Stefan M. Pfister
- Genetics top 0.01%
- Molecular Biology top 0.2%
- Cancer Research top 0.1%
- Neurology top 0.1%
- Pulmonary and Respiratory Medicine top 0.5%
- Co-authors
- Andreas von DeimlingGuido ReifenbergerAndrey KorshunovDavid W. EllisonCynthia HawkinsPieter WesselingDavid N. LouisArie Perry
- Topics
- Glioma Diagnosis and Treatment (190 papers)Chromatin Remodeling and Cancer (70 papers)Epigenetics and DNA Methylation (65 papers)
- Cited by
- GeneticsCancer ResearchNeurology
- Partner nations
- GermanyUnited StatesCanada
In The Last Decade
Stefan M. Pfister
348 papers receiving 25.1k citations
Hit Papers
Peers
Comparison fields: 5 of 172
- Genetics 14.6k
- Molecular Biology 12.4k
- Cancer Research 5.6k
- Neurology 4.4k
- Pulmonary and Respiratory Medicine 3.6k
Countries citing papers authored by Stefan M. Pfister
This map shows the geographic impact of Stefan M. Pfister'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 Stefan M. Pfister with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefan M. Pfister more than expected).
Fields of papers citing papers by Stefan M. Pfister
This network shows the impact of papers produced by Stefan M. Pfister. 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 Stefan M. Pfister. The network helps show where Stefan M. Pfister may publish in the future.
Co-authorship network of co-authors of Stefan M. Pfister
This figure shows the co-authorship network connecting the top 25 collaborators of Stefan M. Pfister. A scholar is included among the top collaborators of Stefan M. Pfister 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 Stefan M. Pfister. Stefan M. Pfister 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 | 6 | |
| 4 | 9 | |
| 5 | 16 | |
| 6 | 11 | |
| 7 | 16 | |
| 8 | 10 | |
| 9 | 3 | |
| 10 | 4 | |
| 11 | 9 | |
| 12 | 29 | |
| 13 | 73 | |
| 14 | 26 | |
| 15 | 25 | |
| 16 | 160 | |
| 17 | Medulloblastoma Comprises Four Distinct Molecular Variantsbreakdown → | 886 |
| 18 | 158 | |
| 19 | 55 | |
| 20 | 198 |
About Stefan M. Pfister
Stefan M. Pfister is a scholar working on Genetics, Cancer Research and Neurology, having authored 371 papers that have together received 25.4k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (190 papers), Chromatin Remodeling and Cancer (70 papers) and Epigenetics and DNA Methylation (65 papers). The work is most often cited by research in Genetics (14.6k citations), Cancer Research (5.6k citations) and Neurology (4.4k citations). Stefan M. Pfister has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Andreas von Deimling, Guido Reifenberger, Andrey Korshunov, David W. Ellison, Cynthia Hawkins, Pieter Wesseling, David N. Louis, Arie Perry, Riccardo Soffietti and Daniel J. Brat. Their work appears in journals such as Nature, Science 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.