Susanne Michel
- Co-authors
- Uwe ClaussenFerdinand von EggelingBettina SchimmelIvan LončarevićKerstin JunkerUlrich HohenleutnerRoland BaumgartnerSvetlana Hamm
- Topics
- Prenatal Screening and Diagnostics (4 papers)Genomic variations and chromosomal abnormalities (4 papers)Genetic Syndromes and Imprinting (2 papers)
In The Last Decade
Susanne Michel
18 papers receiving 392 citations
Peers
Comparison fields: 5 of 56
- Molecular Biology 208
- Genetics 125
- Immunology 78
- Pediatrics, Perinatology and Child Health 72
- Oncology 72
Countries citing papers authored by Susanne Michel
This map shows the geographic impact of Susanne Michel'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 Susanne Michel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susanne Michel more than expected).
Fields of papers citing papers by Susanne Michel
This network shows the impact of papers produced by Susanne Michel. 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 Susanne Michel. The network helps show where Susanne Michel may publish in the future.
Co-authorship network of co-authors of Susanne Michel
This figure shows the co-authorship network connecting the top 25 collaborators of Susanne Michel. A scholar is included among the top collaborators of Susanne Michel 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 Susanne Michel. Susanne Michel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 7 | |
| 2 | 55 | |
| 3 | 37 | |
| 4 | 14 | |
| 5 | 11 | |
| 6 | 66 | |
| 7 | 2 | |
| 8 | 6 | |
| 9 | 8 | |
| 10 | 24 | |
| 11 | 62 | |
| 12 | 45 | |
| 13 | 3 | |
| 14 | 3 | |
| 15 | 16 | |
| 16 | 3 | |
| 17 | 27 | |
| 18 | 16 |
About Susanne Michel
Susanne Michel is a scholar working on Periodontics, Genetics and Pediatrics, Perinatology and Child Health, having authored 18 papers that have together received 405 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (125 citations), Immunology (78 citations) and Pediatrics, Perinatology and Child Health (72 citations). Susanne Michel has collaborated with scholars based in Germany, Russia and Austria. Frequent co-authors include Uwe Claussen, Ferdinand von Eggeling, Bettina Schimmel, Ivan Lončarević, Kerstin Junker, Ulrich Hohenleutner, Roland Baumgartner, Svetlana Hamm, Michael Landthaler and Stefan Böehringer. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Histochemistry & Cytochemistry.
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.