Mireille Castanet

3.6k total citations
56 papers, 2.1k citations indexed

About

Mireille Castanet is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Mireille Castanet has authored 56 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Endocrinology, Diabetes and Metabolism, 27 papers in Molecular Biology and 17 papers in Genetics. Recurrent topics in Mireille Castanet's work include Thyroid Disorders and Treatments (23 papers), Congenital heart defects research (15 papers) and Vitamin D Research Studies (5 papers). Mireille Castanet is often cited by papers focused on Thyroid Disorders and Treatments (23 papers), Congenital heart defects research (15 papers) and Vitamin D Research Studies (5 papers). Mireille Castanet collaborates with scholars based in France, Switzerland and United States. Mireille Castanet's co-authors include Michel Polak, Juliane Léger, Paul Czernichow, Aurore Carré, Stanislas Lyonnet, Gabor Szinnai, Jean Guibourdenche, Elodie Tron, Edith Vuillard and Catherine Bonaïti‐Pellié and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

Mireille Castanet

54 papers receiving 2.0k citations

Peers

Countries citing papers authored by Mireille Castanet

Since Specialization

Citations

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

Fields of papers citing papers by Mireille Castanet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mireille Castanet

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper 2022 ·Archives de Pédiatrie ·Justine Bacchetta, Thomas Édouard, Gilles Laverny, Julie Bernardor, Aurélia Bertholet‐Thomas, Mireille Castanet, (unknown), Isabelle Gennero, (unknown), Alexandre Lapillonne, Arnaud Molin, (unknown), Jean‐Pierre Salles, Sophie Laborie, Patrick Tounian, Agnès Linglart	41
2	The invention of aldosterone, how the past resurfaces in pediatric endocrinology 2021 ·Molecular and Cellular Endocrinology ·Say Viengchareun, Eric Pussard, Mireille Castanet, Laurent M. Sachs, (unknown), Pascal Boileau, Marc Lombès, Laëtitia Martinerie	1
3	Early Effect of Supplemented Infant Formulae on Intestinal Biomarkers and Microbiota: A Randomized Clinical Trial 2020 ·Nutrients ·Mireille Castanet, Christos Costalos, Nadja Haiden, Jean‐Michel Hascoët, Bernard Berger, Norbert Sprenger, Dominik Grathwohl, Harald Brüssow, Nanda de Groot, Philippe Steenhout, Sophie Pecquet, Jalil Benyacoub, Jean‐Charles Picaud	32
4	Molecular Insights into the Possible Role of Kir4.1 and Kir5.1 in Thyroid Hormone Biosynthesis 2015 ·Hormone Research in Paediatrics ·Helton Estrela Ramos, Magnus R. Dias‐da‐Silva, Aurore Carré, (unknown), (unknown), (unknown), Elodie Tron, Mireille Castanet, Michel Polak	5
5	Metallic Profile of Whole Blood and Plasma in a Series of 99 Healthy Children 2015 ·Journal of Analytical Toxicology ·Jean‐Pierre Goullé, P. Le Roux, Mireille Castanet, Loïc Mahieu, (unknown), Michel Guerbet	27
6	Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations 2014 ·European Journal of Endocrinology ·Helton Estrela Ramos, Aurore Carré, L. Chevrier, Gabor Szinnai, Elodie Tron, (unknown), Juliane Léger, S Cabrol, (unknown), (unknown), Nicolás de Roux, Loïc Guillot, Mireille Castanet, Michel Polak	30
7	A Novel FOXE1 Mutation (R73S) in Bamforth–Lazarus Syndrome Causing Increased Thyroidal Gene Expression 2013 ·Thyroid ·Aurore Carré, Rasha T. Hamza, Dulanjalee Kariyawasam, Loïc Guillot, (unknown), Elodie Tron, Mireille Castanet, Corinne Dupuy, Mohamed El Kholy, Michel Polak	31
