Isabelle Rouvet

1.5k total citations
13 papers, 371 citations indexed

About

Isabelle Rouvet is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Epidemiology. According to data from OpenAlex, Isabelle Rouvet has authored 13 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Epidemiology. Recurrent topics in Isabelle Rouvet's work include Mitochondrial Function and Pathology (3 papers), RNA Research and Splicing (3 papers) and Immune Cell Function and Interaction (2 papers). Isabelle Rouvet is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), RNA Research and Splicing (3 papers) and Immune Cell Function and Interaction (2 papers). Isabelle Rouvet collaborates with scholars based in France, United States and Lebanon. Isabelle Rouvet's co-authors include Dominique Bozon, Andoni Echaniz‐Laguna, Bénédicte Mousson de Camaret, Jean Michel Heard, Delphine Bohl, Élise Roy, Stéphanie Bigou, Sandrine Vitry, Roseline Froissart and Stéphane Blanchard and has published in prestigious journals such as Nature Communications, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Isabelle Rouvet

13 papers receiving 368 citations

Peers

Isabelle Rouvet

IMMUN

EPIDE

PHYSI

Yohan Kim United States

David Kunke Czechia

Sonia Benhamida France

Florence Renaldo France

Adi Minis United States

Daniel J. Adams United States

Martina Cesani Italy

João Vasco Ferreira Portugal

Christin Collins United States

Nilesh Pande France

Yohan Kim United States

Isabelle Rouvet

391 ×1.6

59 ×0.8

IMMUN

52 ×0.8

EPIDE

60 ×1.0

PHYSI

14 ×0.2

Citations per year, relative to Isabelle Rouvet Isabelle Rouvet (= 1×) peers Yohan Kim

Countries citing papers authored by Isabelle Rouvet

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Rouvet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Rouvet

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Rouvet. A scholar is included among the top collaborators of Isabelle Rouvet 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 Isabelle Rouvet. Isabelle Rouvet 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

Sun, Xiaona, Ting Liu, Jun Zhao, et al.. (2020). DNA-PK deficiency potentiates cGAS-mediated antiviral innate immunity. Nature Communications. 11(1). 6182–6182. 95 indexed citations

Bourillon, Agnès, Samia Pichard, Jean‐François Benoist, et al.. (2017). Mitochondrial acetoacetyl‐CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis. Journal of Inherited Metabolic Disease. 40(3). 415–422. 11 indexed citations

Zhang, Shu, Corinne Pondarré, Gaëlle Pennarun, et al.. (2016). A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly. The Journal of Experimental Medicine. 213(6). 1011–1028. 19 indexed citations

Millat, Gilles, et al.. (2015). Functional Characterization of Putative Novel Splicing Mutations in the Cardiomyopathy-Causing Genes. DNA and Cell Biology. 34(7). 489–496. 12 indexed citations

Bélot, Alexandre, Anne‐Laure Mathieu, Gillian Rice, et al.. (2014). PRKDC mutations associated with immunodeficiency, granuloma and aire-dependent autoimmunity. Pediatric Rheumatology. 12(S1). 1 indexed citations

Echaniz‐Laguna, Andoni, Daniele Ghezzi, Martine Mayençon, et al.. (2013). SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease. Neurology. 81(17). 1523–1530. 44 indexed citations

Millat, Gilles, Juliette Albuisson, Véronique Bonnet, et al.. (2012). Combined Use of In Silico and In Vitro Splicing Assays for Interpretation of Genomic Variants of Unknown Significance in Cardiomyopathies and Channelopathies. SHILAP Revista de lepidopterología. 2(1). e6–e6. 10 indexed citations

Janoly-Duménil, A., Isabelle Rouvet, Nathalie Bleyzac, et al.. (2012). A Pharmacodynamic Model of Ganciclovir Antiviral Effect and Toxicity for Lymphoblastoid Cells Suggests a New Dosing Regimen To Treat Cytomegalovirus Infection. Antimicrobial Agents and Chemotherapy. 56(7). 3732–3738. 23 indexed citations

Blanchard, Stéphane, Élise Roy, Stéphanie Bigou, et al.. (2011). Modeling neuronal defects associated with a lysosomal disorder using patient-derived induced pluripotent stem cells. Human Molecular Genetics. 20(18). 3653–3666. 69 indexed citations

10.

Echaniz‐Laguna, Andoni, Isabelle Rouvet, Serge Nataf, et al.. (2011). Complete loss of expression of the ANT1 gene causing cardiomyopathy and myopathy. Journal of Medical Genetics. 49(2). 146–150. 53 indexed citations

11.

Camaret, Bénédicte Mousson de, Martine Mayençon, P. Clerc-Renaud, et al.. (2010). POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome. Mitochondrion. 11(1). 223–227. 5 indexed citations

12.

Debret, Romain, Valérie Cenizo, Valérie André, et al.. (2010). Epigenetic Silencing of Lysyl Oxidase-Like-1 through DNA Hypermethylation in an Autosomal Recessive Cutis Laxa Case. Journal of Investigative Dermatology. 130(11). 2594–2601. 17 indexed citations

13.

Janoly-Duménil, A., Isabelle Rouvet, Nathalie Bleyzac, et al.. (2009). Effect of Duration and Intensity of Ganciclovir Exposure on Lymphoblastoid Cell Toxicity. Antiviral chemistry & chemotherapy. 19(6). 257–262. 12 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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