N. de Roux

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Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

E. Génin, E. Milgrom, F. Matsuda, 2003, Proceedings of the National Academy of Sciences of the United States of America.

PRR repeats in the intracellular domain of KISS1R are important for its export to cell membrane.

H. Vaudry, A. D. de Brevern, J. Leprince, 2013, Molecular endocrinology.

Complete Kisspeptin Receptor Inactivation Does Not Impede Exogenous GnRH-Induced LH Surge in Humans

N. de Roux, A. Gompel, J. Hugon-Rodin, 2018, The Journal of clinical endocrinology and metabolism.

Disrupted Academic Careers: The Returns to Time Off after High School

N. de Roux, Evan Riehl, 2020, SSRN Electronic Journal.

PROKR2 and PROK2 mutations cause isolated congenital anosmia without gonadotropic deficiency.

O. Laccourreye, N. de Roux, P. Bonfils, 2012, European journal of endocrinology.

The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindred.

E. Milgrom, N. de Roux, M. Misrahi, 1999, The Journal of clinical endocrinology and metabolism.

Weather Variability, Credit Scores and Access to Credit: Evidence from Colombian Coffee Farmers

N. de Roux, 2020 .

Lack of association between HFE gene mutations and hepatocellular carcinoma in patients with cirrhosis

N. Ganne-Carrié, V. Boige, M. Beaugrand, 2003, Gut.

On the Endogeneity of Inflation Targeting: Preferences Over Inflation

N. de Roux, M. Hofstetter, 2011 .

Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty.

N. de Roux, J. Carel, M. Salerno, 2016, European journal of endocrinology.

Do college students benefit from placement into higher-achieving classes?

N. de Roux, Evan Riehl, 2022, Journal of Public Economics.

Sacrifice Ratios and Inflation Targeting: The Role of Credibility

N. de Roux, M. Hofstetter, 2012 .

Four families with loss of function mutations of the thyrotropin receptor.

E. Milgrom, Y. Le Bouc, N. de Roux, 1996, The Journal of clinical endocrinology and metabolism.

Rabconnectin-3α is required for the morphological maturation of GnRH neurons and kisspeptin responsiveness

S. Peineau, Z. Csaba, N. de Roux, 2017, Scientific Reports.

Absence of GPR54 and TACR3 Mutations in Sporadic Cases of Idiopathic Central Precocious Puberty

G. Chrousos, N. de Roux, C. Kanaka-Gantenbein, 2014, Hormone Research in Paediatrics.

A novel loss-of-function mutation in GPR54/KISS1R leads to hypogonadotropic hypogonadism in a highly consanguineous family.

M. Phillip, R. Nimri, N. de Roux, 2011, The Journal of clinical endocrinology and metabolism.

Isolated Gonadotropic Deficiency with and without Anosmia: A Developmental Defect or a Neuroendocrine Regulation Abnormality of the Gonadotropic Axis

N. de Roux, 2005, Hormone Research in Paediatrics.

New insights in the genetics of isolated hypogonadotropic hypogonadism.

N. de Roux, André Iovane, Chantal Aumas, 2004, European journal of endocrinology.

Pituitary-thyroid feedback in a patient with a sporadic activating thyrotropin (TSH) receptor mutation: implication that thyroid-secreted factors other than thyroid hormones contribute to serum TSH levels.

N. de Roux, J. Carel, D. Chevenne, 2009, The Journal of clinical endocrinology and metabolism.

Congenital Hypogonadotropic Hypogonadism: A Trait Shared by Several Complex Neurodevelopmental Disorders.

N. de Roux, J. Carel, J. Léger, 2016, Endocrine development.

Rational design of triazololipopeptides analogs of kisspeptin inducing a long-lasting increase of gonadotropins.

A. Delmas, A. Caraty, N. de Roux, 2015, Journal of medicinal chemistry.

Negative fetal FSH/LH regulation in late pregnancy is associated with declined kisspeptin/KISS1R expression in the tuberal hypothalamus.

