Louis Vallée

7.0k total citations
157 papers, 2.9k citations indexed

About

Louis Vallée is a scholar working on Psychiatry and Mental health, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Louis Vallée has authored 157 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Psychiatry and Mental health, 41 papers in Molecular Biology and 32 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Louis Vallée's work include Epilepsy research and treatment (31 papers), Metabolism and Genetic Disorders (17 papers) and Neonatal and fetal brain pathology (15 papers). Louis Vallée is often cited by papers focused on Epilepsy research and treatment (31 papers), Metabolism and Genetic Disorders (17 papers) and Neonatal and fetal brain pathology (15 papers). Louis Vallée collaborates with scholars based in France, Belgium and United States. Louis Vallée's co-authors include Stéphane Auvin, Jòseph Vamecq, J. Cuvellier, Jean‐Marie Cuisset, Yann Mikaeloff, Marc Tardieu, Marie‐Dominique Lamblin, Christian Confavreux, Catherine Lubetzki and Samy Suissa and has published in prestigious journals such as Neurology, Annals of Neurology and FEBS Letters.

In The Last Decade

Louis Vallée

149 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louis Vallée France 29 899 728 575 495 409 157 2.9k
Naoto Adachi Japan 36 1.2k 1.4× 796 1.1× 643 1.1× 777 1.6× 384 0.9× 191 4.1k
Alberto Spalice Italy 33 1.3k 1.4× 521 0.7× 1.0k 1.8× 449 0.9× 481 1.2× 173 3.1k
Ki Joong Kim South Korea 28 1.1k 1.3× 892 1.2× 633 1.1× 396 0.8× 490 1.2× 199 3.0k
Kenji Sugai Japan 27 1.0k 1.2× 862 1.2× 760 1.3× 552 1.1× 296 0.7× 213 2.8k
Agustín Legido United States 36 1.4k 1.5× 947 1.3× 1.4k 2.3× 494 1.0× 266 0.7× 138 3.9k
Alfons Macaya Spain 32 630 0.7× 1.3k 1.8× 510 0.9× 909 1.8× 627 1.5× 126 3.5k
Bernhard Schmitt Switzerland 31 733 0.8× 618 0.8× 594 1.0× 427 0.9× 150 0.4× 82 2.3k
Sanjib Sinha India 32 1.3k 1.4× 554 0.8× 641 1.1× 598 1.2× 546 1.3× 252 3.8k
Bruria Ben‐Zeev Israel 33 892 1.0× 1.3k 1.8× 514 0.9× 737 1.5× 268 0.7× 105 3.4k
Ilan Shelef Israel 31 347 0.4× 831 1.1× 274 0.5× 366 0.7× 703 1.7× 181 3.6k

Countries citing papers authored by Louis Vallée

Since Specialization
Citations

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

Fields of papers citing papers by Louis Vallée

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louis Vallée

This figure shows the co-authorship network connecting the top 25 collaborators of Louis Vallée. A scholar is included among the top collaborators of Louis Vallée 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 Louis Vallée. Louis Vallée 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.
2.
Zhang, Peng, Aurélie Cobat, Yoon Seung Lee, et al.. (2021). A computational approach for detecting physiological homogeneity in the midst of genetic heterogeneity. The American Journal of Human Genetics. 108(6). 1012–1025. 8 indexed citations
3.
Jonckheere, Julien De, et al.. (2016). Assessment of Procedural Pain in Children Using Analgesia Nociception Index. Clinical Journal of Pain. 32(12). 1100–1104. 19 indexed citations
4.
Riquet, Audrey, et al.. (2015). Syndrome de Lemierre révélé par un torticolis. Archives de Pédiatrie. 22(5). 540–543.
5.
Cuisset, J., et al.. (2013). Intérêt de la biopsie musculaire chez l’enfant en 2012. Revue Neurologique. 169(8-9). 632–639. 5 indexed citations
6.
Jacquette, Aurélia, David Cohen, Nicolas Bodeau, et al.. (2012). Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1. Developmental Medicine & Child Neurology. 54(10). 905–911. 56 indexed citations
7.
Soto‐Ares, Gustavo, et al.. (2011). Neuropsychological evaluation and follow-up of children with cerebellar cortical dysplasia. Developmental Medicine & Child Neurology. 53(12). 1119–1127. 3 indexed citations
8.
Riquet, Audrey, Marie‐Dominique Lamblin, Maria de Lourdes Bastos, et al.. (2010). Usefulness of video-EEG monitoring in children. Seizure. 20(1). 18–22. 28 indexed citations
9.
Vallée, Louis, Monique Fontaine, Anne‐Frédérique Dessein, et al.. (2009). Comparison of seizure reduction and serum fatty acid levels after receiving the ketogenic and modified Atkins diet. Seizure. 18(5). 359–364. 61 indexed citations
10.
Vallée, Louis, et al.. (2008). Les antiépileptiques dans le traitement préventif de la migraine de l’enfant. Archives de Pédiatrie. 15(11). 1693–1699. 5 indexed citations
11.
Auvin, Stéphane, Louise Devisme, Claude Alain Maurage, et al.. (2007). Neuropathological and MRI findings in an acute presentation of hemiconvulsion-hemiplegia: A report with pathophysiological implications. Seizure. 16(4). 371–376. 25 indexed citations
12.
Cossée, Mireille, Bénédicte Demeer, Patricia Blanchet, et al.. (2006). Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect. European Journal of Human Genetics. 14(4). 418–425. 19 indexed citations
13.
Auvin, Stéphane, et al.. (2006). Varicelle en bracelet: illustration des éruptions varicelleuses atypiques. Archives de Pédiatrie. 14(3). 259–261. 3 indexed citations
14.
Billard, C., et al.. (2002). BREV: une batterie rapide clinique d'évaluation des fonctions cognitives chez les enfants d'âge scolaire et préscolaire.. Revue Neurologique. 158(2). 1 indexed citations
15.
Vallée, Louis, et al.. (2002). Traitements conservatoires chez l'enfant polyhandicapé. Archives de Pédiatrie. 9. 60–65. 3 indexed citations
16.
Motté, Jacques & Louis Vallée. (2002). Diagnostic et traitement des convulsions fébriles. 14(2). 89–94. 3 indexed citations
17.
Manouvrier‐Hanu, Sylvie, Jeanne Amiel, Sylvie Jacquot, et al.. (1999). Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome. Journal of Medical Genetics. 36(10). 775–778. 22 indexed citations
18.
Vallée, Louis, et al.. (1999). Enquête épidémiologique sur les enfants polyhandicapés du département du Nord. Archives de Pédiatrie. 6(8). 832–836. 10 indexed citations
19.
Lesoin, F, Alessandro Cama, Patrick Dhellemmes, et al.. (1987). Extraneural Metastasis of a Pineal Tumor. European Neurology. 27(1). 55–61. 9 indexed citations
20.
Vamecq, Jòseph, Edmond de Hoffmann, Louis Vallée, et al.. (1986). Peroxisomes and Glutaricaciduria Type-i. Archives of Physiology and Biochemistry. 94(1). 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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