Detalhe da pesquisa
1.
Divergent role of Mitochondrial Amidoxime Reducing Component 1 (MARC1) in human and mouse.
PLoS Genet
; 20(3): e1011179, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38437227
2.
Germline Mutations in CIDEB and Protection against Liver Disease.
N Engl J Med
; 387(4): 332-344, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939579
3.
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
4.
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
5.
Ventricular rate in atrial fibrillation and the risk of heart failure and death.
Europace
; 25(5)2023 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37083042
6.
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
7.
Implantable loop recorder detection of atrial fibrillation to prevent stroke (The LOOP Study): a randomised controlled trial.
Lancet
; 398(10310): 1507-1516, 2021 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469766
8.
Associations between primary care electrocardiography and non-Alzheimer dementia.
J Stroke Cerebrovasc Dis
; 31(9): 106640, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35830834
9.
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
10.
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood
; 134(19): 1645-1657, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31420334
11.
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
12.
Mitochondrial genome-wide association study of migraine - the HUNT Study.
Cephalalgia
; 40(6): 625-634, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32056457
13.
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
em Inglês
| MEDLINE | ID: mdl-31596048
14.
Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.
Ann Noninvasive Electrocardiol
; 24(6): e12661, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152482
15.
Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.
Genet Epidemiol
; 41(8): 744-755, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28861891
16.
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
em Inglês
| MEDLINE | ID: mdl-27711072
17.
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.
Circulation
; 130(15): 1225-35, 2014 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25124494
18.
Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population.
Eur Heart J
; 35(20): 1335-44, 2014 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24603310
19.
Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis.
J Mol Cell Cardiol
; 67: 69-76, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24374141
20.
New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome.
BMC Genet
; 15: 74, 2014 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24941995