Thomas Muster

7.5k total citations · 3 hit papers
51 papers, 6.1k citations indexed

About

Thomas Muster is a scholar working on Epidemiology, Immunology and Molecular Biology. According to data from OpenAlex, Thomas Muster has authored 51 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Epidemiology, 28 papers in Immunology and 16 papers in Molecular Biology. Recurrent topics in Thomas Muster's work include Influenza Virus Research Studies (33 papers), Respiratory viral infections research (15 papers) and Immune Response and Inflammation (13 papers). Thomas Muster is often cited by papers focused on Influenza Virus Research Studies (33 papers), Respiratory viral infections research (15 papers) and Immune Response and Inflammation (13 papers). Thomas Muster collaborates with scholars based in Austria, United States and Russia. Thomas Muster's co-authors include Peter Palese, Adolfo Garcı́a-Sastre, Alexandra Trkola, Martin Purtscher, H. Katinger, A. Klima, Andrej Egorov, Franz Steindl, Sabine Brandt and Hongyong Zheng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Cancer Research.

In The Last Decade

Thomas Muster

50 papers receiving 5.9k citations

Hit Papers

Human monoclonal antibody 2G12 defines a distinctive neut... 1993 2026 2004 2015 1996 1993 1998 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
Thomas Muster Austria 30 3.2k 2.8k 2.0k 1.7k 1.6k 51 6.1k
Hana Golding United States 49 4.3k 1.3× 3.5k 1.2× 2.7k 1.3× 2.0k 1.2× 1.8k 1.1× 184 8.2k
Zhi-Yong Yang United States 39 2.4k 0.7× 2.1k 0.7× 2.2k 1.1× 3.1k 1.9× 2.1k 1.2× 54 7.0k
Shan Lu United States 40 2.4k 0.8× 1.6k 0.6× 1.9k 1.0× 1.7k 1.0× 1.6k 1.0× 168 5.3k
Wing-Pui Kong United States 32 1.9k 0.6× 2.4k 0.9× 928 0.5× 2.4k 1.5× 1.4k 0.8× 40 5.4k
Alicia Buckler‐White United States 44 3.0k 0.9× 2.3k 0.8× 5.0k 2.5× 2.9k 1.8× 1.7k 1.0× 107 7.4k
Jody Manischewitz United States 36 2.1k 0.7× 3.1k 1.1× 1.6k 0.8× 1.1k 0.6× 916 0.6× 77 5.0k
Patricia L. Earl United States 54 3.5k 1.1× 3.6k 1.3× 7.0k 3.5× 2.4k 1.4× 3.0k 1.8× 131 9.4k
Gregory R. Reyes United States 39 1.5k 0.5× 2.1k 0.8× 2.3k 1.1× 4.3k 2.6× 1.0k 0.6× 76 8.1k
A J Langlois United States 39 2.8k 0.9× 1.6k 0.6× 5.4k 2.7× 2.5k 1.5× 2.0k 1.2× 83 7.0k
Robin A. Weiss United Kingdom 20 2.5k 0.8× 920 0.3× 3.0k 1.5× 1.5k 0.9× 969 0.6× 40 5.0k

Countries citing papers authored by Thomas Muster

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Muster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Muster

