Els Voorhoeve
- Co-authors
- Egbert BakkerChristine Van BroeckhovenBlas FrangioneM. D. CarmanEfrat LevyIvan LieberburgJ. HaanWim Van Hul
- Topics
- Genomic variations and chromosomal abnormalities (4 papers)Genomics and Rare Diseases (3 papers)Prenatal Screening and Diagnostics (3 papers)
- Cited by
- PhysiologyNeurologyGenetics
- Partner nations
- NetherlandsBelgiumUnited States
In The Last Decade
Els Voorhoeve
12 papers receiving 251 citations
Peers
Comparison fields: 5 of 53
- Molecular Biology 146
- Physiology 98
- Genetics 68
- Neurology 46
- Pediatrics, Perinatology and Child Health 39
Countries citing papers authored by Els Voorhoeve
This map shows the geographic impact of Els Voorhoeve'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 Els Voorhoeve with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Els Voorhoeve more than expected).
Fields of papers citing papers by Els Voorhoeve
This network shows the impact of papers produced by Els Voorhoeve. 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 Els Voorhoeve. The network helps show where Els Voorhoeve may publish in the future.
Co-authorship network of co-authors of Els Voorhoeve
This figure shows the co-authorship network connecting the top 25 collaborators of Els Voorhoeve. A scholar is included among the top collaborators of Els Voorhoeve 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 Els Voorhoeve. Els Voorhoeve is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 25 | |
| 3 | 12 | |
| 4 | 1 | |
| 5 | 22 | |
| 6 | 8 | |
| 7 | 22 | |
| 8 | 36 | |
| 9 | 16 | |
| 10 | 42 | |
| 11 | FINE MAPPING OF KERATOSIS SPINULOSA DECALVANS (KFSD) IN XP22 | 1 |
| 12 | DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type) | 66 |
About Els Voorhoeve
Els Voorhoeve is a scholar working on Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 257 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Physiology (98 citations), Neurology (46 citations) and Genetics (68 citations). Els Voorhoeve has collaborated with scholars based in Netherlands, Belgium and United States. Frequent co-authors include Egbert Bakker, Christine Van Broeckhoven, Blas Frangione, M. D. Carman, Efrat Levy, Ivan Lieberburg, J. Haan, Wim Van Hul, G J van Ommen and Raymund A.C. Roos. Their work appears in journals such as Annals of Neurology, Journal of Medical Genetics and European Journal of Human Genetics.
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.