Marc O. Johnson

2.9k total citations · 3 hit papers
11 papers, 1.7k citations indexed

About

Marc O. Johnson is a scholar working on Molecular Biology, Cancer Research and Immunology. According to data from OpenAlex, Marc O. Johnson has authored 11 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cancer Research and 4 papers in Immunology. Recurrent topics in Marc O. Johnson's work include Cancer, Hypoxia, and Metabolism (5 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and T-cell and B-cell Immunology (2 papers). Marc O. Johnson is often cited by papers focused on Cancer, Hypoxia, and Metabolism (5 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and T-cell and B-cell Immunology (2 papers). Marc O. Johnson collaborates with scholars based in United States and Germany. Marc O. Johnson's co-authors include Jeffrey C. Rathmell, Aaron M. Hosios, Scott R. Manalis, Vivian Hecht, Matthew G. Vander Heiden, Laura V. Danai, Matthew L. Steinhauser, Matt Wachowiak, Daniel W. Wesson and Peter J. Siska and has published in prestigious journals such as Journal of Biological Chemistry, Nature Medicine and Nature Immunology.

In The Last Decade

Marc O. Johnson

11 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Amino Acids Rather than Glucose Account for the Majority of Cell Mass in Proliferating Mammalian Cells

2016 470 citations Aaron M. Hosios, Vivian Hecht et al. Developmental Cell profile →
Foxp3 and Toll-like receptor signaling balance Treg cell anabolic metabolism for suppression

2016 409 citations Valerie A. Gerriets, Rigel J. Kishton et al. Nature Immunology profile →
Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models

2018 379 citations M. Schulte, Allie Fu et al. Nature Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marc O. Johnson United States	8	868	668	476	237	205	11	1.7k
Shun‐ichiro Matsumoto Japan	18	1.1k 1.3×	356 0.5×	673 1.4×	248 1.0×	48 0.2×	23	2.3k
Frank Schnütgen Germany	20	1.4k 1.6×	273 0.4×	191 0.4×	140 0.6×	57 0.3×	50	1.9k
Cheryl B. Bock United States	24	1.5k 1.7×	189 0.3×	1.0k 2.1×	252 1.1×	111 0.5×	35	2.9k
Vincenzo A. Gennarino United States	16	2.0k 2.3×	688 1.0×	204 0.4×	92 0.4×	55 0.3×	25	3.3k
Gianfranco Macchia Italy	16	847 1.0×	223 0.3×	231 0.5×	77 0.3×	31 0.2×	29	1.1k
Heng Wu China	22	1.4k 1.6×	650 1.0×	125 0.3×	102 0.4×	45 0.2×	43	2.2k
Marija Krstic–Demonacos United Kingdom	22	1.2k 1.4×	362 0.5×	233 0.5×	549 2.3×	27 0.1×	59	2.1k
John J. Kelly Canada	22	1.0k 1.2×	77 0.1×	279 0.6×	170 0.7×	27 0.1×	54	1.7k
Julia Janzen United Kingdom	15	620 0.7×	308 0.5×	474 1.0×	187 0.8×	96 0.5×	18	1.2k
Dario De Cesare Italy	23	1.7k 2.0×	353 0.5×	227 0.5×	314 1.3×	48 0.2×	36	2.5k

Countries citing papers authored by Marc O. Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Marc O. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc O. Johnson. 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 Marc O. Johnson. The network helps show where Marc O. Johnson may publish in the future.

Co-authorship network of co-authors of Marc O. Johnson

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

All Works

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11 of 11 papers shown

Dulak, Austin, Marc O. Johnson, Secil Koseoglu, et al.. (2020). Abstract 6639: SRF617, a potent enzymatic inhibitor of CD39, demonstrates single-agent activity and cooperates with various cancer therapies in both solid tumor and hematologic malignancies. Cancer Research. 80(16_Supplement). 6639–6639. 7 indexed citations

Schulte, M., Allie Fu, Ping Zhao, et al.. (2018). Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models. Nature Medicine. 24(2). 194–202. 379 indexed citations breakdown →

Andrejeva, Gabriela, Melissa M. Wolf, Marc O. Johnson, et al.. (2018). Metabolomics analysis reveals differential T cell serine metabolism as a target in autoimmunity.. The Journal of Immunology. 200(Supplement_1). 167.7–167.7. 4 indexed citations

Zhou, Weisong, Jian Zhang, Shinji Toki, et al.. (2018). The PGI2 Analog Cicaprost Inhibits IL-33–Induced Th2 Responses, IL-2 Production, and CD25 Expression in Mouse CD4+ T Cells. The Journal of Immunology. 201(7). 1936–1945. 18 indexed citations

Liberti, Maria V., Ziwei Dai, Suzanne E. Wardell, et al.. (2017). A Predictive Model for Selective Targeting of the Warburg Effect through GAPDH Inhibition with a Natural Product. Cell Metabolism. 26(4). 648–659.e8. 143 indexed citations

Hosios, Aaron M., Vivian Hecht, Laura V. Danai, et al.. (2016). Amino Acids Rather than Glucose Account for the Majority of Cell Mass in Proliferating Mammalian Cells. Developmental Cell. 36(5). 540–549. 470 indexed citations breakdown →

Johnson, Marc O., Peter J. Siska, Diana C. Contreras, & Jeffrey C. Rathmell. (2016). Nutrients and the microenvironment to feed a T cell army. Seminars in Immunology. 28(5). 505–513. 53 indexed citations

Gerriets, Valerie A., Rigel J. Kishton, Marc O. Johnson, et al.. (2016). Foxp3 and Toll-like receptor signaling balance Treg cell anabolic metabolism for suppression. Nature Immunology. 17(12). 1459–1466. 409 indexed citations breakdown →

Hosios, Aaron M., Vivian Hecht, Marc O. Johnson, et al.. (2016). Abstract A36: Amino acids rather than glucose accounts for the majority of cell mass in rapidly proliferating mammalian cells. Molecular Cancer Research. 14(1_Supplement). A36–A36. 1 indexed citations

10.

Wesson, Daniel W., et al.. (2008). Sniffing Behavior of Mice during Performance in Odor-Guided Tasks. Chemical Senses. 33(7). 581–596. 179 indexed citations

11.

Benzing, Thomas, Marc O. Johnson, Bernhard Schermer, et al.. (2002). Interaction of 14-3-3 Protein with Regulator of G Protein Signaling 7 Is Dynamically Regulated by Tumor Necrosis Factor-α. Journal of Biological Chemistry. 277(36). 32954–32962. 52 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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