Marie‐Madeleine Eliot

922 total citations
3 papers, 92 citations indexed

About

Marie‐Madeleine Eliot is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Marie‐Madeleine Eliot has authored 3 papers receiving a total of 92 indexed citations (citations by other indexed papers that have themselves been cited), including 1 paper in Molecular Biology, 1 paper in Genetics and 1 paper in Cognitive Neuroscience. Recurrent topics in Marie‐Madeleine Eliot's work include RNA and protein synthesis mechanisms (1 paper), interferon and immune responses (1 paper) and Cleft Lip and Palate Research (1 paper). Marie‐Madeleine Eliot is often cited by papers focused on RNA and protein synthesis mechanisms (1 paper), interferon and immune responses (1 paper) and Cleft Lip and Palate Research (1 paper). Marie‐Madeleine Eliot collaborates with scholars based in France, Germany and Brazil. Marie‐Madeleine Eliot's co-authors include Claude Jardel, Éréa-Noël Garabédian, Delphine Feldmann, Rémy Couderc, Dominique Weil, Christine Petit, Sandrine Marlin, Élise Chapiro, Françoise Denoyelle and Damien Sternberg and has published in prestigious journals such as Genetics in Medicine, European Journal of Human Genetics and PubMed.

In The Last Decade

Marie‐Madeleine Eliot

3 papers receiving 91 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marie‐Madeleine Eliot France 3 64 29 23 8 8 3 92
Faezeh Mojahedi Iran 6 82 1.3× 64 2.2× 35 1.5× 9 1.1× 14 1.8× 8 160
Jiddeke van de Kamp Netherlands 5 38 0.6× 43 1.5× 15 0.7× 7 0.9× 3 0.4× 6 80
Mariet W. Elting Netherlands 3 44 0.7× 26 0.9× 12 0.5× 5 0.6× 4 0.5× 3 94
Amit Kawalia Germany 6 59 0.9× 23 0.8× 23 1.0× 2 0.3× 14 1.8× 7 112
Thomas Jaworek United States 5 73 1.1× 27 0.9× 47 2.0× 2 0.3× 15 1.9× 7 122
Suzanne E. de Bruijn Netherlands 5 46 0.7× 15 0.5× 13 0.6× 3 0.4× 7 0.9× 13 64
Yoel Hirsch United States 7 93 1.5× 39 1.3× 9 0.4× 4 0.5× 7 0.9× 18 131
Abdullah Üzümcü Türkiye 4 55 0.9× 13 0.4× 32 1.4× 2 0.3× 19 2.4× 5 87
Audrey Mercier France 2 100 1.6× 42 1.4× 9 0.4× 10 1.3× 4 0.5× 2 115
T Derksen Netherlands 2 41 0.6× 43 1.5× 8 0.3× 8 1.0× 3 0.4× 2 104

Countries citing papers authored by Marie‐Madeleine Eliot

Since Specialization
Citations

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

Fields of papers citing papers by Marie‐Madeleine Eliot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie‐Madeleine Eliot. 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 Marie‐Madeleine Eliot. The network helps show where Marie‐Madeleine Eliot may publish in the future.

Co-authorship network of co-authors of Marie‐Madeleine Eliot

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

All Works

3 of 3 papers shown
1.
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
2.
Eliot, Marie‐Madeleine, et al.. (2005). [Autistic-like behavioural disorders and deafness in children].. PubMed. 126(5). 365–7. 3 indexed citations
3.
Chapiro, Élise, Delphine Feldmann, Françoise Denoyelle, et al.. (2002). Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor. European Journal of Human Genetics. 10(12). 851–856. 47 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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Breakdown of academic impact, for papers by Faezeh Mojahedi Breakdown of academic impact, for papers by Jiddeke van de Kamp Breakdown of academic impact, for papers by Mariet W. Elting Breakdown of academic impact, for papers by Amit Kawalia Breakdown of academic impact, for papers by Thomas Jaworek Breakdown of academic impact, for papers by Suzanne E. de Bruijn Breakdown of academic impact, for papers by Yoel Hirsch Breakdown of academic impact, for papers by Abdullah Üzümcü Breakdown of academic impact, for papers by Audrey Mercier Breakdown of academic impact, for papers by T Derksen
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