Martin Münsterkötter

5.8k total citations
38 papers, 1.7k citations indexed

About

Martin Münsterkötter is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, Martin Münsterkötter has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Plant Science, 19 papers in Molecular Biology and 11 papers in Cell Biology. Recurrent topics in Martin Münsterkötter's work include Fungal and yeast genetics research (11 papers), Plant Pathogens and Fungal Diseases (11 papers) and Plant-Microbe Interactions and Immunity (9 papers). Martin Münsterkötter is often cited by papers focused on Fungal and yeast genetics research (11 papers), Plant Pathogens and Fungal Diseases (11 papers) and Plant-Microbe Interactions and Immunity (9 papers). Martin Münsterkötter collaborates with scholars based in Germany, Hungary and Switzerland. Martin Münsterkötter's co-authors include Ulrich Güldener, Wolfram Hörz, Gertrud Mannhaupt, Christian M. K. Sieber, Slobodan Barbarić, Hans‐Werner Mewes, Andrea Schmid, Philip D. Gregory, Jan Schirawski and Regine Kahmann and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Martin Münsterkötter

38 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Münsterkötter Germany 26 935 924 462 214 94 38 1.7k
Zsuzsanna Hamari Hungary 19 1.2k 1.2× 1.1k 1.2× 517 1.1× 395 1.8× 94 1.0× 47 1.9k
Jens Heller Germany 18 682 0.7× 1.0k 1.1× 322 0.7× 197 0.9× 43 0.5× 19 1.4k
Takashi Kamakura Japan 21 840 0.9× 922 1.0× 255 0.6× 179 0.8× 43 0.5× 64 1.5k
Gavin E. Wakley United Kingdom 14 852 0.9× 891 1.0× 458 1.0× 210 1.0× 63 0.7× 24 1.4k
Yasin Dagdas Austria 30 1.4k 1.5× 2.2k 2.4× 837 1.8× 165 0.8× 51 0.5× 61 2.9k
Xiaobo Zheng China 31 1.5k 1.6× 1.9k 2.0× 1.1k 2.3× 386 1.8× 78 0.8× 78 2.4k
Chuck Stäben United States 16 1.1k 1.2× 786 0.9× 430 0.9× 224 1.0× 56 0.6× 27 1.7k
Martine Boccara France 31 992 1.1× 2.2k 2.4× 392 0.8× 129 0.6× 56 0.6× 60 2.8k
Flora Banuett United States 15 1.8k 1.9× 1.1k 1.2× 448 1.0× 296 1.4× 81 0.9× 23 2.2k
Rajagopal Subramaniam Canada 23 787 0.8× 1.4k 1.5× 343 0.7× 88 0.4× 40 0.4× 49 1.7k

Countries citing papers authored by Martin Münsterkötter

Since Specialization
Citations

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

Fields of papers citing papers by Martin Münsterkötter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Münsterkötter

