UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population von Romanet, Pauline, Mohamed, Amira, Giraud, Sophie, Odou, Marie-Françoise, North, Marie-Odile, Pertuit, Morgane, Pasmant, Eric, Coppin, Lucie, Guien, Céline, Calender, Alain, Borson-Chazot, Françoise, Béroud, Christophe, Goudet, Pierre, Barlier, Anne

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Serum Succinate/Fumarate Ratio in Patients With Paraganglioma/Pheochromocytoma Attending an Endocrine Oncogenetic Unit von Bancel, Léo-Paul, Masso, Vincent, Dessein, Anne-Frederique, Aubert, Sébastien, Leteurtre, Emmanuelle, Coppin, Lucie, Odou, Marie-Françoise, Cao, Christine Do, Cardot-Bauters, Catherine, Pigny, Pascal

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Proposition of adjustments to the ACMG‐AMP framework for the interpretation of MEN1 missense variants von Romanet, Pauline, Odou, Marie‐Françoise, North, Marie‐Odile, Saveanu, Alexandru, Coppin, Lucie, Pasmant, Eric, Mohamed, Amira, Goudet, Pierre, Borson‐Chazot, Françoise, Calender, Alain, Béroud, Christophe, Lévy, Nicolas, Giraud, Sophie, Barlier, Anne

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Beyond MEN1, when to think about MEN4? Retrospective study on 5600 patients in the French population & literature review von Chevalier, Benjamin, Coppin, Lucie, Romanet, Pauline, Cuny, Thomas, Maiza, Jean-Christophe, Abeillon, Juliette, Forestier, Julien, Walter, Thomas, Gilly, Olivier, Le Bras, Maëlle, Smati, Sarra, Nunes, Marie Laure, Geslot, Aurore, Grunenwald, Solange, Mouly, Céline, Arnault, Gwenaelle, Wagner, Kathy, Koumakis, Eugénie, Cortet-Rudelli, Christine, Merlen, Émilie, Jannin, Arnaud, Espiard, Stéphanie, Morange, Isabelle, Baudin, Éric, Cavaille, Mathias, Tauveron, Igor, Teissier, Marie-Pierre, Borson-Chazot, Françoise, Mirebeau-Prunier, Delphine, Savagner, Frédérique, Pasmant, Éric, Giraud, Sophie, Vantyghem, Marie-Christine, Goudet, Pierre, Barlier, Anne, Cardot-Bauters, Catherine, Odou, Marie Françoise

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Multiplex targeted high‐throughput sequencing in a series of 352 patients with congenital limb malformations von Jourdain, Anne‐Sophie, Petit, Florence, Odou, Marie‐Françoise, Balduyck, Malika, Brunelle, Perrine, Dufour, William, Boussion, Simon, Brischoux‐Boucher, Elise, Colson, Cindy, Dieux, Anne, Gérard, Marion, Ghoumid, Jamal, Giuliano, Fabienne, Goldenberg, Alice, Khau Van Kien, Philippe, Lehalle, Daphné, Morin, Gilles, Moutton, Sébastien, Smol, Thomas, Vanlerberghe, Clémence, Manouvrier‐Hanu, Sylvie, Escande, Fabienne

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Alpha1 antitrypsin deficiency due to an homozygous PI Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression von Jouhadi, Zineb, Odou, Marie Francoise, Zerimech, Farid, Bousfiha, Ahmed Aziz, Mikou, Nabiha, Porchet, Nicole, Crepin, Michel, Najib, Jilali, Balduyck, Malika

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Mesenteric fat as a source of C reactive protein and as a target for bacterial translocation in Crohn's disease von Peyrin-Biroulet, Laurent, Gonzalez, Florent, Dubuquoy, Laurent, Rousseaux, Christel, Dubuquoy, Caroline, Decourcelle, Cécilia, Saudemont, Alain, Tachon, Mickael, Béclin, Elodie, Odou, Marie-Françoise, Neut, Christel, Colombel, Jean-Frédéric, Desreumaux, Pierre

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Diagnosis of mosaic mutations in the MEN1 gene by next generation sequencing von Coppin, Lucie, Ferrière, Amandine, Crépin, Michel, Haissaguerre, Magalie, Ladsous, Miriam, Tabarin, Antoine, Odou, Marie-Françoise

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Value of Somatostatin Receptor PET/CT in Patients With MEN1 at Various Stages of Their Disease von Mennetrey, Clément, Le Bras, Maëlle, Bando-Delaunay, Aurélie, Al-Mansour, Laure, Haissaguerre, Magalie, Batisse-Lignier, Marie, Ouvrard, Eric, Ansquer, Catherine, Walter, Thomas, de Mestier, Louis, Kelly, Antony, Tlili, Ghoufrane, Giraud, Sophie, North, Marie-Odile, Odou, Marie-Françoise, Goichot, Bernard, Cuny, Thomas, Loundou, Anderson, Romanet, Pauline, Imperiale, Alessio, Taïeb, David

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Genetic biomarkers of life-threatening pheochromocytoma-induced cardiomyopathy von Amar, Jacques, Brunel, Jeremy, Cardot Bauters, Catherine, Jacques, Virginie, Delmas, Clément, Odou, Marie-Françoise, Savagner, Frédérique

