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European Journal of Endocrinology|December 16, 2021
Identification of glucocorticoid-related molecular signature by whole blood methylome analysisRoberta Armignacco, Anne Jouinot, Lucas Bouys, et al.
The Journal of Clinical Endocrinology and Metabolism|August 14, 2025
A Global Approach to the Long-Term Follow-up of 17 Families with Bilateral Macronodular Adrenal DiseaseHelaine Laiz Silva Charchar, Guilherme Asmar Alencar, Beatriz Marinho de Paula Mariani, et al.
European Journal of Endocrinology|March 6, 2026
Clinical Predictors of Outcome in Advanced Adrenocortical Carcinoma: a multicentre international ENSAT studyAlessandra Mangone, Barbara Altieri, Emanuele Ferrante, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
KDM1A inactivation causes hereditary food-dependent Cushing syndromeAnna Vaczlavik, Lucas Bouys, Florian Violon, et al.
European Journal of Endocrinology|February 8, 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlationLucas Bouys, Patricia Vaduva, Anne Jouinot, et al.
Nature Communications|October 6, 2025
Impact of steroid differentiation on tumor microenvironment revealed by single-nucleus atlas of adrenal tumorsAnne Jouinot, Yoann Martin, Florian Violon, et al.
Clinical Epigenetics|November 4, 2022
Whole blood methylome-derived features to discriminate endocrine hypertensionRoberta Armignacco, Parminder S Reel, Smarti Reel, et al.
European Journal of Endocrinology|May 6, 2022
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patientsLucas Bouys, Anna Vaczlavik, Anne Jouinot, et al.
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