Thomas Edouard

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 9

Top Topics

Tyrosine Kinase

Aortic Aneurysm

Top Venues

Orphanet journal of rare diseases

European journal of endocrinology

Human molecular genetics

European journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Thomas Edouard, Marie-Christine Picot, Fernanda Bajanca, Helena Huguet, Aitor Guitarte, Maud Langeois, Bertrand Chesneau, Philippe Khau Van Kien, Eric Garrigue, Yves Dulac, Pascal Amedro
Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Thomas Edouard, Marie-Christine Picot, Fernanda Bajanca, Helena Huguet, Aitor Guitarte, Maud Langeois, Bertrand Chesneau, Philippe Khau Van Kien, Eric Garrigue, Yves Dulac, Pascal Amedro
Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Thomas Edouard, Marie-Christine Picot, Fernanda Bajanca, Helena Huguet, Aitor Guitarte, Maud Langeois, Bertrand Chesneau, Philippe Khau Van Kien, Eric Garrigue, Yves Dulac, Pascal Amedro
Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Alice Broutin, Jean-Pierre Salles, Valérie Porquet-Bordes, Thomas Edouard, Frédéric Vaysse, Emmanuelle Noirrit-Esclassan
Orofacial Features, Oral Health-Related Quality of Life, and Exposure to Bullying in Osteogenesis Imperfecta: A Cross-Sectional Study. Children (Basel, Switzerland) 11 (8) (2024)
Céline Saint-Laurent, Laurène Mazeyrie, Armelle Yart, Thomas Edouard
Novel therapeutic perspectives in Noonan syndrome and RASopathies. European journal of pediatrics (2023)
Rachel Fourneaux, Rachel Reynaud, Gregory Mougel, Sarah Castets, Patricia Bretones, Benjamin Dauriat, Thomas Edouard, Gerald Raverot, Anne Barlier, Thierry Brue, Castinetti Frederic, Alexandru Saveanu
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology 187 (6) (2022)
Gaëlle Nannette, Céline Bar, Gwenaëlle Diene, Catherine Pienkowski, Isabelle Oliver-Petit, Béatrice Jouret, Audrey Cartault, Valérie Porquet-Bordes, Jean Pierre Salles, Solange Grunenwald, Thomas Edouard, Catherine Molinas, Maïthé Tauber
Obesity, overweight and pituitary stalk interruption syndrome in children and young adults. The Journal of clinical endocrinology and metabolism (2022)
Romain Paccoud, Céline Saint-Laurent, Enzo Piccolo, Mylène Tajan, Alizée Dortignac, Ophélie Pereira, Sophie Le Gonidec, Inès Baba, Adélaïde Gélineau, Haoussa Askia, Maxime Branchereau, Julie Charpentier, Jean Personnaz, Sophie Branka, Johanna Auriau, Simon Deleruyelle, Mickaël Canouil, Nicolas Beton, Jean Pierre Salles, Maïthé Tauber, Jacques Weill, Philippe Froguel, Benjamin G Neel, Toshiyuki Araki, Christophe Heymes, Rémy Burcelin, Isabelle Castan-Laurell, Philippe Valet, Cédric Dray, Emmanuel L Gautier, Thomas Edouard, Jean-Philippe Pradère, Armelle Yart
SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations. Science translational medicine 13 (591) (2021)
Caroline Caetano Silva, Thomas Edouard, Melanie Fradin, Marion Aubert-Mucca, Manon Ricquebourg, Ratish Raman, Jean Pierre Salles, Valérie Charon, Pascal Guggenbuhl, Marc Muller, Martine Cohen-Solal, Corinne Collet
WNT11, a new gene associated with early-onset osteoporosis, is required for osteoblastogenesis. Human molecular genetics (2021)