Frédéric Sedel
Impact in
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Papers in
- Physiology 22
- Lysosomal Storage Disorders Research 19
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- Mitochondrial Function and Pathology 5
- Co-authors
- Marie T. Vanier (7 shared papers)Delphine Bernard (3 shared papers)Antoine Triller (4 shared papers)Mark Walterfang (4 shared papers)Ayman Tourbah (11 shared papers)Christian J. Hendriksz (3 shared papers)Frits A. Wijburg (2 shared papers)Marc C. Patterson (2 shared papers)
- Journals
- Neurology (4 papers)Orphanet Journal of Rare Diseases (4 papers)Journal of the Neurological Sciences (3 papers)Journal of Inherited Metabolic Disease (3 papers)Molecular Genetics and Metabolism (3 papers)
- Partner nations
- FranceUnited KingdomGermany
In The Last Decade
Frédéric Sedel
60 papers receiving 3.3k citations
Frédéric Sedel's Hit Papers
Peers
Comparison fields: 5 of 108
- Physiology 1.1k
- Clinical Biochemistry 267
- Developmental Neuroscience 156
- Cancer Research 518
- Neurology 228
Countries citing papers authored by Frédéric Sedel
This map shows the geographic impact of Frédéric Sedel'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 Frédéric Sedel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frédéric Sedel more than expected).
Fields of papers citing papers by Frédéric Sedel
This network shows the impact of papers produced by Frédéric Sedel. 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 Frédéric Sedel. The network helps show where Frédéric Sedel may publish in the future.
Co-authors
The 25 scholars most cited alongside Frédéric Sedel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A long nuclear‐retained non‐coding RNA regulates synaptogenesis by modulating gene expression Hit paper breakdown → | 2010 | 620 |
| 2 | 2012 | 351 | |
| 3 | 2016 | 219 | |
| 4 | 2009 | 184 | |
| 5 | 2015 | 172 | |
| 6 | 2015 | 147 | |
| 7 | 2016 | 118 | |
| 8 | 2013 | 111 | |
| 9 | 2004 | 105 | |
| 10 | 2017 | 104 | |
| 11 | 2012 | 86 | |
| 12 | 2010 | 84 | |
| 13 | 2014 | 74 | |
| 14 | 2012 | 68 | |
| 15 | 2012 | 64 | |
| 16 | 2008 | 58 | |
| 17 | 1999 | 54 | |
| 18 | 2008 | 50 | |
| 19 | 2013 | 43 | |
| 20 | 2014 | 42 |
About Frédéric Sedel
Frédéric Sedel is a scholar working on Physiology, Molecular Biology, Cell Biology, Clinical Biochemistry and Rheumatology, having authored 63 papers that have together received 3.4k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (19 papers), Biotin and Related Studies (13 papers), Metabolism and Genetic Disorders (9 papers), Carbohydrate Chemistry and Synthesis (5 papers), Glycogen Storage Diseases and Myoclonus (5 papers), Trypanosoma species research and implications (5 papers), Mitochondrial Function and Pathology (5 papers) and Neurogenesis and neuroplasticity mechanisms (4 papers). The work is most often cited by research in Physiology (1.1k citations), Clinical Biochemistry (267 citations), Developmental Neuroscience (156 citations), Cancer Research (518 citations) and Neurology (228 citations). Frédéric Sedel has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Marie T. Vanier, Delphine Bernard, Antoine Triller, Mark Walterfang, Ayman Tourbah, Christian J. Hendriksz, Frits A. Wijburg, Marc C. Patterson, Laurent Jourdren and Alain Bessis. Their work appears in journals such as Neurology, Orphanet Journal of Rare Diseases, Journal of the Neurological Sciences, Journal of Inherited Metabolic Disease and Molecular Genetics and Metabolism.
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.