Claire Bouvattier

Inserm — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

42h-index9.6kcitations208works1.72yr avg
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Research Topics

Sexual Differentiation and Disorders(109), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(41), Urological Disorders and Treatments(32), Hypothalamic control of reproductive hormones(31), Hormonal and reproductive studies(29)

Publications199 total

Uneventful pregnancies with homozygous KISS1 frameshift mutation
The Lancet Obstetrics Gynaecology & Women s Health·2025
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants
Endocrine Connections·2025Open Access
Amenorrea en la adolescente
EMC - Ginecología-Obstetricia·2025
Aménorrhée chez l’adolescente
EMC - Gynécologie·2025
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants
Endocrine Abstracts·2025
Hypogonadotropic hypogonadism diagnosis in boys under one year of age based on gonadotrophins, testosterone, antimullerian hormone (AMH) and inhibin B (INHB) measurements
Endocrine Abstracts·2025
Inhibin B and AMH for Diagnosis of Hypogonadotropic Hypogonadism in Boys Under 1 Year of Age: A Case-control Study
The Journal of Clinical Endocrinology & Metabolism·2025· 1 citedOpen Access
Early adolescence assessment of eleven boys treated with continuous subcutaneous infusion of recombinant LH and FSH during infancy
Endocrine Connections·2025Open Access
Pubertad normal. Pubertad precoz y retraso puberal
EMC - Ginecología-Obstetricia·2025Open Access
Contribution of clinical, biological mini-puberty and genetic analysis in 57 46,XY DSD: a monocentric retrospective cohort
Hormone Research in Paediatrics·2025
8577 Gonadal function throughout life in XX and XY patients with a germline WT1 variant - lessons from a cohort of 80 patients
Journal of the Endocrine Society·2024Open Access
8577 Gonadal function throughout life in XX and XY patients with a germline WT1 variant - lessons from a cohort of 80 patients
Journal of the Endocrine Society·2024Open Access
Hyperprolactinémie au décours d’une hypothyroïdie sévère : mythe ou réalité ?
Annales d Endocrinologie·2024Open Access
Variaciones del desarrollo genital
EMC - Ginecología-Obstetricia·2024
Variations isolées du développement génital en maternité
Perfectionnement en Pédiatrie·2024
The role of pre- and postnatal investigations in suspected isolated hypospadias
Journal of Gynecology Obstetrics and Human Reproduction·2024· 3 cited
Organes génitaux externes atypiques et grande prématurité
Réanimation et Soins Intensifs en Néonatologie·2024
Hyperplasie congénitale des surrénales
Réanimation et Soins Intensifs en Néonatologie·2024
Growing heart in congenital hypopituitarism treated in adulthood
The Lancet·2023· 2 cited
Caractéristiques clinico-biologiques des patients avec une aneuploïdie gonosomique en mosaïque 47,XXY/46,XX versus syndrome de Klinefelter homogène (47,XXY) : étude comparative monocentrique
Annales d Endocrinologie·2023
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Frequent Co-authors

Anna Nordenström(12), Birgit Köhler(11), Pierre Bougnères(10), Ute Thyen(10), Jean‐Claude Carel(9), Jacques Young(9), Juliane Léger(8), Hedi L. Claahsen‐van der Grinten(8), Baudewijntje P.C. Kreukels(7), Peggy T. Cohen–Kettenis(7), Catherine Pienkowski(7), R. Coutant(7), Jolanta Słowikowska‐Hilczer(7), Nicole Reisch(7), Robert Roehle(6), A. de Vries(6), Aude Brac de la Perrière(6), Najiba Lahlou(5), Sylvie Cabrol(5), Yves Morel(5)