Antje Labes

2.8k total citations · 2 hit papers
47 papers, 2.0k citations indexed

About

Antje Labes is a scholar working on Pharmacology, Biotechnology and Molecular Biology. According to data from OpenAlex, Antje Labes has authored 47 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pharmacology, 19 papers in Biotechnology and 16 papers in Molecular Biology. Recurrent topics in Antje Labes's work include Microbial Natural Products and Biosynthesis (19 papers), Marine Sponges and Natural Products (9 papers) and Enzyme Production and Characterization (9 papers). Antje Labes is often cited by papers focused on Microbial Natural Products and Biosynthesis (19 papers), Marine Sponges and Natural Products (9 papers) and Enzyme Production and Characterization (9 papers). Antje Labes collaborates with scholars based in Germany, Indonesia and Sweden. Antje Labes's co-authors include Jutta Wiese, Franz Goecke, Johannes F. Imhoff, JF Imhoff, Sergey Dobretsov, Florian Weinberger, Martin Wahl, Peter Schönheit, Deniz Taşdemir and Vera Thiel and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Applied and Environmental Microbiology.

In The Last Decade

Antje Labes

45 papers receiving 2.0k citations

Hit Papers

Chemical interactions between marine macroalgae and bacteria 2010 2026 2015 2020 2010 2012 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antje Labes Germany 23 646 627 569 547 524 47 2.0k
Charles Santhanaraju Vairappan Malaysia 30 446 0.7× 443 0.7× 532 0.9× 702 1.3× 297 0.6× 139 2.8k
Jutta Wiese Germany 33 1.1k 1.7× 1.1k 1.8× 937 1.6× 1.0k 1.9× 1.3k 2.4× 88 3.6k
Olga Maria Lage Portugal 27 910 1.4× 1.1k 1.7× 249 0.4× 327 0.6× 452 0.9× 83 2.0k
Pedro N. Leão Portugal 27 388 0.6× 530 0.8× 291 0.5× 280 0.5× 360 0.7× 68 1.7k
Detmer Sipkema Netherlands 29 762 1.2× 942 1.5× 113 0.2× 1.3k 2.3× 962 1.8× 73 3.2k
Zhiyong Li China 30 506 0.8× 872 1.4× 177 0.3× 1.1k 2.0× 1.1k 2.0× 120 2.5k
Valéria Laneuville Teixeira Brazil 31 175 0.3× 571 0.9× 824 1.4× 1.0k 1.9× 247 0.5× 154 2.8k
Olga I. Nedashkovskaya Russia 34 2.3k 3.5× 2.5k 4.0× 379 0.7× 688 1.3× 219 0.4× 134 3.5k
Valery V. Mikhailov Russia 40 2.5k 3.9× 2.8k 4.4× 325 0.6× 724 1.3× 302 0.6× 128 3.8k
Lyudmila A. Romanenko Russia 29 1.2k 1.9× 1.5k 2.4× 139 0.2× 460 0.8× 270 0.5× 123 2.4k

Countries citing papers authored by Antje Labes

Since Specialization
Citations

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

Fields of papers citing papers by Antje Labes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antje Labes

