Sarah Vergult
- Molecular Biology
- Genetics top 10%
- Cancer Research
- Cellular and Molecular Neuroscience
- Pediatrics, Perinatology and Child Health
- Co-authors
- Björn MentenAnnelies DheedeneTim De MeyerPieter‐Jan VoldersTom SanteRudy Van CosterSandra JanssensWilly Lissens
- Topics
- Genomic variations and chromosomal abnormalities (12 papers)RNA modifications and cancer (6 papers)Genomics and Rare Diseases (4 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Sarah Vergult
28 papers receiving 525 citations
Peers
Comparison fields: 5 of 67
- Molecular Biology 334
- Genetics 218
- Cancer Research 91
- Cellular and Molecular Neuroscience 63
- Pediatrics, Perinatology and Child Health 53
Countries citing papers authored by Sarah Vergult
This map shows the geographic impact of Sarah Vergult'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 Sarah Vergult with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Vergult more than expected).
Fields of papers citing papers by Sarah Vergult
This network shows the impact of papers produced by Sarah Vergult. 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 Sarah Vergult. The network helps show where Sarah Vergult may publish in the future.
Co-authorship network of co-authors of Sarah Vergult
This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Vergult. A scholar is included among the top collaborators of Sarah Vergult 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 Sarah Vergult. Sarah Vergult is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 3 | |
| 4 | 11 | |
| 5 | 7 | |
| 6 | 10 | |
| 7 | 41 | |
| 8 | 14 | |
| 9 | 35 | |
| 10 | 7 | |
| 11 | 42 | |
| 12 | 43 | |
| 13 | 53 | |
| 14 | 25 | |
| 15 | 33 | |
| 16 | 22 | |
| 17 | 27 | |
| 18 | 34 | |
| 19 | 8 | |
| 20 | 20 |
About Sarah Vergult
Sarah Vergult is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 28 papers that have together received 541 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), RNA modifications and cancer (6 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (218 citations), Cancer Research (91 citations) and Clinical Biochemistry (37 citations). Sarah Vergult has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Björn Menten, Annelies Dheedene, Tim De Meyer, Pieter‐Jan Volders, Tom Sante, Rudy Van Coster, Sandra Janssens, Willy Lissens, Frank Speleman and Alfred Meurs. Their work appears in journals such as Nature Communications, PLoS ONE and Scientific Reports.
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.