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.
A saturated map of common genetic variants associated with human height.
Nature
; 610(7933): 704-712, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36224396
3.
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
; 612(7941): 720-724, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36477530
4.
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Nature
; 590(7845): 290-299, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33568819
5.
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Am J Hum Genet
; 109(1): 81-96, 2022 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34932938
6.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods
; 19(12): 1599-1611, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36303018
7.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
; 108(4): 564-582, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713608
8.
Epigenome-wide association study of mitochondrial genome copy number.
Hum Mol Genet
; 31(2): 309-319, 2021 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415308
9.
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
10.
Rare and low-frequency coding variants alter human adult height.
Nature
; 542(7640): 186-190, 2017 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28146470
11.
Rare coding variants in RCN3 are associated with blood pressure.
BMC Genomics
; 23(1): 148, 2022 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35183128
12.
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.
Am J Hum Genet
; 104(2): 260-274, 2019 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30639324
13.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Mol Psychiatry
; 26(6): 2111-2125, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32372009
14.
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
15.
Western Dietary Pattern Derived by Multiple Statistical Methods Is Prospectively Associated with Subclinical Carotid Atherosclerosis in Midlife Women.
J Nutr
; 150(3): 579-591, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31687759
16.
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
17.
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
Am J Epidemiol
; 188(6): 1033-1054, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30698716
18.
A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.
Am J Hum Genet
; 98(3): 525-540, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26942286
19.
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.
Am J Hum Genet
; 99(1): 56-75, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27321945
20.
In utero metal exposures measured in deciduous teeth and birth outcomes in a racially-diverse urban cohort.
Environ Res
; 171: 444-451, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30735952