Fernande Freyermuth
Impact in
Papers in ⓘ
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- RNA Research and Splicing 5
- Muscle Physiology and Disorders 2
- Congenital heart defects research 1
- RNA and protein synthesis mechanisms 1
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- Genetic Neurodegenerative Diseases 3
- Co-authors
- Nicolas Charlet‐Berguerand (4 shared papers)Clotilde Lagier‐Tourenne (3 shared papers)Ricardos Tabet (2 shared papers)Nianwei Lin (1 shared paper)Kevin Drenner (1 shared paper)Melinda S. Beccari (1 shared paper)Moira A. McMahon (1 shared paper)C. Frank Bennett (1 shared paper)
- Journals
- Nature Communications (2 papers)Cell Reports (1 paper)Nature Structural & Molecular Biology (1 paper)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (1 paper)Nature Neuroscience (1 paper)
- Partner nations
- United StatesFranceJapan
In The Last Decade
Fernande Freyermuth
7 papers receiving 946 citations
Hit Papers
Peers
Comparison fields: 5 of 53
- Genetics 257
- Neurology 335
- Cellular and Molecular Neuroscience 308
- Molecular Biology 747
- Genetics 157
Countries citing papers authored by Fernande Freyermuth
This map shows the geographic impact of Fernande Freyermuth'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 Fernande Freyermuth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernande Freyermuth more than expected).
Fields of papers citing papers by Fernande Freyermuth
This network shows the impact of papers produced by Fernande Freyermuth. 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 Fernande Freyermuth. The network helps show where Fernande Freyermuth may publish in the future.
Co-authors
The 25 scholars most cited alongside Fernande Freyermuth, 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 | Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration Hit paper breakdown → | 2019 | 339 |
| 2 | 2011 | 219 | |
| 3 | 2013 | 189 | |
| 4 | 2018 | 100 | |
| 5 | 2018 | 57 | |
| 6 | 2014 | 26 | |
| 7 | 2017 | 23 |
About Fernande Freyermuth
Fernande Freyermuth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Cardiology and Cardiovascular Medicine and Genetics, having authored 7 papers that have together received 953 indexed citations. Recurring topics across this work include RNA Research and Splicing (5 papers), Genetic Neurodegenerative Diseases (3 papers), Cardiomyopathy and Myosin Studies (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Muscle Physiology and Disorders (2 papers), Congenital heart defects research (1 paper), RNA and protein synthesis mechanisms (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (257 citations), Neurology (335 citations), Cellular and Molecular Neuroscience (308 citations), Molecular Biology (747 citations) and Genetics (157 citations). Fernande Freyermuth has collaborated with scholars based in United States, France and Japan. Frequent co-authors include Nicolas Charlet‐Berguerand, Clotilde Lagier‐Tourenne, Ricardos Tabet, Nianwei Lin, Kevin Drenner, Melinda S. Beccari, Moira A. McMahon, C. Frank Bennett, Sandrine Da Cruz and Takuya Ohkubo. Their work appears in journals such as Nature Communications, Cell Reports, Nature Structural & Molecular Biology, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Nature Neuroscience.
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.