Bruno Francou - Concepedia

Author

Bruno Francou

Also Known As

Aude Flechon, B. Francou, Bouligand, Jerome, Bruno Francou, Enrique Schisterman, Francou Bruno, Francou, Bruno, Jérôme Bouligand (101786), Takashi Joh

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Bicêtre Hospital Inserm Assistance Publique – Hôpitaux de Paris Université Paris-Sud Université Paris-Saclay

About

Bruno Francou is an author at Bicêtre Hospital specializing in medicine, health sciences, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	182
2	Health Sciences	3	3	81
3	Public Health	2	2	76
4	Social Sciences	1	1	14
5	Allergy	1	1	11

Bruno Francou

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
<i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans Jacques Young, Jérôme Bouligand, Bruno Francou, The Journal of Clinical Endocrinology & Metabolism	2010	245
Kisspeptin Restores Pulsatile LH Secretion in Patients with Neurokinin B Signaling Deficiencies: Physiological, Pathophysiological and Therapeutic Implications Jacques Young, Jyothis T. George, Javier A. Tello, Neuroendocrinology	2012	155
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development Jacques Young, Corinne Métay, Jérôme Bouligand, Human Reproduction	2012	139
Normosmic Congenital Hypogonadotropic Hypogonadism Due to TAC3/TACR3 Mutations: Characterization of Neuroendocrine Phenotypes and Novel Mutations Bruno Francou, Jérôme Bouligand, Adela Voican, PLoS ONE	2011	99
New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family Nouha Bouali, Bruno Francou, Jérôme Bouligand, Fertility and Sterility New Mcm8 MutationInfertilityMendelian DisorderPremature Ovarian InsufficiencyGenetic Disorder	2017	63
Prevalence of<i>KISS1 Receptor</i>mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study Bruno Francou, Charlotte Paul, Larbi Amazit, Human Reproduction	2016	57
Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity Patrick Hanna, Virginie Grybek, Guiomar Pérez de Nanclares, Journal of Bone and Mineral Research	2018	56
Hyperparathyroidism in Patients With X-Linked Hypophosphatemia Anne-Lise Lecoq, Philippe Chaumet‐Riffaud, Anne Blanchard, Journal of Bone and Mineral Research UrologyBody CompositionX-linked HypophosphatemiaMedicineParathyroid Hormone	2020	54
Familial Multiplicity of Estrogen Insensitivity Associated with a Loss-of-Function <i>ESR1</i> Mutation Valérie Bernard, Sakina Kherra, Bruno Francou, The Journal of Clinical Endocrinology & Metabolism	2016	47
Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Novel Mutation Frédéric Brioude, Jérôme Bouligand, Bruno Francou, PLoS ONE	2013	41

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