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Catherine Dodé

French Institute of Health and Medical Research
Paris Descartes University
University of Paris

159

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7574

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NEXT GENERATION SEQUENCING SHOULD BE PROPOSED TO EVERY WOMAN WITH "IDIOPATHIC" PREMATURE OVARIAN INSUFFICIENCY

2021 Journal of the Endocrine Society
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Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice

2017 Human Molecular Genetics
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Next-generation sequencing of patients with congenital anosmia

2017 European Journal of Human Genetics
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Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome

2017 Annales D Endocrinologie
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First mutation in the FSHR cytoplasmic tail identified in a non-pregnant woman with spontaneous ovarian hyperstimulation syndrome

2017 BMC Medical Genetics
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Insuffisance ovarienne prématurée : analyse génétique par next generation sequencing (NGS) chez 288 patientes

2017 Annales D Endocrinologie
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Première mutation dans la partie C-terminale du récepteur de la FSH (R634H) chez une patiente présentant une hyperstimulation ovarienne spontanée

2016 Annales D Endocrinologie
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New NOBOX Mutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency Decrease KIT-L Expression

2015 The Journal of Clinical Endocrinology and Metabolism
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Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

2015 Nature Reviews Endocrinology
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Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency.

2015 The Journal of Clinical Endocrinology and Metabolism
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