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- 2021
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Mark
Prevalence of Subclinical Coronary Artery Atherosclerosis in the General Population
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- Contribution to journal › Article
- 2012
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Mark
A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events.
(
- Contribution to journal › Article
- 2010
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Mark
Bayesian methods for meta-analysis of causal relationships estimated using genetic instrumental variables.
2010) In Statistics in Medicine(
- Contribution to journal › Article
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Mark
Consequences of orthostatic blood pressure variability in middle-aged men (The Malmö Preventive Project).
(
- Contribution to journal › Article
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Mark
The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes.
(
- Contribution to journal › Article
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Mark
A gene score of nine LDL and HDL regulating genes is associated with fluvastatin induced cholesterol changes in women.
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- Contribution to journal › Article
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Mark
Weak associations between human leucocyte antigen genotype and acute myocardial infarction.
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- Contribution to journal › Article
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Mark
Plasma copeptin and the risk of diabetes mellitus.
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- Contribution to journal › Article
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Mark
Orthostatic hypotension predicts all-cause mortality and coronary events in middle-aged individuals (The Malmo Preventive Project).
(
- Contribution to journal › Article
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Mark
Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes.
(
- Contribution to journal › Article
- 2009
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Mark
Homozygosity for the ephx2 k55r polymorphism increases the long term risk of ischemic stroke in men: a study in swedes
(
- Contribution to journal › Published meeting abstract
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Mark
Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke A Large-Scale Genetic Association Study
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- Contribution to journal › Article
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Mark
The common functional polymorphism-50g > t of the cyp2j2 gene is not associated with coronary and cerebrovascular events in an urban based sample of Swedes
(
- Contribution to journal › Published meeting abstract
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Mark
ION Mobility Analysis Of Lipoprotein Subfractions Suggests Three Independent Mechanisms Of Cardiovascular Risk
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- Contribution to journal › Published meeting abstract
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Mark
Genome-wide association study identifies eight loci associated with blood pressure
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- Contribution to journal › Article
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Mark
Associations Between Human Leukocyte Antigen (HLA) Genotype And Acute Myocardial Infarction
2009) 15th International Symposium on Atherosclerosis In Atherosclerosis Supplements 10(2). p.953-953(
- Contribution to journal › Published meeting abstract
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Mark
Novel and conventional biomarkers for prediction of incident cardiovascular events in the community.
(
- Contribution to journal › Article
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Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies Three Independent Axes of Cardiovascular Risk.
(
- Contribution to journal › Article
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Mark
Relation between human vasopressin 1a gene variance, fat intake, and diabetes.
(
- Contribution to journal › Article
- 2008
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Mark
Phenotype associated with human vasopressin receptor 1a (V1aR) gene variance is dependent on fat intake and resembles the phenotype of the V1aR knock out mouse
2008) 18th Scientific Meeting of the European-Society-of-Hypertension/22nd Scientific Meeting of the International-Society-of-Hypertension In Journal of Hypertension 26(Suppl. 1). p.144-144(
- Contribution to journal › Published meeting abstract
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Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
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Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
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Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
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Mark
Functional variation of the NEDD4L gene predicts ischemic stroke
2008) 18th Scientific Meeting of the European-Society-of-Hypertension/22nd Scientific Meeting of the International-Society-of-Hypertension In Journal of Hypertension 26(Suppl. 1). p.134-134(
- Contribution to journal › Published meeting abstract
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Mark
The Pro12Ala polymorphism of the PPARG gene is not associated with the metabolic syndrome in an urban population of middle-aged Swedish individuals.
(
- Contribution to journal › Article
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Mark
The V433M Variant of the CYP4F2 Is Associated With Ischemic Stroke in Male Swedes Beyond Its Effect on Blood Pressure.
(
- Contribution to journal › Article
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Mark
Job strain, job demands and adrenergic beta1-receptor-polymorphism: a possible interaction affecting blood pressure in men.
(
- Contribution to journal › Article
- 2007
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Mark
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes
(
- Contribution to journal › Article
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Mark
EPIC-Heart: The cardiovascular component of a prospective study of nutritional, lifestyle and biological factors in 520,000 middle-aged participants from 10 European countries
(
- Contribution to journal › Article
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Mark
Increased risk of acute myocardial infarction and elevated levels of C-reactive protein in carriersof the Thr-87 variant of the ATP receptor P2Y11.
(
- Contribution to journal › Article
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Mark
Job strain, decision latitude and alpha2B-adrenergic receptor polymorphism significantly interact, and associate with higher blood pressures in men.
(
- Contribution to journal › Article
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Mark
The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
(
- Contribution to journal › Article
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Mark
Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.
(
- Contribution to journal › Article
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Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article
- 2006
-
Mark
24-hour Ambulatory Blood Pressure is Linked to Chromosome 18q21-22 and Genetic Variation of NEDD4L Associates with Cross-Sectional and Longitudinal Blood Pressure in Swedes.
(
- Contribution to journal › Article
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Mark
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
- 2005
-
Mark
Genetic variance of SGK-1 is associated with blood pressure, blood pressure change over time and strength of the insulin-diastolic blood pressure relationship.
(
- Contribution to journal › Article