8	Accueil en urgence des adolescents pour motif pédopsychiatrique 2013 ·Archives de Pédiatrie ·(unknown), (unknown), (unknown), Sylvain Rigal, (unknown), Mireille Castanet, (unknown), Charles G. Marguet, Priscille Gérardin	6
9	Lightwood Syndrome Revisited with a Novel Mutation in CYP24 and Vitamin D Supplement Recommendations 2013 ·The Journal of Pediatrics ·Mireille Castanet, E. Mallet, Marie‐Laure Kottler	31
10	Multiplex Ligation-Dependent Probe Amplification Improves the Detection Rate of <b><i>NKX2.1</i></b> Mutations in Patients Affected by Brain-Lung-Thyroid Syndrome 2012 ·Hormone Research in Paediatrics ·(unknown), Loïc Guillot, Aurore Carré, (unknown), Chantal Stuckens, H Ythier, Arnold Münnich, Gabor Szinnai, J. de Blic, Annick Clément, Juliane Léger, Mireille Castanet, Ralph Epaud, Michel Polak	14
11	Prescription prophylactique de la vitamine D en France : enquête épidémiologique multicentrique nationale chez 3240 enfants de moins de 6 ans 2012 ·Archives de Pédiatrie ·E. Mallet, J. Gaudelus, P Reinert, J. Stagnara, Jacques Bénichou, Mireille Castanet, (unknown), (unknown), C. Billard, (unknown), (unknown)	6
12	Administration orale hivernale d’une dose unique de 200 000 UI de vitamine D3 chez l’adolescent en région normande : évaluation de sa tolérance et du statut vitaminique D obtenu 2010 ·Archives de Pédiatrie ·E. Mallet, Philippe François, Mireille Castanet, (unknown)	15
13	Minéralisation osseuse et mucoviscidose 2009 ·Archives de Pédiatrie ·Isabelle Sermet‐Gaudelus, Mireille Castanet, (unknown), E. Mallet	7
14	NKX2-1mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome” 2009 ·Human Mutation ·Loïc Guillot, Aurore Carré, Gabor Szinnai, Mireille Castanet, Elodie Tron, Francis Jaubert, Isabelle Broutin, François Counil, Delphine Feldmann, (unknown), Michel Polak, Ralph Epaud	80
15	Familial Forms of Thyroid Dysgenesis 2007 ·Endocrine development ·Mireille Castanet, Michel Polak, Juliane Léger	10
16	Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis 2007 ·Human Genetics ·Aurore Carré, Mireille Castanet, Sylvia Sura‐Trueba, Gabor Szinnai, Guy Van Vliet, Delphine Trochet, Jeanne Amiel, Juliane Léger, Paul Czernichow, Virginie Scotet, Michel Polak	47
17	High Proportion of Pituitary Abnormalities and Other Congenital Defects in Children with Congenital Nasal Pyriform Aperture Stenosis 2006 ·Pediatric Research ·Sophie Guilmin‐Crépon, Cathérine Garel, Clarisse Baumann, Dominique Brémond‐Gignac, Isabelle Bailleul‐Forestier, S Magnier, Mireille Castanet, Paul Czernichow, T. Van Den Abbeele, Juliane Léger	30
18	Congenital Hyperthyroidism: The Fetus as a Patient 2006 ·Hormone Research in Paediatrics ·Michel Polak, (unknown), Edith Vuillard, Jean Guibourdenche, Mireille Castanet, Dominique Luton	65
19	Thyroid Hemiagenesis Is a Rare Variant of Thyroid Dysgenesis with a Familial Component but without Pax8 Mutations in a Cohort of 22 Cases 2005 ·Pediatric Research ·Mireille Castanet, Laurence Leenhardt, Juliane Léger, (unknown), Stanislas Lyonnet, Anna Pelet, Paul Czernichow, Michel Polak	40
20	Nineteen Years of National Screening for Congenital Hypothyroidism: Familial Cases with Thyroid Dysgenesis Suggest the Involvement of Genetic Factors 2001 ·The Journal of Clinical Endocrinology & Metabolism ·Mireille Castanet, Michel Polak, Catherine Bonaïti‐Pellié, Stanislas Lyonnet, Paul Czernichow, Juliane Léger	166

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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