β‐Klotho sustains postnatal GnRH biology and spins the thread of puberty von Misrahi, Micheline

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The Roles of Luteinizing Hormone, Follicle-Stimulating Hormone and Testosterone in Spermatogenesis and Folliculogenesis Revisited von Oduwole, Olayiwola O., Huhtaniemi, Ilpo T., Misrahi, Micheline

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Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency von Heddar, Abdelkader, Misrahi, Micheline

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Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency von Huhtaniemi, Ilpo, Hovatta, Outi, La Marca, Antonio, Livera, Gabriel, Monniaux, Danielle, Persani, Luca, Heddar, Abdelkader, Jarzabek, Katarzyna, Laisk-Podar, Triin, Salumets, Andres, Tapanainen, Juha S., Veitia, Reiner A., Visser, Jenny A., Wieacker, Peter, Wolczynski, Slawomir, Misrahi, Micheline

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Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France von Mariani, Louise-Laure, Lozeron, Pierre, Théaudin, Marie, Mincheva, Zoia, Signate, Aissatou, Ducot, Beatrice, Algalarrondo, Vincent, Denier, Christian, Adam, Clovis, Nicolas, Guillaume, Samuel, Didier, Slama, Michel S., Lacroix, Catherine, Misrahi, Micheline, Adams, David

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A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency von Fouquet, Baptiste, Pawlikowska, Patrycja, Caburet, Sandrine, Guigon, Celine, Mäkinen, Marika, Tanner, Laura, Hietala, Marja, Urbanska, Kaja, Bellutti, Laura, Legois, Bérangère, Bessieres, Bettina, Gougeon, Alain, Benachi, Alexandra, Livera, Gabriel, Rosselli, Filippo, Veitia, Reiner A, Misrahi, Micheline

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Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults von Heddar, Abdelkader, Misrahi, Micheline

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Correction to: Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults von Heddar, Abdelkader, Misrahi, Micheline

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Genetics of primary ovarian insufficiency: a careful step-by-step approach based on solid foundations to bring new knowledge von Heddar, Abdelkader, Misrahi, Micheline

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Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency? von Heddar, Abdelkader, Misrahi, Micheline

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Identification of Variants of Hepatitis C Virus (HCV) Entry Factors in Patients Highly Exposed to HCV but Remaining Uninfected: An ANRS Case-Control Study von Fouquet, Baptiste, Ghosn, Jade, Quertainmont, Yann, Salmon, Dominique, Rioux, Christophe, Duvivier, Claudine, Delfraissy, Jean-François, Misrahi, Micheline

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β‐Klotho sustains postnatal Gn RH biology and spins the thread of puberty von Misrahi, Micheline

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Claudin-6 and Occludin Natural Variants Found in a Patient Highly Exposed but Not Infected with Hepatitis C Virus (HCV) Do Not Confer HCV Resistance In Vitro von Fénéant, Lucie, Ghosn, Jade, Fouquet, Baptiste, Helle, François, Belouzard, Sandrine, Vausselin, Thibaut, Séron, Karin, Delfraissy, Jean-François, Dubuisson, Jean, Misrahi, Micheline, Cocquerel, Laurence

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A Chorionic Gonadotropin–Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation Syndrome von Vasseur, Claudine, Rodien, Patrice, Beau, Isabelle, Desroches, Agnès, Gérard, Capucine, de Poncheville, Loïc, Chaplot, Stéphanie, Savagner, Frédérique, Croué, Anne, Mathieu, Elisabeth, Lahlou, Najiba, Descamps, Philippe, Misrahi, Micheline

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A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation von Heddar, Abdelkader, Beckers, Dominique, Fouquet, Baptiste, Roland, Dominique, Misrahi, Micheline

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Novel STAG3 mutations in a Caucasian family with primary ovarian insufficiency von Heddar, Abdelkader, Dessen, Philippe, Flatters, Delphine, Misrahi, Micheline

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A SPIDR homozygous nonsense pathogenic variant in isolated primary ovarian insufficiency with chromosomal instability von Heddar, Abdelkader, Guichoux, Nathalie, Auger, Nathalie, Misrahi, Micheline

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Power and Pitfalls of Computational Methods to Identify New Genes Responsible for Acute Liver Failure of Indeterminate Etiology in Adults (vol 11, e00180, 2020) von Heddar, Abdelkader, Misrahi, Micheline

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Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girls von Brauner, Raja, Bashamboo, Anu, Rouget, Sébastien, Goulet, Marie, Philibert, Pascal, Sarda-Thibault, Hélène, Trivin, Christine, Misrahi, Micheline, Sultan, Charles, McElreavey, Ken

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Expression of the Thyroid-Stimulating Hormone Receptor in the Folliculo-Stellate Cells of the Human Anterior Pituitary von Prummel, Mark F., Brokken, Leon J. S., Meduri, Geri, Misrahi, Micheline, Bakker, Onno, Wiersinga, Wilmar M.

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