Thomas Schwartz

15.2k total citations · 4 hit papers
90 papers, 11.0k citations indexed

About

Thomas Schwartz is a scholar working on Pollution, Molecular Biology and Molecular Medicine. According to data from OpenAlex, Thomas Schwartz has authored 90 papers receiving a total of 11.0k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Pollution, 42 papers in Molecular Biology and 26 papers in Molecular Medicine. Recurrent topics in Thomas Schwartz's work include Pharmaceutical and Antibiotic Environmental Impacts (45 papers), Bacterial biofilms and quorum sensing (28 papers) and Antibiotic Resistance in Bacteria (26 papers). Thomas Schwartz is often cited by papers focused on Pharmaceutical and Antibiotic Environmental Impacts (45 papers), Bacterial biofilms and quorum sensing (28 papers) and Antibiotic Resistance in Bacteria (26 papers). Thomas Schwartz collaborates with scholars based in Germany, Cyprus and France. Thomas Schwartz's co-authors include Despo Fatta‐Kassinos, Célia M. Manaia, Christophe Merlin, Ursula Obst, Luigi Rizzo, Christophe Dagot, Omolayo M. Ikumapayi, Marie-Cécile Ploy, Johannes Alexander and Christa S. McArdell and has published in prestigious journals such as Environmental Science & Technology, PLoS ONE and The Science of The Total Environment.

In The Last Decade

Thomas Schwartz

88 papers receiving 10.8k citations

Hit Papers

Urban wastewater treatment plants as hotspots fo... 2003 2026 2010 2018 2013 2015 2012 2003 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Schwartz Germany 44 7.2k 3.2k 2.0k 2.0k 1.9k 90 11.0k
Yi Luo China 45 6.9k 1.0× 2.6k 0.8× 1.9k 0.9× 1.1k 0.6× 1.7k 0.9× 154 9.9k
Célia M. Manaia Portugal 59 10.3k 1.4× 4.9k 1.5× 2.6k 1.3× 3.0k 1.5× 2.9k 1.5× 170 16.0k
David W. Graham United Kingdom 54 6.3k 0.9× 2.6k 0.8× 1.5k 0.7× 1.1k 0.6× 2.1k 1.1× 175 10.6k
Olga C. Nunes Portugal 47 4.3k 0.6× 1.5k 0.5× 1.5k 0.7× 2.0k 1.0× 1.7k 0.9× 146 8.7k
Amy Pruden United States 67 10.1k 1.4× 5.0k 1.6× 4.0k 2.0× 2.0k 1.0× 3.7k 1.9× 269 17.4k
Christophe Merlin France 31 4.7k 0.7× 2.2k 0.7× 1.0k 0.5× 1.2k 0.6× 1.5k 0.7× 60 7.6k
Edward Topp Canada 67 8.9k 1.2× 2.8k 0.9× 2.4k 1.2× 2.2k 1.1× 2.6k 1.3× 328 16.7k
Alistair B.A. Boxall United Kingdom 55 10.1k 1.4× 1.2k 0.4× 3.2k 1.6× 1.7k 0.8× 862 0.4× 130 14.1k
Jian‐Qiang Su China 60 8.5k 1.2× 3.1k 1.0× 1.7k 0.8× 696 0.4× 2.8k 1.4× 243 13.6k
Min Qiao China 39 5.9k 0.8× 2.0k 0.6× 1.5k 0.7× 616 0.3× 1.3k 0.7× 87 8.3k

