K. Verhoeven
- Cellular and Molecular Neuroscience top 5%
- Molecular Biology
- Neurology top 5%
- Sensory Systems top 5%
- Cell Biology
- Co-authors
- Guy Van CampVincent TimmermanPeter De JongheIsabelle SchattemanP J WillemsMargriet VerstrekenEls De VriendtMichaela Auer‐Grumbach
- Topics
- Hereditary Neurological Disorders (5 papers)Hearing, Cochlea, Tinnitus, Genetics (4 papers)Neurological diseases and metabolism (3 papers)
- Journals
- BrainNeurologyHuman Genetics
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
K. Verhoeven
13 papers receiving 572 citations
Peers
Comparison fields: 5 of 56
- Cellular and Molecular Neuroscience 319
- Molecular Biology 265
- Neurology 204
- Sensory Systems 131
- Cell Biology 102
Countries citing papers authored by K. Verhoeven
This map shows the geographic impact of K. Verhoeven'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 K. Verhoeven with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Verhoeven more than expected).
Fields of papers citing papers by K. Verhoeven
This network shows the impact of papers produced by K. Verhoeven. 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 K. Verhoeven. The network helps show where K. Verhoeven may publish in the future.
Co-authorship network of co-authors of K. Verhoeven
This figure shows the co-authorship network connecting the top 25 collaborators of K. Verhoeven. A scholar is included among the top collaborators of K. Verhoeven 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 K. Verhoeven. K. Verhoeven is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 62 | |
| 3 | 303 | |
| 4 | Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal Charcot-Marie-Tooth neuropathy | 1 |
| 5 | 33 | |
| 6 | 3 | |
| 7 | Audiometric analysis of a Belgian family linked to the DFNA10 locus. | 15 |
| 8 | 2 | |
| 9 | 38 | |
| 10 | 49 | |
| 11 | A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss. | 26 |
| 12 | A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. | 45 |
| 13 | Early onset maternal inherited hearing loss with late onset neurological symptoms present in a three generation Dutch family. | 2 |
About K. Verhoeven
K. Verhoeven is a scholar working on Sensory Systems, Neurology and Cellular and Molecular Neuroscience, having authored 13 papers that have together received 582 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers) and Neurological diseases and metabolism (3 papers). The work is most often cited by research in Sensory Systems (131 citations), Neurology (204 citations) and Cellular and Molecular Neuroscience (319 citations). K. Verhoeven has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Guy Van Camp, Vincent Timmerman, Peter De Jonghe, Isabelle Schatteman, P J Willems, Margriet Verstreken, Els De Vriendt, Michaela Auer‐Grumbach, F.E. Offeciers and E. Borg. Their work appears in journals such as Brain, Neurology and 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.