Henrik Kaessmann
- Molecular Biology top 1%
- Genetics top 0.2%
- Plant Science top 1%
- Cancer Research top 0.5%
- Cellular and Molecular Neuroscience top 2%
- Co-authors
- Svante PääboNicolas VinckenboschAnamaria NecşuleaMax IngmanUlf GyllenstenAngélica LiechtiDavid BrawandMagali Soumillon
- Topics
- Chromosomal and Genetic Variations (23 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers)Genomics and Chromatin Dynamics (16 papers)
- Partner nations
- SwitzerlandGermanyUnited States
In The Last Decade
Henrik Kaessmann
64 papers receiving 9.3k citations
Hit Papers
Peers
Comparison fields: 5 of 162
- Molecular Biology 5.9k
- Genetics 3.8k
- Plant Science 2.0k
- Cancer Research 1.7k
- Cellular and Molecular Neuroscience 717
Countries citing papers authored by Henrik Kaessmann
This map shows the geographic impact of Henrik Kaessmann'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 Henrik Kaessmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Henrik Kaessmann more than expected).
Fields of papers citing papers by Henrik Kaessmann
This network shows the impact of papers produced by Henrik Kaessmann. 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 Henrik Kaessmann. The network helps show where Henrik Kaessmann may publish in the future.
Co-authorship network of co-authors of Henrik Kaessmann
This figure shows the co-authorship network connecting the top 25 collaborators of Henrik Kaessmann. A scholar is included among the top collaborators of Henrik Kaessmann 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 Henrik Kaessmann. Henrik Kaessmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 16 | |
| 3 | 39 | |
| 4 | 95 | |
| 5 | 23 | |
| 6 | 43 | |
| 7 | 10 | |
| 8 | 33 | |
| 9 | 109 | |
| 10 | 65 | |
| 11 | 85 | |
| 12 | 161 | |
| 13 | Cellular Source and Mechanisms of High Transcriptome Complexity in the Mammalian Testisbreakdown → | 419 |
| 14 | 223 | |
| 15 | 156 | |
| 16 | 125 | |
| 17 | Origins, evolution, and phenotypic impact of new genesbreakdown → | 570 |
| 18 | 286 | |
| 19 | 40 | |
| 20 | 76 |
About Henrik Kaessmann
Henrik Kaessmann is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 67 papers that have together received 9.4k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (23 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Genomics and Chromatin Dynamics (16 papers). The work is most often cited by research in Genetics (3.8k citations), Cancer Research (1.7k citations) and Molecular Biology (5.9k citations). Henrik Kaessmann has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include Svante Pääbo, Nicolas Vinckenbosch, Anamaria Necşulea, Max Ingman, Ulf Gyllensten, Angélica Liechti, David Brawand, Magali Soumillon, Frank Grützner and Maria Warnefors. Their work appears in journals such as Nature, Science and Cell.
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.