Elodie Sanchez

1.3k total citations
15 papers, 272 citations indexed

About

Elodie Sanchez is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Elodie Sanchez has authored 15 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Genetics. Recurrent topics in Elodie Sanchez's work include Inflammasome and immune disorders (5 papers), Genomics and Rare Diseases (3 papers) and interferon and immune responses (2 papers). Elodie Sanchez is often cited by papers focused on Inflammasome and immune disorders (5 papers), Genomics and Rare Diseases (3 papers) and interferon and immune responses (2 papers). Elodie Sanchez collaborates with scholars based in France, Italy and Germany. Elodie Sanchez's co-authors include Isabelle Touitou, David Geneviève, Raffaele Manna, A. Le Quellec, Isabelle Koné‐Paut, Dagmar Wieczorek, Marjolaine Willems, Christian Jørgensen, Sophie Vacher and Philippe Bourin and has published in prestigious journals such as Scientific Reports, Annals of the Rheumatic Diseases and Clinica Chimica Acta.

In The Last Decade

Elodie Sanchez

14 papers receiving 269 citations

Peers

Elodie Sanchez

GENET

IMMUN

ONCOL

GENET

Natália D. Linhares Brazil

Kimihiko Banno Japan

Sara Ekvall Sweden

Ronny Derks Netherlands

Sarina Sulong Malaysia

Margherita Baldassarri Italy

Ola Khalifa Saudi Arabia

Hannah Titheradge United Kingdom

Detlef Trost France

Kyle S. Yau Australia

Natália D. Linhares Brazil

Elodie Sanchez

168 ×1.1

102 ×1.1

GENET

89 ×1.6

IMMUN

29 ×0.7

ONCOL

15 ×0.4

GENET

Citations per year, relative to Elodie Sanchez Elodie Sanchez (= 1×) peers Natália D. Linhares

Countries citing papers authored by Elodie Sanchez

Since Specialization

Citations

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

Fields of papers citing papers by Elodie Sanchez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elodie Sanchez

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

All Works

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15 of 15 papers shown

Sanchez, Elodie, Nathalie Ruiz-Pallares, O. Prodhomme, et al.. (2023). Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephaly. European Journal of Medical Genetics. 66(5). 104733–104733. 3 indexed citations

Rittore, Cécile, Elodie Sanchez, Aude Mallavialle, et al.. (2021). TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS. Scientific Reports. 11(1). 4172–4172. 3 indexed citations

Pérez-Barrios, Clara, Matti Romo, Elodie Sanchez, et al.. (2019). Utility of high sensitivity NGS for EGFR exon 19 mutations detection from circulating-free DNA. Clinica Chimica Acta. 493. S157–S158.

Mau‐Them, Frédéric Tran, Julien Thévenon, Thomas Guignard, et al.. (2018). LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. European Journal of Medical Genetics. 62(3). 161–166. 19 indexed citations

Yauy, Kévin, Frédéric Tran Mau‐Them, Marjolaine Willems, et al.. (2017). B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation. Genetics in Medicine. 20(2). 269–274. 21 indexed citations

Grandemange, Sylvie, Guillaume Sarrabay, Jérôme Pène, et al.. (2017). Clinical dose effect and functional consequences of R92Q in two families presenting with a TRAPS/PFAPA‐like phenotype. Molecular Genetics & Genomic Medicine. 5(2). 110–116. 8 indexed citations

Grandemange, Sylvie, Elodie Sanchez, Pascale Louis‐Plence, et al.. (2015). NLRP1 mutations cause autoinflammatory diseases in human. Pediatric Rheumatology. 13(S1). 5 indexed citations

Bouclier, Céline, Ivan Bièche, Madly Brigitte, et al.. (2015). IL-1β produced by aggressive breast cancer cells is one of the factors that dictate their interactions with mesenchymal stem cells through chemokine production. Oncotarget. 6(30). 29034–29047. 57 indexed citations

Barat‐Houari, Mouna, Vincent Gâtinois, Elodie Sanchez, et al.. (2015). Le syndrome Kabuki : mise au point et revue de la littérature. Archives de Pédiatrie. 22(6). 653–660. 8 indexed citations

10.

Schaefer, Élise, Corinne Collet, David Geneviève, et al.. (2014). Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome. Genetics in Medicine. 16(9). 720–724. 42 indexed citations

11.

Vincent, Marie, Corinne Collet, Alain Verloès, et al.. (2013). Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability. European Journal of Human Genetics. 22(1). 52–56. 15 indexed citations

12.

Rittore, Cécile, Elodie Sanchez, Mouna Barat‐Houari, et al.. (2013). Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene. Annals of the Rheumatic Diseases. 73(1). 290–297. 11 indexed citations

13.

Corsini, Carole, Martin Genčík, Marjolaine Willems, et al.. (2013). Somatic mosaicism in trichorhinophalangeal syndrome: a lesson for genetic counseling. European Journal of Human Genetics. 22(1). 136–139. 2 indexed citations

14.

Mau‐Them, Frédéric Tran, Marjolaine Willems, Beate Albrecht, et al.. (2013). Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability. European Journal of Human Genetics. 22(2). 289–292. 30 indexed citations

15.

Koné‐Paut, Isabelle, Elodie Sanchez, A. Le Quellec, Raffaele Manna, & Isabelle Touitou. (2007). Autoinflammatory gene mutations in Behçet's disease. Annals of the Rheumatic Diseases. 66(6). 832–834. 48 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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