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Muster. A scholar is included among the top collaborators of Thomas Muster 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 Thomas Muster. Thomas Muster 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.
Rathnasinghe, Raveen, Lauren A. Chang, Rebecca L. Pearl, et al.. (2024). Sequential immunization with chimeric hemagglutinin ΔNS1 attenuated influenza vaccines induces broad humoral and cellular immunity. npj Vaccines. 9(1). 169–169. 4 indexed citations
2.
Rathnasinghe, Raveen, Mirella Salvatore, Hongyong Zheng, et al.. (2021). Interferon mediated prophylactic protection against respiratory viruses conferred by a prototype live attenuated influenza virus vaccine lacking non-structural protein 1. Scientific Reports. 11(1). 22164–22164. 10 indexed citations
3.
Jindra, Christoph, et al.. (2021). Influenza virus vector iNS1 expressing bovine papillomavirus 1 (BPV1) antigens efficiently induces tumour regression in equine sarcoid patients. PLoS ONE. 16(11). e0260155–e0260155. 7 indexed citations
5.
Nakowitsch, Sabine, Nina Wressnigg, Emanuele Montomoli, et al.. (2013). Egg‐ or cell culture‐derived hemagglutinin mutations impair virus stability and antigen content of inactivated influenza vaccines. Biotechnology Journal. 9(3). 405–414. 19 indexed citations
6.
Wolzt, Michael, et al.. (2013). Phase I/II trial of a replication-deficient trivalent influenza virus vaccine lacking NS1. Vaccine. 31(52). 6194–6200. 44 indexed citations
7.
Rikxoort, Marijke van, Martin Michaelis, Markus Wolschek, et al.. (2012). Oncolytic Effects of a Novel Influenza A Virus Expressing Interleukin-15 from the NS Reading Frame. PLoS ONE. 7(5). e36506–e36506. 38 indexed citations
8.
Krenn, Brigitte M., Julia Romanova, Sabine Nakowitsch, et al.. (2011). Antimycotic-Antibiotic Amphotericin B Promotes Influenza Virus Replication in Cell Culture. Journal of Virology. 85(21). 11139–11145. 16 indexed citations
9.
Ogbomo, Henry, Martin Michaelis, Janina Geiler, et al.. (2009). Tumor cells infected with oncolytic influenza A virus prime natural killer cells for lysis of resistant tumor cells. Medical Microbiology and Immunology. 199(2). 93–101. 23 indexed citations
10.
Wressnigg, Nina, Daniel Voß, Thorsten Wolff, et al.. (2009). Development of a live-attenuated influenza B ΔNS1 intranasal vaccine candidate. Vaccine. 27(21). 2851–2857. 29 indexed citations
11.
Wressnigg, Nina, Anna-Polina Shurygina, Thorsten Wolff, et al.. (2009). Influenza B mutant viruses with truncated NS1 proteins grow efficiently in Vero cells and are immunogenic in mice. Journal of General Virology. 90(2). 366–374. 20 indexed citations
12.
Ferko, Boris, et al.. (2008). Azidothymidine inhibits melanoma cell growth in vitro and in vivo. Melanoma Research. 18(5). 314–321. 27 indexed citations
13.
Wolff, Klaus, et al.. (2006). Sequence variability of retroviral particles derived from human melanoma cells. Virus Research. 123(2). 211–215. 12 indexed citations
14.
Salvatore, Mirella, Christopher F. Basler, Jean-Patrick Parisien, et al.. (2002). Effects of Influenza A Virus NS1 Protein on Protein Expression: the NS1 Protein Enhances Translation and Is Not Required for Shutoff of Host Protein Synthesis. Journal of Virology. 76(3). 1206–1212. 102 indexed citations
15.
Salvatore, Mirella, Robert E. O’Neill, Hongyong Zheng, et al.. (2000). Influenza A and B viruses expressing altered NS1 proteins: A vaccine approach. Proceedings of the National Academy of Sciences. 97(8). 4309–4314. 260 indexed citations
16.
Palese, Peter, et al.. (1999). Learning from our foes: a novel vaccine concept for influenza virus. PubMed. 15. 131–138. 13 indexed citations
17.
Ferko, Boris, Dietmar Katinger, Andreas Grassauer, et al.. (1998). Chimeric Influenza Virus Replicating Predominantly in the Murine Upper Respiratory Tract Induces Local Immune Responses against Human Immunodeficiency Virus Type 1 in the Genital Tract. The Journal of Infectious Diseases. 178(5). 1359–1368. 42 indexed citations
18.
Egorov, Andrej, Sabine Brandt, Sabine Sereinig, et al.. (1998). Transfectant Influenza A Viruses with Long Deletions in the NS1 Protein Grow Efficiently in Vero Cells. Journal of Virology. 72(8). 6437–6441. 186 indexed citations
19.
Purtscher, Martin, Alexandra Trkola, Andreas Grassauer, et al.. (1996). Restricted antigenic variability of the epitope recognized by the neutralizing gp41 antibody 2F5. AIDS. 10(6). 587–594. 142 indexed citations
20.
Bergmann, Michael & Thomas Muster. (1995). The relative amount of an influenza A virus segment present in the viral particle is not affected by a reduction in replication of that segment. Journal of General Virology. 76(12). 3211–3215. 19 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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