Markus Piotrowski

4.0k total citations
53 papers, 3.1k citations indexed

About

Markus Piotrowski is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Markus Piotrowski has authored 53 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 27 papers in Plant Science and 7 papers in Biochemistry. Recurrent topics in Markus Piotrowski's work include Photosynthetic Processes and Mechanisms (10 papers), Plant nutrient uptake and metabolism (9 papers) and Cassava research and cyanide (7 papers). Markus Piotrowski is often cited by papers focused on Photosynthetic Processes and Mechanisms (10 papers), Plant nutrient uptake and metabolism (9 papers) and Cassava research and cyanide (7 papers). Markus Piotrowski collaborates with scholars based in Germany, United States and Spain. Markus Piotrowski's co-authors include Elmar W. Weiler, Claudia Oecking, Tim Janowitz, Axel Müller, H. Kneifel, Christer Larsson, Marianne Sommarin, Magnus Rosenquist, Gerhard Link and Steffen Reinbothe 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

Markus Piotrowski

52 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Markus Piotrowski Germany 33 2.2k 1.8k 237 227 161 53 3.1k
Alexander Graf Germany 31 1.9k 0.8× 2.1k 1.2× 114 0.5× 155 0.7× 84 0.5× 55 3.4k
Stephan Pollmann Spain 39 2.5k 1.1× 3.5k 1.9× 141 0.6× 117 0.5× 98 0.6× 95 4.3k
Daphné Seigneurin‐Berny France 25 2.8k 1.3× 1.1k 0.6× 240 1.0× 407 1.8× 100 0.6× 42 3.5k
Florence Vignols France 31 2.2k 1.0× 1.6k 0.9× 180 0.8× 222 1.0× 62 0.4× 53 3.2k
Sigrun Reumann Germany 31 2.7k 1.2× 1.1k 0.6× 640 2.7× 197 0.9× 139 0.9× 46 3.2k
Katayoon Dehesh United States 47 3.8k 1.7× 3.9k 2.2× 571 2.4× 273 1.2× 113 0.7× 105 5.6k
Sacha Baginsky Germany 38 3.9k 1.8× 1.9k 1.1× 313 1.3× 464 2.0× 167 1.0× 81 4.8k
Pablo A. Scolnik United States 36 3.2k 1.4× 2.2k 1.2× 113 0.5× 586 2.6× 237 1.5× 49 4.5k
Jean‐Pierre Carde France 22 2.3k 1.0× 1.9k 1.0× 301 1.3× 120 0.5× 51 0.3× 50 3.2k
Zach Adam Israel 38 3.8k 1.7× 1.9k 1.0× 182 0.8× 638 2.8× 124 0.8× 73 4.4k

Countries citing papers authored by Markus Piotrowski

Since Specialization
Citations

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

Fields of papers citing papers by Markus Piotrowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Piotrowski

