Search details
1.
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.
PLoS Genet
; 18(6): e1010193, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35653334
2.
Mendelian randomization in the multivariate general linear model framework.
Genet Epidemiol
; 46(1): 17-31, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34672390
3.
Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.
Int J Obes (Lond)
; 47(2): 109-116, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36463326
4.
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.
Article
in English
| MEDLINE | ID: mdl-37341347
5.
Mendelian randomization study of diabetes and dementia in the Million Veteran Program.
Alzheimers Dement
; 19(10): 4367-4376, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37417779
6.
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.
Article
in English
| MEDLINE | ID: mdl-33910371
7.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Nature
; 518(7537): 102-6, 2015 Feb 05.
Article
in English
| MEDLINE | ID: mdl-25487149
8.
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.
PLoS Genet
; 14(4): e1007275, 2018 04.
Article
in English
| MEDLINE | ID: mdl-29621232
9.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Article
in English
| MEDLINE | ID: mdl-29590102
10.
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.
Article
in English
| MEDLINE | ID: mdl-32143931
11.
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.
Article
in English
| MEDLINE | ID: mdl-29226381
12.
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Am J Hum Genet
; 99(4): 877-885, 2016 Oct 06.
Article
in English
| MEDLINE | ID: mdl-27666373
13.
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Am J Hum Genet
; 99(1): 8-21, 2016 Jul 07.
Article
in English
| MEDLINE | ID: mdl-27346685
14.
Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.
J Electrocardiol
; 55: 1-5, 2019.
Article
in English
| MEDLINE | ID: mdl-31028976
15.
gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.
Genet Epidemiol
; 41(4): 297-308, 2017 05.
Article
in English
| MEDLINE | ID: mdl-28211093
16.
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.
Article
in English
| MEDLINE | ID: mdl-29321517
17.
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.
Article
in English
| MEDLINE | ID: mdl-28912365
18.
Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
Genet Epidemiol
; 40(6): 461-9, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27312771
19.
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.
Article
in English
| MEDLINE | ID: mdl-25224454
20.
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.
Article
in English
| MEDLINE | ID: mdl-24507775