Marie‐Céline Fleury

1.4k total citations
21 papers, 498 citations indexed

About

Marie‐Céline Fleury is a scholar working on Neurology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marie‐Céline Fleury has authored 21 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 7 papers in Pathology and Forensic Medicine and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marie‐Céline Fleury's work include Multiple Sclerosis Research Studies (6 papers), Genetic Neurodegenerative Diseases (5 papers) and Peripheral Neuropathies and Disorders (4 papers). Marie‐Céline Fleury is often cited by papers focused on Multiple Sclerosis Research Studies (6 papers), Genetic Neurodegenerative Diseases (5 papers) and Peripheral Neuropathies and Disorders (4 papers). Marie‐Céline Fleury collaborates with scholars based in France, United States and Canada. Marie‐Céline Fleury's co-authors include Christine Tranchant, J. de Sèze, Frédéric Blanc, Patrick Vermersch, Michel Kœnig, Nicolas Collongues, Hélène Zéphir, Mathieu Anheim, J Warter and Dominique Stoppa‐Lyonnet and has published in prestigious journals such as PLoS ONE, Neurology and Movement Disorders.

In The Last Decade

Marie‐Céline Fleury

20 papers receiving 493 citations

Peers

Marie‐Céline Fleury

CMN

NEURO

PFM

ONCOL

M Craner United Kingdom

Philippe Rondot France

Takayasu Fukudome Japan

Katy Malpass United Kingdom

Sam Horng United States

Sylvain Perriot Switzerland

Ellen Knierim Germany

Sana Eltayeb Sweden

Kunihiro Mizuta Japan

Mondira Kundu United States

M Craner United Kingdom

Marie‐Céline Fleury

97 ×0.4

88 ×0.4

CMN

82 ×0.5

NEURO

220 ×1.4

PFM

139 ×1.5

ONCOL

Citations per year, relative to Marie‐Céline Fleury Marie‐Céline Fleury (= 1×) peers M Craner

Countries citing papers authored by Marie‐Céline Fleury

Since Specialization

Citations

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

Fields of papers citing papers by Marie‐Céline Fleury

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie‐Céline Fleury. 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 Marie‐Céline Fleury. The network helps show where Marie‐Céline Fleury may publish in the future.

Co-authorship network of co-authors of Marie‐Céline Fleury

This figure shows the co-authorship network connecting the top 25 collaborators of Marie‐Céline Fleury. A scholar is included among the top collaborators of Marie‐Céline Fleury 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 Marie‐Céline Fleury. Marie‐Céline Fleury 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

Wirth, Thomas, Céline Bonnet, David Pellerin, et al.. (2024). Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?. Journal of Neurology. 271(4). 2078–2085. 8 indexed citations

Corcia, Philippe, Patrick Vourc’h, E Bernard, et al.. (2023). French National Protocol for genetic of amyotrophic lateral sclerosis. Revue Neurologique. 179(9). 1020–1029. 1 indexed citations

Wirth, Thomas, Céline Bonnet, Jean‐Baptiste Chanson, et al.. (2023). Natural History and Phenotypic Spectrum of GAA‐FGF14 Sporadic Late‐Onset Cerebellar Ataxia (SCA27B). Movement Disorders. 38(10). 1950–1956. 25 indexed citations

Bigaut, Kévin, Laurent Kremer, Thibaut Fabacher, et al.. (2021). Impact of Disease-Modifying Treatments of Multiple Sclerosis on Anti–SARS-CoV-2 Antibodies. Neurology Neuroimmunology & Neuroinflammation. 8(5). 23 indexed citations

Amador, Maria del Mar, François Muratet, Elisa Teyssou, et al.. (2019). Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS. Neurology Genetics. 5(6). e374–e374. 15 indexed citations

Caroppo, Paola, Agnès Camuzat, Anne de Septenville, et al.. (2015). Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 1(4). 481–486. 30 indexed citations

Henriques, Alexandre, Hélène Blasco, Marie‐Céline Fleury, et al.. (2015). Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis. PLoS ONE. 10(7). e0131512–e0131512. 26 indexed citations

Outteryck, Olivier, Hélène Zéphir, Julia Salleron, et al.. (2013). JC-virus seroconversion in multiple sclerosis patients receiving natalizumab. Multiple Sclerosis Journal. 20(7). 822–829. 54 indexed citations

Fleury, Marie‐Céline, et al.. (2013). Therapeutic Decision after JC Virus Testing in a Cohort of Patient Treated with Natalizumab (P01.184). Neurology. 80(7_supplement). 1 indexed citations

10.

Collongues, Nicolas, Hélène Zéphir, Laurent Ballonzoli, et al.. (2013). Longitudinal follow-up of vision in a neuromyelitis optica cohort. Multiple Sclerosis Journal. 19(10). 1320–1322. 19 indexed citations

11.

Outteryck, Olivier, Alain Duhamel, Hélène Zéphir, et al.. (2012). Anti-JCV antibody prevalence in a French cohort of MS patients under natalizumab therapy. Journal of Neurology. 259(11). 2293–2298. 28 indexed citations

12.

Blanc, Frédéric, et al.. (2012). Méningiome et neuropathie optique : un piège diagnostique. Journal Français d Ophtalmologie. 36(3). 221–229. 3 indexed citations

13.

Melin, Anna, Olivier Outteryck, Nicolas Collongues, et al.. (2011). Effect of natalizumab on clinical and radiological disease activity in a French cohort of patients with relapsing-remitting multiple sclerosis. Journal of Neurology. 259(6). 1215–1221. 19 indexed citations

14.

Anheim, Mathieu, Marie‐Céline Fleury, B. Monga, et al.. (2009). Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management. Neurogenetics. 11(1). 1–12. 103 indexed citations

15.

Blanc, Frédéric, Fabrice Berna, Marie‐Céline Fleury, et al.. (2009). Évènements psychotiques inauguraux de sclérose en plaques ?. Revue Neurologique. 166(1). 39–48. 12 indexed citations

16.

Anheim, Mathieu, Marie‐Céline Fleury, J. Franques, et al.. (2008). Clinical and Molecular Findings of Ataxia With Oculomotor Apraxia Type 2 in 4 Families. Archives of Neurology. 65(7). 958–62. 26 indexed citations

17.

Sèze, J. de, Carl Arndt, L. Jeanjean, et al.. (2008). RELAPSING INFLAMMATORY OPTICNEURITIS: IS IT NEUROMYELITIS OPTICA?. Neurology. 70(22). 2075–2076. 37 indexed citations

18.

Fleury, Marie‐Céline, et al.. (2008). Progressive hemianopsia caused by intracranial enchondroma in Ollier disease. Neurology. 71(24). 2018–2018. 2 indexed citations

19.

Blanc, Frédéric, et al.. (2005). Le syndrome de Vogt-Koyanagi-Harada. Revue Neurologique. 161(11). 1079–1090. 7 indexed citations

20.

Tranchant, Christine, et al.. (2003). Phenotypic variability of aprataxin gene mutations. Neurology. 60(5). 868–870. 58 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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