Detalhe da pesquisa
1.
The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance.
PLoS Genet
; 16(9): e1009018, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32925908
2.
ASSOCIATION BETWEEN APOE-ε4 CARRIER STATUS AND QUALITATIVE NEUROIMAGING CHARACTERISTICS IN OLDER ADULTS WITH MILD COGNITIVE IMPAIRMENT.
Rev Invest Clin
; 74(2): 113-120, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35354197
3.
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
Nature
; 506(7486): 97-101, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24390345
4.
A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos.
BMC Genet
; 20(1): 5, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30621578
5.
Frequency of the T307A, N680S, and -29G>A single-nucleotide polymorphisms in the follicle-stimulating hormone receptor in Mexican subjects of Hispanic ancestry.
Reprod Biol Endocrinol
; 16(1): 100, 2018 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30340493
6.
Reconstructing Native American population history.
Nature
; 488(7411): 370-4, 2012 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22801491
7.
Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene.
Arterioscler Thromb Vasc Biol
; 36(7): 1350-5, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27199446
8.
Genome-wide association study of colorectal cancer in Hispanics.
Carcinogenesis
; 37(6): 547-556, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207650
9.
Rare intronic variants of TCF7L2 arising by selective sweeps in an indigenous population from Mexico.
BMC Genet
; 17(1): 68, 2016 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27230431
10.
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
J Med Genet
; 50(5): 298-308, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23505323
11.
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.
JAMA
; 311(22): 2305-14, 2014 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24915262
12.
Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation.
Life Sci Alliance
; 7(8)2024 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-38755006
13.
Local Ancestry at the Major Histocompatibility Complex Region is Not a Major Contributor to Disease Heterogeneity in a Multiethnic Lupus Cohort.
Arthritis Rheumatol
; 76(4): 614-619, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38073021
14.
The fatal contribution of serine protease-related genetic variants to COVID-19 outcomes.
Front Immunol
; 15: 1335963, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38601158
15.
A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.
Hum Mol Genet
; 19(14): 2877-85, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20418488
16.
Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles.
Arterioscler Thromb Vasc Biol
; 31(5): 1201-7, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21393584
17.
A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.
PLoS Genet
; 5(9): e1000642, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19750004
18.
Estimating ethnic admixture from pedigree data.
Am J Hum Genet
; 82(3): 748-55, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18319077
19.
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels.
Am J Hum Genet
; 83(2): 180-92, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18674750
20.
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.
Arterioscler Thromb Vasc Biol
; 30(2): 353-9, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19965785