Agnès Camuzat

6.8k total citations · 1 hit paper
47 papers, 2.9k citations indexed

About

Agnès Camuzat is a scholar working on Neurology, Physiology and Molecular Biology. According to data from OpenAlex, Agnès Camuzat has authored 47 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Neurology, 20 papers in Physiology and 16 papers in Molecular Biology. Recurrent topics in Agnès Camuzat's work include Amyotrophic Lateral Sclerosis Research (25 papers), Alzheimer's disease research and treatments (19 papers) and Parkinson's Disease Mechanisms and Treatments (16 papers). Agnès Camuzat is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (25 papers), Alzheimer's disease research and treatments (19 papers) and Parkinson's Disease Mechanisms and Treatments (16 papers). Agnès Camuzat collaborates with scholars based in France, Italy and United Kingdom. Agnès Camuzat's co-authors include Alexis Brice, Didier Hannequin, Dominique Campion, Catherine Thomas-Antérion, Bruno Dubois, Isabelle Le Ber, Serge Belliard, Françoise Clerget‐Darpoux, Alexandra Dürr and Michèle Puel and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

In The Last Decade

Agnès Camuzat

46 papers receiving 2.8k citations

Hit Papers

Early-Onset Autosomal Dom... 1999 2026 2008 2017 1999 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum
    1999 544 citations Dominique Campion, Cécile Dumanchin et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Agnès Camuzat France 29 1.3k 1.2k 955 708 671 47 2.9k
Coro Paisán‐Ruíz United States 29 1.1k 0.9× 1.9k 1.5× 741 0.8× 987 1.4× 1.3k 2.0× 37 3.1k
Mohamed H. Farah United States 21 1.5k 1.2× 587 0.5× 904 0.9× 1.0k 1.5× 616 0.9× 38 3.3k
Wu-Yen Hung United States 20 1.1k 0.9× 1.5k 1.2× 682 0.7× 697 1.0× 644 1.0× 35 3.0k
Marijke Joosse Netherlands 14 1.4k 1.1× 1.8k 1.5× 1.2k 1.3× 1.1k 1.5× 667 1.0× 16 3.9k
Sigrun Roeber Germany 23 1.1k 0.9× 1.6k 1.3× 878 0.9× 339 0.5× 715 1.1× 50 2.7k
Heather Mortiboys United Kingdom 26 1.4k 1.1× 1.2k 1.0× 671 0.7× 559 0.8× 423 0.6× 48 2.7k
Elizabeth A. Roberts United States 17 1.7k 1.3× 990 0.8× 753 0.8× 628 0.9× 435 0.6× 24 3.3k
Travis L. Unger United States 21 1.5k 1.2× 1000 0.8× 641 0.7× 531 0.8× 335 0.5× 29 3.4k
Bart Dermaut Belgium 31 1.9k 1.5× 872 0.7× 1.3k 1.4× 540 0.8× 416 0.6× 64 3.3k
Elize D. Haasdijk Netherlands 22 910 0.7× 994 0.8× 421 0.4× 405 0.6× 340 0.5× 28 2.1k

Countries citing papers authored by Agnès Camuzat

Since Specialization
Citations

This map shows the geographic impact of Agnès 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 Agnès Camuzat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Agnès Camuzat more than expected).

Fields of papers citing papers by Agnès Camuzat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Agnès 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 Agnès Camuzat. The network helps show where Agnès Camuzat may publish in the future.

