S. Matthíasson

发表

Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior

C. Gieger, A. Hofman, A. Uitterlinden, 2010, Nature Genetics.

Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior

C. Gieger, A. Hofman, A. Uitterlinden, 2010 .

Study of the Interaction of Dextran and Enoxaparin on Haemostasis in Humans

B. Lindblad, D. Bergqvist, T. Mätzsch, 1994, Thrombosis and Haemostasis.

Effect of Low Molecular Weight Heparin, Dextran and Their Combinations on Experimental Venous Thrombosis in Rabbits

B. Lindblad, D. Bergqvist, T. Mätzsch, 1994, Thrombosis and Haemostasis.

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

H. Stefánsson, J. Gulcher, U. Thorsteinsdóttir, 2008, Nature Genetics.

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2004, Nature Genetics.

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

Gerard Tromp, Marylyn D. Ritchie, Dana C. Crawford, 2017, Circulation research.

A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm

Simon C. Potter, Benjamin J. Wright, P. Deloukas, 2013, Circulation. Cardiovascular genetics.

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.

U. Thorsteinsdóttir, K. Stefánsson, N. Samani, 2013, Human molecular genetics.

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

Simon C. Potter, Benjamin J. Wright, T. Assimes, 2011, American journal of human genetics.

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Gerard Tromp, Helena Kuivaniemi, Kari Stefansson, 2010, Nature Genetics.

Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland

Bjarni V. Halldórsson, B. Halldórsson, A. Jonasdottir, 2021, Arteriosclerosis, thrombosis, and vascular biology.

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Dan M Roden, Kari Stefansson, Gudmar Thorleifsson, 2011, Nature Genetics.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, Gao T. Wang, Benjamin J. Wright, 2016, Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease.

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.

P. Tsao, D. Gudbjartsson, U. Thorsteinsdóttir, 2012, Journal of the American College of Cardiology.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Daniel F. Gudbjartsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature.

Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

H. Stefánsson, D. Gudbjartsson, H. Ullum, 2020, European heart journal.

Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2019, Journal of the American College of Cardiology.

Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31.

J. Gulcher, A. Kong, K. Stefánsson, 2002, American journal of human genetics.

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

Vilmundur Gudnason, Kari Stefansson, Arshed A Quyyumi, 2006, Nature Genetics.

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

S. Steinberg, D. Gudbjartsson, T. Thorgeirsson, 2016, Molecular Psychiatry.

Experimental Haemorrhagic Effect of Two-Domain Non-Glycosylated Tissue Factor Pathway Inhibitor Compared to Low Molecular Weight Heparin

B. Lindblad, U. Hedner, J. Holst, 1996, Thrombosis and Haemostasis.