Agnès Camuzat

6.8k citations

47 papers · 2.9k indexed · 1 hit paper · h-index 29

Molecular Biology top 10%
Neurology top 1%
Physiology top 2%
Cellular and Molecular Neuroscience top 2%
Neurology top 1%

Co-authors: Alexis Brice Didier Hannequin Dominique Campion Catherine Thomas-Antérion Bruno Dubois Isabelle Le Ber Serge Belliard Françoise Clerget‐Darpoux
Topics: Amyotrophic Lateral Sclerosis Research (25 papers)Alzheimer's disease research and treatments (19 papers)Parkinson's Disease Mechanisms and Treatments (16 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Journal of Biological Chemistry Nature Genetics PLoS ONE
Partner nations: France Italy United Kingdom

In The Last Decade

Agnès Camuzat

46 papers receiving 2.8k citations

Hit Papers

align trajectories

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.

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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Disease Progression Score Estimation From Multimodal Imaging and MicroRNA Data Using Supervised Variational Autoencoders 2022 ·IEEE Journal of Biomedical and Health Informatics ·(unknown),E. Becker,Dario Saracino,Daisy Rinaldi,Agnès Camuzat,Isabelle Le Ber,Olivier Colliot	10
2	Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study 2019 ·Annals of Neurology ·Giorgia Querin,Peter Bede,Mohamed Mounir El Mendili,Menghan Li,Mélanie Pélégrini‐Issac,Daisy Rinaldi,Martin Catala,Dario Saracino,François Salachas,Agnès Camuzat,Véronique Marchand‐Pauvert,Julien Cohen‐Adad,Olivier Colliot,Isabelle Le Ber,Pierre‐François Pradat,(unknown)	65
3	A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain) 2019 ·Neurobiology of Aging ·Leire Palencia-Madrid,Raquel Sánchez‐Valle,(unknown),(unknown),Oriol Grau‐Rivera,Ramón Reñé,Isabel de la Torre Díez,(unknown),Giacomina Rossi,Paola Caroppo,Veronica Redaelli,Isabelle Le Ber,Agnès Camuzat,Alexis Brice,Anna Antonell,Mircea Balasa,Ellen Gelpí,Albert Lladó,Marian M. de Pancorbo	5
4	Novel VCP mutations expand the mutational spectrum of frontotemporal dementia 2018 ·Neurobiology of Aging ·Dario Saracino,Fabienne Clot,Agnès Camuzat,Vincent Anquetil,Didier Hannequin,Lucie Guyant‐Maréchal,Mira Didic,Léna Guillot‐Noël,Daisy Rinaldi,Morwena Latouche,Sylvie Forlani,(unknown),Cinzia Coppola,Giuseppe Di Iorio,(unknown),E. Le Guern,Alexis Brice,(unknown)	21
5	New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers 2018 ·Frontiers in Neuroscience ·Arthur Viodé,Clémence Fournier,Agnès Camuzat,François Fenaille,(unknown),Morwena Latouche,Fanny M. Elahi,(unknown),Christophe Junot,Foudil Lamari,Vincent Anquetil,(unknown)	23
6	Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients 2014 ·Neurobiology of Aging ·Stéphanie Millecamps,Anne de Septenville,Elisa Teyssou,Maïlys Daniau,Agnès Camuzat,Mélanie Albert,Éric Leguern,Daniela Galimberti,Alexis Brice,Yannick Marie,Isabelle Le Ber	32
7	A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation 2014 ·Journal of Alzheimer s Disease ·Claire Boutoleau‐Bretonnière,Agnès Camuzat,Isabelle Le Ber,(unknown),Rita Guerreiro,(unknown),(unknown),José Brás,(unknown),E. Auffray-Calvier,Amandine Pallardy,John Hardy,Alexis Brice,Pascal Derkinderen,Martine Vercelletto	14
8	Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration 2014 ·Neurogenetics ·Fabienne Clot,Anne Rovelet‐Lecrux,Foudil Lamari,(unknown),Boris Keren,Agnès Camuzat,Agnès Michon,Ludmila Jornéa,Béatrice Laudier,Anne de Septenville,Paola Caroppo,Dominique Campion,Cécile Cazeneuve,Alexis Brice,Éric Leguern,Isabelle Le Ber	7
9	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 2013 ·Neurobiology of Aging ·Serena Lattante,(unknown),Agnès Camuzat,(unknown),Edor Kabashi,(unknown)	0
