Detalhe da pesquisa
1.
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
2.
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
PLoS Genet
; 18(4): e1010068, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35363781
3.
Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data.
Circulation
; 142(6): 546-555, 2020 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32654539
4.
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
N Engl J Med
; 374(12): 1134-44, 2016 03 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26934567
5.
Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.
N Engl J Med
; 374(22): 2131-41, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27192541
6.
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.
Circ Res
; 121(1): 81-88, 2017 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28506971
7.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Nature
; 504(7480): 432-6, 2013 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24213632
8.
Analysis with the exome array identifies multiple new independent variants in lipid loci.
Hum Mol Genet
; 25(18): 4094-4106, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27466198
9.
Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages.
Am J Hum Genet
; 97(2): 228-37, 2015 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26166477
10.
Coronary Artery Disease-Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes.
Arterioscler Thromb Vasc Biol
; 37(6): 1050-1057, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28279971
11.
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.
JAMA
; 317(9): 937-946, 2017 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28267856
12.
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
; 464(7289): 713-20, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20360734
13.
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.
Am J Hum Genet
; 91(5): 823-38, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23063622
14.
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.
Am J Hum Genet
; 90(3): 410-25, 2012 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22325160
15.
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
Am J Hum Genet
; 88(1): 6-18, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21194676
16.
Blood pressure loci identified with a gene-centric array.
Am J Hum Genet
; 89(6): 688-700, 2011 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22100073
17.
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.
PLoS Med
; 10(6): e1001474, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23824655
18.
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies.
Lancet
; 379(9822): 1205-13, 2012 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-22421339
19.
Elucidation of the genetic causes of bicuspid aortic valve disease.
Cardiovasc Res
; 119(3): 857-866, 2023 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35727948
20.
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.
Nat Genet
; 55(6): 964-972, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37248441