PubRank

Maithé Tauber

Author PubWeight™ 23.76‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat Genet 2009 6.39
2 A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Nat Genet 2008 5.49
3 Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human. Nature 2012 3.41
4 Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity. Diabetes 2011 1.12
5 Factors associated with overweight in preschool-age children in southwestern France. Am J Clin Nutr 2007 1.05
6 Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3beta signaling. Mol Cell Biol 2010 1.02
7 New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity. Am J Med Genet A 2014 0.91
8 Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies. Int J Pediatr Endocrinol 2012 0.86
9 Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19. Mol Cell Endocrinol 2011 0.84
10 Analysis of the SIM1 contribution to polygenic obesity in the French population. Obesity (Silver Spring) 2010 0.84
11 Lack of association of CD36 SNPs with early onset obesity: a meta-analysis in 9,973 European subjects. Obesity (Silver Spring) 2010 0.83
12 Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables. J Neurodev Disord 2013 0.79
13 Gonadotropin-Releasing Hormone Agonist Treatment in Sexual Precocity. Endocr Dev 2015 0.77
14 Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndrome. J Pediatr Endocrinol Metab 2007 0.76
15 Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: new cases of "polyvalvular heart disease syndrome" or new association? Eur J Med Genet 2009 0.75
16 Meta-Analysis of Paediatric Patients with Central Precocious Puberty Treated with Intramuscular Triptorelin 11.25 mg 3-Month Prolonged-Release Formulation
. Horm Res Paediatr 2017 0.75