This figure shows the co-authorship network connecting the top 25 collaborators of Antje Labes. A scholar is included among the top collaborators of Antje Labes 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 Antje Labes. Antje Labes 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.
Labes, Antje, et al.. (2024). Molecular characterization of proteolytic bacteria associated with Malaria vectors: Anopheles sundaicus and Anopheles vagus. SHILAP Revista de lepidopterología. 43(2). 202–212.
2.
Labes, Antje, et al.. (2024). Isolation of Lignocellulolytic Bacteria From Erek-erek Geoforest Ijen Geopark, Indonesia. SHILAP Revista de lepidopterología. 101. 2002–2002.
3.
Labes, Antje. (2023). Marine Resources Offer New Compounds and Strategies for the Treatment of Skin and Soft Tissue Infections. Marine Drugs. 21(7). 387–387. 7 indexed citations
4.
Krohn, Steffen, Yu‐Chen Wu, Stefan Veltel, et al.. (2023). Optimised protocols for RNA extraction from a broad taxonomic range of algae. Journal of Applied Phycology. 35(4). 1743–1753. 5 indexed citations
7.
Parrot, Delphine, Corinna Breusing, Heiko Stuckas, et al.. (2018). Combined genotyping, microbial diversity and metabolite profiling studies on farmed Mytilus spp. from Kiel Fjord. Scientific Reports. 8(1). 7983–7983. 27 indexed citations
8.
Parrot, Delphine, et al.. (2018). Molecular Networking-Based Metabolome and Bioactivity Analyses of Marine-Adapted Fungi Co-cultivated With Phytopathogens. Frontiers in Microbiology. 9. 2072–2072. 54 indexed citations
10.
Labes, Antje, et al.. (2016). Phylogenetic Relationship and Secondary Metabolite Production of Marine Fungi Producing the Cyclodepsipeptides Scopularide A and B. Marine Biotechnology. 18(4). 466–474. 4 indexed citations
11.
Beck, Hans Christian, et al.. (2015). Proteomic Analysis of Anti-Cancerous Scopularide Production by a Marine Microascus brevicaulis Strain and Its UV Mutant. PLoS ONE. 10(10). e0140047–e0140047. 13 indexed citations
12.
Yilmaz, Pelin, Michael Weiß, Lothar Reich, et al.. (2015). Identification of Habitat-Specific Biomes of Aquatic Fungal Communities Using a Comprehensive Nearly Full-Length 18S rRNA Dataset Enriched with Contextual Data. PLoS ONE. 10(7). e0134377–e0134377. 58 indexed citations
13.
Ellinger, Bernhard, Anjali Prashar, Johannes Landskron, et al.. (2014). A Phenotypic Screening Approach to Identify Anticancer Compounds Derived from Marine Fungi. Assay and Drug Development Technologies. 12(3). 162–175. 6 indexed citations
14.
Tamminen, Anu, et al.. (2014). Production of scopularide A in submerged culture with Scopulariopsis brevicaulis. Microbial Cell Factories. 13(1). 89–89. 11 indexed citations
15.
Wahl, Martin, Franz Goecke, Antje Labes, Sergey Dobretsov, & Florian Weinberger. (2012). The Second Skin: Ecological Role of Epibiotic Biofilms on Marine Organisms. Frontiers in Microbiology. 3. 292–292. 337 indexed citations breakdown →
16.
Goecke, Franz, et al.. (2012). A Novel Phytomyxean Parasite Associated with Galls on the Bull-Kelp Durvillaea antarctica (Chamisso) Hariot. PLoS ONE. 7(9). e45358–e45358. 19 indexed citations
17.
Staufenberger, Tim, Johannes F. Imhoff, & Antje Labes. (2011). First crenarchaeal chitinase found in Sulfolobus tokodaii. Microbiological Research. 167(5). 262–269. 22 indexed citations
18.
Imhoff, Johannes F., Antje Labes, & Jutta Wiese. (2011). Bio-mining the microbial treasures of the ocean: New natural products. Biotechnology Advances. 29(5). 468–482. 218 indexed citations
19.
Turner, Pernilla, Antje Labes, Ólafur H. Friðjónsson, et al.. (2005). Two novel cyclodextrin-degrading enzymes isolated from thermophilic bacteria have similar domain structures but differ in oligomeric state and activity profile. Journal of Bioscience and Bioengineering. 100(4). 380–390. 28 indexed citations
20.
Labes, Antje & Peter Sch�nheit. (2003). ADP-dependent glucokinase from the hyperthermophilic sulfate-reducing archaeon Archaeoglobus fulgidus strain 7324. Archives of Microbiology. 180(1). 69–75. 28 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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