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MEN1 and the brain: Don’t just look only at the pituitary gland. A case report of anaplastic pleomorphic xanthoastrocytoma in a MEN1 patient, and systematic review von Jannin, Arnaud, Coppin, Lucie, Chevalier, Benjamin, Maurage, Claude-Alain, Odou, Marie Françoise, Bauters, Catherine Cardot

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Frequent Large Germline HRPT2 Deletions in a French National Cohort of Patients With Primary Hyperparathyroidism von Bricaire, Léopoldine, Odou, Marie-Françoise, Cardot-Bauters, Catherine, Delemer, Brigitte, North, Marie-Odile, Salenave, Sylvie, Vezzosi, Delphine, Kuhn, Jean-Marc, Murat, Arnaud, Caron, Philippe, Sadoul, Jean-Louis, Silve, Caroline, Chanson, Philippe, Barlier, Anne, Clauser, Eric, Porchet, Nicole, Groussin, Lionel, the GTE Group

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Multiple endocrine neoplasia type 1 caused by mosaic mutation: clinical follow-up and genetic counseling? von Coppin, Lucie, Giraud, Sophie, Pasmant, Eric, Lagarde, Arnaud, North, Marie-Odile, Le-Collen, Lauriane, Aubert, Valérie, Mougel, Grégory, Ladsous, Miriam, Louboutin, Alyzée, Brixi, Hedia, Haissaguerre, Magalie, Scheyer, Nicolas, Klein, Marc, Tabarin, Antoine, Delemer, Brigitte, Barlier, Anne, Odou, Marie-Françoise, Romanet, Pauline

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Cost of cancer diagnosis using next-generation sequencing targeted gene panels in routine practice: a nationwide French study von Marino, Patricia, Touzani, Rajae, Perrier, Lionel, Rouleau, Etienne, Kossi, Dede Sika, Zhaomin, Zou, Charrier, Nathanaël, Goardon, Nicolas, Preudhomme, Claude, Durand-Zaleski, Isabelle, Borget, Isabelle, Baffert, Sandrine

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Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism? von Coppin, Lucie, Dufosse, Margaux, Romanet, Pauline, Giraud, Sophie, North, Marie-Odile, Cardot Bauters, Catherine, Borson-Chazot, Françoise, Duchesne, Laurence, Métallo, Mélanie, Lovecchio, Tonio, Barlier, Anne, Odou, Marie-Françoise

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Systematic detection of mosaicism by using digital NGS reveals three new MEN1 mosaicisms von Lagarde, Arnaud, Mougel, Grégory, Coppin, Lucie, Haissaguerre, Magalie, Le Collen, Lauriane, Mohamed, Amira, Klein, Marc, Odou, Marie-Françoise, Tabarin, Antoine, Brixi, Hedia, Cuny, Thomas, Delemer, Brigitte, Barlier, Anne, Romanet, Pauline

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Description of 22 new alpha-1 antitrypsin genetic variants von Renoux, Céline, Odou, Marie-Françoise, Tosato, Guillaume, Teoli, Jordan, Abbou, Norman, Lombard, Christine, Zerimech, Farid, Porchet, Nicole, Chapuis Cellier, Colette, Balduyck, Malika, Joly, Philippe

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A Pregnant Woman With Hypercalcemia-Induced Acute Pancreatitis von Fages, Victor, Decaestecker, Antoine, Lessore, Célia, Gaillard, Vianney, Odou, Marie-Françoise, Lemaitre, Madleen, Glowacki, François, Lionet, Arnaud

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Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study von Thevenon, Julien, Bourredjem, Abderrahmane, Faivre, Laurence, Cardot-Bauters, Catherine, Calender, Alain, Murat, Arnaud, Giraud, Sophie, Niccoli, Patricia, Odou, Marie-Françoise, Borson-Chazot, Françoise, Barlier, Anne, Lombard-Bohas, Catherine, Clauser, Eric, Tabarin, Antoine, Parfait, Béatrice, Chabre, Olivier, Castermans, Emilie, Beckers, Albert, Ruszniewski, Philippe, Le Bras, Morgane, Delemer, Brigitte, Bouchard, Philippe, Guilhem, Isabelle, Rohmer, Vincent, Goichot, Bernard, Caron, Philippe, Baudin, Eric, Chanson, Philippe, Groussin, Lionel, Du Boullay, Hélène, Weryha, Georges, Lecomte, Pierre, Penfornis, Alfred, Bihan, Hélène, Archambeaud, Françoise, Kerlan, Véronique, Duron, Françoise, Kuhn, Jean-Marc, Vergès, Bruno, Rodier, Michel, Renard, Michel, Sadoul, Jean-Louis, Binquet, Christine, Goudet, Pierre

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A large extended family with hyperparathyroidism-jaw tumor syndrome due to deletion of the third exon of CDC73: clinical and molecular features von Le Collen, Lauriane, Barraud, Sara, Braconnier, Antoine, Coppin, Lucie, Zachar, Dominique, Boulagnon, Camille, Deguelte, Sophie, Souchon, Pierre François, Spodenkiewicz, Marta, Poirsier, Céline, Aubert, Sébastien, Odou, Marie Françoise, Delemer, Brigitte

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