E. Schleiermacher
- Co-authors
- Almut NebelF. VogelI. Anton‐LamprechtUli SchmidtV. LenhardR MertelsmannT. M. SchroederTrevor Smith
- Topics
- Genomic variations and chromosomal abnormalities (6 papers)Chromosomal and Genetic Variations (6 papers)Carcinogens and Genotoxicity Assessment (5 papers)
In The Last Decade
E. Schleiermacher
38 papers receiving 462 citations
Peers
Comparison fields: 5 of 68
- Molecular Biology 198
- Genetics 161
- Plant Science 134
- Cancer Research 108
- Pediatrics, Perinatology and Child Health 84
Countries citing papers authored by E. Schleiermacher
This map shows the geographic impact of E. Schleiermacher'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 E. Schleiermacher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Schleiermacher more than expected).
Fields of papers citing papers by E. Schleiermacher
This network shows the impact of papers produced by E. Schleiermacher. 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 E. Schleiermacher. The network helps show where E. Schleiermacher may publish in the future.
Co-authorship network of co-authors of E. Schleiermacher
This figure shows the co-authorship network connecting the top 25 collaborators of E. Schleiermacher. A scholar is included among the top collaborators of E. Schleiermacher 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 E. Schleiermacher. E. Schleiermacher is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 16 | |
| 3 | 44 | |
| 4 | 15 | |
| 5 | 23 | |
| 6 | 19 | |
| 7 | 7 | |
| 8 | 5 | |
| 9 | 3 | |
| 10 | 21 | |
| 11 | 1 | |
| 12 | 17 | |
| 13 | 28 | |
| 14 | 34 | |
| 15 | 28 | |
| 16 | 8 | |
| 17 | 15 | |
| 18 | 31 | |
| 19 | 12 | |
| 20 | 38 |
About E. Schleiermacher
E. Schleiermacher is a scholar working on Pharmaceutical Science, Hematology and Reproductive Medicine, having authored 38 papers that have together received 514 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (6 papers) and Carcinogens and Genotoxicity Assessment (5 papers). The work is most often cited by research in Cancer Research (108 citations), Genetics (161 citations) and Reproductive Medicine (43 citations). E. Schleiermacher has collaborated with scholars based in Germany, Thailand and Poland. Frequent co-authors include Almut Nebel, F. Vogel, I. Anton‐Lamprecht, Uli Schmidt, V. Lenhard, R Mertelsmann, T. M. Schroeder, Trevor Smith, Jutta Müller‐Navia and Harry Scherthan. Their work appears in journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and Human Reproduction.
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.