Reinhard Stöger
- Genetics top 1%
- Genetic Syndromes and Imprinting 9
- Genetics and Neurodevelopmental Disorders 8
- Insect and Arachnid Ecology and Behavior 4
-
- Birth, Development, and Health 6
- Molecular Biology top 5%
- Epigenetics and DNA Methylation 24
- Genomics and Chromatin Dynamics 9
- RNA modifications and cancer 3
- Cancer Research top 10%
- Aging top 10%
-
- Insect and Pesticide Research 4
- Co-authors
- Denise P. BarlowBernhard G. HerrmannKoji SaitoNorbert SchweiferCharles D. LairdR. Scott HansenD. WongBrian J. Reid
- 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
- Genetics 1.6k
- Pediatrics, Perinatology and Child Health 806
- Molecular Biology 2.3k
- Cancer Research 260
- Aging 22
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
The 25 scholars most cited alongside Reinhard Stöger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 1 | |
| 2 | 2021 | 39 | |
| 3 | 2021 | 12 | |
| 4 | 2017 | 13 | |
| 5 | 2017 | 49 | |
| 6 | 2017 | 27 | |
| 7 | 2016 | 46 | |
| 8 | 2013 | 116 | |
| 9 | 2011 | 24 | |
| 10 | 2010 | 19 | |
| 11 | 2010 | 47 | |
| 12 | 2008 | 113 | |
| 13 | 2007 | 32 | |
| 14 | 2004 | 56 | |
| 15 | 2004 | 61 | |
| 16 | Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia | 2003 | 7 |
| 17 | 2002 | 40 | |
| 18 | 1999 | 5 | |
| 19 | 1997 | 101 | |
| 20 | 1995 | 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), Genomics and Chromatin Dynamics (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Birth, Development, and Health (6 papers), Insect and Pesticide Research (4 papers), Insect and Arachnid Ecology and Behavior (4 papers) and RNA modifications and cancer (3 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.