Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1666 | 2007 |
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations D Meyre, J Delplanque, JC Chèvre, C Lecoeur, S Lobbens, S Gallina, ... Nature genetics 41 (2), 157-159, 2009 | 778 | 2009 |
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human A Ichimura, A Hirasawa, O Poulain-Godefroy, A Bonnefond, T Hara, ... Nature 483 (7389), 350-354, 2012 | 755 | 2012 |
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk N Bouatia-Naji, A Bonnefond, C Cavalcanti-Proença, T Sparsø, ... Nature genetics 41 (1), 89-94, 2009 | 708 | 2009 |
Recommendations for the diagnosis and management of Prader-Willi syndrome AP Goldstone, AJ Holland, BP Hauffa, AC Hokken-Koelega, M Tauber, ... The Journal of Clinical Endocrinology & Metabolism 93 (11), 4183-4197, 2008 | 503 | 2008 |
A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone C Dos Santos, L Essioux, C Teinturier, M Tauber, V Goffin, P Bougnères Nature genetics 36 (7), 720-724, 2004 | 422 | 2004 |
Growth Hormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome CL Deal, M Tony, C Höybye, DB Allen, M Tauber, JS Christiansen, ... The Journal of Clinical Endocrinology & Metabolism 98 (6), E1072-E1087, 2013 | 359 | 2013 |
Consensus statement on the management of the GH-treated adolescent in the transition to adult care PE Clayton, RC Cuneo, A Juul, JP Monson, SM Shalet, M Tauber European journal of endocrinology 152 (2), 165-170, 2005 | 280 | 2005 |
Growth hormone (GH) retesting and auxological data in 131 GH-deficient patients after completion of treatment M Tauber, P Moulin, C Pienkowski, B Jouret, P Rochiccioli The Journal of Clinical Endocrinology & Metabolism 82 (2), 352-356, 1997 | 263 | 1997 |
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ... Human genetics 131, 565-579, 2012 | 232 | 2012 |
Review of 64 cases of death in children with Prader–Willi syndrome (PWS) M Tauber, G Diene, C Molinas, M Hébert American journal of medical genetics Part A 146 (7), 881-887, 2008 | 232 | 2008 |
Adult height and pubertal growth in Turner syndrome after treatment with recombinant growth hormone L Soriano-Guillen, J Coste, E Ecosse, J Léger, M Tauber, S Cabrol, ... The Journal of Clinical Endocrinology & Metabolism 90 (9), 5197-5204, 2005 | 200 | 2005 |
An early postnatal oxytocin treatment prevents social and learning deficits in adult mice deficient for Magel2, a gene involved in Prader-Willi syndrome and autism H Meziane, F Schaller, S Bauer, C Villard, V Matarazzo, F Riet, G Guillon, ... Biological psychiatry 78 (2), 85-94, 2015 | 193 | 2015 |
Self-esteem and social adjustment in young women with Turner syndrome—influence of pubertal management and sexuality: population-based cohort study JC Carel, C Elie, E Ecosse, M Tauber, J Léger, S Cabrol, M Nicolino, ... The Journal of Clinical Endocrinology & Metabolism 91 (8), 2972-2979, 2006 | 193 | 2006 |
Endocrine disorders in children with Prader-Willi syndrome–data from 142 children of the French database G Diene, E Mimoun, E Feigerlova, S Caula, C Molinas, H Grandjean, ... Hormone research in paediatrics 74 (2), 121-128, 2010 | 188 | 2010 |
Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome E Bieth, S Eddiry, V Gaston, F Lorenzini, A Buffet, F Conte Auriol, ... European Journal of Human Genetics 23 (2), 252-255, 2015 | 179 | 2015 |
Adult height after long term treatment with recombinant growth hormone for idiopathic isolated growth hormone deficiency: observational follow up study of the French population … JC Carel, E Ecosse, M Nicolino, M Tauber, J Leger, S Cabrol, ... Bmj 325 (7355), 70, 2002 | 167 | 2002 |
Factors associated with overweight in preschool-age children in southwestern France B Jouret, N Ahluwalia, C Cristini, M Dupuy, L Nègre-Pages, H Grandjean, ... The American journal of clinical nutrition 85 (6), 1643-1649, 2007 | 162 | 2007 |
Implication of the Pro12Ala polymorphism of the PPAR-gamma 2gene in type 2 diabetes and obesity in the French population M Ghoussaini, D Meyre, S Lobbens, G Charpentier, K Clément, ... BMC medical genetics 6, 1-8, 2005 | 162 | 2005 |
Hyperghrelinemia precedes obesity in Prader-Willi syndrome E Feigerlová, G Diene, F Conte-Auriol, C Molinas, I Gennero, JP Salles, ... The Journal of Clinical Endocrinology & Metabolism 93 (7), 2800-2805, 2008 | 159 | 2008 |