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Head & Neck|December 26, 2018
Tumor multifocality with vagus nerve involvement as a phenotypic marker of SDHD mutation in patients with head and neck paragangliomas: A 18 F-FDOPA PET/CT studyVincent Amodru, Pauline Romanet, Ugo Scemama, et al.
Journal of Neuroendocrinology|June 16, 2023
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reportsThi Thom Mac, Frederic Castinetti, Céline Bar, et al.
Hormone Research in Paediatrics|April 29, 2026
Unraveling the Genetic Heterogeneity of Isolated Growth Hormone Deficiency: Insights from the GENHYPOPIT cohortKarine Aouchiche, Pauline Romanet, Théo Charnay, et al.
European Journal of Endocrinology|November 1, 2019
Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?Lucie Coppin, Margaux Dufosse, Pauline Romanet, et al.
European Journal of Medical Genetics|January 17, 2017
Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of "thyroid-checked" controlsBenjamin Kern, Lucie Coppin, Pauline Romanet, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2026
3D volume growth rate may open new perspectives for the classification of aggressive pituitary adenomasThomas Graillon, Emeline Tabouret, Romain Appay, et al.
Endocrine Connections|September 16, 2022
Systematic detection of mosaicism by using digital NGS reveals three new MEN1 mosaicismsArnaud Lagarde, Grégory Mougel, Lucie Coppin, et al.
Annales De Biologie Clinique|December 21, 2019
[Development of molecular analysis by digital PCR for clinical practice: positioning, current applications and perspectives]Jérôme Alexandre Denis, Alexandre Perrier, Juliette Nectoux, et al.
Human Mutation|March 15, 2019
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variantsPauline Romanet, Marie-Françoise Odou, Marie-Odile North, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2018
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French PopulationPauline Romanet, Amira Mohamed, Sophie Giraud, et al.
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