Renaud Touraine

7.0k total citations
93 papers, 2.0k citations indexed

About

Renaud Touraine is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Renaud Touraine has authored 93 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 33 papers in Genetics and 13 papers in Surgery. Recurrent topics in Renaud Touraine's work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (8 papers) and Allergic Rhinitis and Sensitization (6 papers). Renaud Touraine is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (8 papers) and Allergic Rhinitis and Sensitization (6 papers). Renaud Touraine collaborates with scholars based in France, United States and Belgium. Renaud Touraine's co-authors include Annick Toutain, Michel Goossens, Véronique Pingault, Tania Attié‐Bitach, R. Michael Blaese, Patrick Edery, Viviane Baral, Vincent des Portes, Nadège Bondurand and Nicholas N. Vahanian and has published in prestigious journals such as Science, PLoS ONE and Annals of Neurology.

In The Last Decade

Renaud Touraine

90 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
Renaud Touraine France 25 1.1k 633 354 206 194 93 2.0k
Bruno Leheup France 29 1.1k 1.0× 758 1.2× 239 0.7× 215 1.0× 78 0.4× 97 2.2k
Yasemin Alanay Türkiye 26 994 0.9× 1.0k 1.6× 370 1.0× 155 0.8× 162 0.8× 108 2.1k
Craig B. Woda United States 17 1.4k 1.3× 329 0.5× 275 0.8× 104 0.5× 111 0.6× 21 2.4k
Yoshio Makita Japan 24 916 0.8× 797 1.3× 213 0.6× 131 0.6× 129 0.7× 77 1.8k
Dusica Babovic‐Vuksanovic United States 27 863 0.8× 540 0.9× 294 0.8× 95 0.5× 98 0.5× 99 2.2k
Susan Holder United Kingdom 21 1.1k 1.0× 1.2k 1.9× 525 1.5× 130 0.6× 89 0.5× 43 2.2k
Vincent El Ghouzzi France 27 1.1k 1.0× 1.0k 1.7× 204 0.6× 113 0.5× 233 1.2× 44 2.1k
Shalini N. Jhangiani United States 25 1.1k 1.0× 801 1.3× 142 0.4× 116 0.6× 142 0.7× 80 2.0k
Eva Holmberg Sweden 22 680 0.6× 685 1.1× 234 0.7× 174 0.8× 110 0.6× 40 1.5k
David Mowat Australia 27 1.3k 1.1× 644 1.0× 621 1.8× 129 0.6× 107 0.6× 69 2.4k

Countries citing papers authored by Renaud Touraine

Since Specialization
Citations

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

Fields of papers citing papers by Renaud Touraine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renaud Touraine

This figure shows the co-authorship network connecting the top 25 collaborators of Renaud Touraine. A scholar is included among the top collaborators of Renaud Touraine 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 Renaud Touraine. Renaud Touraine 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.
Callier, Patrick, Renaud Touraine, Antonio Vitobello, et al.. (2024). De Novo Balanced Translocations Disrupting the FBN1 Gene Diagnosed by Genome Sequencing: An Uncommon Cause of Marfan Syndrome Modifying Genetic Counseling. American Journal of Medical Genetics Part A. 197(4). e63923–e63923. 1 indexed citations
2.
Felice, Kevin J., Per Harald Jonson, J. Sarparanta, et al.. (2024). Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation. Annals of Clinical and Translational Neurology. 11(9). 2392–2405. 1 indexed citations
3.
Vaché, Christel, Nicolas Cubedo, David Baux, et al.. (2023). Identification and in vivo functional investigation of a HOMER2 nonstop variant causing hearing loss. European Journal of Human Genetics. 31(7). 834–840. 1 indexed citations
4.
Castaldo, Alice, Céline Delestrain, Renaud Touraine, et al.. (2023). Idiopathic pulmonary fibrosis with benignSFTPCvariant and pathogenicMARS1mutations: can't see the forest for the trees!. ERJ Open Research. 9(6). 472–2023. 2 indexed citations
5.
Touraine, Renaud, et al.. (2022). Tuberous Sclerosis Complex: Genetic counselling and perinatal follow-up. Archives de Pédiatrie. 29(5). 5S3–5S7. 5 indexed citations
6.
Mazzola, Laure, Karen Oliver, Audrey Labalme, et al.. (2020). Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS. Annals of Neurology. 89(2). 402–407. 2 indexed citations
7.
Ramond, Francis, Marlène Rio, Bénédicte Héron, et al.. (2020). AICA‐ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long‐term update on the first case. Journal of Inherited Metabolic Disease. 43(6). 1254–1264. 26 indexed citations
8.
Giraud, Antoine, et al.. (2016). Le phénotype complexe du syndrome ARC : une nouvelle observation. Archives de Pédiatrie. 24(2). 131–134. 1 indexed citations
9.
Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations
10.
Germanaud, David, Massimiliano Rossi, Gérald Bussy, et al.. (2010). The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males. Clinical Genetics. 79(3). 225–235. 36 indexed citations
11.
Schluth‐Bolard, Caroline, Damien Sanlaville, Audrey Labalme, et al.. (2010). 17p13.1 microdeletion involving the TP53 gene in a boy presenting with mental retardation but no tumor. American Journal of Medical Genetics Part A. 152A(5). 1278–1282. 29 indexed citations
12.
Fréminville, Bénédicte de, et al.. (2007). L’accompagnement des enfants porteurs de trisomie 21. MTP. Médecine thérapeutique pédiatrie. 10(4). 272–280. 3 indexed citations
13.
Lesca, Gaëtan, Virginie Bernard, Muriel Bozon, et al.. (2007). Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation. European Journal of Medical Genetics. 50(3). 200–208. 5 indexed citations
14.
Badens, Catherine, Nathalie Martini, Sébastien Courrier, et al.. (2006). ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X‐inactivation pattern. American Journal of Medical Genetics Part A. 140A(20). 2212–2215. 19 indexed citations
15.
Aknin‐Seifer, Isabelle, Renaud Touraine, Anne-Karen Faure, et al.. (2005). Two fast methods for detection of Y-microdeletions. Fertility and Sterility. 84(3). 740–742. 9 indexed citations
16.
Vérot, Lucie, Nicole Alloisio, Laurette Morlé, et al.. (2003). Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24. American Journal of Medical Genetics Part A. 122A(1). 37–41. 5 indexed citations
17.
Amiel, Jeanne, Yolanda Espinosa‐Parrilla, Julie Steffann, et al.. (2001). Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures. The American Journal of Human Genetics. 69(6). 1370–1377. 79 indexed citations
18.
Touraine, Renaud, Tania Attié‐Bitach, E. Manceau, et al.. (2000). Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain. The American Journal of Human Genetics. 66(5). 1496–1503. 124 indexed citations
19.
Morris, John C., Renaud Touraine, Oliver Wildner, & R. Michael Blaese. (1999). 18 Suicide Genes: Gene Therapy Applications Using Enzyme/Prodrug Strategies. Cold Spring Harbor Monograph Archive. 36. 477–526. 4 indexed citations
20.
Prost, Y. De, et al.. (1979). Traitement de la prelade par applications locales de D.N.C.B.. Annales de Dermatologie et de Vénéréologie. 106(5). 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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