Detalhe da pesquisa
1.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature
; 627(8003): 347-357, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374256
2.
Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH.
Diabetologia
; 66(7): 1260-1272, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37233759
3.
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
Diabetologia
; 66(7): 1273-1288, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37148359
4.
Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia.
Lipids Health Dis
; 20(1): 14, 2021 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33588820
5.
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
6.
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
7.
Genome-wide association study of colorectal cancer in Hispanics.
Carcinogenesis
; 37(6): 547-556, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207650
8.
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
9.
Multi-ancestry polygenic mechanisms of type 2 diabetes.
Nat Med
; 30(4): 1065-1074, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38443691
10.
Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes.
medRxiv
; 2023 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37808701
11.
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
; 2023 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37034649
12.
Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes.
Diabetes
; 71(3): 554-565, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34862199
13.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
; 54(5): 560-572, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35551307
14.
Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes.
Front Genet
; 12: 719791, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35046991
15.
Contribution of Known Genetic Risk Variants to Dyslipidemias and Type 2 Diabetes in Mexico: A Population-Based Nationwide Study.
Genes (Basel)
; 11(1)2020 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31968565
16.
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytes.
Eur J Endocrinol
; 180(2): 99-107, 2019 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30475225
17.
Associations of autozygosity with a broad range of human phenotypes.
Nat Commun
; 10(1): 4957, 2019 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31673082
18.
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes.
Diabetes
; 66(11): 2903-2914, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28838971
19.
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.
Nat Commun
; 7: 10531, 2016 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26818947
20.
Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women.
PLoS One
; 10(5): e0126408, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25973943