Matthias Gube

1.5k total citations
28 papers, 972 citations indexed

About

Matthias Gube is a scholar working on Plant Science, Ecology, Evolution, Behavior and Systematics and Pharmacology. According to data from OpenAlex, Matthias Gube has authored 28 papers receiving a total of 972 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Plant Science, 11 papers in Ecology, Evolution, Behavior and Systematics and 8 papers in Pharmacology. Recurrent topics in Matthias Gube's work include Mycorrhizal Fungi and Plant Interactions (17 papers), Lichen and fungal ecology (9 papers) and Fungal Biology and Applications (7 papers). Matthias Gube is often cited by papers focused on Mycorrhizal Fungi and Plant Interactions (17 papers), Lichen and fungal ecology (9 papers) and Fungal Biology and Applications (7 papers). Matthias Gube collaborates with scholars based in Germany, Finland and China. Matthias Gube's co-authors include Johanna Pausch, Yakov Kuzyakov, Erika Kothe, Jie Zhou, Heinrich Dörfelt, Huadong Zang, Sebastian Loeppmann, Jouko Rikkinen, Alexander R. Schmidt and Christina Beimforde and has published in prestigious journals such as Nature Communications, PLoS ONE and Chemosphere.

In The Last Decade

Matthias Gube

28 papers receiving 951 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthias Gube Germany 13 545 290 221 214 200 28 972
Kendall Martin United States 12 638 1.2× 228 0.8× 262 1.2× 150 0.7× 295 1.5× 22 1.1k
Laura Aldrich‐Wolfe United States 13 716 1.3× 220 0.8× 233 1.1× 189 0.9× 196 1.0× 24 1.1k
Sara Hortal Spain 17 697 1.3× 294 1.0× 243 1.1× 243 1.1× 117 0.6× 24 1.0k
Zaida Inês Antoniolli Brazil 18 661 1.2× 433 1.5× 290 1.3× 135 0.6× 105 0.5× 144 1.3k
Jingping Gai China 19 889 1.6× 355 1.2× 245 1.1× 164 0.8× 170 0.8× 46 1.2k
Jean-Charles Munch Germany 17 594 1.1× 478 1.6× 218 1.0× 128 0.6× 148 0.7× 24 1.1k
Komi Assigbetsé France 20 826 1.5× 244 0.8× 148 0.7× 159 0.7× 192 1.0× 47 1.2k
Laura B. Martínez‐García Netherlands 12 664 1.2× 260 0.9× 172 0.8× 144 0.7× 119 0.6× 21 900
Gwen‐Aëlle Grelet New Zealand 12 788 1.4× 203 0.7× 182 0.8× 138 0.6× 122 0.6× 25 1.2k
Sally Hilton United Kingdom 20 731 1.3× 215 0.7× 229 1.0× 144 0.7× 114 0.6× 35 1.2k

