Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
Temporal Changes in Cardiac Troponin I Are Associated with Risk of Cardiovascular Events in the General Population: The Nord-Trøndelag Health Study.
Clin Chem;
65(7): 871-881, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30996050
5.
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
6.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Am J Hum Genet;
94(2): 233-45, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24507775
7.
Loss-of-function mutations in APOC3, triglycerides, and coronary disease.
N Engl J Med;
371(1): 22-31, 2014 Jul 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24941081
8.
Methods for association analysis and meta-analysis of rare variants in families.
Genet Epidemiol;
39(4): 227-38, 2015 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25740221
9.
No large-effect low-frequency coding variation found for myocardial infarction.
Hum Mol Genet;
23(17): 4721-8, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24728188
10.
Impact of sex on the prognostic value of high-sensitivity cardiac troponin I in the general population: the HUNT study.
Clin Chem;
61(4): 646-56, 2015 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25695851
11.
Hypertension after preeclampsia and relation to the C1114G polymorphism (rs4606) in RGS2: data from the Norwegian HUNT2 study.
BMC Med Genet;
15: 28, 2014 Mar 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24593135
12.
Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
PLoS Genet;
7(12): e1002439, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22242009
13.
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.
medRxiv;
2023 Oct 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37873414
14.
Characterization of the genetic architecture of infant and early childhood body mass index.
Nat Metab;
4(3): 344-358, 2022 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35315439
15.
The HUNT study: A population-based cohort for genetic research.
Cell Genom;
2(10): 100193, 2022 Oct 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36777998
16.
Prediction of Ankylosing Spondylitis in the HUNT Study by a Genetic Risk Score Combining 110 Single-nucleotide Polymorphisms of Genome-wide Significance.
J Rheumatol;
47(2): 204-210, 2020 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30936278
17.
Author Correction: Characterization of the genetic architecture of infant and early childhood body mass index.
Nat Metab;
6(2): 378, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38337098
18.
Relative Prognostic Value of Cardiac Troponin I and C-Reactive Protein in the General Population (from the Nord-Trøndelag Health [HUNT] Study).
Am J Cardiol;
121(8): 949-955, 2018 04 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29496193
19.
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.
Commun Biol;
1: 68, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30271950
20.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nat Genet;
50(9): 1234-1239, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30061737