Elizabeth M. Long

736 total citations
9 papers, 615 citations indexed

About

Elizabeth M. Long is a scholar working on Immunology, Molecular Biology and Cancer Research. According to data from OpenAlex, Elizabeth M. Long has authored 9 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Immunology, 4 papers in Molecular Biology and 2 papers in Cancer Research. Recurrent topics in Elizabeth M. Long's work include Immune Response and Inflammation (5 papers), Immune cells in cancer (3 papers) and RNA modifications and cancer (2 papers). Elizabeth M. Long is often cited by papers focused on Immune Response and Inflammation (5 papers), Immune cells in cancer (3 papers) and RNA modifications and cancer (2 papers). Elizabeth M. Long collaborates with scholars based in Canada, United States and Slovakia. Elizabeth M. Long's co-authors include Stephen M. Robbins, Paul Kubes, Graciela Andonegui, Samantha A. Tavener, Holly Van Remmen, R C O Zanardo, Claudine S. Bonder, Michael J. Hickey, Will G. James and Benoît M. Lapointe and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Immunology.

In The Last Decade

Elizabeth M. Long

9 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth M. Long Canada 9 326 224 97 95 57 9 615
Fang Jia-Zhu China 11 191 0.6× 223 1.0× 81 0.8× 54 0.6× 37 0.6× 11 528
Kathy Banahan Ireland 5 401 1.2× 351 1.6× 82 0.8× 98 1.0× 33 0.6× 6 687
Irina Ushach United States 8 298 0.9× 177 0.8× 45 0.5× 99 1.0× 32 0.6× 11 687
Huilan Wang China 17 110 0.3× 292 1.3× 102 1.1× 84 0.9× 24 0.4× 60 722
英俊 猪子 1 210 0.6× 133 0.6× 80 0.8× 72 0.8× 20 0.4× 2 487
Nikolai A. Maianski Netherlands 8 541 1.7× 400 1.8× 55 0.6× 94 1.0× 22 0.4× 8 896
H. Nguyen Belgium 7 357 1.1× 276 1.2× 223 2.3× 86 0.9× 36 0.6× 10 704
Eui Young So United States 13 247 0.8× 166 0.7× 60 0.6× 55 0.6× 33 0.6× 20 520
Bart Everaerdt Belgium 12 366 1.1× 209 0.9× 78 0.8× 106 1.1× 22 0.4× 17 636
Alexander Hooftman Ireland 6 318 1.0× 393 1.8× 36 0.4× 68 0.7× 44 0.8× 8 688

Countries citing papers authored by Elizabeth M. Long

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth M. Long

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth M. Long. 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 Elizabeth M. Long. The network helps show where Elizabeth M. Long may publish in the future.

Co-authorship network of co-authors of Elizabeth M. Long

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

All Works

9 of 9 papers shown
1.
Kruer, Traci, Susan Dougherty, Lindsey Reynolds, et al.. (2016). Expression of the lncRNA Maternally Expressed Gene 3 (MEG3) Contributes to the Control of Lung Cancer Cell Proliferation by the Rb Pathway. PLoS ONE. 11(11). e0166363–e0166363. 65 indexed citations
2.
Long, Elizabeth M., Alexander C. Klimowicz, Heitor A. Paula-Neto, et al.. (2011). A subclass of acylated anti-inflammatory mediators usurp Toll-like receptor 2 to inhibit neutrophil recruitment through peroxisome proliferator-activated receptor γ. Proceedings of the National Academy of Sciences. 108(39). 16357–16362. 12 indexed citations
3.
Long, Elizabeth M., Brandie Millen, Paul Kubes, & Stephen M. Robbins. (2009). Lipoteichoic Acid Induces Unique Inflammatory Responses when Compared to Other Toll-Like Receptor 2 Ligands. PLoS ONE. 4(5). e5601–e5601. 56 indexed citations
4.
Andonegui, Graciela, Hong Zhou, Daniel C. Bullard, et al.. (2009). Mice that exclusively express TLR4 on endothelial cells can efficiently clear a lethal systemic Gram-negative bacterial infection. Journal of Clinical Investigation. 119(7). 1921–30. 138 indexed citations
5.
Smith, E. J., Tuoyu Geng, Elizabeth M. Long, et al.. (2005). Molecular Analysis of the Relatedness of Five Domesticated Turkey Strains. Biochemical Genetics. 43(1-2). 35–47. 18 indexed citations
6.
Tavener, Samantha A., et al.. (2004). Immune Cell Toll-Like Receptor 4 Is Required for Cardiac Myocyte Impairment During Endotoxemia. Circulation Research. 95(7). 700–707. 131 indexed citations
7.
Kerfoot, Steven M., Elizabeth M. Long, Michael J. Hickey, et al.. (2004). TLR4 Contributes to Disease-Inducing Mechanisms Resulting in Central Nervous System Autoimmune Disease. The Journal of Immunology. 173(11). 7070–7077. 170 indexed citations
8.
Long, Elizabeth M., et al.. (2003). Stimulation of the murine Uchl1 gene promoter by the B-Myb transcription factor. Lung Cancer. 42(1). 9–21. 16 indexed citations
9.
Campbell, A. Malcolm, et al.. (2001). IDENTIFICATION AND DNA SEQUENCE OF A NEW H+‐ATPase IN THE UNICELLULAR GREEN ALGA CHLAMYDOMONAS REINHARDTII (CHLOROPHYCEAE). Journal of Phycology. 37(4). 536–542. 9 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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