A. Caraty, N. de Roux, F. Guimiot, 2012, The Journal of clinical endocrinology and metabolism.

Neuroendocrine phenotype analysis in five patients with isolated hypogonadotropic hypogonadism due to a L102P inactivating mutation of GPR54.

N. de Roux, Y. Tenenbaum‐Rakover, O. Admoni, 2007, The Journal of clinical endocrinology and metabolism.

Molecular genetics of isolated hypogonadotropic hypogonadism and Kallmann syndrome.

N. de Roux, B. Karges, 2005, Endocrine development.

TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5.

G. Krause, K. Debatin, N. de Roux, 2005, The Journal of endocrinology.

Na+/H+ antiporter gene expression during monocytic differentiation of HL60 cells.

C. Sardet, J. Pouysségur, G. Rao, 1991, The Journal of biological chemistry.

GnRH receptor and GPR54 inactivation in isolated gonadotropic deficiency.

N. de Roux, 2006, Best practice & research. Clinical endocrinology & metabolism.

Mutation Ala(171)Thr stabilizes the gonadotropin-releasing hormone receptor in its inactive conformation, causing familial hypogonadotropic hypogonadism.

R. Kühne, E. Milgrom, N. de Roux, 2003, The Journal of clinical endocrinology and metabolism.

The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindred.

E. Milgrom, N. de Roux, M. Misrahi, 1999, The Journal of clinical endocrinology and metabolism.

FGFR1 mutations in Kallmann syndrome.

N. de Roux, C. Villanueva, 2010, Frontiers of hormone research.

Transforming a paediatric ICU to an adult ICU for severe Covid-19: lessons learned

J. Timsit, A. Birgy, C. Benzouid, 2021, European Journal of Pediatrics.

Lack of detection of novel nonsense mutations on exon 3 of hemochromatosis gene in patients with hepatic iron overload.

N. de Roux, T. Lazure, G. Pelletier, 2004, Journal of hepatology.

Spectrum of MECP2 mutations in Rett syndrome.

P. Jonveaux, J. Chelly, L. Villard, 2002, Genetic testing.

The incidence of Rett syndrome in France.

L. Pasquier, C. Philippe, P. Jonveaux, 2006, Pediatric neurology.

Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.

M. Polak, L. Guillot, N. de Roux, 2014, European journal of endocrinology.

High prevalence of syndromic disorders in patients with non-isolated central precocious puberty.

N. de Roux, J. Carel, E. Ecosse, 2018, European journal of endocrinology.

Back to Basics: Sticky Prices in the Monetary Transmission Mechanism

N. de Roux, 2011 .

Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomas.

P. Chanson, E. Milgrom, J. Bidart, 1998, European journal of endocrinology.

A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor.

P. Chanson, E. Milgrom, Jacques Young, 1997, The New England journal of medicine.

Clinical and molecular genetics of the human GnRH receptor.

N. de Roux, B. Karges, W. Karges, 2003, Human reproduction update.

IGSF10 mutations dysregulate gonadotropin‐releasing hormone neuronal migration resulting in delayed puberty

M. Sternberg, M. Barnes, R. Quinton, 2016, EMBO molecular medicine.

KISS1 is down-regulated by 17beta-estradiol in MDA-MB-231 cells through a nonclassical mechanism and loss of ribonucleic acid polymerase II binding at the proximal promoter.

N. de Roux, L. Huijbregts, 2010, Endocrinology.

MECP2 mutations account for most cases of typical forms of Rett syndrome.

P. Jonveaux, J. Chelly, A. Arzimanoglou, 2000, Human molecular genetics.

Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations

M. Hauschild, P. Bouloux, M. Polak, 2014, Genetics in Medicine.

Congenital hypogonadotropic hypogonadism

P. Touraine, N. de Roux, N. Roux, 2020, Definitions.

Gonadotropin receptors.

E. Milgrom, N. de Roux, M. Misrahi, 1999, Annales d'endocrinologie.

Gonadotrophin and thyrotrophin receptors.

E. Milgrom, N. de Roux, J. Savouret, 1997, Hormone research.

Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.

N. de Roux, I. Bailleul-Forestier, D. Zénaty, 2010, International journal of paediatric dentistry.

Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update.

