Detalhe da pesquisa
1.
Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.
Int J Obes (Lond)
; 47(2): 109-116, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36463326
2.
Plasma neurofilament light chain concentrations are elevated in youth-onset type 2 diabetes and associated with neuropathy.
J Peripher Nerv Syst
; 28(3): 460-470, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37341347
3.
Mendelian randomization study of diabetes and dementia in the Million Veteran Program.
Alzheimers Dement
; 19(10): 4367-4376, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37417779
4.
Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants.
Arterioscler Thromb Vasc Biol
; 41(6): e369-e378, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33910371
5.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Nature
; 518(7537): 102-6, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25487149
6.
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.
PLoS Genet
; 14(4): e1007275, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29621232
7.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29590102
8.
Genetic Risk for Hepatic Fat among an Ethnically Diverse Cohort of Youth: The Exploring Perinatal Outcomes among Children Study.
J Pediatr
; 220: 146-153.e2, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32143931
9.
A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations.
Genet Epidemiol
; 42(3): 288-302, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29226381
10.
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Am J Hum Genet
; 99(4): 877-885, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666373
11.
Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.
J Electrocardiol
; 55: 1-5, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31028976
12.
Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study.
J Hum Genet
; 63(3): 327-337, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29321517
13.
D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study.
Arterioscler Thromb Vasc Biol
; 37(11): 2220-2227, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28912365
14.
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.
Hum Mol Genet
; 24(2): 572-81, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25224454
15.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Am J Hum Genet
; 94(2): 233-45, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24507775
16.
Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study.
Ann Hum Genet
; 80(5): 294-305, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27530450
17.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
; 135(8): 923-38, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262462
18.
Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan.
Arterioscler Thromb Vasc Biol
; 35(10): 2246-53, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26293465
19.
Exploring the genetic basis of chronic periodontitis: a genome-wide association study.
Hum Mol Genet
; 22(11): 2312-24, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23459936
20.
Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.
Am J Hum Genet
; 91(5): 794-808, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103231