|Mapping autism risk loci using genetic linkage and chromosomal rearrangements|
Nature genetics 39 (3), 319-328, 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
|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
|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
|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
|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
|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
|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
|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
|AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial|
S Allas, A Caixàs, C Poitou, M Coupaye, D Thuilleaux, F Lorenzini, ...
PloS one 13 (1), e0190849, 2018
|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
|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
|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
|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
|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
|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
|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
|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
|Insulin resistance and the metabolic syndrome in obese French children|
C Druet, M Dabbas, V Baltakse, C Payen, B Jouret, C Baud, D Chevenne, ...
Clinical endocrinology 64 (6), 672-678, 2006
|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