Detalhe da pesquisa
1.
Complex effects of sequence variants on lipid levels and coronary artery disease.
Cell
; 186(19): 4085-4099.e15, 2023 09 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37714134
2.
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus.
J Allergy Clin Immunol
; 153(4): 1073-1082, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38300190
3.
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.
Eur Heart J
; 44(21): 1927-1939, 2023 06 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37038246
4.
Genetic risk of fatty liver disease and mortality in the general population: A Mendelian randomization study.
Liver Int
; 43(9): 1955-1965, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37269170
5.
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Eur Heart J
; 43(45): 4707-4718, 2022 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35751511
6.
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Eur Heart J
; 42(44): 4523-4534, 2021 11 21.
Artigo
Inglês
| MEDLINE | ID: mdl-34338756
7.
Associations between primary care electrocardiography and non-Alzheimer dementia.
J Stroke Cerebrovasc Dis
; 31(9): 106640, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-35830834
8.
Effect of diabetes duration on the relationship between glycaemic control and risk of death in older adults with type 2 diabetes.
Diabetes Obes Metab
; 22(2): 231-242, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31596048
9.
Potential Influence of Risk Factor Control on the Association Between Lipoprotein(a) and Atherosclerotic Cardiovascular Disease.
Arterioscler Thromb Vasc Biol
; 44(6): 1455-1457, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38660805
10.
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT.
Circ Res
; 131(10): 862-865, 2022 10 28.
Artigo
Inglês
| MEDLINE | ID: mdl-36205134
11.
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.
Genet Med
; 19(5): 521-528, 2017 05.
Artigo
Inglês
| MEDLINE | ID: mdl-27711072
12.
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
Eur Heart J
; 36(37): 2523-9, 2015 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26159999
13.
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.
Nat Genet
; 56(5): 827-837, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38632349
14.
Variants at the Interleukin 1 Gene Locus and Pericarditis.
JAMA Cardiol
; 9(2): 165-172, 2024 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38150231
15.
Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure.
JAMA Cardiol
; 8(2): 159-166, 2023 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36542369
16.
Association between primary care electrocardiogram markers and Alzheimer's disease.
J Neurol Sci
; 447: 120581, 2023 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-36827718
17.
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Nat Genet
; 55(3): 399-409, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36658437
18.
Effect of Loss-of-Function Genetic Variants in PCSK9 on Glycemic Traits, Neurocognitive Impairment, and Hepatobiliary Function.
Diabetes Care
; 45(1): 251-254, 2022 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34758978
19.
Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.
J Am Heart Assoc
; 11(12): e025361, 2022 06 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35703387
20.
Family Screening in Dilated Cardiomyopathy: Prevalence, Incidence, and Potential for Limiting Follow-Up.
JACC Heart Fail
; 10(11): 792-803, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36328645