Co-authorship network of co-authors of Agnès Camuzat

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

All Works

20 of 20 papers shown
1.
Becker, E., Dario Saracino, Daisy Rinaldi, et al.. (2022). Disease Progression Score Estimation From Multimodal Imaging and MicroRNA Data Using Supervised Variational Autoencoders. IEEE Journal of Biomedical and Health Informatics. 26(12). 6024–6035. 10 indexed citations
2.
Latouche, Morwena, Dario Saracino, Daisy Rinaldi, et al.. (2022). MicroRNAsignatures in genetic frontotemporal dementia and amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 9(11). 1778–1791. 9 indexed citations
3.
Querin, Giorgia, Peter Bede, Mohamed Mounir El Mendili, et al.. (2019). Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study. Annals of Neurology. 86(2). 158–167. 65 indexed citations
4.
Saracino, Dario, Fabienne Clot, Agnès Camuzat, et al.. (2018). Novel VCP mutations expand the mutational spectrum of frontotemporal dementia. Neurobiology of Aging. 72. 187.e11–187.e14. 21 indexed citations
5.
Caroppo, Paola, Agnès Camuzat, Léna Guillot‐Noël, et al.. (2016). Defining the spectrum of frontotemporal dementias associated with TARDBP mutations. Neurology Genetics. 2(3). e80–e80. 52 indexed citations
6.
Millecamps, Stéphanie, Anne de Septenville, Elisa Teyssou, et al.. (2014). Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients. Neurobiology of Aging. 35(12). 2882.e13–2882.e15. 32 indexed citations
7.
Boutoleau‐Bretonnière, Claire, Agnès Camuzat, Isabelle Le Ber, et al.. (2014). A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation. Journal of Alzheimer s Disease. 43(2). 625–630. 14 indexed citations
8.
Caroppo, Paola, Cathérine Belin, David Grabli, et al.. (2014). Posterior Cortical Atrophy as an Extreme Phenotype ofGRNMutations. JAMA Neurology. 72(2). 224–224. 12 indexed citations
9.
Chaussenot, Annabelle, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.. (2014). Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. Neurobiology of Aging. 35(12). 2884.e1–2884.e4. 68 indexed citations
10.
Lattante, Serena, et al.. (2013). 前頭側頭葉変性症および前頭側頭葉変性症‐筋萎縮性側索硬化症のフランス人患者におけるUBQLN‐2のスクリーニング. Neurobiology of Aging. 34(8). 5–2078.
11.
Ber, Isabelle Le, Gaël Nicolas, Agnès Camuzat, et al.. (2013). hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes. Neurobiology of Aging. 35(4). 934.e5–934.e6. 51 indexed citations
12.
Camuzat, Agnès, Léna Guillot‐Noël, Nathalie Guy, et al.. (2010). FUS Mutations in Frontotemporal Lobar Degeneration with Amyotrophic Lateral Sclerosis. Journal of Alzheimer s Disease. 22(3). 765–769. 75 indexed citations
13.
Warrenburg, Bart P.C. van de, Harrie Hendriks, Alexandra Dürr, et al.. (2005). Age at onset variance analysis in spinocerebellar ataxias: A study in a Dutch–French cohort. Annals of Neurology. 57(4). 505–512. 79 indexed citations
14.
Dürr, Alexandra, Agnès Camuzat, Chantal Tallaksen, et al.. (2004). Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia. Archives of Neurology. 61(12). 1867–72. 81 indexed citations
15.
Caparros-Lefèbvre, D, Nicolas Sergeant, Andrew J. Lees, et al.. (2002). Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy‐like tauopathy. Brain. 125(4). 801–811. 109 indexed citations
16.
Verpillat, Patrice, Agnès Camuzat, Didier Hannequin, et al.. (2002). Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis. European Journal of Human Genetics. 10(7). 399–405. 78 indexed citations
17.
Verpillat, Patrice, Agnès Camuzat, Didier Hannequin, et al.. (2002). Association Between the Extended tau Haplotype and Frontotemporal Dementia. Archives of Neurology. 59(6). 935–935. 74 indexed citations
18.
Campion, Dominique, Cécile Dumanchin, Didier Hannequin, et al.. (1999). Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum. The American Journal of Human Genetics. 65(3). 664–670. 544 indexed citations breakdown →
19.
Bonnet, François, Jean-Pierre Périn, Frédéric Charbonnier, et al.. (1996). Structure and Cellular Distribution of Mouse Brain Testican. Journal of Biological Chemistry. 271(8). 4373–4380. 60 indexed citations
20.
Camuzat, Agnès, Hélène Dollfus, Jean‐Michel Rozet, et al.. (1995). A gene for Leber's congenital amaurosis maps to chromosome 17p. Human Molecular Genetics. 4(8). 1447–1452. 33 indexed citations

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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