Detalhe da pesquisa
1.
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Nature
; 586(7831): 749-756, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087929
2.
A fast linkage method for population GWAS cohorts with related individuals.
Genet Epidemiol
; 47(3): 231-248, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739617
3.
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Am J Hum Genet
; 108(9): 1578-1589, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34265237
4.
Identification of cell type specific ACE2 modifiers by CRISPR screening.
PLoS Pathog
; 18(3): e1010377, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35231079
5.
Bicuspid Aortic Valve-Associated Regulatory Regions Reveal GATA4 Regulation and Function During Human-Induced Pluripotent Stem Cell-Based Endothelial-Mesenchymal Transition-Brief Report.
Arterioscler Thromb Vasc Biol
; 43(2): 312-322, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36519469
6.
Genome-scale CRISPR screening for modifiers of cellular LDL uptake.
PLoS Genet
; 17(1): e1009285, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33513160
7.
Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.
Circulation
; 146(8): e93-e118, 2022 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35862132
8.
An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population.
Hum Mol Genet
; 30(9): 836-842, 2021 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693786
9.
Genome-wide association study of cardiac troponin I in the general population.
Hum Mol Genet
; 30(21): 2027-2039, 2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33961016
10.
Incorporating family disease history and controlling case-control imbalance for population-based genetic association studies.
Bioinformatics
; 38(18): 4337-4343, 2022 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35876838
11.
Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study.
Behav Genet
; 53(1): 40-52, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322199
12.
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genet
; 16(6): e1008725, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603359
13.
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility.
Am J Med Genet A
; 188(5): 1448-1456, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35092149
14.
Genetic insight into sick sinus syndrome.
Eur Heart J
; 42(20): 1959-1971, 2021 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36282123
15.
Genetic insight into sick sinus syndrome.
Eur Heart J
; 42(20): 1959-1971, 2021 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33580673
16.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Circulation
; 142(17): 1633-1646, 2020 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32981348
17.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290336
18.
Translating genetic association of lipid levels for biological and clinical application.
Cardiovasc Drugs Ther
; 35(3): 617-626, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33604704
19.
A survey of aortic disease biorepository participants' preferences for return of research genetic results.
J Genet Couns
; 30(3): 645-655, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33319384
20.
Robust meta-analysis of biobank-based genome-wide association studies with unbalanced binary phenotypes.
Genet Epidemiol
; 43(5): 462-476, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30793809