Countries citing papers authored by Matthias Gube

Since Specialization
Citations

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

Fields of papers citing papers by Matthias Gube

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthias Gube

This figure shows the co-authorship network connecting the top 25 collaborators of Matthias Gube. A scholar is included among the top collaborators of Matthias Gube 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 Matthias Gube. Matthias Gube 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.
Zhou, Jie, Sebastian Loeppmann, Haishui Yang, et al.. (2025). Linking microbial community dynamics to rhizosphere carbon flow depend on arbuscular mycorrhizae and nitrogen fertilization. Biology and Fertility of Soils. 61(4). 791–804. 1 indexed citations
2.
Liu, Hongfei, et al.. (2023). Vegetation transition from meadow to forest reduces priming effect on SOM decomposition. Soil Biology and Biochemistry. 184. 109123–109123. 3 indexed citations
3.
Klink, Saskia, Adrienne B. Keller, Vera Baumert, et al.. (2022). Stable isotopes reveal that fungal residues contribute more to mineral-associated organic matter pools than plant residues. Soil Biology and Biochemistry. 168. 108634–108634. 93 indexed citations
4.
Loizides, Michael, Pablo Alvarado, Elias Polemis, et al.. (2020). Multiple evolutionary origins of sequestrate species in the agaricoid genus Chlorophyllum. Mycologia. 112(2). 400–422. 11 indexed citations
5.
Gube, Matthias, Else C. Vellinga, Pablo Alvarado, et al.. (2020). (2749) Proposal to conserve Chlorophyllum nom. cons. against the additional name Secotium (Agaricaceae). Taxon. 69(4). 819–820. 1 indexed citations
6.
Kuhar, Francisco, et al.. (2020). Bovista pezica (Basidiomycota, Agaricales) – A new species with unusually ornamented capillitium, from Patagonia Argentina. Nova Hedwigia. 111(1-2). 173–185. 2 indexed citations
7.
Zhou, Jie, Huadong Zang, Sebastian Loeppmann, et al.. (2019). Arbuscular mycorrhiza enhances rhizodeposition and reduces the rhizosphere priming effect on the decomposition of soil organic matter. Soil Biology and Biochemistry. 140. 107641–107641. 160 indexed citations
8.
Grawunder, Anja & Matthias Gube. (2018). Element distribution in fruiting bodies of Lactarius pubescens with focus on rare earth elements. Chemosphere. 208. 614–625. 13 indexed citations
9.
Miller, Andrew N., Daniel B. Raudabaugh, Teresa Iturriaga, et al.. (2017). First report of the post-fire morelMorchella exuberansin eastern North America. Mycologia. 109(5). 1–5. 7 indexed citations
10.
Beimforde, Christina, Hanna Tuovila, Alexander R. Schmidt, et al.. (2017). Chaenothecopsis schefflerae (Ascomycota: Mycocaliciales): a widespread fungus on semi‐hardened exudates of endemic New Zealand Araliaceae. New Zealand Journal of Botany. 55(4). 387–406. 8 indexed citations
11.
Krause, Katrin, et al.. (2016). Hydrophobins in the Life Cycle of the Ectomycorrhizal Basidiomycete Tricholoma vaccinum. PLoS ONE. 11(12). e0167773–e0167773. 29 indexed citations
12.
Wagner, Katharina, Jörg Linde, Katrin Krause, et al.. (2015). Tricholoma vaccinumhost communication during ectomycorrhiza formation. FEMS Microbiology Ecology. 91(11). fiv120–fiv120. 12 indexed citations
13.
Gube, Matthias, et al.. (2015). Dynein Heavy Chain, Encoded by Two Genes in Agaricomycetes, Is Required for Nuclear Migration in Schizophyllum commune. PLoS ONE. 10(8). e0135616–e0135616. 11 indexed citations
14.
Beimforde, Christina, Kathrin Feldberg, Stephan Nylinder, et al.. (2014). Estimating the Phanerozoic history of the Ascomycota lineages: Combining fossil and molecular data. Molecular Phylogenetics and Evolution. 78. 386–398. 226 indexed citations
15.
Sadowski, Eva‐Maria, Christina Beimforde, Matthias Gube, et al.. (2012). The anamorphic genus Monotosporella (Ascomycota) from Eocene amber and from modern Agathis resin. Fungal Biology. 116(10). 1099–1110. 19 indexed citations
16.
Völksch, Beate, et al.. (2009). Polyphasic study of plant- and clinic-associated Pantoea agglomerans strains reveals indistinguishable virulence potential. Infection Genetics and Evolution. 9(6). 1381–1391. 40 indexed citations
17.
Gube, Matthias & Meike Piepenbring. (2009). Preliminary annotated checklist of Gasteromycetes in Panama. Nova Hedwigia. 89(3-4). 519–543. 12 indexed citations
18.
Gube, Matthias, et al.. (2009). In silico analysis of nickel containing superoxide dismutase evolution and regulation. Journal of Basic Microbiology. 49(1). 109–118. 32 indexed citations
19.
Dörfelt, Heinrich & Matthias Gube. (2007). Secotioid Agaricales (Basidiomycetes) from Mongolia. Feddes Repertorium. 118(3-4). 103–112. 3 indexed citations
20.

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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