Florian Harmuth
Impact in
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- Neurological diseases and metabolism
- Neurological disorders and treatments
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
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- Genetic Neurodegenerative Diseases 4
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- Ion channel regulation and function 1
- Co-authors
- Matthis Synofzik (7 shared papers)Peter Bauer (5 shared papers)Lüdger Schöls (6 shared papers)Dagmar Timmann (4 shared papers)Rebecca Schüle (4 shared papers)Martin A. Giese (3 shared papers)Winfried Ilg (3 shared papers)Holger Hengel (2 shared papers)
- Journals
- Movement Disorders (3 papers)Neurology Genetics (2 papers)Journal of Neurology (2 papers)Breast Cancer Research and Treatment (1 paper)European Journal of Neurology (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Florian Harmuth
11 papers receiving 245 citations
Peers
Comparison fields: 5 of 49
- Neurology 49
- Cellular and Molecular Neuroscience 110
- Neurology 37
- Clinical Biochemistry 16
- Genetics 46
Countries citing papers authored by Florian Harmuth
This map shows the geographic impact of Florian Harmuth'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 Florian Harmuth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florian Harmuth more than expected).
Fields of papers citing papers by Florian Harmuth
This network shows the impact of papers produced by Florian Harmuth. 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 Florian Harmuth. The network helps show where Florian Harmuth may publish in the future.
Co-authors
The 25 scholars most cited alongside Florian Harmuth, 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 | 2016 | 44 | |
| 2 | 2015 | 37 | |
| 3 | 2017 | 36 | |
| 4 | 2018 | 31 | |
| 5 | 2014 | 29 | |
| 6 | 2022 | 26 | |
| 7 | 2015 | 23 | |
| 8 | 2021 | 7 | |
| 9 | 2023 | 6 | |
| 10 | 2019 | 6 | |
| 11 | 2025 | 2 |
About Florian Harmuth
Florian Harmuth is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Neurology and Physiology, having authored 11 papers that have together received 247 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), Lysosomal Storage Disorders Research (2 papers), Neurological diseases and metabolism (2 papers), Genomics and Rare Diseases (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Cancer Genomics and Diagnostics (1 paper), Ion channel regulation and function (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Neurology (49 citations), Cellular and Molecular Neuroscience (110 citations), Neurology (37 citations), Clinical Biochemistry (16 citations) and Genetics (46 citations). Florian Harmuth has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Matthis Synofzik, Peter Bauer, Lüdger Schöls, Dagmar Timmann, Rebecca Schüle, Martin A. Giese, Winfried Ilg, Holger Hengel, Christina Gerth‐Kahlert and Alexander A. Tarnutzer. Their work appears in journals such as Movement Disorders, Neurology Genetics, Journal of Neurology, Breast Cancer Research and Treatment and European Journal 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.