1.2k total citations 106 papers, 996 citations indexed
About
Fryns Jp is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology.
According to data from OpenAlex, Fryns Jp has authored 106 papers receiving a total of 996 indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Genetics, 32 papers in Pediatrics, Perinatology and Child Health and 23 papers in Molecular Biology. Recurrent topics in Fryns Jp's work include Genomic variations and chromosomal abnormalities (48 papers), Prenatal Screening and Diagnostics (27 papers) and Chromosomal and Genetic Variations (14 papers). Fryns Jp is often cited by papers focused on Genomic variations and chromosomal abnormalities (48 papers), Prenatal Screening and Diagnostics (27 papers) and Chromosomal and Genetic Variations (14 papers). Fryns Jp collaborates with scholars based in Belgium, Netherlands and India. Fryns Jp's co-authors include Van den Berghe H, A Kleczkowska, P. Goddeeris, P. Petit, JJ Cassiman, J Jaeken, Kamiel Vandenberghe, Willem Proesmans, F. Moerman and A. Kleczkowska and has published in prestigious journals such as PubMed and Munich Personal RePEc Archive (Ludwig Maximilian University of Munich).
In The Last Decade
Fryns Jp
105 papers
receiving
942 citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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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).
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-authorship network of co-authors of Fryns Jp
This figure shows the co-authorship network connecting the top 25 collaborators of Fryns Jp.
A scholar is included among the top collaborators of Fryns Jp 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 Fryns Jp. Fryns Jp is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Thiry, Paul, et al.. (2000). Angelman syndrome in three adult patients with atypical presentation and severe neurological complications.. PubMed. 11(4). 363–73.8 indexed citations
2.
Moens, Pierre, et al.. (1993). Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.. PubMed. 4(4). 277–80.6 indexed citations
3.
Beemer, F. A., et al.. (1993). VACTERL with hydrocephalus. A distinct entity with a variable spectrum of multiple congenital anomalies.. PubMed. 4(3). 199–201.4 indexed citations
4.
Jp, Fryns, et al.. (1992). The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling.. PubMed. 3(4). 175–7.1 indexed citations
5.
Kleczkowska, A, et al.. (1990). Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.. PubMed. 1(3-4). 227–33.20 indexed citations
6.
Kleczkowska, A, et al.. (1990). Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989.. PubMed. 1(3-4). 241–9.1 indexed citations
7.
Jp, Fryns, et al.. (1990). Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?. PubMed. 1(1). 63–6.3 indexed citations
8.
Gilgenkrantz, S, Fryns Jp, P. Droullé, et al.. (1987). [Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21].. PubMed. 35(1). 51–61.3 indexed citations
Jp, Fryns, et al.. (1980). Dysosteosclerosis in a mentally retarded boy.. PubMed. 33(1). 53–6.6 indexed citations
11.
Jp, Fryns, et al.. (1980). Melorheostosis in a 3-year-old girl.. PubMed. 33(3). 185–7.4 indexed citations
12.
Jp, Fryns, et al.. (1980). Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism.. PubMed. 23(1). 54–6.8 indexed citations
13.
Jp, Fryns & Van den Berghe H. (1979). Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocations.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 125–7.11 indexed citations
14.
Jp, Fryns, et al.. (1979). Partial trisomy 22q with elevated arylsulfatase-A activity.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 168–70.2 indexed citations
15.
Moerman, F., Fryns Jp, P. Goddeeris, et al.. (1979). Complete trisomy 8 in a polymalformed newborn.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 32(4). 283–5.1 indexed citations
16.
Jp, Fryns, et al.. (1979). Familial paracentric inversion of the short arm of chromosome 3.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 163–4.11 indexed citations
17.
Jp, Fryns, et al.. (1978). Tuberous sclerosis. Bourneville disease.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 31(1). suppl V:33–40.16 indexed citations
18.
Jp, Fryns, et al.. (1978). Focal dermal hypoplasia (Goltz syndrome) in a male.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 31(1). 37–9.11 indexed citations
19.
Jp, Fryns, et al.. (1977). The foetal alcohol syndrome.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 30(2). 117–21.13 indexed citations
20.
Jp, Fryns, et al.. (1977). X-linked recessively inherited non-specific mental retardation. Report of a large family.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(4). 263–8.22 indexed citations
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