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Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history

European heart journal, 2016-02, Vol.37 (6), p.561-567

2016

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Twelve–Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke

Stroke (1970), 2014-10, Vol.45 (10), p.2856-2862

2014

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A gene variant in CERS2 is associated with rate of increase in albuminuria in patients with diabetes from ONTARGET and TRANSCEND

PloS one, 2014-09, Vol.9 (9), p.e106631-e106631

2014

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Plasma arginine levels in arginase deficiency in the “real world”

Molecular genetics and metabolism reports, 2024-03, Vol.38, p.101042-101042, Article 101042

2024

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Gaps in Dyslipidemia Care Among Working-Aged Individuals With Employer-Sponsored Health Care

Journal of the American Heart Association, 2020-05, Vol.9 (9), p.e015807

2020

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Predictors of lack of glycemic control in persons with type 2 diabetes

Clinical diabetes and endocrinology, 2024-01, Vol.10 (1), p.2-2, Article 2

2024

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Insulin resistance probability score and incident cardiovascular disease

Journal of internal medicine, 2023-10, Vol.294 (4), p.531-535

2023

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Low-Density Lipoprotein Particle Number Is Associated With Cardiovascular Events Among Those Not Classified Into Statin Benefit Groups

Journal of the American College of Cardiology, 2015-06, Vol.65 (23), p.2571-2573

2015

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A Kinesin Family Member 6 Variant Is Associated With Coronary Heart Disease in the Women’s Health Study

Journal of the American College of Cardiology, 2008-01, Vol.51 (4), p.444-448

2008

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1286-P: Hyperinsulinemia Is Common in Individuals with Normoglycemia in a Nationwide Working-Age Population

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy

PloS one, 2012-05, Vol.7 (5), p.e38240-e38240

2012

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LDL subfractions are associated with incident cardiovascular disease in the Malmö Prevention Project Study

Atherosclerosis, 2017-08, Vol.263, p.287-292

2017

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965-P: Factors Associated with Poor Glycemic Control in Persons with Type 2 Diabetes and Employer-Based Health Care Coverage

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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945-P: Predictors of Lack of Improvement in Glycemic Control in Persons with Type 2 Diabetes

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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An Insulin Resistance Score Improved Diabetes Risk Assessment in the Malmö Prevention Project-A Longitudinal Population-Based Study of Older Europeans

Diabetes care, 2021-10, Vol.44 (10), p.e186-e187

2021

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Effect of Pravastatin Therapy on Coronary Events in Carriers of the KIF6 719Arg Allele from the Cholesterol and Recurrent Events Trial

The American journal of cardiology, 2010-05, Vol.105 (9), p.1300-1305

2010

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Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction

PloS one, 2008-08, Vol.3 (8), p.e2895-e2895

2008

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Concordance of Cardiovascular Risk Factors and Behaviors in a Multiethnic US Nationwide Cohort of Married Couples and Domestic Partners

JAMA network open, 2020-10, Vol.3 (10), p.e2022119

2020

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Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy

Atherosclerosis, 2009-04, Vol.203 (2), p.371-376

2009

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The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study

BMC cardiovascular disorders, 2011-03, Vol.11 (1), p.10-10, Article 10

2011

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Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study

Arteriosclerosis, thrombosis, and vascular biology, 2008-01, Vol.28 (1), p.173-179

2008

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Maternal red blood cell alloimmunization prevalence in the United States

Blood advances, 2024-08, Vol.8 (16), p.4311-4319

2024

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Genetic risk for atrial fibrillation could motivate patient adherence to warfarin therapy: a cost effectiveness analysis

BMC cardiovascular disorders, 2015-09, Vol.15 (1), p.104-104, Article 104

2015

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Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction

Arteriosclerosis, thrombosis, and vascular biology, 2006-07, Vol.26 (7), p.1613-1618

2006

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Single variants can explain the association between coronary heart disease and haplotypes in the apolipoprotein(a) locus

Atherosclerosis, 2010-09, Vol.212 (1), p.193-196

2010

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Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history

Twelve–Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke

A gene variant in CERS2 is associated with rate of increase in albuminuria in patients with diabetes from ONTARGET and TRANSCEND

Plasma arginine levels in arginase deficiency in the “real world”

Gaps in Dyslipidemia Care Among Working-Aged Individuals With Employer-Sponsored Health Care

Predictors of lack of glycemic control in persons with type 2 diabetes

Insulin resistance probability score and incident cardiovascular disease

Low-Density Lipoprotein Particle Number Is Associated With Cardiovascular Events Among Those Not Classified Into Statin Benefit Groups

A Kinesin Family Member 6 Variant Is Associated With Coronary Heart Disease in the Women’s Health Study

1286-P: Hyperinsulinemia Is Common in Individuals with Normoglycemia in a Nationwide Working-Age Population

Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy

LDL subfractions are associated with incident cardiovascular disease in the Malmö Prevention Project Study

965-P: Factors Associated with Poor Glycemic Control in Persons with Type 2 Diabetes and Employer-Based Health Care Coverage

945-P: Predictors of Lack of Improvement in Glycemic Control in Persons with Type 2 Diabetes

An Insulin Resistance Score Improved Diabetes Risk Assessment in the Malmö Prevention Project-A Longitudinal Population-Based Study of Older Europeans

Effect of Pravastatin Therapy on Coronary Events in Carriers of the KIF6 719Arg Allele from the Cholesterol and Recurrent Events Trial

Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction

Concordance of Cardiovascular Risk Factors and Behaviors in a Multiethnic US Nationwide Cohort of Married Couples and Domestic Partners

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy

The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study

Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study

Maternal red blood cell alloimmunization prevalence in the United States

Genetic risk for atrial fibrillation could motivate patient adherence to warfarin therapy: a cost effectiveness analysis

Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction

Single variants can explain the association between coronary heart disease and haplotypes in the apolipoprotein(a) locus

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