Seth A. Brooks

1.2k total citations
17 papers, 943 citations indexed

About

Seth A. Brooks is a scholar working on Molecular Biology, Immunology and Cancer Research. According to data from OpenAlex, Seth A. Brooks has authored 17 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Immunology and 4 papers in Cancer Research. Recurrent topics in Seth A. Brooks's work include RNA Research and Splicing (10 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (4 papers). Seth A. Brooks is often cited by papers focused on RNA Research and Splicing (10 papers), RNA modifications and cancer (5 papers) and RNA and protein synthesis mechanisms (4 papers). Seth A. Brooks collaborates with scholars based in United States and Lebanon. Seth A. Brooks's co-authors include Perry J. Blackshear, William F. C. Rigby, John E. Connolly, S.J.M. Skinner, Robert Gross, Roy A. Fava, W. H. Davin Townley-Tilson, Michael L. Whitfield, Jane Collins and Karl E. Griswold and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Seth A. Brooks

17 papers receiving 931 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seth A. Brooks United States 14 736 220 209 108 42 17 943
Dmitry N. Lyabin Russia 17 1.0k 1.4× 215 1.0× 160 0.8× 94 0.9× 75 1.8× 32 1.2k
Bruce Fowler United States 12 428 0.6× 222 1.0× 172 0.8× 90 0.8× 25 0.6× 12 902
Stefan Teigelkamp Germany 15 1.0k 1.4× 151 0.7× 169 0.8× 77 0.7× 67 1.6× 19 1.2k
John L. McElwee United States 12 360 0.5× 114 0.5× 197 0.9× 151 1.4× 16 0.4× 16 719
Delphine Durand United States 5 397 0.5× 237 1.1× 491 2.3× 154 1.4× 18 0.4× 8 786
Mathieu Durand Canada 19 1.4k 1.9× 260 1.2× 115 0.6× 81 0.8× 53 1.3× 26 1.6k
Katia Fecchi Italy 13 600 0.8× 164 0.7× 142 0.7× 88 0.8× 37 0.9× 22 928
Xinjun Ji United States 14 887 1.2× 379 1.7× 72 0.3× 45 0.4× 40 1.0× 23 1.1k
Sung‐Yul Lee South Korea 10 916 1.2× 679 3.1× 101 0.5× 81 0.8× 35 0.8× 29 1.1k
Uwe Galli Germany 10 622 0.8× 372 1.7× 71 0.3× 122 1.1× 18 0.4× 11 812

Countries citing papers authored by Seth A. Brooks

Since Specialization
Citations

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

Fields of papers citing papers by Seth A. Brooks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seth A. Brooks

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

All Works

17 of 17 papers shown
1.
Eszterhas, Susan K., Seth A. Brooks, Susan Zolla‐Pazner, et al.. (2020). Induction of cross-reactive HIV-1 specific antibody responses by engineered V1V2 immunogens with reduced conformational plasticity. Vaccine. 38(18). 3436–3446. 4 indexed citations
2.
Li, Liang, Seth A. Brooks, Susan K. Eszterhas, et al.. (2020). Deimmunized Lysostaphin Synergizes with Small-Molecule Chemotherapies and Resensitizes Methicillin-Resistant Staphylococcus aureus to β-Lactam Antibiotics. Antimicrobial Agents and Chemotherapy. 65(3). 11 indexed citations
3.
Zhao, Hongliang, Seth A. Brooks, Susan K. Eszterhas, et al.. (2020). Globally deimmunized lysostaphin evades human immune surveillance and enables highly efficacious repeat dosing. Science Advances. 6(36). 27 indexed citations
4.
Verma, Deeptak, et al.. (2017). Computationally optimized deimmunization libraries yield highly mutated enzymes with low immunogenicity and enhanced activity. Proceedings of the National Academy of Sciences. 114(26). E5085–E5093. 31 indexed citations
5.
Brooks, Seth A. & Perry J. Blackshear. (2013). Tristetraprolin (TTP): Interactions with mRNA and proteins, and current thoughts on mechanisms of action. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1829(6-7). 666–679. 318 indexed citations
6.
Brooks, Seth A., et al.. (2012). Cullin 4B Is Recruited to Tristetraprolin-Containing Messenger Ribonucleoproteins and Regulates TNF-α mRNA Polysome Loading. The Journal of Immunology. 188(4). 1828–1839. 26 indexed citations
7.
Nichols, Ralph C., et al.. (2010). A Flexible Approach to Studying Post-Transcriptional Gene Regulation in Stably Transfected Mammalian Cells. Molecular Biotechnology. 48(3). 210–217. 4 indexed citations
8.
Brooks, Seth A.. (2010). Functional interactions between mRNA turnover and surveillance and the ubiquitin proteasome system. Wiley Interdisciplinary Reviews - RNA. 1(2). 240–252. 18 indexed citations
9.
Brooks, Seth A., et al.. (2010). CARHSP1 Is Required for Effective Tumor Necrosis Factor Alpha mRNA Stabilization and Localizes to Processing Bodies and Exosomes. Molecular and Cellular Biology. 31(2). 277–286. 40 indexed citations
10.
Townley-Tilson, W. H. Davin, et al.. (2008). Identification of TTP mRNA targets in human dendritic cells reveals TTP as a critical regulator of dendritic cell maturation. RNA. 14(5). 888–902. 76 indexed citations
11.
Skinner, S.J.M., et al.. (2007). Extracellular Signal-regulated Kinase Regulation of Tumor Necrosis Factor-α mRNA Nucleocytoplasmic Transport Requires TAP-NxT1 Binding and the AU-rich Element. Journal of Biological Chemistry. 283(6). 3191–3199. 21 indexed citations
12.
13.
Rigby, William F. C., et al.. (2005). Structure/Function Analysis of Tristetraprolin (TTP): p38 Stress-Activated Protein Kinase and Lipopolysaccharide Stimulation Do Not Alter TTP Function. The Journal of Immunology. 174(12). 7883–7893. 52 indexed citations
14.
Brooks, Seth A., John E. Connolly, & William F. C. Rigby. (2004). The Role of mRNA Turnover in the Regulation of Tristetraprolin Expression: Evidence for an Extracellular Signal-Regulated Kinase-Specific, AU-Rich Element-Dependent, Autoregulatory Pathway. The Journal of Immunology. 172(12). 7263–7271. 112 indexed citations
15.
Brooks, Seth A., et al.. (2002). Analysis of the function, expression, and subcellular distribution of human tristetraprolin. Arthritis & Rheumatism. 46(5). 1362–1370. 57 indexed citations
16.
Brooks, Seth A.. (2000). Characterization of the mRNA ligands bound by the RNA binding protein hnRNP A2 utilizing a novel in vivo technique. Nucleic Acids Research. 28(10). 49e–49. 19 indexed citations
17.
Cohen, Jeffrey A., et al.. (1992). Characterization of a novel mRNA expressed by neurons in mature brain. Journal of Neuroscience Research. 31(2). 273–284. 16 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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