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1.
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.
Nature;
483(7389): 350-4, 2012 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22343897
2.
Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.
Cerebrovasc Dis;
37(1): 57-63, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24401931
3.
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.
Cerebrovasc Dis;
38(6): 433-40, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25472749
4.
Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites.
J Clin Psychopharmacol;
33(2): 206-10, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23422394
5.
Examination of rare missense variants in the CHRNA5-A3-B4 gene cluster to level of response to alcohol in the San Diego Sibling Pair study.
Alcohol Clin Exp Res;
37(8): 1311-6, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23458267
6.
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects.
Hum Mol Genet;
18(13): 2495-501, 2009 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19377085
7.
Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets.
Mol Genet Metab;
100(1): 77-82, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20138556
8.
Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study.
J Mol Med (Berl);
86(3): 341-8, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18210030
9.
Clinical implications of recent advances in primary open-angle glaucoma genetics.
Eye (Lond);
2019 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31645673
10.
Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications.
Sci Rep;
9(1): 17123, 2019 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31748580
11.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Nat Genet;
51(2): 237-244, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30643251
12.
The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies.
BMC Med Genet;
9: 45, 2008 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-18498634
13.
TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis.
J Mol Med (Berl);
85(7): 777-82, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17476472
14.
Common Mitochondrial Haplogroups and Cutaneous Squamous Cell Carcinoma Risk.
Cancer Epidemiol Biomarkers Prev;
27(7): 838-841, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29695379
15.
A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci.
Genetics;
210(2): 499-515, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30108127
16.
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
Nat Commun;
9(1): 2278, 2018 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29891935
17.
TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study.
Diabetes;
55(11): 3189-92, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17065361
18.
Transcription factor TCF7L2 genetic study in the French population: expression in human beta-cells and adipose tissue and strong association with type 2 diabetes.
Diabetes;
55(10): 2903-8, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17003360
19.
TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population.
BMC Med Genet;
8: 37, 2007 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-17593304
20.
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure.
Nat Commun;
8(1): 2108, 2017 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29235454