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Münsterkötter. A scholar is included among the top collaborators of Martin Münsterkötter 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 Martin Münsterkötter. Martin Münsterkötter 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.
Rigling, Daniel, et al.. (2020). Chromosomal assembly and analyses of genome-wide recombination rates in the forest pathogenic fungus Armillaria ostoyae. Heredity. 124(6). 699–713. 13 indexed citations
2.
Kappel, Lisa, Martin Münsterkötter, György Sipos, Carolina Escobar Rodríguez, & Sabine Gruber. (2020). Chitin and chitosan remodeling defines vegetative development and Trichoderma biocontrol. PLoS Pathogens. 16(2). e1008320–e1008320. 46 indexed citations
3.
Boenisch, Marike Johanne, Bernard Henrissat, Rasmus John Normand Frandsen, et al.. (2020). Infection cushions of Fusarium graminearum are fungal arsenals for wheat infection. Molecular Plant Pathology. 21(8). 1070–1087. 54 indexed citations
4.
Chen, Liqiong, Bettina Bóka, Orsolya Kedves, et al.. (2019). Towards the Biological Control of Devastating Forest Pathogens from the Genus Armillaria. Forests. 10(11). 1013–1013. 25 indexed citations
5.
Atanasova, Lea, Sabine Gruber, Alexander Lichius, et al.. (2018). The Gpr1-regulated Sur7 family protein Sfp2 is required for hyphal growth and cell wall stability in the mycoparasite Trichoderma atroviride. Scientific Reports. 8(1). 12064–12064. 29 indexed citations
6.
Stam, Remco, Martin Münsterkötter, Saurabh D. Pophaly, et al.. (2018). A New Reference Genome Shows the One-Speed Genome Structure of the Barley PathogenRamularia collo-cygni. Genome Biology and Evolution. 10(12). 3243–3249. 20 indexed citations
7.
Niehaus, Eva‐Maria, Hee-Kyoung Kim, Martin Münsterkötter, et al.. (2017). Comparative genomics of geographically distant Fusarium fujikuroi isolates revealed two distinct pathotypes correlating with secondary metabolite profiles. PLoS Pathogens. 13(10). e1006670–e1006670. 62 indexed citations
8.
Croll, Daniel, Stefan Zoller, György Sipos, et al.. (2017). High-density genetic mapping identifies the genetic basis of a natural colony morphology mutant in the root rot pathogen Armillaria ostoyae. Fungal Genetics and Biology. 108. 44–54. 6 indexed citations
9.
Niehaus, Eva‐Maria, Julia Schumacher, Immo Burkhardt, et al.. (2017). The GATA-Type Transcription Factor Csm1 Regulates Conidiation and Secondary Metabolism in Fusarium fujikuroi. Frontiers in Microbiology. 8. 1175–1175. 37 indexed citations
10.
Niehaus, Eva‐Maria, et al.. (2017). Analysis of the global regulator Lae1 uncovers a connection between Lae1 and the histone acetyltransferase HAT1 in Fusarium fujikuroi. Applied Microbiology and Biotechnology. 102(1). 279–295. 36 indexed citations
11.
Palma, Margarida, Martin Münsterkötter, João Peça, Ulrich Güldener, & Isabel Sá‐Correia. (2017). Genome sequence of the highly weak-acid-tolerant Zygosaccharomyces bailii IST302, amenable to genetic manipulations and physiological studies. FEMS Yeast Research. 17(4). 12 indexed citations
12.
Mira, Nuno P., Martin Münsterkötter, Júlia Santos, et al.. (2014). The Genome Sequence of the Highly Acetic Acid-Tolerant Zygosaccharomyces bailii-Derived Interspecies Hybrid Strain ISA1307, Isolated From a Sparkling Wine Plant. DNA Research. 21(3). 299–313. 38 indexed citations
13.
Frangoulidis, Dimitrios, Mathias C. Walter, Markus Antwerpen, et al.. (2014). Molecular analysis of Coxiella burnetii in Germany reveals evolution of unique clonal clusters. International Journal of Medical Microbiology. 304(7). 868–876. 31 indexed citations
14.
Wong, P., Mathias C. Walter, Wanseon Lee, et al.. (2010). FGDB: revisiting the genome annotation of the plant pathogen Fusarium graminearum. Nucleic Acids Research. 39(Database). D637–D639. 76 indexed citations
15.
Feldbrügge, Michael, Kathi Zarnack, Evelyn Vollmeister, et al.. (2008). The posttranscriptional machinery of Ustilago maydis. Fungal Genetics and Biology. 45. S40–S46. 24 indexed citations
16.
Mewes, Hans‐Werner, Sabine Dietmann, Dmitrij Frishman, et al.. (2007). MIPS: analysis and annotation of genome information in 2007. Nucleic Acids Research. 36(Database). D196–D201. 131 indexed citations
17.
Briza, Peter, Edith Bogengruber, Michael Rützler, et al.. (2002). Systematic analysis of sporulation phenotypes in 624 non‐lethal homozygous deletion strains of Saccharomyces cerevisiae. Yeast. 19(5). 403–422. 45 indexed citations
18.
Münsterkötter, Martin, Slobodan Barbarić, & Wolfram Hörz. (2000). Transcriptional Regulation of the Yeast PHO8 Promoter in Comparison to the Coregulated PHO5 Promoter. Journal of Biological Chemistry. 275(30). 22678–22685. 26 indexed citations
19.
Gregory, Philip D., et al.. (1999). Chromatin remodelling at the PHO8 promoter requires SWI–SNF and SAGA at a step subsequent to activator binding. The EMBO Journal. 18(22). 6407–6414. 113 indexed citations
20.
Evers, Jürgen, et al.. (1990). Natriumdinitridoborat mit dem linear gebauten, symmetrischen BN23− -Anion. Journal of the Less Common Metals. 162(1). L17–L22. 23 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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