Jurgen Del‐Favero
- Molecular Biology top 5%
- Genetics top 1%
- Psychiatry and Mental health top 0.5%
- Cellular and Molecular Neuroscience top 1%
- Physiology top 5%
- Co-authors
- Christine Van BroeckhovenPeter De JongheLieve ClaesBerten CeulemansLieven LagaePeter De RijkStephan ClaesD. Goossens
- Topics
- Genetics and Neurodevelopmental Disorders (23 papers)Genomic variations and chromosomal abnormalities (18 papers)Genomics and Rare Diseases (15 papers)
- Partner nations
- BelgiumSwedenUnited States
In The Last Decade
Jurgen Del‐Favero
140 papers receiving 6.6k citations
Hit Papers
Peers
Comparison fields: 5 of 148
- Molecular Biology 2.5k
- Genetics 1.7k
- Psychiatry and Mental health 1.5k
- Cellular and Molecular Neuroscience 1.4k
- Physiology 664
Countries citing papers authored by Jurgen Del‐Favero
This map shows the geographic impact of Jurgen Del‐Favero'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 Jurgen Del‐Favero with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jurgen Del‐Favero more than expected).
Fields of papers citing papers by Jurgen Del‐Favero
This network shows the impact of papers produced by Jurgen Del‐Favero. 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 Jurgen Del‐Favero. The network helps show where Jurgen Del‐Favero may publish in the future.
Co-authorship network of co-authors of Jurgen Del‐Favero
This figure shows the co-authorship network connecting the top 25 collaborators of Jurgen Del‐Favero. A scholar is included among the top collaborators of Jurgen Del‐Favero 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 Jurgen Del‐Favero. Jurgen Del‐Favero is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 11 | |
| 2 | 58 | |
| 3 | 4 | |
| 4 | 5 | |
| 5 | 139 | |
| 6 | 53 | |
| 7 | 21 | |
| 8 | 72 | |
| 9 | Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS | 3 |
| 10 | 34 | |
| 11 | 50 | |
| 12 | 2 | |
| 13 | 88 | |
| 14 | 22 | |
| 15 | 214 | |
| 16 | 126 | |
| 17 | Heritability and genetics of personality in healthy families and families with affective disorders from Sweden | 1 |
| 18 | De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancybreakdown → | 916 |
| 19 | No CAG or CCG repeats within 18Q2133-q23 involved in bipolar disorder | 1 |
| 20 | Manic depressive disorder and chromosome 18 | 4 |
About Jurgen Del‐Favero
Jurgen Del‐Favero is a scholar working on Behavioral Neuroscience, Biological Psychiatry and Genetics, having authored 141 papers that have together received 6.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (18 papers) and Genomics and Rare Diseases (15 papers). The work is most often cited by research in Biological Psychiatry (379 citations), Behavioral Neuroscience (456 citations) and Psychiatry and Mental health (1.5k citations). Jurgen Del‐Favero has collaborated with scholars based in Belgium, Sweden and United States. Frequent co-authors include Christine Van Broeckhoven, Peter De Jonghe, Lieve Claes, Berten Ceulemans, Lieven Lagae, Peter De Rijk, Stephan Claes, D. Goossens, Cornelia M. van Duijn and Rolf Adolfsson. Their work appears in journals such as New England Journal of Medicine, Nucleic Acids Research and Journal of Biological Chemistry.
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.