Kathrin Müller
- Neurology top 2%
- Molecular Biology
- Genetics top 2%
- Physiology
- Neurology top 5%
- Co-authors
- Jochen H. WeishauptAlbert C. LudolphAxel FreischmidtPeter M. AndersenMarkus OttoPatrick WeydtAlexander E. VolkPeter Wiegand
- Topics
- Amyotrophic Lateral Sclerosis Research (17 papers)Neurogenetic and Muscular Disorders Research (15 papers)Parkinson's Disease Mechanisms and Treatments (6 papers)
- Journals
- PLoS ONEBrainAnnals of Neurology
- Partner nations
- GermanySwedenUnited States
In The Last Decade
Kathrin Müller
39 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 93
- Neurology 593
- Molecular Biology 482
- Genetics 356
- Physiology 168
- Neurology 159
Countries citing papers authored by Kathrin Müller
This map shows the geographic impact of Kathrin Müller'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 Kathrin Müller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kathrin Müller more than expected).
Fields of papers citing papers by Kathrin Müller
This network shows the impact of papers produced by Kathrin Müller. 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 Kathrin Müller. The network helps show where Kathrin Müller may publish in the future.
Co-authorship network of co-authors of Kathrin Müller
This figure shows the co-authorship network connecting the top 25 collaborators of Kathrin Müller. A scholar is included among the top collaborators of Kathrin Müller 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 Kathrin Müller. Kathrin Müller is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 7 | |
| 2 | 7 | |
| 3 | 31 | |
| 4 | 3 | |
| 5 | 3 | |
| 6 | 4 | |
| 7 | 5 | |
| 8 | 15 | |
| 9 | 9 | |
| 10 | 53 | |
| 11 | 7 | |
| 12 | 15 | |
| 13 | 20 | |
| 14 | 42 | |
| 15 | 50 | |
| 16 | 48 | |
| 17 | 10 | |
| 18 | 27 | |
| 19 | 9 | |
| 20 | 24 |
About Kathrin Müller
Kathrin Müller is a scholar working on Genetics, Neurology and Aging, having authored 39 papers that have together received 1.2k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (17 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). The work is most often cited by research in Neurology (593 citations), Genetics (356 citations) and Neurology (159 citations). Kathrin Müller has collaborated with scholars based in Germany, Sweden and United States. Frequent co-authors include Jochen H. Weishaupt, Albert C. Ludolph, Axel Freischmidt, Peter M. Andersen, Markus Otto, Patrick Weydt, Alexander E. Volk, Peter Wiegand, Karin M. Danzer and Michael N. Smolka. Their work appears in journals such as PLoS ONE, Brain and Annals of Neurology.
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.