Stefanie Belet
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
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- RNA modifications and cancer
- Ubiquitin and proteasome pathways
Papers in
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- Congenital heart defects research 2
- RNA modifications and cancer 2
- Genetics 8
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Genomics and Rare Diseases 1
- Co-authors
- Guy Froyen (10 shared papers)Nathalie Fieremans (5 shared papers)Jelle Verbeeck (5 shared papers)Hilde Van Esch (4 shared papers)Marijke Bauters (3 shared papers)Kevin J. Verstrepen (1 shared paper)Peter Marynen (3 shared papers)Jorge Duitama (1 shared paper)
- Journals
- Human Genetics (2 papers)Human Mutation (2 papers)European Journal of Medical Genetics (1 paper)European Journal of Human Genetics (1 paper)PLoS ONE (1 paper)
- Partner nations
- BelgiumUnited StatesBrazil
In The Last Decade
Stefanie Belet
10 papers receiving 241 citations
Peers
Comparison fields: 5 of 48
- Genetics 145
- Molecular Biology 124
- Cell Biology 29
- Aging 2
- Cellular and Molecular Neuroscience 20
Countries citing papers authored by Stefanie Belet
This map shows the geographic impact of Stefanie Belet'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 Stefanie Belet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefanie Belet more than expected).
Fields of papers citing papers by Stefanie Belet
This network shows the impact of papers produced by Stefanie Belet. 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 Stefanie Belet. The network helps show where Stefanie Belet may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefanie Belet, 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 | 2013 | 47 | |
| 2 | 2014 | 41 | |
| 3 | 2014 | 33 | |
| 4 | 2013 | 27 | |
| 5 | 2015 | 25 | |
| 6 | 2013 | 22 | |
| 7 | 2013 | 22 | |
| 8 | 2015 | 16 | |
| 9 | 2011 | 14 | |
| 10 | 2013 | 6 |
About Stefanie Belet
Stefanie Belet is a scholar working on Molecular Biology, Genetics, Cell Biology, Cellular and Molecular Neuroscience and Epidemiology, having authored 10 papers that have together received 253 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (2 papers), Cellular transport and secretion (2 papers), RNA modifications and cancer (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genomics and Rare Diseases (1 paper) and Trypanosoma species research and implications (1 paper). The work is most often cited by research in Genetics (145 citations), Molecular Biology (124 citations), Cell Biology (29 citations), Aging (2 citations) and Cellular and Molecular Neuroscience (20 citations). Stefanie Belet has collaborated with scholars based in Belgium, United States and Brazil. Frequent co-authors include Guy Froyen, Nathalie Fieremans, Jelle Verbeeck, Hilde Van Esch, Marijke Bauters, Kevin J. Verstrepen, Peter Marynen, Jorge Duitama, Joris Vermeesch and An Jansen. Their work appears in journals such as Human Genetics, Human Mutation, European Journal of Medical Genetics, European Journal of Human Genetics and PLoS ONE.
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.