Gudrun Schottmann
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
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- Neurogenetic and Muscular Disorders Research
Papers in
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- RNA modifications and cancer 2
- Mitochondrial Function and Pathology 2
- Ubiquitin and proteasome pathways 2
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- Hereditary Neurological Disorders 3
- Genetic Neurodegenerative Diseases 2
- Co-authors
- Markus Schuelke (6 shared papers)Esther Gill (4 shared papers)Denise Horn (1 shared paper)Peter Meinecke (1 shared paper)Susanne Morales-Gonzalez (3 shared papers)Ulrike Schara (2 shared papers)Klaus Rüther (1 shared paper)G. Stoltenburg (1 shared paper)
- Journals
- Movement Disorders (2 papers)The American Journal of Human Genetics (1 paper)Frontiers in Neuroscience (1 paper)Neurology (1 paper)Mitochondrion (1 paper)
- Partner nations
- GermanyNetherlandsUnited Kingdom
In The Last Decade
Gudrun Schottmann
9 papers receiving 194 citations
Peers
Comparison fields: 5 of 40
- Clinical Biochemistry 41
- Genetics 55
- Neurology 36
- Cellular and Molecular Neuroscience 39
- Molecular Biology 123
Countries citing papers authored by Gudrun Schottmann
This map shows the geographic impact of Gudrun Schottmann'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 Gudrun Schottmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gudrun Schottmann more than expected).
Fields of papers citing papers by Gudrun Schottmann
This network shows the impact of papers produced by Gudrun Schottmann. 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 Gudrun Schottmann. The network helps show where Gudrun Schottmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Gudrun Schottmann, 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 | 2019 | 31 | |
| 2 | 2015 | 27 | |
| 3 | 2009 | 26 | |
| 4 | 2013 | 24 | |
| 5 | 2016 | 23 | |
| 6 | 2010 | 22 | |
| 7 | 2015 | 20 | |
| 8 | 2017 | 15 | |
| 9 | 2019 | 11 | |
| 10 | 2024 | 0 |
About Gudrun Schottmann
Gudrun Schottmann is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Genetics and Cell Biology, having authored 10 papers that have together received 199 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (3 papers), Hereditary Neurological Disorders (3 papers), RNA modifications and cancer (2 papers), Genetic Neurodegenerative Diseases (2 papers), Mitochondrial Function and Pathology (2 papers), Ubiquitin and proteasome pathways (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Hippo pathway signaling and YAP/TAZ (1 paper). The work is most often cited by research in Clinical Biochemistry (41 citations), Genetics (55 citations), Neurology (36 citations), Cellular and Molecular Neuroscience (39 citations) and Molecular Biology (123 citations). Gudrun Schottmann has collaborated with scholars based in Germany, Netherlands and United Kingdom. Frequent co-authors include Markus Schuelke, Esther Gill, Denise Horn, Peter Meinecke, Susanne Morales-Gonzalez, Ulrike Schara, Klaus Rüther, G. Stoltenburg, Werner Stenzel and Katja von Au. Their work appears in journals such as Movement Disorders, The American Journal of Human Genetics, Frontiers in Neuroscience, Neurology and Mitochondrion.
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.