Olov Sterner
About
In The Last Decade
Olov Sterner
420 papers receiving 8.9k citations
Hit Papers
Peers
Comparison fields: 5 of 141
- Molecular Biology 3.1k
- Pharmacology 2.8k
- Plant Science 2.5k
- Organic Chemistry 2.2k
- Sensory Systems 804
Countries citing papers authored by Olov Sterner
This map shows the geographic impact of Olov Sterner'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 Olov Sterner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Olov Sterner more than expected).
Fields of papers citing papers by Olov Sterner
This network shows the impact of papers produced by Olov Sterner. 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 Olov Sterner. The network helps show where Olov Sterner may publish in the future.
Co-authorship network of co-authors of Olov Sterner
This figure shows the co-authorship network connecting the top 25 collaborators of Olov Sterner. A scholar is included among the top collaborators of Olov Sterner 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 Olov Sterner. Olov Sterner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 8 | |
| 2 | 7 | |
| 3 | 1 | |
| 4 | 3 | |
| 5 | 3 | |
| 6 | ENT- KAURANE DITERPENOIDS FROM BACCHARIS LEPTOPHYLLA | 1 |
| 7 | SPECTROSCOPIC STUDIES OF LICHEN DEPSIDES AND DEPSIDONES | 3 |
| 8 | Activation of the free fatty acid receptor GPR40 by (+)-curcuphenol and related synthetic compounds | 2 |
| 9 | Prenylated protocatechuic acid derivatives with anti-oxidant activity from Piper heterophyllum | 0 |
| 10 | PHENOLIC COMPOUNDS FROM BACCHARIS PAPILLOSA SUBSP. PAPILLOSA | 4 |
| 11 | A 5-methylcoumarin glucoside and a coumestan derivative from Mutisia orbignyana. | 3 |
| 12 | 7 | |
| 13 | MORE INVESTIGATIONS IN POTENT ACTIVITY AND RELATIONSHIP STRUCTURE OF THE LICHEN ANTIBIOTIC (+)-USNIC ACID AND ITS DERIVATE DIBENZOYLUSNIC ACID | 12 |
| 14 | PHYTOCHEMICAL RESEARCH OF PLANTS USED BY THE ASSOCIATION OF TRADITIONAL MEDICINE AT APILLAPAMPA | 3 |
| 15 | OLEANANE-TYPE TRITERPENES AND DERIVATIVES FROM SEED COAT OF BOLIVIAN CHENOPODIUM QUINOA GENOTYPE “SALAR” | 5 |
| 16 | Aislamiento de flavonoides y estudio de la actividad toxica y antibacteriana de extractos de Baccaria latifolia. | 1 |
| 17 | Picranitine, a new indole alkaloid from Picralima nitida (Apocynaceae) | 7 |
| 18 | Metabolites with Nematicidal and Antimicrobial Activities from the Ascomycete Lachnum papyraceum(Karst.) Karst. III. Production of Novel Isocoumarin Derivatives, Isolation, and Biological Activities.:III. Production of Novel Isocoumarin Derivatives, Isolation, and Biological Activities | 1 |
| 19 | 28 | |
| 20 | Mutagens in larger fungi 1. 48 species screened for mutagenic activity in the salmonella microsome assay | 29 |
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.