Guy Van Camp
Impact in
- Sensory Systems top 0.01%
- Hearing, Cochlea, Tinnitus, Genetics
- Otorhinolaryngology top 0.5%
- Ear Surgery and Otitis Media
Papers in
- Sensory Systems 242
- Hearing, Cochlea, Tinnitus, Genetics 242
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- Ear Surgery and Otitis Media 34
- Co-authors
- Richard J. Smith (63 shared papers)Lut Van Laer (49 shared papers)Erik Fransén (86 shared papers)Ken Op de Beeck (66 shared papers)Paul Van de Heyning (48 shared papers)Patrick J. Willems (27 shared papers)Nele Hilgert (12 shared papers)Cor W. R. J. Cremers (45 shared papers)
- Journals
- European Journal of Human Genetics (21 papers)The American Journal of Human Genetics (18 papers)Journal of Medical Genetics (17 papers)Human Genetics (16 papers)Otology & Neurotology (15 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Guy Van Camp
432 papers receiving 19.1k citations
Guy Van Camp's Hit Papers
Peers
Comparison fields: 5 of 161
- Sensory Systems 10.5k
- Otorhinolaryngology 973
- Neurology 510
- Genetics 1.8k
- Genetics 519
Countries citing papers authored by Guy Van Camp
This map shows the geographic impact of Guy Van Camp'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 Guy Van Camp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Guy Van Camp more than expected).
Fields of papers citing papers by Guy Van Camp
This network shows the impact of papers produced by Guy Van Camp. 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 Guy Van Camp. The network helps show where Guy Van Camp may publish in the future.
Co-authors
The 25 scholars most cited alongside Guy Van Camp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 440 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma Hit paper breakdown → | 2018 | 549 |
| 2 | 1998 | 471 | |
| 3 | 2005 | 451 | |
| 4 | 2008 | 385 | |
| 5 | Congenital hearing loss Hit paper breakdown → | 2017 | 379 |
| 6 | 1998 | 331 | |
| 7 | Nonsyndromic hearing impairment: unparalleled heterogeneity. | 1997 | 295 |
| 8 | 1998 | 284 | |
| 9 | 2005 | 272 | |
| 10 | 2006 | 268 | |
| 11 | 2003 | 254 | |
| 12 | 1999 | 252 | |
| 13 | 2007 | 241 | |
| 14 | 2008 | 228 | |
| 15 | 1998 | 219 | |
| 16 | 1999 | 212 | |
| 17 | 1995 | 192 | |
| 18 | 2017 | 184 | |
| 19 | 2004 | 177 | |
| 20 | The hereditary hearing loss homepage | 1997 | 170 |
About Guy Van Camp
Guy Van Camp is a scholar working on Sensory Systems, Otorhinolaryngology, Genetics, Molecular Biology and Oncology, having authored 440 papers that have together received 19.8k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (242 papers), Ear Surgery and Otitis Media (34 papers), Epigenetics and DNA Methylation (20 papers), Genomics and Rare Diseases (13 papers), Vestibular and auditory disorders (10 papers), Colorectal Cancer Treatments and Studies (10 papers), Genetic Associations and Epidemiology (10 papers) and Hearing Loss and Rehabilitation (9 papers). The work is most often cited by research in Sensory Systems (10.5k citations), Otorhinolaryngology (973 citations), Neurology (510 citations), Genetics (1.8k citations) and Genetics (519 citations). Guy Van Camp has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Richard J. Smith, Lut Van Laer, Erik Fransén, Ken Op de Beeck, Paul Van de Heyning, Patrick J. Willems, Nele Hilgert, Cor W. R. J. Cremers, Paul J. Coucke and Marc Peeters. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Medical Genetics, Human Genetics and Otology & Neurotology.
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.