Reinhard Stöger
- Molecular Biology top 5%
- Genetics top 1%
- Pediatrics, Perinatology and Child Health top 1%
- Cancer Research top 10%
- Physiology
- Co-authors
- Denise P. BarlowBernhard G. HerrmannKoji SaitoNorbert SchweiferCharles D. LairdR. Scott HansenD. WongBrian J. Reid
- Topics
- Epigenetics and DNA Methylation (24 papers)Genetic Syndromes and Imprinting (9 papers)Genomics and Chromatin Dynamics (9 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Reinhard Stöger
46 papers receiving 3.0k citations
Hit Papers
Peers
Comparison fields: 5 of 121
- Molecular Biology 2.3k
- Genetics 1.6k
- Pediatrics, Perinatology and Child Health 806
- Cancer Research 260
- Physiology 170
Countries citing papers authored by Reinhard Stöger
This map shows the geographic impact of Reinhard Stöger'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 Reinhard Stöger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reinhard Stöger more than expected).
Fields of papers citing papers by Reinhard Stöger
This network shows the impact of papers produced by Reinhard Stöger. 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 Reinhard Stöger. The network helps show where Reinhard Stöger may publish in the future.
Co-authorship network of co-authors of Reinhard Stöger
This figure shows the co-authorship network connecting the top 25 collaborators of Reinhard Stöger. A scholar is included among the top collaborators of Reinhard Stöger 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 Reinhard Stöger. Reinhard Stöger 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 | 39 | |
| 3 | 12 | |
| 4 | 13 | |
| 5 | 49 | |
| 6 | 27 | |
| 7 | 46 | |
| 8 | 116 | |
| 9 | 24 | |
| 10 | 19 | |
| 11 | 47 | |
| 12 | 113 | |
| 13 | 32 | |
| 14 | 56 | |
| 15 | 61 | |
| 16 | Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia | 7 |
| 17 | 40 | |
| 18 | 5 | |
| 19 | 101 | |
| 20 | 103 |
About Reinhard Stöger
Reinhard Stöger is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 46 papers that have together received 3.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (24 papers), Genetic Syndromes and Imprinting (9 papers) and Genomics and Chromatin Dynamics (9 papers). The work is most often cited by research in Genetics (1.6k citations), Pediatrics, Perinatology and Child Health (806 citations) and Molecular Biology (2.3k citations). Reinhard Stöger has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Denise P. Barlow, Bernhard G. Herrmann, Koji Saito, Norbert Schweifer, Charles D. Laird, R. Scott Hansen, D. Wong, Brian J. Reid, Mary J. Emond and Eugene F. Schuster. Their work appears in journals such as Nature, Cell and Proceedings of the National Academy of Sciences.
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.