A. Camuzat

1.5k total citations
12 papers, 598 citations indexed

About

A. Camuzat is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, A. Camuzat has authored 12 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in A. Camuzat's work include Genetic Neurodegenerative Diseases (4 papers), Neurological diseases and metabolism (2 papers) and Retinal Development and Disorders (2 papers). A. Camuzat is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Neurological diseases and metabolism (2 papers) and Retinal Development and Disorders (2 papers). A. Camuzat collaborates with scholars based in France, India and United States. A. Camuzat's co-authors include Alexis Brice, Giovanni Stévanin, Dominique Campion, Didier Hannequin, A. Dürr, Cosette Martin, Thierry Frébourg, Pascale Saugier-Véber, Patrice Verpillat and Bruno Dubois and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

A. Camuzat

11 papers receiving 584 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
A. Camuzat France 9 351 299 274 171 99 12 598
Maureen Gatherer United Kingdom 12 164 0.5× 176 0.6× 169 0.6× 206 1.2× 127 1.3× 22 531
Mustafa Batbayli Denmark 9 235 0.7× 76 0.3× 129 0.5× 125 0.7× 49 0.5× 10 411
Viviana Pensato Italy 12 182 0.5× 176 0.6× 280 1.0× 85 0.5× 149 1.5× 26 530
Johanne Bertrand Canada 7 267 0.8× 317 1.1× 32 0.1× 162 0.9× 64 0.6× 10 528
Jimena Baleriola Spain 10 291 0.8× 140 0.5× 45 0.2× 152 0.9× 90 0.9× 18 551
Kenji Sakagami Japan 11 246 0.7× 116 0.4× 69 0.3× 72 0.4× 103 1.0× 22 521
Kotaro Endo Japan 8 400 1.1× 577 1.9× 465 1.7× 78 0.5× 70 0.7× 16 862
Seung‐Pil Yang Canada 8 200 0.6× 73 0.2× 88 0.3× 114 0.7× 92 0.9× 10 396
Michael Niblock United Kingdom 7 225 0.6× 74 0.2× 80 0.3× 110 0.6× 26 0.3× 7 324
Esteban Luna United States 7 186 0.5× 155 0.5× 262 1.0× 129 0.8× 55 0.6× 7 458

Countries citing papers authored by A. Camuzat

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of A. Camuzat

This figure shows the co-authorship network connecting the top 25 collaborators of A. Camuzat. A scholar is included among the top collaborators of A. Camuzat 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 A. Camuzat. A. Camuzat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Charles, Perrine, A. Camuzat, N. Benammar, et al.. (2007). Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?. Neurology. 69(21). 1970–1975. 110 indexed citations
2.
Ber, Isabelle Le, F. Clot, Laurent Vercueil, et al.. (2006). Predominant dystonia with marked cerebellar atrophy. Neurology. 67(10). 1769–1773. 60 indexed citations
3.
Martinaud, Olivier, A. Laquérrière, Lucie Guyant‐Maréchal, et al.. (2005). Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. Acta Neuropathologica. 110(1). 84–92. 18 indexed citations
4.
Stévanin, Giovanni, A. Camuzat, Susan E. Holmes, et al.. (2002). CAG/CTG repeat expansions at the Huntington’s disease–like 2 locus are rare in Huntington’s disease patients. Neurology. 58(6). 965–967. 38 indexed citations
5.
Fujigasaki, Hiroto, Ishwar C. Verma, A. Camuzat, et al.. (2001). SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family. Annals of Neurology. 49(1). 117–121. 72 indexed citations
6.
Dumanchin, Cécile, A. Camuzat, Dominique Campion, et al.. (1998). Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism. Human Molecular Genetics. 7(11). 1825–1829. 184 indexed citations
7.
Charbonnier, Frédéric, J.-P. Périn, Marie‐Geneviève Mattéi, et al.. (1998). Genomic Organization of the Human SPOCK Gene and Its Chromosomal Localization to 5q31. Genomics. 48(3). 377–380. 28 indexed citations
8.
Camuzat, A., Jean‐Michel Rozet, Hélène Dollfus, et al.. (1996). Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13. Human Genetics. 97(6). 798–801. 35 indexed citations
9.
Kaplan, Josseline, A. Camuzat, Hélène Dollfus, et al.. (1995). 3235 A gene for Leber's congenital amaurosis maps to chromosome 17p. Vision Research. 35. S132–S132. 1 indexed citations
10.
Gerber, S., Jean‐Michel Rozet, Dominique Bonneau, et al.. (1995). A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.. PubMed. 56(2). 396–9. 50 indexed citations
11.
Souied, Eric, S. Gerber, Jean‐Michel Rozet, et al.. (1995). P 367 Two novel missense mutations of peripherin/RDS gene in autosomal dominant retinitis pigmentosa (ADRP), in pedigrees from France. Vision Research. 35. S221–S221. 2 indexed citations
12.
Kaplan, Josseline, Jean‐Michel Rozet, S. Gerber, et al.. (1995). Des gènes pour les dystrophies rétiniennes des enfants. médecine/sciences. 11(3). 325–325.

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.

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