Claude Cancès

1.6k total citations
15 papers, 574 citations indexed

About

Claude Cancès is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Claude Cancès has authored 15 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Psychiatry and Mental health. Recurrent topics in Claude Cancès's work include Epilepsy research and treatment (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Claude Cancès is often cited by papers focused on Epilepsy research and treatment (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Claude Cancès collaborates with scholars based in France, Belgium and United States. Claude Cancès's co-authors include Alexis Arzimanoglou, Nadia Bahi‐Buisson, Mathieu Milh, Nathalie Boddaert, Thierry Bienvenu, Christophe Philippe, Jamel Chelly, Marlène Rio, Dorothée Ville and Alexandra Afenjar and has published in prestigious journals such as Brain, Annals of Neurology and Epilepsia.

In The Last Decade

Claude Cancès

15 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claude Cancès France	10	310	293	115	89	71	15	574
Stefania Bigoni Italy	14	255 0.8×	190 0.6×	82 0.7×	90 1.0×	53 0.7×	33	520
Maria Teresa Bonati Italy	14	330 1.1×	327 1.1×	97 0.8×	208 2.3×	35 0.5×	44	756
Tetsushi Yamagata Japan	12	276 0.9×	448 1.5×	196 1.7×	82 0.9×	33 0.5×	14	736
Matthieu Raveau Japan	10	229 0.7×	232 0.8×	70 0.6×	99 1.1×	28 0.4×	13	535
Shino Shimada Japan	15	318 1.0×	315 1.1×	43 0.4×	35 0.4×	23 0.3×	36	545
Amanda Lindy United States	8	328 1.1×	225 0.8×	146 1.3×	23 0.3×	21 0.3×	13	517
Elizabeth Zuniga United States	5	276 0.9×	372 1.3×	28 0.2×	105 1.2×	73 1.0×	5	696
Bernardo Dalla Bernardina Italy	16	573 1.8×	486 1.7×	255 2.2×	208 2.3×	23 0.3×	31	972
Aurélia Jacquette France	11	191 0.6×	276 0.9×	71 0.6×	40 0.4×	38 0.5×	23	498
Madeleine Fannemel Norway	11	196 0.6×	173 0.6×	98 0.9×	58 0.7×	18 0.3×	18	386

Countries citing papers authored by Claude Cancès

Since Specialization

Citations

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

Fields of papers citing papers by Claude Cancès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claude Cancès

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

All Works

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15 of 15 papers shown

Lagrue, Emmanuelle, Claude Cancès, & Juliette Ropars. (2021). Micro/mini-dystrophines et dystrophie musculaire de Duchenne : entre espoirs et défis. Springer Link (Chiba Institute of Technology). 12–17. 1 indexed citations

Van‐Gils, Julien, et al.. (2020). Early-onset epileptic encephalopathy related to germline PIGA mutations: A series of 5 cases. European Journal of Paediatric Neurology. 28. 214–220. 4 indexed citations

Villega, Frédéric, et al.. (2019). Early-Onset Epileptic Encephalopathy Related to Germline PIGA Mutations: A Series of Four Patients. Neuropediatrics. 1 indexed citations

Dorboz, Imen, Hélène Dumay‐Odelot, Yosra Bouyacoub, et al.. (2018). Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation. Neurology Genetics. 4(6). e289–e289. 55 indexed citations

Siegfried, Aurore, Claude Cancès, Marie Denuelle, et al.. (2017). Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature. American Journal of Medical Genetics Part A. 173(4). 1061–1065. 23 indexed citations

Mancini, Josette, J.‐C. Dubus, Élisabeth Jouve, et al.. (2017). Effect of desipramine on patients with breathing disorders in RETT syndrome. Annals of Clinical and Translational Neurology. 5(2). 118–127. 17 indexed citations

Rheims, Sylvain, Vania Herbillon, Nathalie Villeneuve, et al.. (2016). ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate. Epilepsia. 57(7). 1069–1077. 27 indexed citations

Plaisancié, Julie, Pascale Kleinfinger, Claude Cancès, et al.. (2014). Constitutional chromoanasynthesis: description of a rare chromosomal event in a patient. European Journal of Medical Genetics. 57(10). 567–570. 28 indexed citations

Plaisancié, Julie, Laurence Bouneau, Claude Cancès, et al.. (2013). Distal 10q monosomy: New evidence for a neurobehavioral condition?. European Journal of Medical Genetics. 57(1). 47–53. 30 indexed citations

10.

Dellatolas, Georges, Monika Eisermann, Nathalie Boddaert, et al.. (2013). Children often present with infantile spasms after herpetic encephalitis. Epilepsia. 54(9). 1571–1576. 5 indexed citations

11.

Bahi‐Buisson, Nadia, Juliette Nectoux, Haydeé Rosas‐Vargas, et al.. (2008). Key clinical features to identify girls with CDKL5 mutations. Brain. 131(10). 2647–2661. 209 indexed citations

12.

Rooryck, Caroline, Jean‐François Chateil, Claude Cancès, et al.. (2007). Bardet-Biedl Syndrome and Brain Abnormalities. Neuropediatrics. 38(1). 5–9. 24 indexed citations

13.

Bitoun, Marc, Jorge A. Bevilacqua, Bernard Prudhon, et al.. (2007). Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset. Annals of Neurology. 62(6). 666–670. 104 indexed citations

14.

Chaix, Yves, Valérie Lauwers‐Cancès, Géraldine Daquin, et al.. (2005). Reading abilities and cognitive functions of children with epilepsy: Influence of epileptic syndrome. Brain and Development. 28(2). 122–130. 44 indexed citations

15.

Chaix, Yves, et al.. (2004). Étude des capacités de lecture dans une population d’enfants épileptiques. 16(4). 205–212. 2 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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