Tom C. Hobman

5.9k total citations
112 papers, 4.1k citations indexed

About

Tom C. Hobman is a scholar working on Molecular Biology, Epidemiology and Infectious Diseases. According to data from OpenAlex, Tom C. Hobman has authored 112 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 39 papers in Epidemiology and 31 papers in Infectious Diseases. Recurrent topics in Tom C. Hobman's work include Virology and Viral Diseases (33 papers), Mosquito-borne diseases and control (31 papers) and Viral Infections and Vectors (19 papers). Tom C. Hobman is often cited by papers focused on Virology and Viral Diseases (33 papers), Mosquito-borne diseases and control (31 papers) and Viral Infections and Vectors (19 papers). Tom C. Hobman collaborates with scholars based in Canada, United States and France. Tom C. Hobman's co-authors include Zaikun Xu, Anil Kumar, Daniel Limonta, Nasser Tahbaz, Marilyn G. Farquhar, Christopher Power, L. Woodward, Adriana M. Airo, Shangmei Hou and Shirley Gillam and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Tom C. Hobman

111 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tom C. Hobman Canada 39 1.8k 1.4k 1.0k 947 677 112 4.1k
Christopher K. E. Bleck United States 30 1.6k 0.9× 1.1k 0.7× 759 0.7× 737 0.8× 600 0.9× 71 4.0k
Nolwenn Jouvenet France 28 1.1k 0.6× 1.4k 1.0× 790 0.8× 846 0.9× 954 1.4× 58 3.5k
Christopher T. Jones United States 35 1.9k 1.1× 2.0k 1.4× 2.4k 2.3× 2.0k 2.1× 1.6k 2.3× 69 7.7k
Nihal Altan‐Bonnet United States 27 1.8k 1.0× 1.1k 0.8× 705 0.7× 292 0.3× 457 0.7× 43 3.7k
Matthew J. Evans United States 37 2.1k 1.2× 1.4k 1.0× 4.5k 4.4× 1.3k 1.3× 789 1.2× 75 8.7k
Nicolás Fasel Switzerland 39 1.4k 0.8× 500 0.3× 1.7k 1.7× 2.6k 2.8× 943 1.4× 117 4.5k
Ching C. Wang United States 37 2.7k 1.5× 699 0.5× 1.8k 1.8× 649 0.7× 218 0.3× 122 4.3k
R. Padmanabhan United States 31 2.3k 1.3× 1.0k 0.7× 443 0.4× 1.3k 1.3× 424 0.6× 84 4.6k
Raymond A. Koski United States 35 2.1k 1.2× 1.2k 0.8× 302 0.3× 1.0k 1.1× 620 0.9× 58 4.8k
Eiji Morita Japan 29 2.1k 1.2× 944 0.7× 1.5k 1.4× 513 0.5× 653 1.0× 75 4.8k

Countries citing papers authored by Tom C. Hobman

Since Specialization
Citations

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

Fields of papers citing papers by Tom C. Hobman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tom C. Hobman. 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 Tom C. Hobman. The network helps show where Tom C. Hobman may publish in the future.

