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Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

American journal of human genetics, 2009-04, Vol.84 (4), p.468-476

2009

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Incidence and Risk Factors for Invasive Pneumococcal Disease and Community-acquired Pneumonia in Human Immunodeficiency Virus–Infected Individuals in a High-income Setting

Clinical infectious diseases, 2020-06, Vol.71 (1), p.41-50

2020

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Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans

Diabetes (New York, N.Y.), 2006-06, Vol.55 (6), p.1807-1812

2006

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Human ATP-binding cassette G1 controls macrophage lipoprotein lipase bioavailability and promotes foam cell formation

Arteriosclerosis, thrombosis, and vascular biology, 2012-09, Vol.32 (9), p.2223

2012

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Nuclear Receptor Nurr1 Is Expressed In and Is Associated With Human Restenosis and Inhibits Vascular Lesion Formation In Mice Involving Inhibition of Smooth Muscle Cell Proliferation and Inflammation

Circulation (New York, N.Y.), 2010-05, Vol.121 (18), p.2023-2032

2010

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Both paraoxonase-1 genotype and activity do not predict the risk of future coronary artery disease; the EPIC-Norfolk Prospective Population Study

PloS one, 2009-08, Vol.4 (8), p.e6809-e6809

2009

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Assessment of coagulation and fibrinolysis in families with unexplained thrombophilia

Thrombosis and haemostasis, 2009-03, Vol.101 (3), p.465

2009

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Striatal Dopamine Transporter Availability Associated with Polymorphisms in the Dopamine Transporter Gene SLC6A3

Journal of Nuclear Medicine, 2009-01, Vol.50 (1), p.45-52

2009

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Genetic variation in thrombin-activatable fibrinolysis inhibitor (TAFI) is associated with the risk of splanchnic vein thrombosis

Thrombosis and haemostasis, 2007-02, Vol.97 (2), p.181

2007

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Risk scores for outcome in bacterial meningitis: Systematic review and external validation study

The Journal of infection, 2016-11, Vol.73 (5), p.393-401

2016

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Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death

Journal of molecular and cellular cardiology, 2012-03, Vol.52 (3), p.620-629

2012

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Nonclassical FCGR2C haplotype is associated with protection from red blood cell alloimmunization in sickle cell disease

Blood, 2017-11, Vol.130 (19), p.2121-2130

2017

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SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

International journal of cardiology, 2018-09, Vol.266, p.128-132

2018

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SNP rs688 within the low‐density lipoprotein receptor (LDL‐R) gene associates with HCV susceptibility

Liver international, 2019-03, Vol.39 (3), p.463-469

2019

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Red cell distribution width is associated with physical inactivity and heart failure, independent of established risk factors, inflammation or iron metabolism; the EPIC—Norfolk study

International journal of cardiology, 2013-10, Vol.168 (4), p.3550-3555

2013

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Relative risk for cardiovascular atherosclerotic events after smoking cessation: 6-9 years excess risk in individuals with familial hypercholesterolemia

BMC public health, 2006-10, Vol.6 (1), p.262-262, Article 262

2006

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Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Circulation. Cardiovascular genetics, 2015-06, Vol.8 (3), p.447

2015

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Familial sudden death is an important risk factor for primary ventricular fibrillation : A case-control study in acute myocardial infarction patients

Circulation (New York, N.Y.), 2006-09, Vol.114 (11), p.1140-1145

2006

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Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

European heart journal, 2006-09, Vol.27 (18), p.2240-2246

2006

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Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2005-07, Vol.25 (7), p.1475

2005

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The association between the gene encoding 5-lipoxygenase activating protein and abdominal aortic aneurysms

Atherosclerosis, 2012-02, Vol.220 (2), p.425-428

2012

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Common genetic variants do not associate with CAD in familial hypercholesterolemia

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.809-813

2014

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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature genetics, 2021-02, Vol.53 (2), p.128-134

2021

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Chemokine ligand 2 genetic variants, serum monocyte chemoattractant protein-1 levels, and the risk of coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 2010-07, Vol.30 (7), p.1460

2010

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Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

Incidence and Risk Factors for Invasive Pneumococcal Disease and Community-acquired Pneumonia in Human Immunodeficiency Virus–Infected Individuals in a High-income Setting

Large genome-wide association study identifies three novel risk variants for restless legs syndrome

Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans

Human ATP-binding cassette G1 controls macrophage lipoprotein lipase bioavailability and promotes foam cell formation

Nuclear Receptor Nurr1 Is Expressed In and Is Associated With Human Restenosis and Inhibits Vascular Lesion Formation In Mice Involving Inhibition of Smooth Muscle Cell Proliferation and Inflammation

Both paraoxonase-1 genotype and activity do not predict the risk of future coronary artery disease; the EPIC-Norfolk Prospective Population Study

Assessment of coagulation and fibrinolysis in families with unexplained thrombophilia

Striatal Dopamine Transporter Availability Associated with Polymorphisms in the Dopamine Transporter Gene SLC6A3

Genetic variation in thrombin-activatable fibrinolysis inhibitor (TAFI) is associated with the risk of splanchnic vein thrombosis

Risk scores for outcome in bacterial meningitis: Systematic review and external validation study

Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death

Nonclassical FCGR2C haplotype is associated with protection from red blood cell alloimmunization in sickle cell disease

SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

SNP rs688 within the low‐density lipoprotein receptor (LDL‐R) gene associates with HCV susceptibility

Red cell distribution width is associated with physical inactivity and heart failure, independent of established risk factors, inflammation or iron metabolism; the EPIC—Norfolk study

Relative risk for cardiovascular atherosclerotic events after smoking cessation: 6-9 years excess risk in individuals with familial hypercholesterolemia

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Familial sudden death is an important risk factor for primary ventricular fibrillation : A case-control study in acute myocardial infarction patients

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia

The association between the gene encoding 5-lipoxygenase activating protein and abdominal aortic aneurysms

Common genetic variants do not associate with CAD in familial hypercholesterolemia

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Chemokine ligand 2 genetic variants, serum monocyte chemoattractant protein-1 levels, and the risk of coronary artery disease

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