Detalhe da pesquisa
1.
A central role for GRB10 in regulation of islet function in man.
PLoS Genet
; 10(4): e1004235, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24699409
2.
Variation in FTO contributes to childhood obesity and severe adult obesity.
Nat Genet
; 39(6): 724-6, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17496892
3.
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
Nat Genet
; 37(8): 863-7, 2005 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16025115
4.
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
PLoS Genet
; 6(4): e1000916, 2010 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-20421936
5.
A POMC variant implicates beta-melanocyte-stimulating hormone in the control of human energy balance.
Cell Metab
; 3(2): 135-40, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16459314
6.
Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications.
Sci Rep
; 9(1): 17123, 2019 11 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31748580
7.
Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity.
J Clin Endocrinol Metab
; 92(11): 4403-9, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17698913
8.
Genetic analysis of ADIPOR1 and ADIPOR2 candidate polymorphisms for type 2 diabetes in the Caucasian population.
Diabetes
; 55(3): 856-61, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16505255
9.
Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.
BMC Med Genet
; 8: 44, 2007 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-17617923
10.
Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetes.
Diabetes
; 51(5): 1640-3, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11978668
11.
A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2.
Diabetes
; 53(3): 803-11, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14988267
12.
Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p.
Diabetes
; 51(4): 1247-55, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11916952
13.
Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population.
BMC Genet
; 6: 19, 2005 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-15823203
14.
Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
J Clin Invest
; 123(7): 3037-41, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23778136
15.
Loss-of-function mutations in MC4R are very rare in the Greek severely obese adult population.
Obesity (Silver Spring)
; 20(11): 2278-82, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22447289
16.
Common variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 show evidence of association with adult obesity in the Greek population.
Obesity (Silver Spring)
; 20(2): 389-95, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21720444
17.
Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.
PLoS One
; 7(6): e37423, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22701567
18.
Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity.
Diabetes
; 61(2): 383-90, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22210313
19.
Estimation of newborn risk for child or adolescent obesity: lessons from longitudinal birth cohorts.
PLoS One
; 7(11): e49919, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23209618
20.
Study of TNFalpha -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population.
Clin Biochem
; 43(6): 549-52, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20132806