Sabrina Eichler

478 citations
15 papers · 336 · h-index 10

Impact in

  • Physiology top 10%
    • Lysosomal Storage Disorders Research
    • Calcium signaling and nucleotide metabolism
    • Cellular transport and secretion

Papers in

Sabrina Eichler

14 papers receiving 327 citations

Peers

Sabrina Eichler
Comparison fields: 5 of 48
  • Physiology 255
  • Cell Biology 69
  • Physiology 19
  • Epidemiology 69
  • Hematology 22
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Tomo Sawada Japan
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Jacobo Villalobos Venezuela
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Mici Phillips Israel
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Citations per field
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Citations per year

Countries citing papers authored by Sabrina Eichler

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Sabrina Eichler Line = papers co-authored together Sabrina Eichler links everyone, so they are left out of the graph.

All Works

15 of 15 papers shown
#Work
1 2015102
2 201556
3 201737
4 201730
5 201724
6 201620
7 201216
8 201516
9 201514
10 201712
11 20195
12
Morquio syndrome: new heterozygous mutation of the GALNS gene in two siblings from south-west Colombia. Clinical, molecular, and bioinformatic analysis
20162
13 20171
14
Síndrome de Morquio: nueva mutación del gen GALNS en dos hermanos del sur-occidente colombiano. Análisis clínico, molecular y bioinformático
20161
15 20150

About Sabrina Eichler

Sabrina Eichler is a scholar working on Physiology, Cell Biology, Rheumatology, Molecular Biology and Organic Chemistry, having authored 15 papers that have together received 336 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 (3 papers), Trypanosoma species research and implications (2 papers), Carbohydrate Chemistry and Synthesis (2 papers), Folate and B Vitamins Research (1 paper), Genetic and rare skin diseases. (1 paper) and Family and Disability Support Research (1 paper). The work is most often cited by research in Physiology (255 citations), Cell Biology (69 citations), Physiology (19 citations), Epidemiology (69 citations) and Hematology (22 citations). Sabrina Eichler has collaborated with scholars based in Germany, Colombia and United States. Frequent co-authors include Arndt Rolfs, Anne‐Katrin Giese, Jan Lukáš, Claudia Cozma, Nada Al Eisa, Hermann Mascher, Mario Cortina‐Borja, Forbes D. Porter, Daniëlle te Vruchte and Tobias Böttcher. Their work appears in journals such as PLoS ONE, Molecular Genetics and Metabolism, Scientific Reports, Human Mutation and International Journal of Molecular Sciences.

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.

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