Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene von Quilichini, Juliette, Perol, Sandrine, Cuisset, Laurence, Grotto, Sarah, Fouveaut, Corinne, Barbot, Jean Claude, Verebi, Camille, Jordan, Pénélope, Héron, Delphine, Molina‐Gomes, Denise, Pipiras, Eva, Grynberg, Michael, Catteau‐Jonard, Sophie, Touraine, Philippe, Christin‐Maître, Sophie, Plu‐Bureau, Geneviève, El Khattabi, Laila, Bienvenu, Thierry

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Fertility care among people with primary ciliary dyskinesia von Schreck, Leonie D., Goutaki, Myrofora, Jörger, Philippa, Dexter, Katie, Manion, Michele, Christin‐Maitre, Sophie, Maitre, Bernard, Kuehni, Claudia E., Pedersen, Eva S. L.

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Shifting the landscape: Dominant C‐terminal rare missense FOXL2 variants in non‐syndromic primary ovarian failure etiology von Jordan, Pénélope, Verebi, Camille, Hervé, Bérénice, Perol, Sandrine, Chakhtoura, Zeina, Courtillot, Carine, Bachelot, Anne, Karila, Daphné, Renard, Céline, Grouthier, Virginie, Croix, Stanislas Mulot, Bernard, Valérie, Fouveaut, Corinne, Perrière, Aude Brac, Jonard‐Catteau, Sophie, Touraine, Philippe, Plu‐Bureau, Geneviève, Dupont, Jean Michel, Christin‐Maitre, Sophie, Bienvenu, Thierry

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History of oral contraceptive drugs and their use worldwide von Christin-Maitre, Sophie, MD, PhD

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An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature von Lerat, Justine, Jonard, Laurence, Loundon, Natalie, Christin-Maitre, Sophie, Lacombe, Didier, Goizet, Cyril, Rouzier, Cécile, Van Maldergem, Lionel, Gherbi, Souad, Garabedian, Eréa-Nöel, Bonnefont, Jean- Paul, Touraine, Philippe, Mosnier, Isabelle, Munnich, Arnold, Denoyelle, Françoise, Marlin, Sandrine

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Infertility in an adult cohort with primary ciliary dyskinesia: phenotype-gene association von Vanaken, Gert Jan, Bassinet, Laurence, Boon, Mieke, Mani, Rahma, Honoré, Isabelle, Papon, Jean-Francois, Cuppens, Harry, Jaspers, Martine, Lorent, Natalie, Coste, André, Escudier, Estelle, Amselem, Serge, Maitre, Bernard, Legendre, Marie, Christin-Maitre, Sophie

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Intraadrenal Corticotropin in Bilateral Macronodular Adrenal Hyperplasia von Louiset, Estelle, Duparc, Céline, Young, Jacques, Renouf, Sylvie, Tetsi Nomigni, Milène, Boutelet, Isabelle, Libé, Rossella, Bram, Zakariae, Groussin, Lionel, Caron, Philippe, Tabarin, Antoine, Grunenberger, Fabienne, Christin-Maitre, Sophie, Bertagna, Xavier, Kuhn, Jean-Marc, Anouar, Youssef, Bertherat, Jérôme, Lefebvre, Hervé

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Diagnostic and referral pathways in patients with rare lipodystrophy and insulin-resistance syndromes: key milestones assessed from a national reference center von Donadille, Bruno, Janmaat, Sonja, Mosbah, Héléna, Belalem, Inès, Lamothe, Sophie, Nedelcu, Mariana, Jannot, Anne-Sophie, Christin-Maitre, Sophie, Fève, Bruno, Vatier, Camille, Vigouroux, Corinne

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Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey von Bouvattier, Claire, Esterle, Laure, Renoult-Pierre, Peggy, de la Perrière, Aude Brac, Illouz, Frederic, Kerlan, Véronique, Pascal-Vigneron, Veronique, Drui, Delphine, Christin-Maitre, Sophie, Galland, Françoise, Brue, Thierry, Reznik, Yves, Schillo, Frank, Pinsard, Denis, Piguel, Xavier, Chabrier, Gérard, Decoudier, Bénédicte, Emy, Philippe, Tauveron, Igor, Raffin-Sanson, Marie-Laure, Bertherat, Jerôme, Kuhn, Jean-Marc, Caron, Philippe, Cartigny, Maryse, Chabre, Olivier, Dewailly, Didier, Morel, Yves, Touraine, Philippe, Tardy-Guidollet, Véronique, Young, Jacques

