Immunology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Janet Jackman has authored 15 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Immunology, 6 papers in Molecular Biology and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Janet Jackman's work include Asthma and respiratory diseases (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers) and T-cell and B-cell Immunology (4 papers). Janet Jackman is often cited by papers focused on Asthma and respiratory diseases (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers) and T-cell and B-cell Immunology (4 papers). Janet Jackman collaborates with scholars based in United States, United Kingdom and Germany. Janet Jackman's co-authors include Paul R. Findell, Gary A. Koretzky, David G. Motto, Gary Peltz, Guanghui Kong, Sandra E. Wilkinson, Juliane Bubeck Wardenburg, Horst Flotow, Andrew C. Chan and D. H. Williams and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and The Journal of Immunology.

In The Last Decade

Janet Jackman

14 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janet Jackman United States 12 763 464 306 227 198 15 1.3k
Tohru Takashi Japan 16 433 0.6× 312 0.7× 193 0.6× 311 1.4× 184 0.9× 35 1.0k
Jami Willette‐Brown United States 20 914 1.2× 367 0.8× 79 0.3× 80 0.4× 228 1.2× 34 1.3k
Günter Brittinger Germany 18 551 0.7× 253 0.5× 130 0.4× 51 0.2× 424 2.1× 27 1.6k
Sharon J. Hyduk Canada 18 731 1.0× 503 1.1× 69 0.2× 532 2.3× 171 0.9× 26 1.4k
Seiichiro Tarui Japan 17 375 0.5× 523 1.1× 108 0.4× 112 0.5× 118 0.6× 40 1.3k
Dolores Vázquez‐Abad United States 12 409 0.5× 545 1.2× 51 0.2× 155 0.7× 197 1.0× 17 1.1k
Masamichi Inami Japan 17 472 0.6× 331 0.7× 218 0.7× 68 0.3× 173 0.9× 41 1.0k
Debra M. Meyer United States 11 411 0.5× 195 0.4× 70 0.2× 57 0.3× 393 2.0× 13 1.2k
Abhishek Aphale United States 13 880 1.2× 370 0.8× 208 0.7× 38 0.2× 283 1.4× 16 1.3k
Julie Stockis Belgium 17 589 0.8× 505 1.1× 43 0.1× 74 0.3× 418 2.1× 21 1.3k

Countries citing papers authored by Janet Jackman

Since Specialization
Citations

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

Fields of papers citing papers by Janet Jackman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janet Jackman. 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 Janet Jackman. The network helps show where Janet Jackman may publish in the future.

Co-authorship network of co-authors of Janet Jackman

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

All Works

15 of 15 papers shown
1.
Maun, Henry R., Rajesh Vij, Benjamin T. Walters, et al.. (2020). Bivalent antibody pliers inhibit β-tryptase by an allosteric mechanism dependent on the IgG hinge. Nature Communications. 11(1). 6435–6435. 38 indexed citations
2.
Choy, David F., Neil N. Trivedi, Amy Dressen, et al.. (2018). Tryptase loss-of-function mutations reduce tryptase expression and predict asthmatic response to anti-IgE therapy. OA1652–OA1652. 2 indexed citations
3.
Shikotra, Aarti, David F. Choy, Salman Siddiqui, et al.. (2017). A CEACAM6-High Airway Neutrophil Phenotype and CEACAM6-High Epithelial Cells Are Features of Severe Asthma. The Journal of Immunology. 198(8). 3307–3317. 24 indexed citations
4.
Brightbill, Hans D., Janet Jackman, Eric Suto, et al.. (2015). Conditional Deletion of NF-κB–Inducing Kinase (NIK) in Adult Mice Disrupts Mature B Cell Survival and Activation. The Journal of Immunology. 195(3). 953–964. 47 indexed citations
5.
Shikotra, Aarti, David F. Choy, Salman Siddiqui, et al.. (2015). CEACAM6-high airway neutrophils and epithelial cells are a feature of severe asthma. PA910–PA910. 1 indexed citations
6.
Chandriani, Sanjay, Daryle J. DePianto, Alexander R. Abbas, et al.. (2014). Endogenously Expressed IL-13Rα2 Attenuates IL-13–Mediated Responses but Does Not Activate Signaling in Human Lung Fibroblasts. The Journal of Immunology. 193(1). 111–119. 56 indexed citations
7.
Shikotra, A, David F. Choy, Chandra Ohri, et al.. (2012). Increased expression of immunoreactive thymic stromal lymphopoetin in severe asthma. Journal of Allergy and Clinical Immunology.
8.
Wranik, Bernd J., et al.. (2012). LUZ-Y, a Novel Platform for the Mammalian Cell Production of Full-length IgG-bispecific Antibodies. Journal of Biological Chemistry. 287(52). 43331–43339. 29 indexed citations
9.
Abbas, Alexander R., Janet Jackman, Sherron Bullens, et al.. (2011). Lung Gene Expression in a Rhesus Allergic Asthma Model Correlates with Physiologic Parameters of Disease and Exhibits Common and Distinct Pathways with Human Asthma and a Mouse Asthma Model. American Journal Of Pathology. 179(4). 1667–1680. 12 indexed citations
10.
Shikotra, Aarti, David F. Choy, Chandra Ohri, et al.. (2011). Increased expression of immunoreactive thymic stromal lymphopoietin in patients with severe asthma. Journal of Allergy and Clinical Immunology. 129(1). 104–111.e9. 257 indexed citations
11.
Jackman, Janet, Yongmei Chen, Arthur Huang, et al.. (2010). Development of a Two-part Strategy to Identify a Therapeutic Human Bispecific Antibody That Inhibits IgE Receptor Signaling. Journal of Biological Chemistry. 285(27). 20850–20859. 68 indexed citations
12.
Wardenburg, Juliane Bubeck, Chong Fu, Janet Jackman, et al.. (1996). Phosphorylation of SLP-76 by the ZAP-70 Protein-tyrosine Kinase Is Required for T-cell Receptor Function. Journal of Biological Chemistry. 271(33). 19641–19644. 393 indexed citations
13.
Jackman, Janet, David G. Motto, Qiming Sun, et al.. (1995). Molecular Cloning of SLP-76, a 76-kDa Tyrosine Phosphoprotein Associated with Grb2 in T Cells. Journal of Biological Chemistry. 270(13). 7029–7032. 301 indexed citations
14.
Lahesmaa, Riitta, et al.. (1995). Modulation of the Grb2-associated protein complex in human CD4+ T cells by receptor activation. The Journal of Immunology. 155(8). 3815–3822. 27 indexed citations
15.
Motto, David G., Susan Ross, Janet Jackman, et al.. (1994). In vivo association of Grb2 with pp116, a substrate of the T cell antigen receptor-activated protein tyrosine kinase.. Journal of Biological Chemistry. 269(34). 21608–21613. 73 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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