A. Camuzat
Impact in
- Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
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- Genetic Neurodegenerative Diseases
Papers in
-
- Retinal Development and Disorders 2
-
- Genetic Neurodegenerative Diseases 3
- Co-authors
- Alexis Brice (5 shared papers)Didier Hannequin (3 shared papers)Giovanni Stévanin (3 shared papers)Dominique Campion (2 shared papers)A. Dürr (2 shared papers)Isabelle Le Ber (2 shared papers)Pascale Saugier-Véber (1 shared paper)F. Charbonnier (1 shared paper)
- Journals
- Neurology (3 papers)Vision Research (2 papers)Human Genetics (1 paper)Genomics (1 paper)Acta Neuropathologica (1 paper)
- Partner nations
- France
In The Last Decade
A. Camuzat
11 papers receiving 579 citations
Peers
Comparison fields: 5 of 45
- Neurology 258
- Cellular and Molecular Neuroscience 240
- Neurology 80
- Physiology 165
- Ophthalmology 41
Countries citing papers authored by A. Camuzat
This map shows the geographic impact of A. Camuzat'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 A. Camuzat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Camuzat more than expected).
Fields of papers citing papers by A. Camuzat
This network shows the impact of papers produced by A. Camuzat. 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 A. Camuzat. The network helps show where A. Camuzat may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Camuzat, 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 | 1998 | 185 | |
| 2 | 2007 | 116 | |
| 3 | 2006 | 60 | |
| 4 | 2005 | 58 | |
| 5 | A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13. | 1995 | 50 |
| 6 | 2002 | 38 | |
| 7 | 1996 | 35 | |
| 8 | 1998 | 28 | |
| 9 | 2005 | 18 | |
| 10 | 1995 | 2 | |
| 11 | 1995 | 1 | |
| 12 | 1995 | 0 |
About A. Camuzat
A. Camuzat is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Ophthalmology, Neurology and Physiology, having authored 12 papers that have together received 591 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (3 papers), Alzheimer's disease research and treatments (2 papers), Retinal Diseases and Treatments (2 papers), Retinal Development and Disorders (2 papers), Neurological diseases and metabolism (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Amyotrophic Lateral Sclerosis Research (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Neurology (258 citations), Cellular and Molecular Neuroscience (240 citations), Neurology (80 citations), Physiology (165 citations) and Ophthalmology (41 citations). A. Camuzat has collaborated with scholars based in France. Frequent co-authors include Alexis Brice, Didier Hannequin, Giovanni Stévanin, Dominique Campion, A. Dürr, Isabelle Le Ber, Pascale Saugier-Véber, F. Charbonnier, Bruno Dubois and Patrice Verpillat. Their work appears in journals such as Neurology, Vision Research, Human Genetics, Genomics and Acta Neuropathologica.
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.