691 total citations 45 papers, 562 citations indexed
About
Van den Berghe H is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health.
According to data from OpenAlex, Van den Berghe H has authored 45 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Van den Berghe H's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Van den Berghe H is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Van den Berghe H collaborates with scholars based in Belgium, Netherlands and Italy. Van den Berghe H's co-authors include Fryns Jp, Cristina Mecucci, Roland Berger, Olivier Bernard, M Mauchauffé, Willem Proesmans, P Malvaux, P. Denys, W Tanghe and P. Goddeeris and has published in prestigious journals such as Blood, PubMed and Munich Personal RePEc Archive (Ludwig Maximilian University of Munich).
In The Last Decade
Van den Berghe H
43 papers
receiving
538 citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
hero ref
Countries citing papers authored by Van den Berghe H
Since
Specialization
Citations
This map shows the geographic impact of Van den Berghe H'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 Van den Berghe H with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Van den Berghe H more than expected).
Fields of papers citing papers by Van den Berghe H
This network shows the impact of papers produced by Van den Berghe H. 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 Van den Berghe H. The network helps show where Van den Berghe H may publish in the future.
Co-authorship network of co-authors of Van den Berghe H
This figure shows the co-authorship network connecting the top 25 collaborators of Van den Berghe H.
A scholar is included among the top collaborators of Van den Berghe H 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 Van den Berghe H. Van den Berghe H 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.
Pauwels, Patrick, et al.. (1996). Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma.. PubMed. 29(1). 84–7.33 indexed citations
2.
Kleczkowska, A, et al.. (1987). Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.. PubMed. 30(1). 47–51.7 indexed citations
3.
Aventı́n, Anna, Cristina Mecucci, Guido Tricot, & Van den Berghe H. (1987). Burkitt-type ALL with variant t(2;8) and complex additional rearrangements at diagnosis.. PubMed. 30(1). 52–5.1 indexed citations
4.
Jp, Fryns, et al.. (1986). Ring chromosome 15 syndrome. Further delineation of the adult phenotype.. PubMed. 29(1). 45–8.12 indexed citations
5.
Barbieri, Dario & Van den Berghe H. (1984). Chromosome change in prolymphocytic leukemia.. Blood. 63(5). 1258–1258.2 indexed citations
6.
Jp, Fryns, et al.. (1982). The elfin face syndrome and the short arm of chromosome 15.. PubMed. 25(3). 181–2.13 indexed citations
7.
Jp, Fryns, P. Petit, F. Moerman, JJ Cassiman, & Van den Berghe H. (1982). 8p trisomy in a malformed foetus.. PubMed. 25(3). 162–3.20 indexed citations
8.
Jp, Fryns, Robin P. Peeters, P. Petit, & Van den Berghe H. (1981). New chromosomal syndromes. III. The 13q deletion syndrome.. PubMed. 33(4). 261–4.3 indexed citations
9.
Jp, Fryns & Van den Berghe H. (1981). The Cohen syndrome.. PubMed. 29(4). 449–53.13 indexed citations
10.
Cassiman, JJ, et al.. (1981). Application of crossed immunoelectrophoresis to the visualization and characterization of human fibroblast antigens.. PubMed. 27(1). 39–48.4 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, et al.. (1980). Unusual translocation in Down syndrome.. PubMed. 33(1). 47–9.2 indexed citations
14.
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
15.
Cassiman, JJ, et al.. (1979). Anomalous alpha 2-macroglobulin-protease complexes in cystic fibrosis: decreased uptake of the complexes by fibroblasts in culture.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 13(12). 1384–6.12 indexed citations
16.
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
17.
Jp, Fryns, et al.. (1977). A patient with Langer type of mesomelic dwarfism.. PubMed. 29(3). 193–6.2 indexed citations
18.
H, Van den Berghe, et al.. (1977). Pre- and postnatal growth retardation with severe mental retardation, acral limb deficiencies and ocular anomalies: a new syndrome of inherited intrauterine dwarfism?. PubMed. 30(4). 227–32.2 indexed citations
19.
H, Van den Berghe. (1974). Clastogenic effects of haloperidol in vivo and of haloperidol, droperidol, and pipamperone in vitro. A negative study.. PubMed. 24(12). 2055–8.1 indexed citations
20.
Denys, P., P Malvaux, Van den Berghe H, W Tanghe, & Willem Proesmans. (1967). [Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism].. PubMed. 24(7). 729–39.88 indexed citations
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.