Fabienne Clot

2.9k total citations
27 papers, 1.1k citations indexed

About

Fabienne Clot is a scholar working on Neurology, Physiology and Gastroenterology. According to data from OpenAlex, Fabienne Clot has authored 27 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 9 papers in Physiology and 7 papers in Gastroenterology. Recurrent topics in Fabienne Clot's work include Parkinson's Disease Mechanisms and Treatments (13 papers), Amyotrophic Lateral Sclerosis Research (11 papers) and Alzheimer's disease research and treatments (7 papers). Fabienne Clot is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (13 papers), Amyotrophic Lateral Sclerosis Research (11 papers) and Alzheimer's disease research and treatments (7 papers). Fabienne Clot collaborates with scholars based in France, Italy and Tunisia. Fabienne Clot's co-authors include Luigi Greco, Kati Karell, A.S. Louka, Jukka Partanen, Henry Ascher, Paul J. Ciclitira, Ludvig M. Sollid, Simon Moodie, Marie Vidailhet and Emmanuel Roze and has published in prestigious journals such as SLEEP, Neurobiology of Aging and Movement Disorders.

In The Last Decade

Fabienne Clot

27 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabienne Clot France 14 511 389 379 262 158 27 1.1k
Mary Ambler United States 18 68 0.1× 113 0.3× 161 0.4× 123 0.5× 113 0.7× 34 984
JuliaM. Polak United Kingdom 6 170 0.3× 511 1.3× 104 0.3× 494 1.9× 82 0.5× 6 1.3k
S.A. Wank United States 8 62 0.1× 400 1.0× 180 0.5× 209 0.8× 24 0.2× 9 1.2k
Svend Knuhtsen Denmark 20 133 0.3× 220 0.6× 23 0.1× 653 2.5× 56 0.4× 37 1.4k
Tiina Keränen Finland 11 32 0.1× 55 0.1× 211 0.6× 25 0.1× 109 0.7× 12 681
Irmlind Geerling Germany 10 144 0.3× 35 0.1× 15 0.0× 173 0.7× 80 0.5× 15 553
Edward J. Parr Canada 12 136 0.3× 13 0.0× 52 0.1× 118 0.5× 25 0.2× 22 535
Tetsuya Matsuura Japan 15 77 0.2× 23 0.1× 153 0.4× 90 0.3× 26 0.2× 37 595
Priya Shanmugarajah United Kingdom 14 70 0.1× 74 0.2× 254 0.7× 20 0.1× 52 0.3× 23 529
A. Weber United Kingdom 13 66 0.1× 44 0.1× 27 0.1× 177 0.7× 134 0.8× 18 796

Countries citing papers authored by Fabienne Clot

Since Specialization
Citations

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

Fields of papers citing papers by Fabienne Clot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabienne Clot

This figure shows the co-authorship network connecting the top 25 collaborators of Fabienne Clot. A scholar is included among the top collaborators of Fabienne Clot 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 Fabienne Clot. Fabienne Clot 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.
Saracino, Dario, Vincent Huin, Fabienne Clot, et al.. (2020). Isolated parkinsonism is an atypical presentation of GRN and C9orf72 gene mutations. Parkinsonism & Related Disorders. 80. 73–81. 11 indexed citations
2.
Saracino, Dario, Leila Sellami, Fabienne Clot, et al.. (2019). The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency. Neurobiology of Aging. 85. 154.e9–154.e11. 4 indexed citations
3.
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
4.
Trimouille, Aurélien, Émilie Obre, Guillaume Banneau, et al.. (2018). An in-frame deletion in BICD2 associated with a non-progressive form of SMALED. Clinical Neurology and Neurosurgery. 166. 1–3. 7 indexed citations
5.
Barbier, Mathieu, Agnès Camuzat, Marion Houot, et al.. (2017). Factors influencing the age at onset in familial frontotemporal lobar dementia. Neurology Genetics. 3(6). e203–e203. 5 indexed citations
6.
7.
Clot, Fabienne, Anne Rovelet‐Lecrux, Foudil Lamari, et al.. (2014). Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15(2). 95–100. 7 indexed citations
8.
Caroppo, Paola, Isabelle Le Ber, Fabienne Clot, et al.. (2014). DCTN1Mutation Analysis in Families With Progressive Supranuclear Palsy–Like Phenotypes. JAMA Neurology. 71(2). 208–208. 40 indexed citations
9.
Roze, Emmanuel, Marie‐Laure Welter, Soledad Navarro, et al.. (2011). Bilateral Deep Brain Stimulation of the Pallidum for Myoclonus-Dystonia Due to ε-Sarcoglycan Mutations. Archives of Neurology. 68(1). 94–8. 59 indexed citations
10.
Leu‐Semenescu, Smaranda, Isabelle Arnulf, Caroline Decaix, et al.. (2010). Sleep and Rhythm Consequences of a Genetically Induced Loss of Serotonin. SLEEP. 33(3). 307–314. 38 indexed citations
11.
Kinugawa, Kiyoka, Marie Vidailhet, Fabienne Clot, et al.. (2009). Myoclonus‐dystonia: An update. Movement Disorders. 24(4). 479–489. 99 indexed citations
12.
Clot, Fabienne, Arnaud Blanchard, Claire‐Marie Dhaenens, et al.. (2009). The p.Asp216His TOR1A allele effect is not found in the French population. Movement Disorders. 24(6). 919–921. 12 indexed citations
13.
Zanotti‐Fregonara, Paolo, Marie Vidailhet, Aurélie Kas, et al.. (2008). [123I]-FP-CIT and [99mTc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia–parkinsonism. Journal of the Neurological Sciences. 273(1-2). 148–151. 35 indexed citations
14.
Karell, Kati, A.S. Louka, Simon Moodie, et al.. (2003). Hla types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the european genetics cluster on celiac disease. Human Immunology. 64(4). 469–477. 455 indexed citations
15.
Clot, Fabienne, Marie‐Claude Babron, Selvaggia Percopo, et al.. (2000). Study of Two Ectopeptidases in the Susceptibility to Celiac Disease: Two Newly Identified Polymorphisms of Dipeptidylpeptidase IV. Journal of Pediatric Gastroenterology and Nutrition. 30(4). 464–466. 7 indexed citations
16.
Clot, Fabienne & Marie‐Claude Babron. (2000). Genetics of Celiac Disease. Molecular Genetics and Metabolism. 71(1-2). 76–80. 26 indexed citations
17.
Clot, Fabienne, Carmen Gianfrani, Marie‐Claude Babron, et al.. (1999). HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides. Immunogenetics. 49(9). 800–807. 27 indexed citations
18.
Greco, Luigi, Selvaggia Percopo, Fabienne Clot, et al.. (1998). Lack of Correlation Between Genotype and Phenotype in Celiac Disease. Journal of Pediatric Gastroenterology and Nutrition. 26(3). 286–290. 1 indexed citations
19.
Greco, Luigi, Selvaggia Percopo, Fabienne Clot, et al.. (1998). Lack of Correlation Between Genotype and Phenotype in Celiac Disease. Journal of Pediatric Gastroenterology and Nutrition. 26(3). 286–290. 28 indexed citations
20.
Bouguerra, F., et al.. (1996). Synergistic effect of two HLA heterodimers in celiac disease. Human Immunology. 47(1-2). 29–29. 5 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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