Fryns Jp
Impact in
- Genetics top 5%
- 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 77
- Genomic variations and chromosomal abnormalities 47
- 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
- Co-authors
- H Van den Berghe (27 shared papers)Alice Kleczkowska (23 shared papers)P. Goddeeris (5 shared papers)Ph. Petit (6 shared papers)J Jaeken (6 shared papers)Kamiel Vandenberghe (2 shared papers)Willem Proesmans (1 shared paper)JJ Cassiman (3 shared papers)
- Journals
- PubMed (104 papers)
- Partner nations
- BelgiumIndiaNetherlands
In The Last Decade
Fryns Jp
102 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 70
- Genetics 764
- Pediatrics, Perinatology and Child Health 293
- Developmental Biology 29
- Genetics 88
- Urology 36
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 104 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Interstitial deletion of the long arm of chromosome 15. | 1982 | 65 |
| 2 | Complex chromosomal rearrangements (CCR) and their genetic consequences. | 1982 | 62 |
| 3 | Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989. | 1990 | 34 |
| 4 | Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome. | 1980 | 33 |
| 5 | Interstitial 16q deletion with typical dysmorphic syndrome. | 1981 | 29 |
| 6 | Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum. | 1993 | 24 |
| 7 | X-linked recessively inherited non-specific mental retardation. Report of a large family. | 1977 | 22 |
| 8 | Partial duplication of the long arm of chromosome 4. | 1980 | 21 |
| 9 | 8p trisomy in a malformed foetus. | 1982 | 20 |
| 10 | Distal 10p deletion syndrome. | 1981 | 19 |
| 11 | Melnick-Needles syndrome (osteodysplasty). Clinical and radiological heterogeneity. | 1986 | 19 |
| 12 | Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6. | 1991 | 19 |
| 13 | Partial distal 12q trisomy. | 1980 | 18 |
| 14 | Tuberous sclerosis. Bourneville disease. | 1978 | 17 |
| 15 | The lethal multiple pterygium syndrome: a nosological approach. | 1990 | 17 |
| 16 | Cystic hygroma and multiple pterygium syndrome. | 1984 | 17 |
| 17 | The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large family. | 1992 | 17 |
| 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 | 17 |
| 19 | Familial partial distal 18q (18q22-18q23) trisomy. | 1981 | 16 |
| 20 | Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood. | 1980 | 15 |
About Fryns Jp
Fryns Jp is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Genetics and Plant Science, having authored 104 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (47 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 Congenital Anomalies and Fetal Surgery (6 papers). The work is most often cited by research in Genetics (764 citations), Pediatrics, Perinatology and Child Health (293 citations), Developmental Biology (29 citations), Genetics (88 citations) and Urology (36 citations). Fryns Jp has collaborated with scholars based in Belgium, India and Netherlands. Frequent co-authors include H Van den Berghe, Alice Kleczkowska, P. Goddeeris, Ph. Petit, J Jaeken, Kamiel Vandenberghe, Willem Proesmans, JJ Cassiman, Alicja Kleczkowska and Frank Theo Moerman. Their work appears in journals such as 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.