J. P. Fryns
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities 92
- Genetics and Neurodevelopmental Disorders 71
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 24
- Connective tissue disorders research 19
- Developmental Biology top 1%
- Congenital limb and hand anomalies 31
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- Prenatal Screening and Diagnostics 40
- Cognitive Neuroscience top 2%
- Molecular Biology top 2%
- Congenital heart defects research 17
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- Chromosomal and Genetic Variations 36
- Co-authors
- Herman Van den BergheA KleczkowskaKoenraad DevriendtT. LukusaMartine BorghgraefC. T. R. M. Schrander‐StumpelP. PetitAnnick Vogels
- Journals
- Human Genetics (55 papers)Clinical Genetics (49 papers)Journal of Medical Genetics (25 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
J. P. Fryns
278 papers receiving 5.9k citations
Peers
Comparison fields: 5 of 128
- Genetics 4.3k
- Developmental Biology 240
- Pediatrics, Perinatology and Child Health 997
- Cognitive Neuroscience 893
- Molecular Biology 2.8k
Countries citing papers authored by J. P. Fryns
This map shows the geographic impact of J. P. 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 J. P. Fryns with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. P. Fryns more than expected).
Fields of papers citing papers by J. P. Fryns
This network shows the impact of papers produced by J. P. 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 J. P. Fryns. The network helps show where J. P. Fryns may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J. P. Fryns, 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 | 2007 | 131 | |
| 2 | 2006 | 8 | |
| 3 | 2006 | 31 | |
| 4 | 2005 | 63 | |
| 5 | 2004 | 57 | |
| 6 | Costello syndrome in two siblings and minor manifestations in their mother. Further evidence for autosomal dominant inheritance? | 2002 | 8 |
| 7 | 2001 | 8 | |
| 8 | 2001 | 298 | |
| 9 | 2001 | 5 | |
| 10 | 2001 | 8 | |
| 11 | 1994 | 1 | |
| 12 | 1993 | 15 | |
| 13 | 1993 | 3 | |
| 14 | Hypomelanosis of Ito and severe sensorineural deafness. | 1992 | 2 |
| 15 | 1992 | 23 | |
| 16 | 1990 | 20 | |
| 17 | 1989 | 2 | |
| 18 | 1988 | 10 | |
| 19 | 1988 | 15 | |
| 20 | 1987 | 16 |
About J. P. Fryns
J. P. Fryns is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 280 papers that have together received 6.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (92 papers), Genetics and Neurodevelopmental Disorders (71 papers), Prenatal Screening and Diagnostics (40 papers), Chromosomal and Genetic Variations (36 papers), Congenital limb and hand anomalies (31 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers), Connective tissue disorders research (19 papers) and Congenital heart defects research (17 papers). The work is most often cited by research in Genetics (4.3k citations), Developmental Biology (240 citations) and Pediatrics, Perinatology and Child Health (997 citations). J. P. Fryns has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Herman Van den Berghe, A Kleczkowska, Koenraad Devriendt, T. Lukusa, Martine Borghgraef, C. T. R. M. Schrander‐Stumpel, P. Petit, Annick Vogels, Joris Vermeesch and Leopold Curfs. Their work appears in journals such as Human Genetics, Clinical Genetics, Journal of Medical Genetics, European Journal of Pediatrics and Journal of Intellectual Disability Research.
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.