10	hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes 2013 ·Neurobiology of Aging ·Isabelle Le Ber,(unknown),Gaël Nicolas,(unknown),Agnès Camuzat,David Wallon,Anne de Septenville,Morwena Latouche,Serena Lattante,Edor Kabashi,Ludmila Jornéa,Didier Hannequin,Alexis Brice	51
11	Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France 2012 ·Neurobiology of Aging ·Serena Lattante,Isabelle Le Ber,Agnès Camuzat,Alexis Brice,Edor Kabashi	21
12	FUS Mutations in Frontotemporal Lobar Degeneration with Amyotrophic Lateral Sclerosis 2010 ·Journal of Alzheimer s Disease ·(unknown),Agnès Camuzat,Léna Guillot‐Noël,Nathalie Guy,Stéphanie Millecamps,(unknown),Lucette Lacomblez,Véronique Golfier,Didier Hannequin,François Salachas,William Camu,Mira Didic,Bruno Dubois,Vincent Meininger,Isabelle Le Ber,Alexis Brice	75
13	TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration 2009 ·Annals of Neurology ·Lina Benajiba,Isabelle Le Ber,Agnès Camuzat,(unknown),Catherine Thomas-Antérion,Philippe Couratier,Solenn Legallic,François Salachas,Didier Hannequin,M. Décousus,Lucette Lacomblez,Eric Guedj,Véronique Golfier,William Camu,Bruno Dubois,Dominique Campion,Vincent Meininger,Alexis Brice	239
14	The PSP‐associated MAPT H1 subhaplotype in Guadeloupean atypical Parkinsonism 2008 ·Movement Disorders ·Agnès Camuzat,Marc Romana,Alexandra Dürr,Josué Feingold,Alexis Brice,Merle Ruberg,Annie Lannuzel	10
15	Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia 2004 ·Archives of Neurology ·Alexandra Dürr,Agnès Camuzat,(unknown),Chantal Tallaksen,Didier Hannequin,Paula Coutinho,Bertrand Fontaine,Annick Rossi,Roger Gil,Christophe Rousselle,Merle Ruberg,Giovanni Stévanin,Alexis Brice	81
16	Prevalence of Dentatorubral-Pallidoluysian Atrophy in a Large Series of White Patients With Cerebellar Ataxia 2003 ·Archives of Neurology ·Isabelle Le Ber,Agnès Camuzat,Giovanni Castelnovo,Jean‐Philippe Azulay,Pierre Genton,J L Gastaut,D Broglin,Pierre Labauge,Alexis Brice,Alexandra Dürr	34
17	Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy‐like tauopathy 2002 ·Brain ·D Caparros-Lefèbvre,Nicolas Sergeant,Andrew J. Lees,Agnès Camuzat,Susan E. Daniel,Annie Lannuzel,Alexis Brice,Eduardo Tolosa,André Delacourte,Charles Duyckaerts	109
18	Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrumbreakdown → 1999 ·The American Journal of Human Genetics ·Dominique Campion,Cécile Dumanchin,Didier Hannequin,Bruno Dubois,Serge Belliard,Michèle Puel,Catherine Thomas-Antérion,Agnès Michon,Cosette Martin,Françoise Charbonnier,Grégory Raux,Agnès Camuzat,Christiane Penet,Valérie Mesnage,María Martínez,Françoise Clerget‐Darpoux,Alexis Brice,Thierry Frébourg	544
19	Structure and Cellular Distribution of Mouse Brain Testican 1996 ·Journal of Biological Chemistry ·François Bonnet,Jean-Pierre Périn,Frédéric Charbonnier,Agnès Camuzat,G. Roussel,Jean‐Louis Nussbaum,Patrick M. Alliel	60
20	Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis 1996 ·Nature Genetics ·Isabelle Perrault,Jean‐Michel Rozet,Patrick Calvas,S. Gerber,Agnès Camuzat,Hélène Dollfus,Sophie Châtelin,Eric H. Souied,(unknown),Corinne Leowski,(unknown),Denis Le Paslier,J Frézal,Jean‐Louis Dufier,Steven J. Pittler,Arnold Munnich,Josseline Kaplan	353

About Agnès Camuzat

Agnès Camuzat is a scholar working on Neurology, Neurology and Genetics, having authored 47 papers that have together received 2.9k indexed citations. Recurring topics across this 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). The work is most often cited by research in Neurology (1.2k citations), Neurology (671 citations) and Cellular and Molecular Neuroscience (708 citations). Agnès Camuzat has collaborated with scholars based in France, Italy and United Kingdom. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

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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