Erik Huys
- Genetics top 1%
- Molecular Biology top 10%
- Genetics top 2%
- Pulmonary and Respiratory Medicine top 10%
- Plant Science top 10%
- Co-authors
- Eric SchoenmakersAd Geurts van KesselIrene M. JanssenJoris A. VeltmanBert B.A. de VriesHan G. BrunnerLisenka E.L.M. VissersR.J.C. Admiraal
- Topics
- Cancer Genomics and Diagnostics (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Acute Myeloid Leukemia Research (4 papers)
- Partner nations
- NetherlandsBelgiumUnited States
In The Last Decade
Erik Huys
20 papers receiving 1.9k citations
Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 1.2k
- Molecular Biology 808
- Genetics 496
- Pulmonary and Respiratory Medicine 344
- Plant Science 340
Countries citing papers authored by Erik Huys
This map shows the geographic impact of Erik Huys'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 Erik Huys with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erik Huys more than expected).
Fields of papers citing papers by Erik Huys
This network shows the impact of papers produced by Erik Huys. 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 Erik Huys. The network helps show where Erik Huys may publish in the future.
Co-authorship network of co-authors of Erik Huys
This figure shows the co-authorship network connecting the top 25 collaborators of Erik Huys. A scholar is included among the top collaborators of Erik Huys 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 Erik Huys. Erik Huys 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 | 1 | |
| 3 | 3 | |
| 4 | 25 | |
| 5 | 11 | |
| 6 | 9 | |
| 7 | 27 | |
| 8 | 14 | |
| 9 | 7 | |
| 10 | 37 | |
| 11 | 12 | |
| 12 | 3 | |
| 13 | 413 | |
| 14 | Mutations in a new member of the chromodomain gene family cause CHARGE syndromebreakdown → | 876 |
| 15 | 348 | |
| 16 | 83 | |
| 17 | 1 | |
| 18 | 10 | |
| 19 | 32 | |
| 20 | Selection of CD34-positive cells using immunomagnetic beads results in more than 15 log reduction of malignant cells in myeloma PBC autografts | 1 |
About Erik Huys
Erik Huys is a scholar working on Genetics, Hematology and Obstetrics and Gynecology, having authored 20 papers that have together received 1.9k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Acute Myeloid Leukemia Research (4 papers). The work is most often cited by research in Genetics (496 citations), Genetics (1.2k citations) and Pediatrics, Perinatology and Child Health (293 citations). Erik Huys has collaborated with scholars based in Netherlands, Belgium and United States. Frequent co-authors include Eric Schoenmakers, Ad Geurts van Kessel, Irene M. Janssen, Joris A. Veltman, Bert B.A. de Vries, Han G. Brunner, Lisenka E.L.M. Vissers, R.J.C. Admiraal, Conny M.A. van Ravenswaaij and Ben C.J. Hamel. Their work appears in journals such as Nature Genetics, Blood and The American 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.