Detalhe da pesquisa
1.
Actionable Genotypes and Their Association with Life Span in Iceland.
N Engl J Med
; 389(19): 1741-1752, 2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937776
2.
Genetic variants associated with syncope implicate neural and autonomic processes.
Eur Heart J
; 44(12): 1070-1080, 2023 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36747475
3.
Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.
JAMA
; 330(8): 725-735, 2023 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37606673
4.
Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.
Arterioscler Thromb Vasc Biol
; 41(10): 2616-2628, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34407635
5.
Sequence variants associating with urinary biomarkers.
Hum Mol Genet
; 28(7): 1199-1211, 2019 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30476138
6.
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.
Eur Heart J
; 41(28): 2618-2628, 2020 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702746
7.
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
8.
FTO genotype is associated with phenotypic variability of body mass index.
Nature
; 490(7419): 267-72, 2012 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22982992
9.
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.
PLoS Genet
; 11(9): e1005379, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26327206
10.
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.
PLoS Genet
; 11(7): e1005230, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26132169
11.
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.
PLoS Genet
; 9(6): e1003530, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23754956
12.
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
PLoS Genet
; 9(6): e1003500, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23754948
13.
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
Nat Genet
; 39(6): 770-5, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17460697
14.
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.
Nat Genet
; 39(8): 977-83, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17603485
15.
Parental origin of sequence variants associated with complex diseases.
Nature
; 462(7275): 868-74, 2009 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20016592
16.
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.
PLoS Genet
; 8(5): e1002741, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22693455
17.
Genetics of gene expression and its effect on disease.
Nature
; 452(7186): 423-8, 2008 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-18344981
18.
A common inversion under selection in Europeans.
Nat Genet
; 37(2): 129-37, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15654335
19.
InterPregGen: genetic studies of pre-eclampsia in three continents.
Nor Epidemiol
; 24(1-2): 141-146, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-26568652
20.
Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.
medRxiv
; 2024 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38633783