Geert Vandeweyer
- Co-authors
- R. Frank KooyNathalie Van der AaEdwin ReyniersGeert MortierLut Van LaerBart LoeysLiesbeth RoomsWim Wuyts
- Topics
- Genomic variations and chromosomal abnormalities (14 papers)Genetics and Neurodevelopmental Disorders (14 papers)Genomics and Rare Diseases (13 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Geert Vandeweyer
46 papers receiving 947 citations
Peers
Comparison fields: 5 of 95
- Molecular Biology 496
- Genetics 414
- Oncology 93
- Epidemiology 92
- Pulmonary and Respiratory Medicine 90
Countries citing papers authored by Geert Vandeweyer
This map shows the geographic impact of Geert Vandeweyer'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 Geert Vandeweyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Geert Vandeweyer more than expected).
Fields of papers citing papers by Geert Vandeweyer
This network shows the impact of papers produced by Geert Vandeweyer. 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 Geert Vandeweyer. The network helps show where Geert Vandeweyer may publish in the future.
Co-authorship network of co-authors of Geert Vandeweyer
This figure shows the co-authorship network connecting the top 25 collaborators of Geert Vandeweyer. A scholar is included among the top collaborators of Geert Vandeweyer 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 Geert Vandeweyer. Geert Vandeweyer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 3 | |
| 3 | 2 | |
| 4 | 12 | |
| 5 | 1 | |
| 6 | 47 | |
| 7 | 5 | |
| 8 | 6 | |
| 9 | 15 | |
| 10 | 17 | |
| 11 | 9 | |
| 12 | ADNP-Related Intellectual Disability and Autism Spectrum Disorder | 2 |
| 13 | 78 | |
| 14 | 29 | |
| 15 | 90 | |
| 16 | 20 | |
| 17 | 3 | |
| 18 | 12 | |
| 19 | 55 | |
| 20 | 20 |
About Geert Vandeweyer
Geert Vandeweyer is a scholar working on Genetics, Developmental Neuroscience and Otorhinolaryngology, having authored 48 papers that have together received 980 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Genomics and Rare Diseases (13 papers). The work is most often cited by research in Genetics (414 citations), Sensory Systems (65 citations) and Otorhinolaryngology (34 citations). Geert Vandeweyer has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include R. Frank Kooy, Nathalie Van der Aa, Edwin Reyniers, Geert Mortier, Lut Van Laer, Bart Loeys, Liesbeth Rooms, Wim Wuyts, Céline Helsmoortel and Guy Van Camp. Their work appears in journals such as Bioinformatics, PLoS ONE and Scientific Reports.
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.