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First Birth Achieved After In Vitro Maturation of Oocytes From a Woman Endowed With Multiple Antral Follicles Unresponsive to Follicle-stimulating Hormone von Grynberg, Michaël, Peltoketo, Hellevi, Christin-Maître, Sophie, Poulain, Marine, Bouchard, Philippe, Fanchin, Renato

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Toward a multi-country monitoring system of reproductive health in the context of endocrine disrupting chemical exposure von Le Moal, Joëlle, Sharpe, Richard M, Jϕrgensen, Niels, Levine, Hagai, Jurewicz, Joanna, Mendiola, Jaime, Swan, Shanna H, Virtanen, Helena, Christin-Maître, Sophie, Cordier, Sylvaine, Toppari, Jorma, Hanke, Wojciech

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Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases von Kallali, Wafa, Messiaen, Claude, Saidi, Roumaisah, Lessim, Soucounda, Viaud, Magali, Dulon, Jerome, Nedelcu, Mariana, Samara, Dinane, Houang, Muriel, Donadille, Bruno, Courtillot, Carine, de Filippo, GianPaolo, Carel, Jean-Claude, Christin-Maitre, Sophie, Touraine, Philippe, Netchine, Irene, Polak, Michel, Leger, Juliane

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Clinical Characteristics and Outcome of Acromegaly Induced by Ectopic Secretion of Growth Hormone-Releasing Hormone (GHRH): A French Nationwide Series of 21 Cases von Garby, Laetitia, Caron, Philippe, Claustrat, Francine, Chanson, Philippe, Tabarin, Antoine, Rohmer, Vincent, Arnault, Gwenaëlle, Bonnet, Fabrice, Chabre, Olivier, Christin-Maitre, Sophie, du-Boullay, Hélène, Murat, Arnaud, Nakib, Ihab, Sadoul, Jean-Louis, Sassolas, Geneviève, Claustrat, Bruno, Raverot, Gérald, Borson-Chazot, Françoise, the GTE Group

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Preface: What should be known about oral contraceptive drugs von Christin-Maitre, Sophie, MD, PhD

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Monitoring gestational diabetes mellitus patients with the telemedicine application MyDiabby decreases the rate of foetal macrosomia von Meykiechel, Tiphaine, de Carne, Céline, Gueguen, Isabelle, Vatier, Camille, Girard, Guillaume, Buzzi, Jean-Claude, Christin-Maitre, Sophie, Bourcigaux, Nathalie

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Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene von Knauff, Erik A.H., Franke, Lude, van Es, Michael A., van den Berg, Leonard H., van der Schouw, Yvonne T., Laven, Joop S.E., Lambalk, Cornelius B., Hoek, Annemieke, Goverde, Angelique J., Christin-Maitre, Sophie, Hsueh, Aaron J., Wijmenga, Cisca, Fauser, Bart C.J.M.

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Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure von Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner A, Fellous, Marc

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Human 3beta-hydroxysteroid dehydrogenase deficiency associated with normal spermatic numeration despite a severe enzyme deficit von Donadille, Bruno, Houang, Muriel, Netchine, Irène, Siffroi, Jean-Pierre, Christin-Maitre, Sophie

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Looking at New Unexpected Disease Targets in LMNA-Linked Lipodystrophies in the Light of Complex Cardiovascular Phenotypes: Implications for Clinical Practice von Mosbah, Helena, Vatier, Camille, Boccara, Franck, Jeru, Isabelle, Lascols, Olivier, Vantyghem, Marie-Christine, Feve, Bruno, Donadille, Bruno, Sarrazin, Elisabeth, Benabbou, Sophie, Inamo, Jocelyn, Ederhy, Stephane, Cohen, Ariel, Neraud, Barbara, Richard, Pascale, Picard, Fabien, Christin-Maitre, Sophie, Redheuil, Alban, Wahbi, Karim, Vigouroux, Corinne

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FOXO3a variants in patients with premature ovarian failure von Vinci, Giovanna, Christin-Maitre, Sophie, Pasquier, Maud, Bouchard, Philippe, Fellous, Marc, Veitia, Reiner A.

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