G Chazot

5.6k total citations · 1 hit paper
119 papers, 4.0k citations indexed

About

G Chazot is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, G Chazot has authored 119 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Neurology, 29 papers in Cellular and Molecular Neuroscience and 23 papers in Physiology. Recurrent topics in G Chazot's work include Circadian rhythm and melatonin (21 papers), Migraine and Headache Studies (20 papers) and Hereditary Neurological Disorders (16 papers). G Chazot is often cited by papers focused on Circadian rhythm and melatonin (21 papers), Migraine and Headache Studies (20 papers) and Hereditary Neurological Disorders (16 papers). G Chazot collaborates with scholars based in France, United States and Switzerland. G Chazot's co-authors include Bruno Claustrat, Jocelyne Brun, M. Geoffriau, P. Henry, Michel Lantéri‐Minet, Christian Lucas, Radwan Zaidan, D. C. Jordan, Abdelkader El Hasnaoui and G. Sassolas and has published in prestigious journals such as The Lancet, Neurology and Biological Psychiatry.

In The Last Decade

G Chazot

115 papers receiving 3.8k citations

Hit Papers

The basic physiology and pathophysiology of melatonin 2004 2026 2011 2018 2004 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G Chazot France 33 1.5k 1.3k 906 652 650 119 4.0k
Tetsuo Shimizu Japan 35 1.2k 0.8× 721 0.6× 601 0.7× 1.4k 2.2× 188 0.3× 175 4.4k
Diana N. Krause United States 47 1.4k 1.0× 914 0.7× 1.7k 1.8× 347 0.5× 635 1.0× 100 6.4k
Alfredo Costa Italy 32 558 0.4× 1.3k 1.0× 1.1k 1.2× 240 0.4× 544 0.8× 168 4.1k
A. Wauquier Belgium 36 485 0.3× 1.0k 0.8× 474 0.5× 1.1k 1.7× 182 0.3× 131 3.9k
Ronald A. Remick Canada 32 427 0.3× 1.3k 1.0× 286 0.3× 355 0.5× 427 0.7× 103 3.4k
Holger Jahn Germany 37 303 0.2× 794 0.6× 1.1k 1.3× 444 0.7× 196 0.3× 118 4.5k
Philip R. Holland United Kingdom 38 1.1k 0.7× 3.9k 3.0× 1.7k 1.8× 552 0.8× 1.9k 2.9× 85 5.1k
E. Rüther Germany 35 468 0.3× 1.2k 0.9× 919 1.0× 719 1.1× 66 0.1× 174 3.8k
E. Martignoni Italy 41 367 0.3× 1.3k 1.0× 1.2k 1.3× 733 1.1× 483 0.7× 172 6.1k
Raffaella Molteni Italy 46 661 0.5× 545 0.4× 1.5k 1.6× 745 1.1× 324 0.5× 100 7.7k

Countries citing papers authored by G Chazot

Since Specialization
Citations

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

Fields of papers citing papers by G Chazot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Chazot

This figure shows the co-authorship network connecting the top 25 collaborators of G Chazot. A scholar is included among the top collaborators of G Chazot 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 G Chazot. G Chazot 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.
Gonnaud, Pierre‐Marie, Franck Sturtz, Christine Tranchant, et al.. (2009). DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations. Acta Neurologica Scandinavica. 92(4). 313–318. 3 indexed citations
2.
Giraud, P., et al.. (2002). Increased Detection of 14-3-3 Protein in Cerebrospinal Fluid in Sporadic Creutzfeldt-Jakob Disease during the Disease Course. European Neurology. 48(4). 218–221. 16 indexed citations
3.
Demarquay, Geneviève, et al.. (2000). Clinical report of three patients with hereditary hemochromatosis and movement disorders. Movement Disorders. 15(6). 1204–1209. 34 indexed citations
4.
Geoffriau, M., Jocelyne Brun, G Chazot, & Bruno Claustrat. (1998). The Physiology and Pharmacology of Melatonin in Humans. Hormone Research in Paediatrics. 49(3-4). 136–141. 131 indexed citations
5.
Latour, Philippe, Catherine Ressot, J.‐C. Antoine, et al.. (1997). New Mutations in the X-Linked Form of Charcot-Marie-Tooth Disease. European Neurology. 37(1). 38–42. 13 indexed citations
6.
Claustrat, Bruno, et al.. (1997). Nocturnal Plasma Melatonin Profile and Melatonin Kinetics During Infusion in Status Migrainosus. Cephalalgia. 17(4). 511–517. 49 indexed citations
7.
Broussolle, Emmanuel, Serge Bakchine, M Tommasi, et al.. (1996). Slowly progressive anarthria with late anterior opercular syndrome: a variant form of frontal cortical atrophy syndromes. Journal of the Neurological Sciences. 144(1-2). 44–58. 85 indexed citations
8.
Ryvlin, Philippe, et al.. (1995). Magnetic Resonance Imaging Evidence of Decreased Putamenal Iron Content in Idiopathic Parkinson's Disease. Archives of Neurology. 52(6). 583–588. 73 indexed citations
9.
Bost, Muriel, et al.. (1995). Restriction polymorphisms of the ceruloplasmin gene on chromosome 3. Human Genetics. 96(2). 239–240. 4 indexed citations
10.
Boureau, F., et al.. (1995). Comparison of Subcutaneous Sumatriptan with Usual Acute Treatments for Migraine. European Neurology. 35(5). 264–269. 20 indexed citations
11.
Latour, Philippe, Eva Nelis, André Dautigny, et al.. (1995). Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B. Human Mutation. 6(1). 50–54. 31 indexed citations
12.
Broussolle, E., et al.. (1993). [Treatment of Wilson's disease with zinc. 5 cases].. PubMed. 149(6-7). 393–7. 3 indexed citations
13.
Claustrat, Bruno, Jocelyne Brun, & G Chazot. (1990). Melatonin in humans, neuroendocrinological and pharmacological aspects. International Journal of Radiation Applications and Instrumentation Part B Nuclear Medicine and Biology. 17(7). 625–632. 11 indexed citations
14.
Chazot, G, et al.. (1989). Current trends in trace elements research. 11 indexed citations
15.
Zaidan, Radwan, et al.. (1988). Effects of a four-day nocturnal melatonin treatment on the 24 h plasma melatonin, cortisol and prolactin profiles in humans. European Journal of Endocrinology. 119(4). 474–480. 43 indexed citations
16.
Daléry, J, et al.. (1985). [Daily profiles of melatonin, cortisol and gonadotropins in 8 adolescents with anorexia nervosa].. PubMed. 11(1). 25–8. 6 indexed citations
17.
Laurent, B., et al.. (1983). Chutes cataplectiques révélant une hypercalcémie.. La Presse Médicale. 12(12). 1 indexed citations
18.
Confavreux, Christian, Elisabetta Gianazza, P Arnaud, et al.. (1982). [Silver stain of unconcentrated cerebrospinal fluid. Preliminary results in multiple sclerosis and other neurological diseases].. PubMed. 138(4). 317–25. 6 indexed citations
19.
Chazot, G, et al.. (1980). Radio-immunofixation: une nouvelle technique de caractérisation des immunoglobulines dans le liquide céphalo-rachidien non concentré. Résultats préliminaires.. Revue Neurologique. 136(11). 2 indexed citations
20.
Chazot, G, Benjamin Berger, H Carrier, et al.. (1976). [Neurological manifestations in monoclonal gammapathies. Pure neurological manifestations. Immunofluorescence study].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 132(3). 195–212. 36 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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