Thomas Maskow

2.5k total citations
101 papers, 1.9k citations indexed

About

Thomas Maskow is a scholar working on Physical and Theoretical Chemistry, Molecular Biology and Pollution. According to data from OpenAlex, Thomas Maskow has authored 101 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Physical and Theoretical Chemistry, 53 papers in Molecular Biology and 19 papers in Pollution. Recurrent topics in Thomas Maskow's work include thermodynamics and calorimetric analyses (66 papers), Microbial Metabolic Engineering and Bioproduction (26 papers) and Viral Infectious Diseases and Gene Expression in Insects (12 papers). Thomas Maskow is often cited by papers focused on thermodynamics and calorimetric analyses (66 papers), Microbial Metabolic Engineering and Bioproduction (26 papers) and Viral Infectious Diseases and Gene Expression in Insects (12 papers). Thomas Maskow collaborates with scholars based in Germany, China and Hungary. Thomas Maskow's co-authors include Hauke Harms, Urs von Stockar, W. Babel, J. Lerchner, Torsten Schubert, Rodrigo Patiño, Jingsong Liu, I. W. Marison, Uta Breuer and G. Wolf and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Energy & Environmental Science and The Science of The Total Environment.

In The Last Decade

Thomas Maskow

97 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Maskow Germany 26 829 789 304 277 201 101 1.9k
I. W. Marison Switzerland 44 2.8k 3.4× 871 1.1× 1.3k 4.2× 207 0.7× 107 0.5× 150 5.0k
Oense M. Neijssel Netherlands 27 1.5k 1.8× 179 0.2× 483 1.6× 232 0.8× 167 0.8× 63 2.3k
Aurora Pinazo Spain 33 1.3k 1.6× 229 0.3× 234 0.8× 738 2.7× 67 0.3× 88 3.9k
Abdul Matin United States 37 2.5k 3.1× 94 0.1× 395 1.3× 270 1.0× 615 3.1× 118 4.6k
D. Naumann Germany 23 1.1k 1.3× 108 0.1× 517 1.7× 103 0.4× 166 0.8× 48 3.4k
D. W. Tempest Netherlands 34 2.0k 2.5× 203 0.3× 527 1.7× 304 1.1× 301 1.5× 70 3.3k
Sven‐Olof Enfors Sweden 40 3.3k 3.9× 146 0.2× 1.2k 4.1× 153 0.6× 203 1.0× 119 4.6k
J.P. Belaïch France 25 807 1.0× 168 0.2× 902 3.0× 78 0.3× 79 0.4× 55 1.8k
Tsukasa Ikeda Japan 34 2.3k 2.8× 103 0.1× 343 1.1× 294 1.1× 462 2.3× 126 4.0k
P. Mañas Spain 35 639 0.8× 81 0.1× 393 1.3× 84 0.3× 98 0.5× 81 3.6k

Countries citing papers authored by Thomas Maskow

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Maskow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Maskow

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Maskow. A scholar is included among the top collaborators of Thomas Maskow 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 Maskow. Thomas Maskow 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.
Blagodatskaya, Еvgenia, et al.. (2025). Carbon and energy utilization in microbial cell extracts from soil. European Journal of Soil Biology. 124. 103713–103713.
2.
Maskow, Thomas, et al.. (2025). Deciphering guanidine assimilation and riboswitch-based gene regulation in cyanobacteria for synthetic biology applications. Proceedings of the National Academy of Sciences. 122(49). e2519335122–e2519335122.
4.
Harms, Hauke, et al.. (2025). Soil microbial metabolism: Insights from heat, CO2 emission and isotope analysis using a novel macrocalorespirometer. Soil Biology and Biochemistry. 212. 109994–109994.
6.
Harms, Hauke, et al.. (2024). Enhancing insights: exploring the information content of calorespirometric ratio in dynamic soil microbial growth processes through calorimetry. Frontiers in Microbiology. 15. 1321059–1321059. 12 indexed citations
8.
Held, Christoph, et al.. (2020). Thermodynamics and Kinetics of Glycolytic Reactions. Part I: Kinetic Modeling Based on Irreversible Thermodynamics and Validation by Calorimetry. International Journal of Molecular Sciences. 21(21). 8341–8341. 4 indexed citations
9.
Held, Christoph, et al.. (2020). Thermodynamics and Kinetics of Glycolytic Reactions. Part II: Influence of Cytosolic Conditions on Thermodynamic State Variables and Kinetic Parameters. International Journal of Molecular Sciences. 21(21). 7921–7921. 4 indexed citations
11.
Verevkin, Sergey P., et al.. (2020). Standard Gibbs energy of metabolic reactions: V. Enolase reaction. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1868(4). 140365–140365. 15 indexed citations
12.
Harms, Hauke, et al.. (2019). Rapid Calorimetric Detection of Bacterial Contamination: Influence of the Cultivation Technique. Frontiers in Microbiology. 10. 2530–2530. 21 indexed citations
13.
Russel, Mohammad, Marios Sophocleous, Jiajia Shan, et al.. (2018). High-frequency, dielectric spectroscopy for the detection of electrophysiological/biophysical differences in different bacteria types and concentrations. Analytica Chimica Acta. 1028. 86–95. 17 indexed citations
15.
Mühling, Martin, Antje Wolf, Thomas Maskow, et al.. (2013). A chip-calorimetric approach to the analysis of Ag nanoparticle caused inhibition and inactivation of beads-grown bacterial biofilms. Journal of Microbiological Methods. 95(2). 129–137. 11 indexed citations
16.
Yao, Jun, et al.. (2009). Acute toxic effects of three pesticides onPseudomonas putidamonitored by microcalorimeter. Journal of Environmental Science and Health Part B. 44(2). 157–163. 7 indexed citations
17.
Zhou, Yong, Jun Yao, Martin M. F. Choi, et al.. (2009). A combination method to study microbial communities and activities in zinc contaminated soil. Journal of Hazardous Materials. 169(1-3). 875–881. 46 indexed citations
18.
Maskow, Thomas, et al.. (2009). What heat is telling us about microbial conversions in nature and technology: from chip‐ to megacalorimetry. Microbial Biotechnology. 3(3). 269–284. 46 indexed citations
19.
Yao, Jun, Fei Wang, Yong Zhou, et al.. (2008). Toxic Effect of Inorganic Arsenite [As(III)] on Metabolic Activity of Bacillus subtilis by Combined Methods. Current Microbiology. 57(3). 258–263. 13 indexed citations
20.
Yao, Jun, Yong Zhou, Fei Wang, et al.. (2008). Investigation of the toxic effect of cadmium on Candida humicola and Bacillus subtilis using a microcalorimetric method. Journal of Hazardous Materials. 159(2-3). 465–470. 22 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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