Cyril Mignot

16.6k total citations
101 papers, 2.0k citations indexed

About

Cyril Mignot is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Cyril Mignot has authored 101 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 29 papers in Genetics and 16 papers in Cell Biology. Recurrent topics in Cyril Mignot's work include Genetics and Neurodevelopmental Disorders (21 papers), Cellular transport and secretion (15 papers) and Genomics and Rare Diseases (11 papers). Cyril Mignot is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Cellular transport and secretion (15 papers) and Genomics and Rare Diseases (11 papers). Cyril Mignot collaborates with scholars based in France, United States and Germany. Cyril Mignot's co-authors include Thierry Billette de Villemeur, Irène Maire, A. Gélot, Gaëtan Lesca, Diana Rodriguez, Stanislas Lyonnet, Danielle Pham-Dinh, Odile Boespflug‐Tanguy, F. X. Coudé and M. Lambert and has published in prestigious journals such as Circulation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Cyril Mignot

88 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cyril Mignot France 26 844 520 464 339 321 101 2.0k
Paul Renbaum Israel 28 1.6k 1.9× 296 0.6× 976 2.1× 413 1.2× 114 0.4× 87 3.2k
Grazia M.S. Mancini Netherlands 26 849 1.0× 216 0.4× 681 1.5× 134 0.4× 285 0.9× 46 1.9k
D. Goossens Belgium 25 797 0.9× 455 0.9× 548 1.2× 91 0.3× 170 0.5× 75 1.9k
Robert Y. Chen United States 16 584 0.7× 224 0.4× 248 0.5× 459 1.4× 86 0.3× 27 1.8k
Jennifer Robertson Canada 21 1.4k 1.6× 206 0.4× 308 0.7× 536 1.6× 281 0.9× 32 2.9k
Annick Raas‐Rothschild Israel 34 1.7k 2.0× 982 1.9× 898 1.9× 140 0.4× 781 2.4× 108 3.8k
Donna M. Krasnewich United States 28 1.3k 1.6× 671 1.3× 362 0.8× 90 0.3× 488 1.5× 59 2.4k
Marcela V. Karpuj United States 20 1.3k 1.5× 192 0.4× 370 0.8× 254 0.7× 170 0.5× 26 2.9k
Jun Tohyama Japan 29 1.2k 1.4× 332 0.6× 992 2.1× 79 0.2× 263 0.8× 108 2.8k
Richard P. Morse United States 19 427 0.5× 679 1.3× 319 0.7× 144 0.4× 140 0.4× 36 1.8k

Countries citing papers authored by Cyril Mignot

Since Specialization
Citations

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

Fields of papers citing papers by Cyril Mignot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyril Mignot

This figure shows the co-authorship network connecting the top 25 collaborators of Cyril Mignot. A scholar is included among the top collaborators of Cyril Mignot 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 Cyril Mignot. Cyril Mignot 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.
Srivastava, Siddharth, Lindsay C. Swanson, Boris Keren, et al.. (2024). Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder. Pediatric Neurology. 160. 45–53.
2.
Keren, Boris, et al.. (2023). A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report. Acta Neuropathologica Communications. 11(1). 131–131. 3 indexed citations
3.
Hähner, Antje, et al.. (2022). Der Einfluss eines Riechtrainings auf die Schmerzwahrnehmung und das Riechvermögen bei Patienten mit Migräne mit und ohne Aura. Nervenheilkunde. 41(5). 355–355. 1 indexed citations
4.
Patat, Olivier, Sandra Whalen, Lionel Arnaud, et al.. (2021). Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome. Journal of Medical Genetics. 59(5). 505–510. 8 indexed citations
5.
Doummar, Diane, Thierry Bienvenu, Perrine Charles, et al.. (2021). Tremor-like subcortical myoclonus in STXBP1 encephalopathy. European Journal of Paediatric Neurology. 34. 62–66. 4 indexed citations
6.
Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations
7.
Besnard, Thomas, Mathilde Nizon, Christel Thauvin‐Robinet, et al.. (2021). Loss‐of‐function variants in ARHGEF9 are associated with an X‐linked intellectual disability dominant disorder. Human Mutation. 42(5). 498–505. 2 indexed citations
8.
Maire, Albane le, Natacha Bouhours‐Nouet, Delphine Mirebeau‐Prunier, et al.. (2020). Two Novel Cases of Resistance to Thyroid Hormone Due to THRA Mutation. Thyroid. 30(8). 1217–1221. 19 indexed citations
9.
Valence, Stéphanie, Hélène Maurey, Sarah Weckhuysen, et al.. (2019). Three novel patients with epileptic encephalopathy due to biallelic mutations in the PLCB1 gene. Clinical Genetics. 97(3). 477–482. 11 indexed citations
10.
Larcher, Lise, Joy Norris, Julien Buratti, et al.. (2019). The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome. European Journal of Medical Genetics. 63(4). 103777–103777. 21 indexed citations
11.
Hiatt, Susan M., Michelle L. Thompson, Jeremy W. Prokop, et al.. (2019). Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. The American Journal of Human Genetics. 104(4). 701–708. 15 indexed citations
12.
Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations
13.
Guinchat, Vincent, Jean Xavier, Cyril Mignot, et al.. (2017). Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self‐Injurious Blindness. Case Reports in Psychiatry. 2017(1). 7582780–7582780. 6 indexed citations
14.
Mahlaoui, Nizar, Isabelle Pellier, Cyril Mignot, et al.. (2012). Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome. Blood. 121(9). 1510–1516. 48 indexed citations
15.
Muller, Cécile, Cyril Mignot, N. Belarbi, Dominique Berrebi, & Arnaud Bonnard. (2012). Does the radiographic transition zone correlate with the level of aganglionosis on the specimen in Hirschsprung’s disease?. Pediatric Surgery International. 28(6). 597–601. 27 indexed citations
16.
Bratosin, Daniela & Cyril Mignot. (2011). In Memoriam: Professor Emeritus Jean Montreuil (1920–2010). A Lifetime Dedicated to the Progress of Science and Education. Cytometry Part B Clinical Cytometry. 80B(2). 69–70. 1 indexed citations
17.
Mignot, Cyril, Marie‐Laure Moutard, Oriane Trouillard, et al.. (2011). STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Epilepsia. 52(10). 1820–1827. 76 indexed citations
18.
Ronce, Nathalie, Éric Bieth, Lydie Bürglen, et al.. (2010). Twenty-five novel mutations including duplications in the ATP7A gene. Clinical Genetics. 79(3). 243–253. 15 indexed citations
19.
Mignot, Cyril, et al.. (2003). Maladie de Gaucher, une maladie multisystémique et un traitement enzymatique substitutif. MTP. Médecine thérapeutique pédiatrie. 6(2). 75–79.
20.
Mignot, Cyril. (2003). Éloigner ? Séparer ? Placer ?. Cairn.info. 39–46. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Paul Renbaum Breakdown of academic impact, for papers by Grazia M.S. Mancini Breakdown of academic impact, for papers by D. Goossens Breakdown of academic impact, for papers by Robert Y. Chen Breakdown of academic impact, for papers by Jennifer Robertson Breakdown of academic impact, for papers by Annick Raas‐Rothschild Breakdown of academic impact, for papers by Donna M. Krasnewich Breakdown of academic impact, for papers by Marcela V. Karpuj Breakdown of academic impact, for papers by Jun Tohyama Breakdown of academic impact, for papers by Richard P. Morse
Rankless by CCL
2026