Gabriele Senger
- Molecular Biology top 10%
- Genetics top 2%
- Plant Science top 5%
- Immunology top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Co-authors
- Uwe ClaussenBernhard HorsthemkeDenise SheerRichard A. KroczekHans Werner MagesJohn TrowsdaleHermann‐Josef LüdeckeUlf Korthäuer
- Topics
- Genomic variations and chromosomal abnormalities (26 papers)Chromosomal and Genetic Variations (17 papers)Prenatal Screening and Diagnostics (8 papers)
- Cited by
- GeneticsImmunologyMolecular Biology
- Partner nations
- GermanyUnited KingdomFrance
In The Last Decade
Gabriele Senger
54 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 102
- Molecular Biology 1.3k
- Genetics 1.1k
- Plant Science 596
- Immunology 526
- Pediatrics, Perinatology and Child Health 291
Countries citing papers authored by Gabriele Senger
This map shows the geographic impact of Gabriele Senger'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 Gabriele Senger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gabriele Senger more than expected).
Fields of papers citing papers by Gabriele Senger
This network shows the impact of papers produced by Gabriele Senger. 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 Gabriele Senger. The network helps show where Gabriele Senger may publish in the future.
Co-authorship network of co-authors of Gabriele Senger
This figure shows the co-authorship network connecting the top 25 collaborators of Gabriele Senger. A scholar is included among the top collaborators of Gabriele Senger 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 Gabriele Senger. Gabriele Senger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 23 | |
| 2 | 35 | |
| 3 | 3 | |
| 4 | 17 | |
| 5 | 16 | |
| 6 | 169 | |
| 7 | 30 | |
| 8 | 21 | |
| 9 | 48 | |
| 10 | 14 | |
| 11 | 41 | |
| 12 | 6 | |
| 13 | 13 | |
| 14 | 43 | |
| 15 | 232 | |
| 16 | 7 | |
| 17 | 17 | |
| 18 | 9 | |
| 19 | 81 | |
| 20 | 261 |
About Gabriele Senger
Gabriele Senger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 56 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (8 papers). The work is most often cited by research in Genetics (1.1k citations), Immunology (526 citations) and Molecular Biology (1.3k citations). Gabriele Senger has collaborated with scholars based in Germany, United Kingdom and France. Frequent co-authors include Uwe Claussen, Bernhard Horsthemke, Denise Sheer, Richard A. Kroczek, Hans Werner Mages, John Trowsdale, Hermann‐Josef Lüdecke, Ulf Korthäuer, U. Claussen and Daniel Graf. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Current Biology.
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.