Detalhe da pesquisa
1.
Major Facilitator Superfamily Domain Containing 5 Inhibition Reduces Lipoprotein(a) Uptake and Calcification in Valvular Heart Disease.
Circulation
; 149(5): 391-401, 2024 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937463
2.
Toll-Like Receptor 3 Mediates Aortic Stenosis Through a Conserved Mechanism of Calcification.
Circulation
; 147(20): 1518-1533, 2023 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37013819
3.
Sortilin enhances fibrosis and calcification in aortic valve disease by inducing interstitial cell heterogeneity.
Eur Heart J
; 44(10): 885-898, 2023 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36660854
4.
Interplay of Atherogenic Particle Number and Particle Size and the Risk of Coronary Heart Disease.
Clin Chem
; 69(1): 48-55, 2023 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36331823
5.
Genome-Wide Association Study Highlights APOH as a Novel Locus for Lipoprotein(a) Levels-Brief Report.
Arterioscler Thromb Vasc Biol
; 41(1): 458-464, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33115273
6.
Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution.
Am J Hum Genet
; 101(6): 925-938, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220676
7.
Hypertension, brain imaging phenotypes, and cognitive impairment: lessons from Mendelian randomization.
Eur Heart J
; 44(23): 2126-2128, 2023 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36994899
8.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
Hum Mol Genet
; 24(12): 3582-94, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25784503
9.
Association Between Family History, a Genetic Risk Score, and Severity of Coronary Artery Disease in Patients With Premature Acute Coronary Syndromes.
Arterioscler Thromb Vasc Biol
; 36(6): 1286-92, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27102964
10.
Periodontitis and hypertension: causally linked by immune mechanisms.
Eur Heart J
; 40(42): 3471-3473, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31589300
11.
Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI.
Diabetologia
; 57(4): 738-45, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24362726
12.
Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis.
JAMA
; 312(17): 1764-71, 2014 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25344734
13.
Large-Scale Proteomics Identifies Novel Biomarkers and Circulating Risk Factors for Aortic Stenosis.
J Am Coll Cardiol
; 83(5): 577-591, 2024 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38296402
14.
A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a): Meta-Analysis of Published and Novel Data.
Circulation
; 135(12): 1181-1183, 2017 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-28320808
15.
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.
Lancet
; 380(9841): 572-80, 2012 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22607825
16.
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
N Engl J Med
; 363(23): 2220-7, 2010 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20942659
17.
P2RX7 gene knockout or antagonism reduces angiotensin II-induced hypertension, vascular injury and immune cell activation.
J Hypertens
; 41(11): 1701-1712, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37796207
18.
Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias.
PLoS Med
; 9(2): e1001177, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22363213
19.
BRCA2 variants and cardiovascular disease in a multi-ethnic study.
BMC Med Genet
; 13: 56, 2012 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22809218
20.
NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage.
J Med Genet
; 48(8): 540-8, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21659348