L. Pasquier, C. Philippe, P. Jonveaux, 2006, European journal of medical genetics.

Analysis of the thyrotropin receptor as a candidate gene in familial Graves' disease.

E. Milgrom, D. Shields, N. de Roux, 1996, The Journal of clinical endocrinology and metabolism.

A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism.

M. Polak, P. Czernichow, E. Milgrom, 1996, The Journal of clinical endocrinology and metabolism.

High tumoral levels of Kiss1 and G-protein-coupled receptor 54 expression are correlated with poor prognosis of estrogen receptor-positive breast tumors.

Didier Marot, Rosette Lidereau, M. Perricaudet, 2007, Endocrine-related cancer.

DLK1 Is a Somato-Dendritic Protein Expressed in Hypothalamic Arginine-Vasopressin and Oxytocin Neurons

N. de Roux, Sandrine Jacquier, C. Villanueva, 2012, PloS one.

Somatostatin receptors type 2 and 5 expression and localization during human pituitary development.

P. Gressens, S. Peineau, S. Schulz, 2014, Endocrinology.

Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases

L. Vallée, O. Boespflug-Tanguy, M. Tardieu, 2004, Journal of Medical Genetics.

An inactivating mutation within the first extracellular loop of the thyrotropin receptor impedes normal posttranslational maturation of the extracellular domain.

M. Polak, N. de Roux, Sylvia Sura-Trueba, 2009, Endocrinology.

Haploinsufficiency of Dmxl2, Encoding a Synaptic Protein, Causes Infertility Associated with a Loss of GnRH Neurons in Mouse

E. Génin, J. Dupont, Z. Csaba, 2014, PLoS biology.

Estimating Production Functions in Differentiated-Product Industries with Quantity Information and External Instruments

Nicolás de Roux, Marcela Eslava, Santiago Franco, 2021, SSRN Electronic Journal.

Forgone Investment: Civil Conflict and Agricultural Credit in Colombia

N. de Roux, L. Mart́ınez, 2021, SSRN Electronic Journal.

Conflict Reduces Investment: Evidence from the Demand for Agricultural Credit in Colombia

N. de Roux, L. Mart́ınez, 2020, SSRN Electronic Journal.

Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population

R. Touraine, C. Elie, J. Auger, 2016, Hormone Research in Paediatrics.

Response to letter to the editor (from De Zegher and Ibanes) (On the rising incidence of early breast development: puberty as an adaptive escape from ectopic adiposity in mismatch girls).

N. de Roux, J. Carel, J. Léger, 2021, European journal of endocrinology.

Deposit Insurance and Depositor Behavior: Evidence from Colombia

N. de Roux, Nicola Limodio, 2021, SSRN Electronic Journal.

Is it my money or not? An experiment on risk aversion and the house-money effect

J. Cárdenas, N. de Roux, Christian R. Jaramillo, 2013, Experimental Economics.

Zero-length cross-linking reveals that tight interactions between the extracellular and transmembrane domains of the luteinizing hormone receptor persist during receptor activation.

P. Kelly, E. Milgrom, N. de Roux, 2005, Molecular endocrinology.

Labor Market Power in Developing Countries: Evidence from Colombian Plants

N. de Roux, Francesco Amodio, 2021, SSRN Electronic Journal.

Isolating Peer Effects in the Returns to College Selectivity

N. de Roux, Evan Riehl, 2019, SSRN Electronic Journal.

Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion.

M. Polak, N. de Roux, G. Szinnai, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Loss of function mutations of the GnRH receptor: a new cause of hypogonadotropic hypogonadism.

E. Milgrom, N. de Roux, M. Misrahi, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Absence of GPR54 and TACR3 Mutations in Sporadic Cases of Idiopathic Central Precocious Puberty

G. Chrousos, N. de Roux, C. Kanaka-Gantenbein, 2014, Hormone Research in Paediatrics.

It’s Not My Money: An Experiment on Risk Aversion and the House-Money Effect

Juan-Camilo Cardenas, N. de Roux, Christian R. Jaramillo, 2010 .