Sylvia Redon

837 total citations
12 papers, 227 citations indexed

About

Sylvia Redon is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Sylvia Redon has authored 12 papers receiving a total of 227 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Oncology. Recurrent topics in Sylvia Redon's work include Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Melanoma and MAPK Pathways (2 papers). Sylvia Redon is often cited by papers focused on Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Melanoma and MAPK Pathways (2 papers). Sylvia Redon collaborates with scholars based in France and Monaco. Sylvia Redon's co-authors include Claude Férec, Caroline Bénech, Jian‐Min Chen, I. Quéré, Yannick Le Meur, Marie‐Pierre Audrézet, Émilie Cornec-Le Gall, Arnaud Uguen, Gaëlle Friocourt and Pascale Marcorelles and has published in prestigious journals such as PLoS ONE, Thrombosis and Haemostasis and Human Mutation.

In The Last Decade

Sylvia Redon

11 papers receiving 216 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sylvia Redon France 8 158 139 33 24 23 12 227
Kristen L. Sund United States 9 171 1.1× 193 1.4× 56 1.7× 23 1.0× 19 0.8× 15 326
Caroline Bénech France 8 196 1.2× 132 0.9× 41 1.2× 28 1.2× 5 0.2× 14 278
Xingbo Cheng China 7 148 0.9× 167 1.2× 58 1.8× 19 0.8× 11 0.5× 21 295
Cynthia Lim United States 5 145 0.9× 126 0.9× 39 1.2× 17 0.7× 8 0.3× 9 231
Laurence Faivre France 6 188 1.2× 117 0.8× 27 0.8× 9 0.4× 15 0.7× 7 252
Philip L. Beales United Kingdom 7 152 1.0× 102 0.7× 32 1.0× 48 2.0× 4 0.2× 8 263
Mamiko Yamada Japan 9 102 0.6× 111 0.8× 15 0.5× 6 0.3× 17 0.7× 59 216
M. Cecilia Cirio United States 10 163 1.0× 330 2.4× 122 3.7× 25 1.0× 13 0.6× 15 394
Eugene W. Taylor United States 9 189 1.2× 159 1.1× 25 0.8× 34 1.4× 10 0.4× 17 335
Patrick Yap Australia 7 131 0.8× 99 0.7× 16 0.5× 18 0.8× 8 0.3× 9 186

Countries citing papers authored by Sylvia Redon

Since Specialization
Citations

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

Fields of papers citing papers by Sylvia Redon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvia Redon

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

All Works

12 of 12 papers shown
1.
Uguen, Kévin, Sylvia Redon, Karen Rouault, et al.. (2024). An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation. American Journal of Medical Genetics Part A. 194(5). e63532–e63532.
2.
Quintin‐Roué, Isabelle, Sylvia Redon, Elsa Magro, et al.. (2019). Transformation d’un mélanocytome méningé en mélanome : étude clinique, histopathologique et cytogénétique. Annales de Pathologie. 39(5). 352–356. 2 indexed citations
3.
Bénéteau, Claire, Sylvia Redon, Céline Dupont, et al.. (2019). Prenatal findings in 1p36 deletion syndrome: New cases and a literature review. Prenatal Diagnosis. 39(10). 871–882. 11 indexed citations
4.
Redon, Sylvia, et al.. (2017). A Diagnostic Algorithm Combining Immunohistochemistry and Molecular Cytogenetics to Diagnose Challenging Melanocytic Tumors. Applied immunohistochemistry & molecular morphology. 26(10). 714–720. 17 indexed citations
5.
Guéguen, Paul, Sylvia Redon, & Cédric Le Maréchal. (2015). Puces à ADN (microArrays) et séquençage de nouvelle génération. Revue Francophone des Laboratoires. 2015(473). 63–70. 1 indexed citations
6.
Masson, Emmanuelle, Pascal Hammel, Caroline Bénech, et al.. (2013). Characterization of two deletions of the CTRC locus. Molecular Genetics and Metabolism. 109(3). 296–300. 8 indexed citations
7.
Redon, Sylvia, Caroline Bénech, Séverine Audebert‐Bellanger, et al.. (2013). A small de novo 16q24.1 duplication in a woman with severe clinical features. European Journal of Medical Genetics. 56(4). 211–215. 16 indexed citations
8.
Audrézet, Marie‐Pierre, Émilie Cornec-Le Gall, Jian‐Min Chen, et al.. (2012). Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients. Human Mutation. 33(8). 1239–1250. 122 indexed citations
9.
Talagas, Matthieu, Pascale Marcorelles, Arnaud Uguen, et al.. (2012). Identification of a novel population in high-grade oligodendroglial tumors not deleted on 1p/19q using array CGH. Journal of Neuro-Oncology. 109(2). 405–413. 9 indexed citations
10.
Redon, Sylvia, Edouard Hirchaud, Daniel Barón, et al.. (2011). High-Throughput Analysis of Promoter Occupancy Reveals New Targets for Arx, a Gene Mutated in Mental Retardation and Interneuronopathies. PLoS ONE. 6(9). e25181–e25181. 29 indexed citations
11.
Guéguen, Paul, Sylvia Redon, Brigitte Pan‐Petesch, et al.. (2011). Revisiting the molecular epidemiology of factor XI deficiency: Nine new mutations and an original large 4qTer deletion in western Brittany (France). Thrombosis and Haemostasis. 107(1). 44–50. 11 indexed citations
12.
Azzalin, Claus M., Sylvia Redon, & Joachim Lingner. (2005). S. Cerevisiae Est1/H. sapiens SMG6 protein family members function in telomere metabolism. Infoscience (Ecole Polytechnique Fédérale de Lausanne). 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.

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