| Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene RS Jackson, JWM Creemers, S Ohagi, ML Raffin-Sanson, L Sanders, ... Nature genetics 16 (3), 303-306, 1997 | 1360 | 1997 |
| Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency RS Jackson, JWM Creemers, IS Farooqi, ML Raffin-Sanson, A Varro, ... The Journal of clinical investigation 112 (10), 1550-1560, 2003 | 411 | 2003 |
| Proopiomelanocortin, a polypeptide precursor with multiple functions: from physiology to pathological conditions ML Raffin-Sanson, Y De Keyzer, X Bertagna European Journal of Endocrinology 149 (2), 79-90, 2003 | 335 | 2003 |
| Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin P Rodien, C Brémont, MLR Sanson, J Parma, J Van Sande, S Costagliola, ... New England Journal of Medicine 339 (25), 1823-1826, 1998 | 319 | 1998 |
| Structural and functional abnormalities at 11p15 are associated with the malignant phenotype in sporadic adrenocortical tumors: study on a series of 82 tumors C Gicquel, ML Raffin-Sanson, V Gaston, X Bertagna, PF Plouin, ... The Journal of Clinical Endocrinology & Metabolism 82 (8), 2559-2565, 1997 | 273 | 1997 |
| TAC3 and TACR3 Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans J Young, J Bouligand, B Francou, ML Raffin-Sanson, S Gaillez, ... The Journal of Clinical Endocrinology & Metabolism 95 (5), 2287-2295, 2010 | 250 | 2010 |
| Pangenomic classification of pituitary neuroendocrine tumors M Neou, C Villa, R Armignacco, A Jouinot, ML Raffin-Sanson, A Septier, ... Cancer cell 37 (1), 123-134. e5, 2020 | 223 | 2020 |
| ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences S Espiard, L Drougat, R Libé, G Assié, K Perlemoine, L Guignat, ... The Journal of Clinical Endocrinology & Metabolism 100 (6), E926-E935, 2015 | 162 | 2015 |
| Germline inactivating mutations of the aryl hydrocarbon receptor-interacting protein gene in a large cohort of sporadic acromegaly: mutations are found in a subset … L Cazabat, R Libe, K Perlemoine, F René-Corail, N Burnichon, ... European Journal of Endocrinology 157 (1), 1-8, 2007 | 159 | 2007 |
| Phosphodiesterase 11A (PDE11A) and genetic predisposition to adrenocortical tumors R Libé, A Fratticci, J Coste, F Tissier, A Horvath, B Ragazzon, ... Clinical Cancer Research 14 (12), 4016-4024, 2008 | 119 | 2008 |
| Frequent Phosphodiesterase 11A Gene (PDE11A) Defects in Patients with Carney Complex (CNC) Caused by PRKAR1A Mutations: PDE11A May Contribute to … R Libé, A Horvath, D Vezzosi, A Fratticci, J Coste, K Perlemoine, ... The Journal of Clinical Endocrinology & Metabolism 96 (1), E208-E214, 2011 | 116 | 2011 |
| Clinical outcome, hormonal status, gonadotrope axis, and testicular function in 219 adult men born with classic 21-hydroxylase deficiency. A French national survey C Bouvattier, L Esterle, P Renoult-Pierre, AB de La Perrière, F Illouz, ... The Journal of Clinical Endocrinology & Metabolism 100 (6), 2303-2313, 2015 | 114 | 2015 |
| The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects C Beldjord, F Desclaux-Arramond, M Raffin-Sanson, JC Corvol, ... The Journal of Clinical Endocrinology & Metabolism 80 (7), 2063-2068, 1995 | 98 | 1995 |
| Functional phosphodiesterase 11A mutations may modify the risk of familial and bilateral testicular germ cell tumors A Horvath, L Korde, MH Greene, R Libe, P Osorio, FR Faucz, ... Cancer research 69 (13), 5301-5306, 2009 | 94 | 2009 |
| Variable expression of the V1 vasopressin receptor modulates the phenotypic response of steroid-secreting adrenocortical tumors G Arnaldi, JM Gasc, Y de Keyzer, ML Raffin-Sanson, V Perraudin, ... The Journal of Clinical Endocrinology & Metabolism 83 (6), 2029-2035, 1998 | 92 | 1998 |
| High plasma proopiomelanocortin in aggressive adrenocorticotropin-secreting tumors ML Raffin-Sanson, JF Massias, C Dumont, MC Raux-Demay, ... The Journal of Clinical Endocrinology & Metabolism 81 (12), 4272-4277, 1996 | 78 | 1996 |
| Progestin-associated shift of meningioma mutational landscape M Peyre, S Gaillard, C de Marcellus, M Giry, F Bielle, C Villa, AL Boch, ... Annals of Oncology 29 (3), 681-686, 2018 | 77 | 2018 |
| Identification of novel genetic variants in phosphodiesterase 8B ( PDE8B ), a cAMP‐specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort … A Rothenbuhler, A Horvath, R Libé, FR Faucz, A Fratticci, ... Clinical endocrinology 77 (2), 195-199, 2012 | 74 | 2012 |
| Phosphodiesterase 11A (PDE11A) Genetic Variants May Increase Susceptibility to Prostatic Cancer FR Faucz, A Horvath, A Rothenbuhler, MQ Almeida, R Libe, ... The Journal of Clinical Endocrinology & Metabolism 96 (1), E135-E140, 2011 | 71 | 2011 |
| Cushing's syndrome and pregnancy: aetiologies and prognosis in twenty-two patients. B Guilhaume, ML Sanson, L Billaud, X Bertagna, MH Laudat, JP Luton The European journal of medicine 1 (2), 83-89, 1992 | 69 | 1992 |
