Ganesh Kolumam

4.7k total citations · 1 hit paper
37 papers, 2.9k citations indexed

About

Ganesh Kolumam is a scholar working on Molecular Biology, Immunology and Physiology. According to data from OpenAlex, Ganesh Kolumam has authored 37 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Immunology and 10 papers in Physiology. Recurrent topics in Ganesh Kolumam's work include Adipose Tissue and Metabolism (8 papers), Immune Cell Function and Interaction (7 papers) and T-cell and B-cell Immunology (7 papers). Ganesh Kolumam is often cited by papers focused on Adipose Tissue and Metabolism (8 papers), Immune Cell Function and Interaction (7 papers) and T-cell and B-cell Immunology (7 papers). Ganesh Kolumam collaborates with scholars based in United States, France and Australia. Ganesh Kolumam's co-authors include Kaja Murali‐Krishna, Sunil Thomas, Lucas Thompson, Jonathan Sprent, Colin Havenar‐Daughton, Jose Zavala‐Solorio, Lance Kates, Wyne P. Lee, Nicholas van Bruggen and Wenjun Ouyang and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Ganesh Kolumam

37 papers receiving 2.9k citations

Hit Papers

Type I interferons act directly on CD8 T cells to allow c... 2005 2026 2012 2019 2005 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
Ganesh Kolumam United States 26 1.5k 788 490 393 388 37 2.9k
Niklas Beyersdorf Germany 28 1.4k 1.0× 1.2k 1.5× 569 1.2× 388 1.0× 334 0.9× 80 3.4k
Toru Miyazaki Japan 34 2.2k 1.5× 1.1k 1.4× 562 1.1× 528 1.3× 444 1.1× 89 3.9k
Enric Esplugues United States 24 2.3k 1.6× 1.1k 1.4× 352 0.7× 510 1.3× 288 0.7× 31 3.8k
Ming-Hong Xie United States 14 2.1k 1.4× 709 0.9× 292 0.6× 657 1.7× 185 0.5× 31 3.3k
Peter Oliver United States 25 1.6k 1.1× 1.0k 1.3× 350 0.7× 320 0.8× 372 1.0× 44 3.6k
Wing Y. Lam United States 12 2.2k 1.5× 1.1k 1.3× 478 1.0× 338 0.9× 244 0.6× 13 3.2k
Hidechika Okada Japan 32 1.7k 1.1× 987 1.3× 376 0.8× 407 1.0× 351 0.9× 142 3.7k
Pravin B. Sehgal United States 32 1.3k 0.9× 1.3k 1.7× 442 0.9× 893 2.3× 246 0.6× 79 3.5k
Joseph M. Reynolds United States 27 2.5k 1.7× 1.1k 1.4× 426 0.9× 503 1.3× 182 0.5× 48 3.8k
Greg Elson Switzerland 27 1.9k 1.3× 787 1.0× 394 0.8× 702 1.8× 212 0.5× 53 3.1k

Countries citing papers authored by Ganesh Kolumam

Since Specialization
Citations

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

Fields of papers citing papers by Ganesh Kolumam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ganesh Kolumam

