Kyle L. Dunbar
- Molecular Biology top 10%
- Pharmacology top 1%
- Organic Chemistry top 5%
- Biotechnology top 5%
- Oncology
- Co-authors
- Douglas A. MitchellChristian HertweckAgnieszka LitomskaDaniel H. ScharfBrandon J. BurkhartGraham A. HudsonJoel O. MelbyCourtney Cox
- Topics
- Microbial Natural Products and Biosynthesis (18 papers)Biochemical and Structural Characterization (13 papers)Antimicrobial Peptides and Activities (6 papers)
- Journals
- Chemical ReviewsProceedings of the National Academy of SciencesJournal of the American Chemical Society
- Partner nations
- GermanyUnited States
In The Last Decade
Kyle L. Dunbar
27 papers receiving 1.3k citations
Hit Papers
Peers
Comparison fields: 5 of 73
- Molecular Biology 799
- Pharmacology 641
- Organic Chemistry 587
- Biotechnology 118
- Oncology 90
Countries citing papers authored by Kyle L. Dunbar
This map shows the geographic impact of Kyle L. Dunbar'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 Kyle L. Dunbar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kyle L. Dunbar more than expected).
Fields of papers citing papers by Kyle L. Dunbar
This network shows the impact of papers produced by Kyle L. Dunbar. 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 Kyle L. Dunbar. The network helps show where Kyle L. Dunbar may publish in the future.
Co-authorship network of co-authors of Kyle L. Dunbar
This figure shows the co-authorship network connecting the top 25 collaborators of Kyle L. Dunbar. A scholar is included among the top collaborators of Kyle L. Dunbar 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 Kyle L. Dunbar. Kyle L. Dunbar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 8 | |
| 3 | 3 | |
| 4 | 2 | |
| 5 | 1 | |
| 6 | 3 | |
| 7 | 17 | |
| 8 | 29 | |
| 9 | 3 | |
| 10 | 23 | |
| 11 | 11 | |
| 12 | 6 | |
| 13 | 22 | |
| 14 | 5 | |
| 15 | 28 | |
| 16 | 11 | |
| 17 | 32 | |
| 18 | 288 | |
| 19 | 65 | |
| 20 | 104 |
About Kyle L. Dunbar
Kyle L. Dunbar is a scholar working on Pharmacology, Microbiology and Biotechnology, having authored 27 papers that have together received 1.3k indexed citations. Recurring topics across this work include Microbial Natural Products and Biosynthesis (18 papers), Biochemical and Structural Characterization (13 papers) and Antimicrobial Peptides and Activities (6 papers). The work is most often cited by research in Pharmacology (641 citations), Organic Chemistry (587 citations) and Microbiology (89 citations). Kyle L. Dunbar has collaborated with scholars based in Germany and United States. Frequent co-authors include Douglas A. Mitchell, Christian Hertweck, Agnieszka Litomska, Daniel H. Scharf, Brandon J. Burkhart, Graham A. Hudson, Joel O. Melby, Courtney Cox, Evelyn M. Molloy and Jonathan R. Chekan. Their work appears in journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.
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.