Florian Eichler
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Neurology top 2%
- Neuroinflammation and Neurodegeneration Mechanisms
Papers in
-
- Peroxisome Proliferator-Activated Receptors 43
- RNA regulation and disease 21
- Sphingolipid Metabolism and Signaling 6
- Physiology 30
- Lysosomal Storage Disorders Research 15
- Co-authors
- Eric E. Smith (2 shared papers)Jeremy D. Schmahmann (3 shared papers)Christopher M. Filley (1 shared paper)Robert H. Brown (6 shared papers)Thorsten Hornemann (8 shared papers)Matthew P. Frosch (7 shared papers)Gerald V. Raymond (6 shared papers)Arnold von Eckardstein (3 shared papers)
- Journals
- Neurology (17 papers)Molecular Genetics and Metabolism (13 papers)Muscle & Nerve (6 papers)Orphanet Journal of Rare Diseases (5 papers)Human Gene Therapy (5 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Florian Eichler
122 papers receiving 4.3k citations
Peers
Comparison fields: 5 of 125
- Clinical Biochemistry 412
- Neurology 455
- Physiology 944
- Biochemistry 244
- Microbiology 24
Countries citing papers authored by Florian Eichler
This map shows the geographic impact of Florian Eichler'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 Eichler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florian Eichler more than expected).
Fields of papers citing papers by Florian Eichler
This network shows the impact of papers produced by Florian Eichler. 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 Eichler. The network helps show where Florian Eichler may publish in the future.
Co-authors
The 25 scholars most cited alongside Florian Eichler, 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 136 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 389 | |
| 2 | 2010 | 300 | |
| 3 | 2009 | 231 | |
| 4 | 2015 | 165 | |
| 5 | 2011 | 160 | |
| 6 | 2008 | 141 | |
| 7 | 2005 | 122 | |
| 8 | 2011 | 116 | |
| 9 | 2015 | 115 | |
| 10 | 2009 | 106 | |
| 11 | 2002 | 103 | |
| 12 | 2007 | 103 | |
| 13 | 2018 | 98 | |
| 14 | 2018 | 95 | |
| 15 | 2019 | 79 | |
| 16 | 2009 | 78 | |
| 17 | 2002 | 75 | |
| 18 | 2011 | 70 | |
| 19 | 2001 | 69 | |
| 20 | Diffuse metabolic abnormalities in reversible posterior leukoencephalopathy syndrome. | 2002 | 68 |
About Florian Eichler
Florian Eichler is a scholar working on Molecular Biology, Physiology, Clinical Biochemistry, Neurology and Epidemiology, having authored 136 papers that have together received 4.4k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (43 papers), RNA regulation and disease (21 papers), Metabolism and Genetic Disorders (17 papers), Lysosomal Storage Disorders Research (15 papers), Neuroinflammation and Neurodegeneration Mechanisms (9 papers), Virus-based gene therapy research (8 papers), Biomedical Research and Pathophysiology (6 papers) and Sphingolipid Metabolism and Signaling (6 papers). The work is most often cited by research in Clinical Biochemistry (412 citations), Neurology (455 citations), Physiology (944 citations), Biochemistry (244 citations) and Microbiology (24 citations). Florian Eichler has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Eric E. Smith, Jeremy D. Schmahmann, Christopher M. Filley, Robert H. Brown, Thorsten Hornemann, Matthew P. Frosch, Gerald V. Raymond, Arnold von Eckardstein, Anke Penno and Alfried Kohlschütter. Their work appears in journals such as Neurology, Molecular Genetics and Metabolism, Muscle & Nerve, Orphanet Journal of Rare Diseases and Human Gene Therapy.
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.