Karen Rouault

655 total citations
13 papers, 286 citations indexed

About

Karen Rouault is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Karen Rouault has authored 13 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Karen Rouault's work include Forensic and Genetic Research (3 papers), Genomics and Rare Diseases (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Karen Rouault is often cited by papers focused on Forensic and Genetic Research (3 papers), Genomics and Rare Diseases (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Karen Rouault collaborates with scholars based in France, Portugal and Spain. Karen Rouault's co-authors include Claude Férec, F. Dubrana, François Gaucher, D. Tanguy, Virginie Scotet, Gaël Erauso, Didier Flament, Daniël Prieur, Claire Geslin and M. Le Romancer and has published in prestigious journals such as PLoS ONE, Scientific Reports and Journal of Bacteriology.

In The Last Decade

Karen Rouault

12 papers receiving 281 citations

Peers

Karen Rouault

GENET

SURGE

ECOLO

GENET

F S Collins United States

Tetsuya Oda Japan

Wenzhu Li China

Gang Sun China

Sang-Beom Seo South Korea

Sara Zamora‐Caballero Spain

M Li China

Wenjing Tang China

Eglė Gineikienė Lithuania

Geneviève Pont-Kingdon United States

F S Collins United States

Karen Rouault

187 ×1.9

108 ×1.3

GENET

28 ×0.4

SURGE

26 ×0.4

ECOLO

27 ×0.6

GENET

Citations per year, relative to Karen Rouault Karen Rouault (= 1×) peers F S Collins

Countries citing papers authored by Karen Rouault

Since Specialization

Citations

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

Fields of papers citing papers by Karen Rouault

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Rouault

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

All Works

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13 of 13 papers shown

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.

Mekki, Najla, Imen Ben‐Mustapha, Karen Rouault, et al.. (2017). A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients. Molecular Immunology. 90. 57–63. 21 indexed citations

Solé‐Morata, Neus, Laura Valverde, Francesca Tassi, et al.. (2017). Analysis of the R1b-DF27 haplogroup shows that a large fraction of Iberian Y-chromosome lineages originated recently in situ. Scientific Reports. 7(1). 7341–7341. 23 indexed citations

Ben‐Mustapha, Imen, Meriem Ben‐Ali, Karen Rouault, et al.. (2016). A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients. Journal of Clinical Immunology. 36(6). 547–554. 13 indexed citations

Baeta, Miriam, Carolina Núńez, Sellama Nadifi, et al.. (2016). A genetic overview of Atlantic coastal populations from Europe and North-West Africa based on a 17 X-STR panel. Forensic Science International Genetics. 27. 167–171. 12 indexed citations

Valverde, Laura, Sergio Cardoso, Jaime Algorta, et al.. (2015). New clues to the evolutionary history of the main European paternal lineage M269: dissection of the Y-SNP S116 in Atlantic Europe and Iberia. European Journal of Human Genetics. 24(3). 437–441. 21 indexed citations

Farrell, Philip M., Emmanuelle Génin, Claude Férec, et al.. (2015). WS17.1 The ancient origin of F508del-CF: When and where the mutation arose. Journal of Cystic Fibrosis. 14. S31–S31. 1 indexed citations

Guéguen, Paul, Karen Rouault, Jian‐Min Chen, et al.. (2013). A Missense Mutation in the Alpha-Actinin 1 Gene (ACTN1) Is the Cause of Autosomal Dominant Macrothrombocytopenia in a Large French Family. PLoS ONE. 8(9). e74728–e74728. 34 indexed citations

Saliou, Philippe, Gérald Le Gac, Paul Guéguen, et al.. (2013). Evidence for the High Importance of Co-Morbid Factors in HFE C282Y/H63D Patients Cared by Phlebotomies: Results from an Observational Prospective Study. PLoS ONE. 8(12). e81128–e81128. 5 indexed citations

10.

Rouault, Karen, Virginie Scotet, François Gaucher, et al.. (2010). Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian population. Osteoarthritis and Cartilage. 18(9). 1144–1149. 58 indexed citations

11.

Rouault, Karen, Virginie Scotet, François Gaucher, et al.. (2009). Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian population. Osteoarthritis and Cartilage. 17(8). 1099–1105. 31 indexed citations

12.

Geslin, Claire, Didier Flament, Karen Rouault, et al.. (2007). Analysis of the First Genome of a Hyperthermophilic Marine Virus-Like Particle, PAV1, Isolated fromPyrococcus abyssi. Journal of Bacteriology. 189(12). 4510–4519. 54 indexed citations

13.

Prieur, Daniël, Gaël Erauso, Claire Geslin, et al.. (2004). Genetic elements of Thermococcales. Biochemical Society Transactions. 32(2). 184–187. 13 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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