Cardiovascular Research - Hypertension
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- 2010
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Mark
Atrial fibrillation in the Malmö diet and cancer study: a study of occurrence, risk factors and diagnostic validity.
(
- Contribution to journal › Article
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Mark
Weak associations between human leucocyte antigen genotype and acute myocardial infarction.
(
- Contribution to journal › Article
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Mark
Vanin-1 I26T Polymorphism And Hypertension In Two Large Urban-Based Prospective Studies In Swedes
2010) 20th Annual Meeting of the European-Society-of-Hypertension In Journal of Hypertension 28. p.341-341(
- Contribution to journal › Published meeting abstract
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Mark
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension
(
- Contribution to journal › Article
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Mark
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
(
- Contribution to journal › Article
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
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Mark
A dedicated investigation unit improves management of syncopal attacks (Syncope Study of Unselected Population in Malmo--SYSTEMA I).
(
- Contribution to journal › Article
- 2009
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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
(
- Contribution to journal › Published meeting abstract
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Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
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Mark
Orthostatic hypotension: revision of the definition is needed Reply
(
- Contribution to journal › Letter
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Mark
Gastroparesis is associated with oxytocin deficiency, oesophageal dysmotility with hyperCCKemia, and autonomic neuropathy with hypergastrinemia
(
- Contribution to journal › Article
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Mark
Biomarkers for Prediction of Cardiovascular Events Reply
(
- Contribution to journal › Letter
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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
Gender differences in the association between NT proBNP and glucometabolic disturbances in a population-based cohort
(
- Contribution to journal › Published meeting abstract
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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
Genetic variation in serum and glucocortocoid regulated kinase 1 (SGK-1), a regulator of the epithelial sodium channel, is associated with ischemic stroke
(
- Contribution to journal › Published meeting abstract
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Mark
Overexpression of cytochrome P450 4F2 in mice increases 20-hydroxyeicosatetraenoic acid production and arterial blood pressure
(
- Contribution to journal › Letter
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Mark
European GWAS strategy using extremes of blood pressure distribution
(
- Contribution to journal › Published meeting abstract
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Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies 3 Independent Axes of Cardiovascular Risk
2009) Joint Nutrition, Physical Activity and Metabolism Conference/49th Cardiovascular Disease Epidemiology and Prevention, 2009 In Circulation 119(10). p.282-283(
- Contribution to journal › Published meeting abstract
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Mark
New susceptibility locus for coronary artery disease on chromosome 3q22.3
(
- Contribution to journal › Article
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Mark
The metabolic syndrome and risk of myocardial infarction in familial hypertension (Hypertension Heredity in Malmö Evaluation study).
(
- Contribution to journal › Article
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Mark
The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
(
- Contribution to journal › Article
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Mark
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- Contribution to journal › Article
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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
Orthostatic hypotension in genetically related hypertensive and normotensive individuals.
(
- Contribution to journal › Article
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Mark
Distribution and Correlates of Midregional Proadrenomedullin in the General Population.
(
- 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
Carotid Intima-Media Thickness, Systemic Inflammation, and Incidence of Heart Failure Hospitalizations.
(
- Contribution to journal › Article
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Mark
Fasting insulin has a stronger association with an adverse cardiometabolic risk profile than insulin resistance: the RISC study
(
- 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
2009) 10th Annual Conference on Arteriosclerosis, Thrombosis and Vascular Biology In Arteriosclerosis, Thrombosis, and Vascular Biology 29(7). p.23-24(
- Contribution to journal › Published meeting abstract
-
Mark
Increased pulse pressure is a marker for aortic stiffness independent of mean arterial pressure, age, sex, and other well-known cardiovascular risk factors
(
- Contribution to journal › Published meeting abstract
-
Mark
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
(
- Contribution to journal › Article
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Mark
Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip
(
- Contribution to journal › Article
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Mark
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
(
- Contribution to journal › Article
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Mark
Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke A Large-Scale Genetic Association Study
(
- Contribution to journal › Article
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Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
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Mark
Relation between human vasopressin 1a gene variance, fat intake, and diabetes.
(
- Contribution to journal › Article
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Mark
Leukocyte Count and Incidence of Hospitalizations Due to Heart Failure
(
- Contribution to journal › Article
- 2008
-
Mark
Functional polymorphism of the NEDD4L gene strongly influences cardiovascular outcome in hypertensive patients treated with beta-blockers and diuretics
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.143-144(
- Contribution to journal › Published meeting abstract
-
Mark
Determinants of kidney function in Swedish families. Role of heritable factors
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.131-131(
- Contribution to journal › Published meeting abstract
-
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
-
Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
-
Mark
The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of cardiovascular risk factors and coronary events in patients with hypertension
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.141-142(
- Contribution to journal › Published meeting abstract
-
Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
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Mark
Telomere Length Is Associated With Obesity Parameters but With a Gender Difference
(
- Contribution to journal › Article
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Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
(
- Contribution to journal › Article
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Mark
An association between Type 2 diabetes and alpha(1)-antitrypsin deficiency
(
- Contribution to journal › Article
-
Mark
Determinants of kidney function in Swedish families: role of heritable factors.
