Elodie Tron

665 total citations
10 papers, 388 citations indexed

About

Elodie Tron is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Endocrine and Autonomic Systems. According to data from OpenAlex, Elodie Tron has authored 10 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 3 papers in Endocrine and Autonomic Systems. Recurrent topics in Elodie Tron's work include Thyroid Disorders and Treatments (6 papers), Congenital heart defects research (5 papers) and Neuroscience of respiration and sleep (3 papers). Elodie Tron is often cited by papers focused on Thyroid Disorders and Treatments (6 papers), Congenital heart defects research (5 papers) and Neuroscience of respiration and sleep (3 papers). Elodie Tron collaborates with scholars based in France, Switzerland and Brazil. Elodie Tron's co-authors include Aurore Carré, Mireille Castanet, Gabor Szinnai, Isabelle Broutin, Michel Polak, Juliane Léger, Loïc Guillot, Cyril Goizet, M.L. Moutard and Serge Romana and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Journal of Investigative Dermatology.

In The Last Decade

Elodie Tron

10 papers receiving 377 citations

Peers

Elodie Tron

EDM

GENET

PRM

SURGE

Sylvia Sura‐Trueba France

Michael J McPhaul United States

Andrew Lane United States

Martine Sinico France

Sarah Brickwood United Kingdom

Esther M. Nitsche Germany

Monique De Vroede Netherlands

Jing W. Hughes United States

Stefano Maio United Kingdom

Shuntaro Morikawa Japan

Sylvia Sura‐Trueba France

Elodie Tron

199 ×0.9

116 ×0.8

EDM

145 ×1.1

GENET

61 ×0.6

PRM

59 ×0.7

SURGE

Citations per year, relative to Elodie Tron Elodie Tron (= 1×) peers Sylvia Sura‐Trueba

Countries citing papers authored by Elodie Tron

Since Specialization

Citations

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

Fields of papers citing papers by Elodie Tron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elodie Tron

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

All Works

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10 of 10 papers shown

Ramos, Helton Estrela, Magnus R. Dias‐da‐Silva, Aurore Carré, et al.. (2015). Molecular Insights into the Possible Role of Kir4.1 and Kir5.1 in Thyroid Hormone Biosynthesis. Hormone Research in Paediatrics. 83(2). 141–147. 5 indexed citations

Ramos, Helton Estrela, Aurore Carré, L. Chevrier, et al.. (2014). Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations. European Journal of Endocrinology. 171(4). 499–507. 30 indexed citations

Carré, Aurore, L. Chevrier, Gabor Szinnai, et al.. (2014). Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion. Journal of Pediatric Endocrinology and Metabolism. 28(7-8). 777–84. 5 indexed citations

Carré, Aurore, Rasha T. Hamza, Dulanjalee Kariyawasam, et al.. (2013). A Novel FOXE1 Mutation (R73S) in Bamforth–Lazarus Syndrome Causing Increased Thyroidal Gene Expression. Thyroid. 24(4). 649–654. 31 indexed citations

Lacroix, Matthieu, Laetitia Furio, Elodie Tron, et al.. (2011). Clinical Expression and New SPINK5 Splicing Defects in Netherton Syndrome: Unmasking a Frequent Founder Synonymous Mutation and Unconventional Intronic Mutations. Journal of Investigative Dermatology. 132(3). 575–582. 27 indexed citations

Carré, Aurore, Latif Rachdi, Elodie Tron, et al.. (2011). Hes1 Is Required for Appropriate Morphogenesis and Differentiation during Mouse Thyroid Gland Development. PLoS ONE. 6(2). e16752–e16752. 37 indexed citations

Ramos, Helton Estrela, Aurore Carré, Elodie Tron, et al.. (2010). Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care. European Journal of Endocrinology. 164(2). 309–314. 16 indexed citations

Ramos, Helton Estrela, Aurore Carré, Mireille Castanet, et al.. (2010). New Cases of Isolated Congenital Central Hypothyroidism Due to Homozygous Thyrotropin Beta Gene Mutations: A Pitfall to Neonatal Screening. Thyroid. 20(6). 639–645. 12 indexed citations

Guillot, Loïc, Aurore Carré, Gabor Szinnai, et al.. (2009). NKX2-1mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome”. Human Mutation. 31(2). E1146–E1162. 80 indexed citations

10.

Carré, Aurore, Gabor Szinnai, Mireille Castanet, et al.. (2009). Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case. Human Molecular Genetics. 18(12). 2266–2276. 145 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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