Co-authorship network of co-authors of Tom C. Hobman

This figure shows the co-authorship network connecting the top 25 collaborators of Tom C. Hobman. A scholar is included among the top collaborators of Tom C. Hobman 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 Tom C. Hobman. Tom C. Hobman 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.
Makio, Tadashi, Ke Zhang, Fred D. Mast, et al.. (2024). SARS-CoV-2 Orf6 is positioned in the nuclear pore complex by Rae1 to inhibit nucleocytoplasmic transport. Molecular Biology of the Cell. 35(5). ar62–ar62. 5 indexed citations
2.
Xu, Zaikun, Mohamed Elaish, Bardes B. Hassan, et al.. (2024). The Wnt/β-catenin pathway is important for replication of SARS-CoV-2 and other pathogenic RNA viruses. PubMed. 2(1). 6–6. 7 indexed citations
3.
Moitra, Subhabrata, Desmond Pink, John D. Lewis, et al.. (2023). SARS-CoV-2-Induced TSLP Is Associated with Duration of Hospital Stay in COVID-19 Patients. Viruses. 15(2). 556–556. 7 indexed citations
4.
Kumar, Anil, Joaquín López-Orozco, Mohamed Elaish, et al.. (2021). SARS-CoV-2 Nonstructural Protein 1 Inhibits the Interferon Response by Causing Depletion of Key Host Signaling Factors. Journal of Virology. 95(13). e0026621–e0026621. 69 indexed citations
5.
Knoblach, Barbara, et al.. (2021). Peroxisomes exhibit compromised structure and matrix protein content in SARS-CoV-2-infected cells. Molecular Biology of the Cell. 32(14). 1273–1282. 26 indexed citations
6.
Heindel, Daniel W., Yue Zhang, Brian Kasper, et al.. (2020). Glycomic analysis of host response reveals high mannose as a key mediator of influenza severity. Proceedings of the National Academy of Sciences. 117(43). 26926–26935. 39 indexed citations
7.
Glasgow, Anum, Jeff E. Glasgow, Daniel Limonta, et al.. (2020). Engineered ACE2 receptor traps potently neutralize SARS-CoV-2. Proceedings of the National Academy of Sciences. 117(45). 28046–28055. 160 indexed citations
8.
Branton, William G., et al.. (2020). Human Pegivirus-1 is Neurotropic and Associated with Neuroinflammation (4656). Neurology. 94(15_supplement). 1 indexed citations
9.
Griffiths, Cameron, Leanne M. Bilawchuk, John E. McDonough, et al.. (2020). Publisher Correction: IGF1R is an entry receptor for respiratory syncytial virus. Nature. 583(7815). E22–E22. 5 indexed citations
10.
Joyce, Michael, et al.. (2019). HCV and flaviviruses hijack cellular mechanisms for nuclear STAT2 degradation: Up-regulation of PDLIM2 suppresses the innate immune response. PLoS Pathogens. 15(8). e1007949–e1007949. 24 indexed citations
11.
Airo, Adriana M., Joaquín López-Orozco, Charles F.B. Holmes, et al.. (2018). Expression of flavivirus capsids enhance the cellular environment for viral replication by activating Akt-signalling pathways. Virology. 516. 147–157. 19 indexed citations
12.
Singaravelu, Ragunath, Daniel M. Jones, Ran Chen, et al.. (2015). MicroRNAs regulate the immunometabolic response to viral infection in the liver. Nature Chemical Biology. 11(12). 988–993. 56 indexed citations
13.
Wang, Yang, Rebecca Mercier, Tom C. Hobman, & Paul LaPointe. (2013). Regulation of RNA interference by Hsp90 is an evolutionarily conserved process. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(12). 2673–2681. 11 indexed citations
14.
Pare, Justin M., Paul LaPointe, & Tom C. Hobman. (2013). Hsp90 cochaperones p23 and FKBP4 physically interact with hAgo2 and activate RNA interference–mediated silencing in mammalian cells. Molecular Biology of the Cell. 24(15). 2303–2310. 33 indexed citations
15.
Ilkow, Carolina S., Ing Swie Goping, & Tom C. Hobman. (2011). The Rubella Virus Capsid Is an Anti-Apoptotic Protein that Attenuates the Pore-Forming Ability of Bax. PLoS Pathogens. 7(2). e1001291–e1001291. 35 indexed citations
16.
Provost, Patrick, et al.. (2003). Ago1 and Dcr1, Two Core Components of the RNA Interference Pathway, Functionally Diverge from Rdp1 in Regulating Cell Cycle Events inSchizosaccharomyces pombe. Molecular Biology of the Cell. 15(3). 1425–1435. 36 indexed citations
17.
Abousalham, Abdelkarim, Tom C. Hobman, Jay Dewald, Michael Garbutt, & David N. Brindley. (2002). Cell-permeable ceramides preferentially inhibit coated vesicle formation and exocytosis in Chinese hamster ovary compared with Madin‒Darby canine kidney cells by preventing the membrane association of ADP-ribosylation factor. Biochemical Journal. 361(3). 653–653. 16 indexed citations
18.
Nakhasi, Hira L., Meera Ramanujam, Chintamani D. Atreya, et al.. (2001). Rubella virus glycoprotein interaction with the endoplasmic reticulum calreticulin and calnexin. Archives of Virology. 146(1). 1–14. 38 indexed citations
19.
Hobman, Tom C., Baoping Zhao, Honey Chan, & Marilyn G. Farquhar. (1998). Immunoisolation and Characterization of a Subdomain of the Endoplasmic Reticulum That Concentrates Proteins Involved in COPII Vesicle Biogenesis. Molecular Biology of the Cell. 9(6). 1265–1278. 42 indexed citations
20.
Hobman, Tom C., et al.. (1994). Assembly of Rubella Virus Structural Proteins into Virus-like Particles in Transfected Cells. Virology. 202(2). 574–585. 66 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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