L. Van Laer
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Neurology top 5%
- Vestibular and auditory disorders
Papers in
-
- Hearing, Cochlea, Tinnitus, Genetics 13
-
- Vestibular and auditory disorders 6
- Co-authors
- Guy Van Camp (15 shared papers)Els Van Eyken (5 shared papers)Paul Van de Heyning (7 shared papers)Richard J. Smith (6 shared papers)Erik Fransén (6 shared papers)Ann Vandevelde (3 shared papers)Vedat Topsakal (2 shared papers)S. D. Smith (2 shared papers)
- Journals
- Mitochondrion (2 papers)Journal of Medical Genetics (2 papers)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
L. Van Laer
17 papers receiving 792 citations
Peers
Comparison fields: 5 of 78
- Sensory Systems 629
- Neurology 260
- Otorhinolaryngology 83
- Speech and Hearing 112
- Cognitive Neuroscience 316
Countries citing papers authored by L. Van Laer
This map shows the geographic impact of L. Van Laer'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 L. Van Laer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L. Van Laer more than expected).
Fields of papers citing papers by L. Van Laer
This network shows the impact of papers produced by L. Van Laer. 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 L. Van Laer. The network helps show where L. Van Laer may publish in the future.
Co-authors
The 25 scholars most cited alongside L. Van Laer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 220 | |
| 2 | 2001 | 152 | |
| 3 | 1995 | 79 | |
| 4 | 2006 | 74 | |
| 5 | 2009 | 64 | |
| 6 | 2004 | 51 | |
| 7 | A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. | 1997 | 45 |
| 8 | 1997 | 36 | |
| 9 | Prevalence of tinnitus and audiometric shape. | 2007 | 35 |
| 10 | 1997 | 19 | |
| 11 | 2010 | 10 | |
| 12 | 2011 | 7 | |
| 13 | 2011 | 6 | |
| 14 | 2009 | 5 | |
| 15 | 2007 | 3 | |
| 16 | 1999 | 3 | |
| 17 | 2000 | 2 |
About L. Van Laer
L. Van Laer is a scholar working on Sensory Systems, Neurology, Molecular Biology, Cognitive Neuroscience and Speech and Hearing, having authored 17 papers that have together received 811 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (6 papers), Hearing Loss and Rehabilitation (4 papers), Connexins and lens biology (2 papers), Noise Effects and Management (2 papers), Mitochondrial Function and Pathology (2 papers), Metabolism and Genetic Disorders (1 paper) and Neuroscience of respiration and sleep (1 paper). The work is most often cited by research in Sensory Systems (629 citations), Neurology (260 citations), Otorhinolaryngology (83 citations), Speech and Hearing (112 citations) and Cognitive Neuroscience (316 citations). L. Van Laer has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Guy Van Camp, Els Van Eyken, Paul Van de Heyning, Richard J. Smith, Erik Fransén, Ann Vandevelde, Vedat Topsakal, S. D. Smith, Wendy Balemans and Matthew Brown. Their work appears in journals such as Mitochondrion, Journal of Medical Genetics, Human Mutation, The American Journal of Human Genetics and Annals 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.