JP Fryns
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Plant Science
- Cellular and Molecular Neuroscience
- Co-authors
- Koenraad DevriendtJoris VermeeschFemke HannesGriet Van BuggenhoutPeter MarynenRegina ReganAnnick VogelsHelen Stewart
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Chromosomal and Genetic Variations (4 papers)Congenital heart defects research (4 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
JP Fryns
13 papers receiving 538 citations
Peers
Comparison fields: 5 of 46
- Genetics 427
- Molecular Biology 284
- Pediatrics, Perinatology and Child Health 108
- Plant Science 107
- Cellular and Molecular Neuroscience 80
Countries citing papers authored by JP Fryns
This map shows the geographic impact of JP Fryns'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 JP Fryns with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites JP Fryns more than expected).
Fields of papers citing papers by JP Fryns
This network shows the impact of papers produced by JP Fryns. 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 JP Fryns. The network helps show where JP Fryns may publish in the future.
Co-authorship network of co-authors of JP Fryns
This figure shows the co-authorship network connecting the top 25 collaborators of JP Fryns. A scholar is included among the top collaborators of JP Fryns 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 JP Fryns. JP Fryns is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 0 | |
| 3 | 23 | |
| 4 | 17 | |
| 5 | 207 | |
| 6 | 99 | |
| 7 | 25 | |
| 8 | 16 | |
| 9 | 49 | |
| 10 | 32 | |
| 11 | 10 | |
| 12 | 25 | |
| 13 | 2 | |
| 14 | 55 |
About JP Fryns
JP Fryns is a scholar working on Genetics, Developmental Neuroscience and Urology, having authored 14 papers that have together received 563 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Genetics (427 citations), Developmental Biology (15 citations) and Pediatrics, Perinatology and Child Health (108 citations). JP Fryns has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Koenraad Devriendt, Joris Vermeesch, Femke Hannes, Griet Van Buggenhout, Peter Marynen, Regina Regan, Annick Vogels, Helen Stewart, Thomy de Ravel and Heather C. Mefford. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics and Clinical 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.