(
- Contribution to journal › Article
-
Mark
Association between an estrogen receptor alpha polymorphism (ERA : rs2234693) and the metabolic syndrome and cardiovascular and cerebrovascular morbidity and mortality
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.341-341(
- Contribution to journal › Published meeting abstract
-
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
-
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
-
Mark
Hypertension and genome-wide association studies: combining high fidelity phenotyping and hypercontrols.
(
- Contribution to journal › Article
-
Mark
The P2Y(13) Met-158-Thr Polymorphism, Which Is in Linkage Disequilibrium with the P2Y(12) Locus, Is Not Associated with Acute Myocardial Infarction.
(
- Contribution to journal › Article
-
Mark
Job strain, job demands and adrenergic beta1-receptor-polymorphism: a possible interaction affecting blood pressure in men.
(
- Contribution to journal › Article
-
Mark
Determinants of increasing pulse pressure during 23 years' follow-up as a marker of arterial stiffness and vascular ageing.
(
- Contribution to journal › Article
-
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
Genetics of cardiovascular disease: interplay between common and rare alleles.
(
- Contribution to journal › Article
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Mark
Interaction Between Renal Function and Microalbuminuria for Cardiovascular Risk in Hypertension The Nordic Diltiazem Study
(
- Contribution to journal › Article
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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
Determinants of increasing pulse pressure during 26 years' follow-up, as a marker of arterial stiffness and early vascular ageing (EVA)
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.117-117(
- Contribution to journal › Published meeting abstract
-
Mark
Gender Differences in Predictors of Heart Failure Morbidity and Mortality in an Urban Swedish Population: The Malmo Preventive Project
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 2007
-
Mark
Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes
(
- Contribution to journal › Article
-
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
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article
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Mark
hTERT T-1327/C polymorphism is not associated with age-related telomere attrition in peripheral blood
(
- Contribution to journal › Article
-
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
Are minor gene effects of clinical importance?
(
- Contribution to journal › Letter
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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
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
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- 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
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Mark
Moderate salt restriction effectively lowers blood pressure and degree of salt sensitivity is related to baseline concentration of renin and N-terminal atrial natriuretic peptide in plasma.
(
- Contribution to journal › Article
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Mark
Oesophageal dysmotility, delayed gastric emptying and gastrointestinal symptoms in patients with diabetes mellitus.
(
- Contribution to journal › Article
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Mark
Polymorphism in NEDD4L Is Associated with Increased Salt Sensitivity, Reduced Levels of P-renin and Increased Levels of Nt-proANP.
(
- 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
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes
(
- Contribution to journal › Article
- 2006
-
Mark
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
-
Mark
Salt sensitivity: a consequence of the metabolic syndrome?
(
- Contribution to journal › Letter
-
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
-
Mark
Glycemic and non-glycemic effects of pioglitazone in triple oral therapy in patients with type 2 diabetes mellitus
(
- Contribution to journal › Article
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Mark
Oesophageal dysmotility, delayed gastric emptying and autonomic neuropathy correlate to disturbed glucose homeostasis.
(
- 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
-
Mark
Nt-proANP in plasma, a marker of salt sensitivity, is reduced in type 2 diabetes patients.
(
- Contribution to journal › Article
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Mark
Detailed MALDI-MS/MS analysis of 2D gel spots: Results comparable to LC-MS in a fraction of the time without the need for LC-MS separation.
2005) HUPO 4th annual world congress, 2005(
- Contribution to conference › Abstract
- 2004
-
Mark
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3.
(
- Contribution to journal › Article
-
Mark
Elevated Plasma Levels of Nt-proBNP in Patients With Type 2 Diabetes Without Overt Cardiovascular Disease.
(
- Contribution to journal › Article
-
Mark
Urinary excretion rate of tamm-horsfall protein is related to salt intake in humans.
(
- Contribution to journal › Article
-
Mark
C-reactive protein as a marker of heart failure.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 2003
-
Mark
Peroxisome proliferator-activated receptor-gammaPro12Ala polymorphism and the association with blood pressure in type 2 diabetes: Skaraborg Hypertension and Diabetes Project.
(
- Contribution to journal › Article
-
Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
-
Mark
No evidence of a relation between 11beta-hydroxysteroid dehydrogenasetype 2 activity and salt sensitivity.
(
- Contribution to journal › Article
- 2002
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
From linkage to genes in human hypertension
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Improved cardiac function and quality of life following upgrade to dual chamber pacing after long-term ventricular stimulation.
(
- Contribution to journal › Article
- 2001
-
Mark
Beta(2)-adrenergic receptor gene variation and hypertension in subjects with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The ACE gene I/D polymorphism is associated with higher mortality in men with hypertension and type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Measurements of the gastric emptying rate by use of ultrasonography: studies in humans using bread with added sodium propionate
(
- Contribution to journal › Article
- 2000
-
Mark
Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells
(
- Contribution to journal › Article
- 1999
-
Mark
Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and diabetes project
(
- Contribution to journal › Article