Bernhard Erdlenbruch
- Molecular Biology
- Genetics top 5%
- Oncology
- Pulmonary and Respiratory Medicine
- Pediatrics, Perinatology and Child Health top 10%
- Co-authors
- M. LakomekWilfried KuglerVerena JendrossekArnulf PekrunHansjörg EiblOlaf WittDirk ReinhardtWolfgang Kern
- Topics
- Glioma Diagnosis and Treatment (7 papers)Drug Transport and Resistance Mechanisms (4 papers)PI3K/AKT/mTOR signaling in cancer (3 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Bernhard Erdlenbruch
31 papers receiving 949 citations
Peers
Comparison fields: 5 of 97
- Molecular Biology 448
- Genetics 210
- Oncology 175
- Pulmonary and Respiratory Medicine 126
- Pediatrics, Perinatology and Child Health 104
Countries citing papers authored by Bernhard Erdlenbruch
This map shows the geographic impact of Bernhard Erdlenbruch'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 Bernhard Erdlenbruch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernhard Erdlenbruch more than expected).
Fields of papers citing papers by Bernhard Erdlenbruch
This network shows the impact of papers produced by Bernhard Erdlenbruch. 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 Bernhard Erdlenbruch. The network helps show where Bernhard Erdlenbruch may publish in the future.
Co-authorship network of co-authors of Bernhard Erdlenbruch
This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Erdlenbruch. A scholar is included among the top collaborators of Bernhard Erdlenbruch 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 Bernhard Erdlenbruch. Bernhard Erdlenbruch 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 | 3 | |
| 3 | 92 | |
| 4 | 34 | |
| 5 | 20 | |
| 6 | 15 | |
| 7 | 16 | |
| 8 | 51 | |
| 9 | 81 | |
| 10 | 64 | |
| 11 | 14 | |
| 12 | 16 | |
| 13 | 26 | |
| 14 | 28 | |
| 15 | 61 | |
| 16 | 21 | |
| 17 | 4 | |
| 18 | 35 | |
| 19 | 57 | |
| 20 | 34 |
About Bernhard Erdlenbruch
Bernhard Erdlenbruch is a scholar working on Genetics, Neurology and Internal Medicine, having authored 32 papers that have together received 965 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (7 papers), Drug Transport and Resistance Mechanisms (4 papers) and PI3K/AKT/mTOR signaling in cancer (3 papers). The work is most often cited by research in Genetics (210 citations), Neurology (84 citations) and Pharmaceutical Science (51 citations). Bernhard Erdlenbruch has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include M. Lakomek, Wilfried Kugler, Verena Jendrossek, Arnulf Pekrun, Hansjörg Eibl, Olaf Witt, Dirk Reinhardt, Wolfgang Kern, Gert Fricker and Holger Schiffmann. Their work appears in journals such as SHILAP Revista de lepidopterología, Blood and Cancer.
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.