Countries citing papers authored by Thomas Schwartz

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Schwartz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Schwartz. A scholar is included among the top collaborators of Thomas Schwartz 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 Schwartz. Thomas Schwartz 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.
Mazierski, Paweł, Magdalena Miodyńska, Adriana Zaleska‐Medynska, et al.. (2024). The role of TiO2 and gC3N4 bimetallic catalysts in boosting antibiotic resistance gene removal through photocatalyst assisted peroxone process. Scientific Reports. 14(1). 22897–22897. 9 indexed citations
2.
Khan, Umer, et al.. (2023). Antibiotic resistances from slaughterhouse effluents and enhanced antimicrobial blue light technology for wastewater decontamionation. Environmental Science and Pollution Research. 30(50). 109315–109330. 6 indexed citations
3.
Gmurek, Marta, Johannes Alexander, Paweł Mazierski, et al.. (2023). Enhancement of photocatalytic-based processes by mono- and bimetallic (CuPd) rutile loaded nanoparticles for antibiotic resistance genes and facultative pathogenic bacteria removal. Chemical Engineering Journal. 462. 142243–142243. 8 indexed citations
4.
Savin, Mykhailo, Jens A. Hammerl, Julia Hassa, et al.. (2023). Free-floating extracellular DNA (exDNA) in different wastewaters: Status quo on exDNA-associated antimicrobial resistance genes. Environmental Pollution. 337. 122560–122560. 10 indexed citations
5.
Lei, Wenxi, Anna A. Popova, Markus Reischl, et al.. (2022). Droplet Microarray as a Powerful Platform for Seeking New Antibiotics Against Multidrug‐Resistant Bacteria. Advanced Biology. 6(12). e2200166–e2200166. 10 indexed citations
6.
Hilgert, Stephan, et al.. (2021). Determination of antibiotic resistance genes in a WWTP-impacted river in surface water, sediment, and biofilm: Influence of seasonality and water quality. The Science of The Total Environment. 768. 144526–144526. 72 indexed citations
7.
Lei, Wenxi, et al.. (2020). Controlling Geometry and Flow Through Bacterial Bridges on Patterned Lubricant‐Infused Surfaces (pLIS). Small. 16(52). e2004575–e2004575. 10 indexed citations
8.
Sib, Esther, Mykhailo Savin, Norman Hembach, et al.. (2020). Bacteria isolated from hospital, municipal and slaughterhouse wastewaters show characteristic, different resistance profiles. The Science of The Total Environment. 746. 140894–140894. 42 indexed citations
9.
Lei, Wenxi, et al.. (2019). Biofilm Bridges Forming Structural Networks on Patterned Lubricant‐Infused Surfaces. Advanced Science. 6(13). 1900519–1900519. 40 indexed citations
10.
Brown, Philip C., et al.. (2019). Decay of elevated antibiotic resistance genes in natural river sediments after sedimentation of wastewater particles. The Science of The Total Environment. 705. 135861–135861. 25 indexed citations
11.
Voigt, Alexander, Nicole Zacharias, Esther Sib, et al.. (2019). Association between antibiotic residues, antibiotic resistant bacteria and antibiotic resistance genes in anthropogenic wastewater – An evaluation of clinical influences. Chemosphere. 241. 125032–125032. 88 indexed citations
12.
Jäger, Thomas, Johannes Alexander, Silke Kirchen, et al.. (2017). Live-dead discrimination analysis, qPCR assessment for opportunistic pathogens, and population analysis at ozone wastewater treatment plants. Environmental Pollution. 232. 571–579. 59 indexed citations
13.
Kirchen, Silke, et al.. (2013). Sub-inhibitory concentrations of antibiotics and wastewater influencing biofilm formation and gene expression of multi-resistant Pseudomonas aeruginosa wastewater isolates. Environmental Science and Pollution Research. 20(6). 3539–3549. 43 indexed citations
14.
Proia, Lorenzo, Victoria Osorio, Sandra Pérez, et al.. (2013). Response of biofilm bacterial communities to antibiotic pollutants in a Mediterranean river. Chemosphere. 92(9). 1126–1135. 86 indexed citations
15.
Henkel, Marius, et al.. (2013). Expression of genes involved in rhamnolipid synthesis in Pseudomonas aeruginosa PAO1 in a bioreactor cultivation. Applied Microbiology and Biotechnology. 97(13). 5779–5791. 14 indexed citations
16.
Rizzo, Luigi, Célia M. Manaia, Christophe Merlin, et al.. (2013). Urban wastewater treatment plants as hotspots for antibiotic resistant bacteria and genes spread into the environment: A review. The Science of The Total Environment. 447. 345–360. 1824 indexed citations breakdown →
17.
Henkel, Marius, Christian Kühnert, Thomas Bernard, et al.. (2013). Kinetic modeling of the time course of N-butyryl-homoserine lactone concentration during batch cultivations of Pseudomonas aeruginosa PAO1. Applied Microbiology and Biotechnology. 97(17). 7607–7616. 24 indexed citations
18.
Rieder, Annika, et al.. (2011). The impact of recombinant fusion-hydrophobin coated surfaces onE. coliand natural mixed culture biofilm formation. Biofouling. 27(10). 1073–1085. 11 indexed citations
19.
Berensmeier, Sonja, et al.. (2009). In vivo labeling and specific magnetic bead separation of RNA for biofilm characterization and stress-induced gene expression analysis in bacteria. Journal of Microbiological Methods. 79(3). 344–352. 2 indexed citations
20.
Schwartz, Thomas, et al.. (2004). Investigation of natural biofilms formed during the production of drinking water from surface water embankment filtration. Water Research. 38(5). 1197–1206. 135 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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