Jean-Claude Carel

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 5

Top Venues

The Journal of clinical endocrinology and metabolism

Human mutation

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Linda Humbert, Emmanuelle Proust-Lemoine, Sylvain Dubucquoi, Elisabeth Helen Kemp, Pascale Saugier-Veber, Nicole Fabien, Isabelle Raymond-Top, Catherine Cardot-Bauters, Jean-Claude Carel, Maryse Cartigny, Olivier Chabre, Philippe Chanson, Brigitte Delemer, Christine Do Cao, Laurence Guignat, Jean Emmanuel Kahn, Veronique Kerlan, Herve Lefebvre, Agnès Linglart, Roberto Mallone, Rachel Reynaud, Boualem Sendid, Pierre-François Souchon, Philippe A Touraine, Jean-Louis Wémeau, Marie-Christine Vantyghem
Lessons from prospective longitudinal follow-up of a French APECED cohort. The Journal of clinical endocrinology and metabolism (2024)
Juliane Léger, Clemence Delcour, Jean-Claude Carel
APPROACH TO THE PATIENT Fetal and neonatal thyroid dysfunction. The Journal of clinical endocrinology and metabolism (2021)
Sophie Courbage, Christine Poitou, Johanne Le Beyec-Le Bihan, Alexandra Karsenty, Julie Lemale, Véronique Pelloux, Jean-Marc Lacorte, Jean-Claude Carel, Nathalie Lecomte, Caroline Storey, Gianpaolo De Filippo, Muriel Coupaye, Jean-Michel Oppert, Patrick Tounian, Karine Clément, Beatrice Dubern
Implication of Heterozygous Variants in Genes of the Leptin-Melanocortin Pathway in Severe Obesity. The Journal of clinical endocrinology and metabolism 106 (10) (2021)
Enzo Cohen, Sabrina Belkacem, Soumeya Fedala, Nathalie Collot, Eliane Khallouf, Florence Dastot, Michel Polak, Philippe Duquesnoy, Frederic Brioude, Sophie Rose, Géraldine Viot, Aude Soleyan, Jean-Claude Carel, Marie-Laure Sobrier, Philippe Chanson, Frédérique Gatelais, Claudine Heinrichs, Noureddine Kaffel, Regis Coutant, Senay Savas Erdeve, Erdal Kurnaz, Zehra Aycan, Caroline Thalassinos, Stanislas Lyonnet, Zeynep Şıklar, Merih Berberoglu, Cécile Brachet, Serge Amselem, Marie Legendre
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations. Human mutation 40 (11) (2019)
Kenneth McElreavey, Anne Jørgensen, Caroline Eozenou, Tiphanie Merel, Joelle Bignon-Topalovic, Daisylyn Senna Tan, Denis Houzelstein, Federica Buonocore, Nick Warr, Raissa G G Kay, Matthieu Peycelon, Jean-Pierre Siffroi, Inas Mazen, John C Achermann, Yuliya Shcherbak, Juliane Leger, Agnes Sallai, Jean-Claude Carel, Laetitia Martinerie, Romain Le Ru, Gerard S Conway, Brigitte Mignot, Lionel Van Maldergem, Rita Bertalan, Evgenia Globa, Raja Brauner, Ralf Jauch, Serge Nef, Andy Greenfield, Anu Bashamboo
Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)

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Publication Activity (10 Years)

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Top Venues

Jean-Claude Carel