Van den Berghe H
- Molecular Biology
- Genetics top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Pulmonary and Respiratory Medicine
- Hematology top 10%
- Co-authors
- Fryns JpCristina MecucciOlivier BernardM MauchaufféRoland BergerWillem ProesmansP MalvauxW Tanghe
- Topics
- Genomic variations and chromosomal abnormalities (15 papers)Prenatal Screening and Diagnostics (5 papers)Chromosomal and Genetic Variations (4 papers)
- Journals
- BloodPubMedMunich Personal RePEc Archive (Ludwig Maximilian University of Munich)
- Partner nations
- BelgiumNetherlandsItaly
In The Last Decade
Van den Berghe H
43 papers receiving 538 citations
Peers
Comparison fields: 5 of 63
- Molecular Biology 267
- Genetics 257
- Pediatrics, Perinatology and Child Health 98
- Pulmonary and Respiratory Medicine 89
- Hematology 87
Countries citing papers authored by Van den Berghe H
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
| # | Work | Indexed citations |
|---|---|---|
| 1 | Cytogenetics revealing the diagnosis in a metastatic endometrial stromal sarcoma. | 33 |
| 2 | A new t(2;5) translocation in a null cell type CD30 positive anaplastic large cell lymphoma case. | 6 |
| 3 | Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism. | 1 |
| 4 | Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood. | 7 |
| 5 | Chromosome change in prolymphocytic leukemia. | 2 |
| 6 | The elfin face syndrome and the short arm of chromosome 15. | 13 |
| 7 | New chromosomal syndromes. III. The 13q deletion syndrome. | 3 |
| 8 | Application of crossed immunoelectrophoresis to the visualization and characterization of human fibroblast antigens. | 4 |
| 9 | The Cohen syndrome. | 13 |
| 10 | Mosaic supernumerary small ring chromosome. | 1 |
| 11 | Melorheostosis in a 3-year-old girl. | 4 |
| 12 | Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism. | 8 |
| 13 | Unusual translocation in Down syndrome. | 2 |
| 14 | Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy. | 1 |
| 15 | Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocations. | 11 |
| 16 | Anomalous alpha 2-macroglobulin-protease complexes in cystic fibrosis: decreased uptake of the complexes by fibroblasts in culture. | 12 |
| 17 | Focal dermal hypoplasia (Goltz syndrome) in a male. | 11 |
| 18 | Pre- and postnatal growth retardation with severe mental retardation, acral limb deficiencies and ocular anomalies: a new syndrome of inherited intrauterine dwarfism? | 2 |
| 19 | A patient with Langer type of mesomelic dwarfism. | 2 |
| 20 | Clastogenic effects of haloperidol in vivo and of haloperidol, droperidol, and pipamperone in vitro. A negative study. | 1 |
About Van den Berghe H
Van den Berghe H is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 45 papers that have together received 562 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (257 citations), Hematology (87 citations) and Pediatrics, Perinatology and Child Health (98 citations). Van den Berghe H has collaborated with scholars based in Belgium, Netherlands and Italy. Frequent co-authors include Fryns Jp, Cristina Mecucci, Olivier Bernard, M Mauchauffé, Roland Berger, Willem Proesmans, P Malvaux, W Tanghe, P. Denys and P. Goddeeris. Their work appears in journals such as Blood, PubMed and Munich Personal RePEc Archive (Ludwig Maximilian University of Munich).
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.