This figure shows the co-authorship network connecting the top 25 collaborators of Ganesh Kolumam. A scholar is included among the top collaborators of Ganesh Kolumam 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 Ganesh Kolumam. Ganesh Kolumam 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.
Maile, Tobias M, Jonathon J. O’Brien, Sean R. Hackett, et al.. (2024). Automated preparation of plasma lipids, metabolites, and proteins for LC/MS-based analysis of a high-fat diet in mice. Journal of Lipid Research. 65(9). 100607–100607. 1 indexed citations
2.
Choy, Lisa, Stephen R. Norris, Xiumin Wu, et al.. (2024). Inhibition of Aurora Kinase Induces Endogenous Retroelements to Induce a Type I/III IFN Response via RIG-I. Cancer Research Communications. 4(2). 540–555. 4 indexed citations
3.
Zhang, Guozhu, Anil Raj, Baby Martin-McNulty, et al.. (2021). Intermittent fasting and caloric restriction interact with genetics to shape physiological health in mice. Genetics. 220(1). 4 indexed citations
4.
Sousa‐Victor, Pedro, Joana Neves, Patrick Ventura, et al.. (2019). MANF regulates metabolic and immune homeostasis in ageing and protects against liver damage. Nature Metabolism. 1(2). 276–290. 97 indexed citations
5.
Kolumam, Ganesh, Xiumin Wu, Wyne P. Lee, et al.. (2017). IL-22R Ligands IL-20, IL-22, and IL-24 Promote Wound Healing in Diabetic db/db Mice. PLoS ONE. 12(1). e0170639–e0170639. 68 indexed citations
6.
Chen, Mark Z., Joshua C. Chang, Jose Zavala‐Solorio, et al.. (2017). FGF21 mimetic antibody stimulates UCP1-independent brown fat thermogenesis via FGFR1/βKlotho complex in non-adipocytes. Molecular Metabolism. 6(11). 1454–1467. 44 indexed citations
7.
Solloway, Mark J., Azadeh Madjidi, Chunyan Gu, et al.. (2015). Glucagon Couples Hepatic Amino Acid Catabolism to mTOR-Dependent Regulation of α-Cell Mass. Cell Reports. 12(3). 495–510. 144 indexed citations
8.
Wu, Lindsay E., Christopher C. Meoli, Salvatore Mangiafico, et al.. (2014). Systemic VEGF-A Neutralization Ameliorates Diet-Induced Metabolic Dysfunction. Diabetes. 63(8). 2656–2667. 27 indexed citations
9.
Tonks, Katherine, Yi Zhen Ng, Adelle C.F. Coster, et al.. (2013). Impaired Akt phosphorylation in insulin-resistant human muscle is accompanied by selective and heterogeneous downstream defects. Diabetologia. 56(4). 875–885. 87 indexed citations
10.
Mukund, Susmith, Holly J. Clarke, Azadeh Madjidi, et al.. (2013). Inhibitory Mechanism of an Allosteric Antibody Targeting the Glucagon Receptor. Journal of Biological Chemistry. 288(50). 36168–36178. 33 indexed citations
11.
Chiang, Eugene Y., Ganesh Kolumam, Krista McCutcheon, et al.. (2012). In Vivo Depletion of Lymphotoxin-Alpha Expressing Lymphocytes Inhibits Xenogeneic Graft-versus-Host-Disease. PLoS ONE. 7(3). e33106–e33106. 17 indexed citations
12.
Zhang, Yingnan, Lijuan Zhou, Monica Kong-Beltran, et al.. (2012). Calcium-Independent Inhibition of PCSK9 by Affinity-Improved Variants of the LDL Receptor EGF(A) Domain. Journal of Molecular Biology. 422(5). 685–696. 31 indexed citations
13.
Belcik, J. Todd, Yue Qi, Beat A. Kaufmann, et al.. (2012). Cardiovascular and Systemic MicrovascularEffects of Anti-Vascular Endothelial Growth Factor Therapy for Cancer. Journal of the American College of Cardiology. 60(7). 618–625. 42 indexed citations
14.
Lipari, Michael T., Wei Li, Paul Moran, et al.. (2012). Furin-cleaved Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Is Active and Modulates Low Density Lipoprotein Receptor and Serum Cholesterol Levels. Journal of Biological Chemistry. 287(52). 43482–43491. 75 indexed citations
15.
Ganesan, Rajkumar, Ganesh Kolumam, Seh‐Ching Lin, et al.. (2011). Proteolytic Activation of Pro-Macrophage-Stimulating Protein by Hepsin. Molecular Cancer Research. 9(9). 1175–1186. 55 indexed citations
16.
Young, Judy, Xin Yu, Kristen Wolslegel, et al.. (2010). Lymphotoxin-αβ heterotrimers are cleaved by metalloproteinases and contribute to synovitis in rheumatoid arthritis. Cytokine. 51(1). 78–86. 38 indexed citations
17.
Grogan, Jane L., et al.. (2009). Targeted depletion of lymphotoxin-alpha-expressing Th1 and Th17 cells inhibits autoimmune disease (48.22). The Journal of Immunology. 182(Supplement_1). 48.22–48.22. 5 indexed citations
18.
Thomas, Sunil, Ganesh Kolumam, & Kaja Murali‐Krishna. (2007). Antigen Presentation by Nonhemopoietic Cells Amplifies Clonal Expansion of Effector CD8 T Cells in a Pathogen-Specific Manner. The Journal of Immunology. 178(9). 5802–5811. 26 indexed citations
19.
Havenar‐Daughton, Colin, Ganesh Kolumam, & Kaja Murali‐Krishna. (2006). Cutting Edge: The Direct Action of Type I IFN on CD4 T Cells Is Critical for Sustaining Clonal Expansion in Response to a Viral but Not a Bacterial Infection. The Journal of Immunology. 176(6). 3315–3319. 176 indexed citations
20.
Kolumam, Ganesh, Sunil Thomas, Lucas Thompson, Jonathan Sprent, & Kaja Murali‐Krishna. (2005). Type I interferons act directly on CD8 T cells to allow clonal expansion and memory formation in response to viral infection. The Journal of Experimental Medicine. 202(5). 637–650. 768 indexed citations breakdown →

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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