This figure shows the co-authorship network connecting the top 25 collaborators of Markus Piotrowski. A scholar is included among the top collaborators of Markus Piotrowski 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 Markus Piotrowski. Markus Piotrowski 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.
Schulz, Frank, et al.. (2023). Arabidopsis nicotianamine synthases comprise a common core-NAS domain fused to a variable autoinhibitory C terminus. Journal of Biological Chemistry. 299(6). 104732–104732. 6 indexed citations
2.
Woodward, Jeremy, et al.. (2018). Substrate specificity of plant nitrilase complexes is affected by their helical twist. Communications Biology. 1(1). 186–186. 29 indexed citations
3.
Stauber, Einar J., Birgit Vogt, Tim Janowitz, et al.. (2012). Turning the ‘Mustard Oil Bomb’ into a ‘Cyanide Bomb’: Aromatic Glucosinolate Metabolism in a Specialist Insect Herbivore. PLoS ONE. 7(4). e35545–e35545. 51 indexed citations
4.
Piotrowski, Markus, Ashley Lloyd, Thorsten Forster, et al.. (2012). Exploiting Parallel R in the Cloud with SPRINT. Methods of Information in Medicine. 52(1). 80–90. 2 indexed citations
5.
Kong, Fanjiang, Jun Abe, Baohui Liu, et al.. (2009). Expression of Allene Oxide Cyclase fromPharbitis nilupon Theobroxide Treatment. Bioscience Biotechnology and Biochemistry. 73(5). 1007–1013. 6 indexed citations
6.
Bals, Thomas, Irene L. Gügel, Markus Piotrowski, et al.. (2009). Alb4 of Arabidopsis Promotes Assembly and Stabilization of a Non Chlorophyll-Binding Photosynthetic Complex, the CF1CF0–ATP Synthase. Molecular Plant. 2(6). 1410–1424. 50 indexed citations
7.
Piotrowski, Markus. (2008). Primary or secondary? Versatile nitrilases in plant metabolism. Phytochemistry. 69(15). 2655–2667. 87 indexed citations
8.
Kriechbaumer, Verena, et al.. (2007). Maize nitrilases have a dual role in auxin homeostasis and -cyanoalanine hydrolysis. Journal of Experimental Botany. 58(15-16). 4225–4233. 48 indexed citations
9.
Baumann, Sascha, et al.. (2006). Chlorella viruses contain genes encoding a complete polyamine biosynthetic pathway. Virology. 360(1). 209–217. 35 indexed citations
10.
Piotrowski, Markus, et al.. (2006). Cyanide Metabolism in Higher Plants: Cyanoalanine Hydratase is a NIT4 Homolog. Plant Molecular Biology. 61(1-2). 111–122. 58 indexed citations
12.
Depping, Reinhard, et al.. (2004). Bacteriophage T4 α-glucosyltransferase: a novel interaction with gp45 and aspects of the catalytic mechanism. Biochemical and Biophysical Research Communications. 323(3). 809–815. 9 indexed citations
13.
Hoffmeister, Michael, et al.. (2004). Mitochondrial trans-2-Enoyl-CoA Reductase of Wax Ester Fermentation from Euglena gracilis Defines a New Family of Enzymes Involved in Lipid Synthesis. Journal of Biological Chemistry. 280(6). 4329–4338. 65 indexed citations
14.
Piotrowski, Markus, Tim Janowitz, & H. Kneifel. (2003). Plant C-N Hydrolases and the Identification of a Plant N-Carbamoylputrescine Amidohydrolase Involved in Polyamine Biosynthesis. Journal of Biological Chemistry. 278(3). 1708–1712. 72 indexed citations
15.
Pollmann, Stephan, Axel Müller, Markus Piotrowski, & Elmar W. Weiler. (2002). Occurrence and formation of indole-3-acetamide in Arabidopsis thaliana. Planta. 216(1). 155–161. 74 indexed citations
16.
Müller, Axel, et al.. (2002). A role for nitrilase 3 in the regulation of root morphology in sulphur‐starving Arabidopsis thaliana. The Plant Journal. 30(1). 95–106. 171 indexed citations
17.
Piotrowski, Markus, et al.. (2001). The Arabidopsis thaliana Isogene NIT4 and Its Orthologs in Tobacco Encode β-Cyano-l-alanine Hydratase/Nitrilase. Journal of Biological Chemistry. 276(4). 2616–2621. 163 indexed citations
19.
Piotrowski, Markus, Pierre Morsomme, Marc Boutry, & Claudia Oecking. (1998). Complementation of the Saccharomyces cerevisiaePlasma Membrane H+-ATPase by a Plant H+-ATPase Generates a Highly Abundant Fusicoccin Binding Site. Journal of Biological Chemistry. 273(45). 30018–30023. 48 indexed citations
20.
Piotrowski, Markus & Claudia Oecking. (1997). Five new 14-3-3 isoforms from Nicotiana tabacum L.: implications for the phylogeny of plant 14-3-3 proteins. Planta. 204(1). 127–130. 26 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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