Sabrina Eichler
Impact in
- Physiology top 10%
- Lysosomal Storage Disorders Research
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- Cellular transport and secretion
Papers in
- Physiology 11
- Lysosomal Storage Disorders Research 11
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- Glycogen Storage Diseases and Myoclonus 4
- Co-authors
- Arndt Rolfs (12 shared papers)Anne‐Katrin Giese (6 shared papers)Jan Lukáš (4 shared papers)Claudia Cozma (5 shared papers)Tobias Böttcher (3 shared papers)Daniëlle te Vruchte (1 shared paper)Mario Cortina‐Borja (1 shared paper)Forbes D. Porter (1 shared paper)
- Journals
- PLoS ONE (2 papers)Human Mutation (1 paper)Scientific Reports (1 paper)Orphanet Journal of Rare Diseases (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- GermanyUnited KingdomColombia
In The Last Decade
Sabrina Eichler
14 papers receiving 317 citations
Peers
Comparison fields: 5 of 51
- Physiology 251
- Cell Biology 87
- Physiology 20
- Hematology 35
- Epidemiology 94
Countries citing papers authored by Sabrina Eichler
This map shows the geographic impact of Sabrina 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 Sabrina Eichler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sabrina Eichler more than expected).
Fields of papers citing papers by Sabrina Eichler
This network shows the impact of papers produced by Sabrina 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 Sabrina Eichler. The network helps show where Sabrina Eichler may publish in the future.
Co-authors
The 25 scholars most cited alongside Sabrina 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
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 96 | |
| 2 | 2015 | 54 | |
| 3 | 2017 | 37 | |
| 4 | 2017 | 27 | |
| 5 | 2017 | 24 | |
| 6 | 2016 | 20 | |
| 7 | 2012 | 16 | |
| 8 | 2015 | 16 | |
| 9 | 2015 | 13 | |
| 10 | 2017 | 12 | |
| 11 | 2019 | 5 | |
| 12 | Morquio syndrome: new heterozygous mutation of the GALNS gene in two siblings from south-west Colombia. Clinical, molecular, and bioinformatic analysis | 2016 | 2 |
| 13 | 2017 | 1 | |
| 14 | Síndrome de Morquio: nueva mutación del gen GALNS en dos hermanos del sur-occidente colombiano. Análisis clínico, molecular y bioinformático | 2016 | 1 |
| 15 | 2015 | 0 |
About Sabrina Eichler
Sabrina Eichler is a scholar working on Physiology, Rheumatology, Cell Biology, Epidemiology and Molecular Biology, having authored 15 papers that have together received 324 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Trypanosoma species research and implications (4 papers), Carbohydrate Chemistry and Synthesis (2 papers), Metabolism and Genetic Disorders (1 paper), Genetic and rare skin diseases. (1 paper) and Cystic Fibrosis Research Advances (1 paper). The work is most often cited by research in Physiology (251 citations), Cell Biology (87 citations), Physiology (20 citations), Hematology (35 citations) and Epidemiology (94 citations). Sabrina Eichler has collaborated with scholars based in Germany, United Kingdom and Colombia. Frequent co-authors include Arndt Rolfs, Anne‐Katrin Giese, Jan Lukáš, Claudia Cozma, Tobias Böttcher, Daniëlle te Vruchte, Mario Cortina‐Borja, Forbes D. Porter, Ulrike Grittner and Hermann Mascher. Their work appears in journals such as PLoS ONE, Human Mutation, Scientific Reports, Orphanet Journal of Rare Diseases 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.