Steffen Uebe
- Molecular Biology top 10%
- Genetics top 5%
- Immunology
- Cancer Research
- Cell Biology top 10%
- Co-authors
- Arif B. EkiciAndré ReisHeinrich StichtJuliane HoyerGeorgia VasileiouChristiane ZweierRami Abou JamraCornelia Kraus
- Topics
- Genetics and Neurodevelopmental Disorders (10 papers)Genomics and Rare Diseases (8 papers)Genomic variations and chromosomal abnormalities (6 papers)
- Partner nations
- GermanySwitzerlandNetherlands
In The Last Decade
Steffen Uebe
57 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 94
- Molecular Biology 819
- Genetics 507
- Immunology 138
- Cancer Research 137
- Cell Biology 134
Countries citing papers authored by Steffen Uebe
This map shows the geographic impact of Steffen Uebe'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 Steffen Uebe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steffen Uebe more than expected).
Fields of papers citing papers by Steffen Uebe
This network shows the impact of papers produced by Steffen Uebe. 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 Steffen Uebe. The network helps show where Steffen Uebe may publish in the future.
Co-authorship network of co-authors of Steffen Uebe
This figure shows the co-authorship network connecting the top 25 collaborators of Steffen Uebe. A scholar is included among the top collaborators of Steffen Uebe 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 Steffen Uebe. Steffen Uebe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 0 | |
| 3 | 10 | |
| 4 | 42 | |
| 5 | 56 | |
| 6 | 16 | |
| 7 | 13 | |
| 8 | 27 | |
| 9 | 5 | |
| 10 | 29 | |
| 11 | 40 | |
| 12 | Expression of CACNA1A in Patients with Pseudoexfoliation Syndrome | 1 |
| 13 | 28 | |
| 14 | 9 | |
| 15 | 64 | |
| 16 | 26 | |
| 17 | 9 | |
| 18 | 112 | |
| 19 | 63 | |
| 20 | 45 |
About Steffen Uebe
Steffen Uebe is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 58 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Genetics (507 citations), Molecular Biology (819 citations) and Clinical Biochemistry (69 citations). Steffen Uebe has collaborated with scholars based in Germany, Switzerland and Netherlands. Frequent co-authors include Arif B. Ekici, André Reis, Heinrich Sticht, Juliane Hoyer, Georgia Vasileiou, Christiane Zweier, Rami Abou Jamra, Cornelia Kraus, Christian T. Thiel and Mandy Krumbiegel. Their work appears in journals such as Journal of Clinical Investigation, The Journal of Experimental Medicine and PLoS ONE.
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.