Fryns Jp
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 79
- Genomic variations and chromosomal abnormalities 48
- Genetics and Neurodevelopmental Disorders 12
- Genetic Syndromes and Imprinting 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
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- Prenatal Screening and Diagnostics 27
- Fetal and Pediatric Neurological Disorders 6
- Co-authors
- Van den Berghe H (28 shared papers)A Kleczkowska (24 shared papers)P. Goddeeris (4 shared papers)P. Petit (6 shared papers)JJ Cassiman (4 shared papers)J Jaeken (6 shared papers)Kamiel Vandenberghe (2 shared papers)A. Kleczkowska (3 shared papers)
- Journals
- Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) (8 papers)PubMed (98 papers)
- Partner nations
- BelgiumNetherlandsIndia
In The Last Decade
Fryns Jp
105 papers receiving 942 citations
Peers
Comparison fields: 5 of 72
- Genetics 728
- Pediatrics, Perinatology and Child Health 297
- Developmental Biology 28
- Genetics 85
- Plant Science 241
Countries citing papers authored by Fryns Jp
This map shows the geographic impact of Fryns Jp'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 Fryns Jp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fryns Jp more than expected).
Fields of papers citing papers by Fryns Jp
This network shows the impact of papers produced by Fryns Jp. 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 Fryns Jp. The network helps show where Fryns Jp may publish in the future.
Co-authors
The 25 scholars most cited alongside Fryns Jp, 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 106 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Complex chromosomal rearrangements (CCR) and their genetic consequences. | 1982 | 61 |
| 2 | Interstitial deletion of the long arm of chromosome 15. | 1982 | 56 |
| 3 | Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome. | 1980 | 31 |
| 4 | X-linked recessively inherited non-specific mental retardation. Report of a large family. | 1977 | 22 |
| 5 | Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989. | 1990 | 20 |
| 6 | Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum. | 1993 | 20 |
| 7 | Partial duplication of the long arm of chromosome 4. | 1980 | 20 |
| 8 | 8p trisomy in a malformed foetus. | 1982 | 20 |
| 9 | Interstitial 16q deletion with typical dysmorphic syndrome. | 1981 | 18 |
| 10 | Partial distal 12q trisomy. | 1980 | 18 |
| 11 | [Ring chromosome 6. Karotype 46, XY, r (6)-45, XY,-6]. | 1974 | 17 |
| 12 | Melnick-Needles syndrome (osteodysplasty). Clinical and radiological heterogeneity. | 1986 | 17 |
| 13 | Tuberous sclerosis. Bourneville disease. | 1978 | 16 |
| 14 | Familial partial distal 18q (18q22-18q23) trisomy. | 1981 | 16 |
| 15 | Distal 10p deletion syndrome. | 1981 | 15 |
| 16 | Ring chromosome 14. A distinct clinical entity. | 1983 | 15 |
| 17 | Cystic hygroma and multiple pterygium syndrome. | 1984 | 15 |
| 18 | Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3). | 1994 | 15 |
| 19 | Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6. | 1991 | 15 |
| 20 | De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24). | 1980 | 15 |
About Fryns Jp
Fryns Jp is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Surgery, having authored 106 papers that have together received 996 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (48 papers), Prenatal Screening and Diagnostics (27 papers), Chromosomal and Genetic Variations (14 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genetic Syndromes and Imprinting (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital limb and hand anomalies (7 papers) and Fetal and Pediatric Neurological Disorders (6 papers). The work is most often cited by research in Genetics (728 citations), Pediatrics, Perinatology and Child Health (297 citations), Developmental Biology (28 citations), Genetics (85 citations) and Plant Science (241 citations). Fryns Jp has collaborated with scholars based in Belgium, Netherlands and India. Frequent co-authors include Van den Berghe H, A Kleczkowska, P. Goddeeris, P. Petit, JJ Cassiman, J Jaeken, Kamiel Vandenberghe, A. Kleczkowska, Willem Proesmans and F. Moerman. Their work appears in journals such as Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and PubMed.
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.