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

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

#	Work	Indexed citations
1	Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephaly 2023 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), Elodie Sanchez, Nathalie Ruiz-Pallares, (unknown), (unknown), (unknown), O. Prodhomme, Nicolas Leboucq, Isabelle Meunier, D. Bessis, (unknown), Mouna Barat‐Houari, Marjolaine Willems	3
2	TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS 2021 ·Scientific Reports ·Cécile Rittore, (unknown), Elodie Sanchez, (unknown), (unknown), (unknown), (unknown), Aude Mallavialle, Eric Richard, Isabelle Duroux-Richard, Florence Apparailly, Isabelle Touitou, Sylvie Grandemange	3
3	Utility of high sensitivity NGS for EGFR exon 19 mutations detection from circulating-free DNA 2019 ·Clinica Chimica Acta ·Clara Pérez-Barrios, Matti Romo, Elodie Sanchez, Raquel Laza‐Briviesca, (unknown), (unknown), Mariano Provencio, Angélica Romero	0
4	LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters 2018 ·European Journal of Medical Genetics ·(unknown), Frédéric Tran Mau‐Them, Julien Thévenon, Thomas Guignard, Vincent Gâtinois, Jean‐Baptiste Rivière, Anne Boland, Vincent Meyer, Jean‐François Deleuze, Elodie Sanchez, Florence Apparailly, David Geneviève, Marjolaine Willems	19
5	B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation 2017 ·Genetics in Medicine ·Kévin Yauy, Frédéric Tran Mau‐Them, Marjolaine Willems, Christine Coubes, Patricia Blanchet, Christian Herlin, (unknown), Elodie Sanchez, Jean-Michel Faure, (unknown), O. Prodhomme, Anne Boland, Vincent Meyer, Jean‐Baptiste Rivière, Yannis Duffourd, Jean‐François Deleuze, Thomas Guignard, Guillaume Captier, Mouna Barat‐Houari, David Geneviève	21
6	Clinical dose effect and functional consequences of R92Q in two families presenting with a TRAPS/PFAPA‐like phenotype 2017 ·Molecular Genetics & Genomic Medicine ·Sylvie Grandemange, (unknown), Guillaume Sarrabay, Jérôme Pène, Cécile Rittore, Elodie Sanchez, (unknown), (unknown), Pascal Pillet, Isabelle Touitou	8
7	NLRP1 mutations cause autoinflammatory diseases in human 2015 ·Pediatric Rheumatology ·Sylvie Grandemange, Elodie Sanchez, Pascale Louis‐Plence, Cécile Rittore, JC Reed, Isabelle Touitou, David Geneviève	5
8	IL-1β produced by aggressive breast cancer cells is one of the factors that dictate their interactions with mesenchymal stem cells through chemokine production 2015 ·Oncotarget ·(unknown), Céline Bouclier, (unknown), Ivan Bièche, Madly Brigitte, Andrés Caicedo, Elodie Sanchez, Sophie Vacher, Marie‐Luce Vignais, Philippe Bourin, David Geneviève, Franck Molina, Christian Jørgensen, Gwendal Lazennec	57
9	Le syndrome Kabuki : mise au point et revue de la littérature 2015 ·Archives de Pédiatrie ·(unknown), Mouna Barat‐Houari, Vincent Gâtinois, Elodie Sanchez, Stanislas Lyonnet, Isabelle Touitou, David Geneviève	8
10	Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome 2014 ·Genetics in Medicine ·Élise Schaefer, Corinne Collet, David Geneviève, Marie Vincent, Dietmar Lohmann, Elodie Sanchez, (unknown), Marie‐Madeleine Eliot, Gudrun Nürnberg, Maria-Rita Passos-Bueno, Dagmar Wieczorek, Lionel Van Maldergem, Bérénice Doray	42
11	Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability 2013 ·European Journal of Human Genetics ·Marie Vincent, Corinne Collet, Alain Verloès, Laëtitia Lambert, Christian Herlin, Catherine Blanchet, Elodie Sanchez, Séverine Drunat, Jacqueline Vigneron, Jean Laplanche, Jacques Puechberty, Pierre Sarda, David Geneviève	15
12	Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene 2013 ·Annals of the Rheumatic Diseases ·Cécile Rittore, Elodie Sanchez, (unknown), Mouna Barat‐Houari, (unknown), Laura Obici, Michael McDermott, Isabelle Touitou, Sylvie Grandemange	11
13	Somatic mosaicism in trichorhinophalangeal syndrome: a lesson for genetic counseling 2013 ·European Journal of Human Genetics ·Carole Corsini, Martin Genčík, Marjolaine Willems, Eva L. Decker, Elodie Sanchez, Jacques Puechberty, Anouck Schneider, Manon Girard, Patrick Edery, (unknown), J. Cottalorda, Geneviève Lefort, Claire Jeandel, Pierre Sarda, David Geneviève	2
14	Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability 2013 ·European Journal of Human Genetics ·Frédéric Tran Mau‐Them, Marjolaine Willems, Beate Albrecht, Elodie Sanchez, Jacques Puechberty, Sabine Endele, Anouck Schneider, (unknown), Chantal Missirian, François Rivier, Manon Girard, Muriel Holder, Sylvie Manouvrier, Isabelle Touitou, Geneviève Lefort, Pierre Sarda, Anne Moncla, Séverine Drunat, Dagmar Wieczorek, David Geneviève	30
15	Autoinflammatory gene mutations in Behçet's disease 2007 ·Annals of the Rheumatic Diseases ·Isabelle Koné‐Paut, Elodie Sanchez, A. Le Quellec, Raffaele Manna, Isabelle Touitou	48

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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