Detalhe da pesquisa
1.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046083
2.
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 586(7831): 763-768, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057201
3.
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.
Hum Mol Genet
; 32(6): 1048-1060, 2023 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36444934
4.
METRO: Multi-ancestry transcriptome-wide association studies for powerful gene-trait association detection.
Am J Hum Genet
; 109(5): 783-801, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35334221
5.
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.
Brain
; 146(2): 492-506, 2023 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943854
6.
Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction.
Hum Mol Genet
; 30(15): 1443-1456, 2021 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33856023
7.
Genetic Architecture of Gene Expression in European and African Americans: An eQTL Mapping Study in GENOA.
Am J Hum Genet
; 106(4): 496-512, 2020 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32220292
8.
US Residents' Preferences for Sharing of Electronic Health Record and Genetic Information: A Discrete Choice Experiment.
Value Health
; 26(9): 1301-1307, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36736697
9.
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 591(7851): E27, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33707633
10.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
PLoS Genet
; 15(12): e1008500, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31869403
11.
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program.
Am J Epidemiol
; 190(10): 1977-1992, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33861317
12.
Bayesian hierarchical models for high-dimensional mediation analysis with coordinated selection of correlated mediators.
Stat Med
; 40(27): 6038-6056, 2021 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34404112
13.
DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.
Am J Hum Genet
; 101(6): 888-902, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29198723
14.
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis.
Blood
; 132(17): 1842-1850, 2018 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30042098
15.
Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples.
J Nutr
; 150(10): 2635-2645, 2020 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32840624
16.
Bayesian shrinkage estimation of high dimensional causal mediation effects in omics studies.
Biometrics
; 76(3): 700-710, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31733066
17.
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
PLoS Genet
; 13(3): e1006678, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28346479
18.
Religion as a Health Promoter During the 2019/2020 COVID Outbreak: View from Detroit.
J Relig Health
; 59(5): 2243-2255, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32548832
19.
Testing cross-phenotype effects of rare variants in longitudinal studies of complex traits.
Genet Epidemiol
; 42(4): 320-332, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29601641
20.
The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus.
Hum Genet
; 138(4): 375-388, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30852652