Rachel Schot
- Molecular Biology
- Genetics top 10%
- Cell Biology
- Pediatrics, Perinatology and Child Health top 10%
- Surgery
- Co-authors
- Frans W. VerheijenI.F.M. de CooMaarten H. LequinGrazia M.S. ManciniCathryn PoultonMarie‐Claire Y. de WitRenske OegemaPeter J. van der Spek
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (8 papers)Genomics and Rare Diseases (7 papers)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Rachel Schot
32 papers receiving 676 citations
Peers
Comparison fields: 5 of 77
- Molecular Biology 355
- Genetics 260
- Cell Biology 107
- Pediatrics, Perinatology and Child Health 100
- Surgery 78
Countries citing papers authored by Rachel Schot
This map shows the geographic impact of Rachel Schot'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 Rachel Schot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Schot more than expected).
Fields of papers citing papers by Rachel Schot
This network shows the impact of papers produced by Rachel Schot. 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 Rachel Schot. The network helps show where Rachel Schot may publish in the future.
Co-authorship network of co-authors of Rachel Schot
This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Schot. A scholar is included among the top collaborators of Rachel Schot based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rachel Schot. Rachel Schot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 11 | |
| 3 | 0 | |
| 4 | 8 | |
| 5 | 1 | |
| 6 | 7 | |
| 7 | 11 | |
| 8 | 73 | |
| 9 | 55 | |
| 10 | 6 | |
| 11 | 39 | |
| 12 | 8 | |
| 13 | 21 | |
| 14 | 5 | |
| 15 | 24 | |
| 16 | 17 | |
| 17 | 28 | |
| 18 | 13 | |
| 19 | 25 | |
| 20 | 2 |
About Rachel Schot
Rachel Schot is a scholar working on Genetics, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 686 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (260 citations), Immunology and Allergy (53 citations) and Cell Biology (107 citations). Rachel Schot has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Frans W. Verheijen, I.F.M. de Coo, Maarten H. Lequin, Grazia M.S. Mancini, Cathryn Poulton, Grazia M.S. Mancini, Marie‐Claire Y. de Wit, Renske Oegema, Peter J. van der Spek and Elly Verbeek. Their work appears in journals such as Cell, Neurology and The American Journal of Human Genetics.
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.