Ulrike Gamerdinger
- Co-authors
- Thomas DreyerU. StahlJoachim WoenckhausEva PeneloIrina FenicKlaus StegerHartmut EngelsM. Hansmann
- Topics
- Genomic variations and chromosomal abnormalities (7 papers)Chromosomal and Genetic Variations (7 papers)Prenatal Screening and Diagnostics (3 papers)
- Cited by
- GeneticsOtorhinolaryngology
In The Last Decade
Ulrike Gamerdinger
19 papers receiving 389 citations
Peers
Comparison fields: 5 of 64
- Molecular Biology 190
- Genetics 105
- Oncology 94
- Pulmonary and Respiratory Medicine 74
- Plant Science 60
Countries citing papers authored by Ulrike Gamerdinger
This map shows the geographic impact of Ulrike Gamerdinger'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 Ulrike Gamerdinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ulrike Gamerdinger more than expected).
Fields of papers citing papers by Ulrike Gamerdinger
This network shows the impact of papers produced by Ulrike Gamerdinger. 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 Ulrike Gamerdinger. The network helps show where Ulrike Gamerdinger may publish in the future.
Co-authorship network of co-authors of Ulrike Gamerdinger
This figure shows the co-authorship network connecting the top 25 collaborators of Ulrike Gamerdinger. A scholar is included among the top collaborators of Ulrike Gamerdinger 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 Ulrike Gamerdinger. Ulrike Gamerdinger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 5 | |
| 3 | 10 | |
| 4 | 7 | |
| 5 | 53 | |
| 6 | 10 | |
| 7 | 0 | |
| 8 | 3 | |
| 9 | 10 | |
| 10 | 1 | |
| 11 | 31 | |
| 12 | 7 | |
| 13 | 4 | |
| 14 | 15 | |
| 15 | 2 | |
| 16 | 30 | |
| 17 | 125 | |
| 18 | 21 | |
| 19 | 49 | |
| 20 | 10 |
About Ulrike Gamerdinger
Ulrike Gamerdinger is a scholar working on Genetics, Otorhinolaryngology and Oncology, having authored 20 papers that have together received 398 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (55 citations), Genetics (105 citations) and Otorhinolaryngology (16 citations). Ulrike Gamerdinger has collaborated with scholars based in Germany, Iran and Poland. Frequent co-authors include Thomas Dreyer, U. Stahl, Joachim Woenckhaus, Eva Penelo, Irina Fenic, Klaus Steger, Hartmut Engels, M. Hansmann, Gabriele Lasczkowski and Stefan Gattenlöhner. Their work appears in journals such as Cancer Research, The Journal of Pathology and Oral Oncology.
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.