Eric Noé

656 total citations
10 papers, 354 citations indexed

About

Eric Noé is a scholar working on Psychiatry and Mental health, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eric Noé has authored 10 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Psychiatry and Mental health, 3 papers in Molecular Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eric Noé's work include Epilepsy research and treatment (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Eric Noé is often cited by papers focused on Epilepsy research and treatment (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Eric Noé collaborates with scholars based in France, Tunisia and Saudi Arabia. Eric Noé's co-authors include Stéphanie Baulac, Éric Leguern, Guillaume Achaz, Emeline Mundwiller, Fabienne Picard, Pierre Thomas, Christian Marescaux, Markus Wolff, Richard Miles and Édouard Hirsch and has published in prestigious journals such as Nature Genetics, Neurology and Experimental Cell Research.

In The Last Decade

Eric Noé

9 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Noé France 8 168 119 83 76 63 10 354
Elena I. Ilina Germany 9 184 1.1× 66 0.6× 123 1.5× 70 0.9× 46 0.7× 13 340
Marcello Scala Italy 15 207 1.2× 178 1.5× 53 0.6× 91 1.2× 35 0.6× 61 513
Sinan Çomu Türkiye 8 165 1.0× 87 0.7× 91 1.1× 29 0.4× 62 1.0× 15 404
Monica Traverso Italy 13 348 2.1× 122 1.0× 66 0.8× 53 0.7× 81 1.3× 32 488
Mariëlle E.M. Swinkels Netherlands 10 285 1.7× 357 3.0× 132 1.6× 109 1.4× 65 1.0× 11 639
Sımona Baldassari Italy 10 247 1.5× 91 0.8× 94 1.1× 53 0.7× 79 1.3× 22 399
Marc D’Hooghe Belgium 12 337 2.0× 63 0.5× 95 1.1× 123 1.6× 44 0.7× 18 580
Emanuela Dazzo Italy 13 154 0.9× 72 0.6× 57 0.7× 64 0.8× 57 0.9× 20 370
Krzysztof Szczałuba Poland 15 328 2.0× 369 3.1× 63 0.8× 40 0.5× 28 0.4× 57 638
Takuya Hiraide Japan 12 271 1.6× 185 1.6× 82 1.0× 26 0.3× 56 0.9× 34 441

Countries citing papers authored by Eric Noé

Since Specialization
Citations

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

Fields of papers citing papers by Eric Noé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Noé

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

All Works

10 of 10 papers shown
1.
Lee, Ju‐Yeun, Eric Noé, Chang Ki Yoon, et al.. (2024). INCIDENCE OF CENTRAL SEROUS CHORIORETINOPATHY AND ITS ASSOCIATION WITH GYNECOLOGICAL DISEASES IN WOMEN. Retina. 45(3). 541–547.
2.
Baldassari, Sara, Guillaume Achaz, Stéphanie Baulac, et al.. (2021). Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy. Frontiers in Neurology. 12. 9 indexed citations
3.
Landoulsi, Zied, Eric Noé, Saloua Mrabet, et al.. (2018). Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes. Neurogenetics. 19(3). 165–178. 13 indexed citations
4.
Baulac, Stéphanie, Guy M. Lenk, Bouchra Ouled Amar Bencheikh, et al.. (2014). Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria. Neurology. 82(12). 1068–1075. 64 indexed citations
5.
Ishida, Saeko, Fabienne Picard, Gabrielle Rudolf, et al.. (2013). Mutations of DEPDC5 cause autosomal dominant focal epilepsies. Nature Genetics. 45(5). 552–555. 167 indexed citations
6.
Mignot, Cyril, Cécile Delarasse, Bruno Della Gaspera, et al.. (2007). Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease. Experimental Cell Research. 313(13). 2766–2779. 32 indexed citations
7.
Cournu‐Rebeix, Isabelle, Emmanuelle Génin, Gaëtan Lesca, et al.. (2003). Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis. Genes and Immunity. 4(7). 518–523. 27 indexed citations
8.
Eurin, Joëlle, C. Barthélémy, Françoise Masson, et al.. (2000). Release of neuropeptide Y and hemodynamic changes during surgical removal of human pheochromocytomas. Regulatory Peptides. 86(1-3). 95–102. 15 indexed citations
9.
Carayon, A., F. Masson, Eric Noé, et al.. (1993). Mechanisms of isoproterenol-induced atrial natriuretic peptide release from superfused rabbit atria. American Journal of Physiology-Heart and Circulatory Physiology. 265(4). H1283–H1288. 6 indexed citations
10.
Carayon, A., Françoise Masson, G. Maistre, et al.. (1991). Effects of arginine vasopressin and extracellular osmolarity on atrial natriuretic peptide release by superfused rat atria. European Journal of Pharmacology. 209(1-2). 45–55. 21 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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