Wouter Steyaert
Impact in
Papers in
- Genetics 28
- Genomics and Rare Diseases 12
- Connective tissue disorders research 11
- Genomic variations and chromosomal abnormalities 5
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- CRISPR and Genetic Engineering 5
- Genomics and Phylogenetic Studies 3
- RNA modifications and cancer 3
- RNA regulation and disease 3
- Co-authors
- Paul J. Coucke (22 shared papers)Anne De Paepe (10 shared papers)Bert Louis Callewaert (6 shared papers)Andy Willaert (6 shared papers)Fransiska Malfait (5 shared papers)Annekatrien Boel (4 shared papers)Sofie Symoens (6 shared papers)Björn Menten (2 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (5 papers)Disease Markers (2 papers)European Journal of Medical Genetics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Wouter Steyaert
45 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 85
- Genetics 563
- Aging 29
- Molecular Biology 583
- Rheumatology 89
- Cancer Research 85
Countries citing papers authored by Wouter Steyaert
This map shows the geographic impact of Wouter Steyaert'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 Wouter Steyaert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wouter Steyaert more than expected).
Fields of papers citing papers by Wouter Steyaert
This network shows the impact of papers produced by Wouter Steyaert. 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 Wouter Steyaert. The network helps show where Wouter Steyaert may publish in the future.
Co-authors
The 25 scholars most cited alongside Wouter Steyaert, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 104 | |
| 2 | 2017 | 91 | |
| 3 | 2018 | 84 | |
| 4 | 2021 | 80 | |
| 5 | 2016 | 77 | |
| 6 | 2018 | 70 | |
| 7 | 2016 | 52 | |
| 8 | 2015 | 50 | |
| 9 | 2014 | 46 | |
| 10 | 2014 | 45 | |
| 11 | 2015 | 40 | |
| 12 | 2016 | 35 | |
| 13 | 2015 | 29 | |
| 14 | 2022 | 27 | |
| 15 | 2019 | 25 | |
| 16 | 2014 | 24 | |
| 17 | 2018 | 23 | |
| 18 | 2015 | 23 | |
| 19 | 2018 | 21 | |
| 20 | 2019 | 20 |
About Wouter Steyaert
Wouter Steyaert is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Rheumatology, having authored 45 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Connective tissue disorders research (11 papers), CRISPR and Genetic Engineering (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Phylogenetic Studies (3 papers), RNA modifications and cancer (3 papers) and RNA regulation and disease (3 papers). The work is most often cited by research in Genetics (563 citations), Aging (29 citations), Molecular Biology (583 citations), Rheumatology (89 citations) and Cancer Research (85 citations). Wouter Steyaert has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Paul J. Coucke, Anne De Paepe, Bert Louis Callewaert, Andy Willaert, Fransiska Malfait, Annekatrien Boel, Sofie Symoens, Björn Menten, Sanne D’hondt and Nina De Rocker. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Disease Markers, European Journal of Medical Genetics and Genetics in Medicine.
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.