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- 2009
-
Mark
The metabolic syndrome and risk of myocardial infarction in familial hypertension (Hypertension Heredity in Malmö Evaluation study).
(
- Contribution to journal › Article
-
Mark
Carotid Intima-Media Thickness, Systemic Inflammation, and Incidence of Heart Failure Hospitalizations.
(
- Contribution to journal › Article
-
Mark
Distribution and Correlates of Midregional Proadrenomedullin in the General Population.
(
- Contribution to journal › Article
-
Mark
Orthostatic hypotension in genetically related hypertensive and normotensive individuals.
(
- Contribution to journal › Article
-
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
-
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
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
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
-
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
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
-
Mark
Interaction Between Renal Function and Microalbuminuria for Cardiovascular Risk in Hypertension The Nordic Diltiazem Study
(
- Contribution to journal › Article
-
Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
(
- Contribution to journal › Article
-
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
Determinants of kidney function in Swedish families: role of heritable factors.
(
- Contribution to journal › Article
-
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
An association between Type 2 diabetes and alpha(1)-antitrypsin deficiency
(
- 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
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
Telomere Length Is Associated With Obesity Parameters but With a Gender Difference
(
- 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
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Mark
Genetics of cardiovascular disease: interplay between common and rare alleles.
(
- 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
-
Mark
Job strain, job demands and adrenergic beta1-receptor-polymorphism: a possible interaction affecting blood pressure in men.
(
- Contribution to journal › Article
-
Mark
Hypertension and genome-wide association studies: combining high fidelity phenotyping and hypercontrols.
(
- 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
Heritability of the ambulatory arterial stiffness index in Swedish families.
(
- Contribution to journal › Article
- 2007
-
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
-
Mark
Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes
(
- Contribution to journal › Article
-
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
-
Mark
Job strain, decision latitude and alpha2B-adrenergic receptor polymorphism significantly interact, and associate with higher blood pressures in men.
(
- Contribution to journal › Article
-
Mark
The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
(
- Contribution to journal › Article
-
Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article
-
Mark
hTERT T-1327/C polymorphism is not associated with age-related telomere attrition in peripheral blood
(
- Contribution to journal › Article
-
Mark
Are minor gene effects of clinical importance?
(
- Contribution to journal › Letter
-
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
-
Mark
Interaction between the angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea as a mechanism for hypertension.
(
- Contribution to journal › Article
-
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
-
Mark
Oesophageal dysmotility, delayed gastric emptying and gastrointestinal symptoms in patients with diabetes mellitus.
(
- Contribution to journal › Article
-
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
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
- 2006
-
Mark
Oesophageal dysmotility, delayed gastric emptying and autonomic neuropathy correlate to disturbed glucose homeostasis.
(
- 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
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
-
Mark
Multilevel analysis of systolic blood pressure and ACE gene I/D polymorphism in 438 Swedish families - a public health perspective
(
- Contribution to journal › Article
- 2005
-
Mark
Dipping and variability of blood pressure and heart rate at night are heritable traits.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
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
- 2004
-
Mark
A Functional Variant in the {alpha}2B Adrenoceptor Gene, a Positional Candidate on Chromosome 2, Associates With Hypertension.
(
- Contribution to journal › Article
-
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
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- 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
- 2003
-
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
-
Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
-
Mark
Inhibition of lipolysis during acute GH exposure increases insulin sensitivity in previously untreated GH-deficient adults.
(
- Contribution to journal › Article
-
Mark
Intrauterine growth and blood pressure: what causes the relationship?
(
- Contribution to journal › Debate/Note/Editorial
-
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
- 2002
-
Mark
Plasma ProANP(1-30) reflects salt sensitivity in subjects with heredity for hypertension
(
- Contribution to journal › Article
-
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
- 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
Polymorphism in the beta(1)-adrenergic receptor gene and hypertension
(
- Contribution to journal › Article
- 2000
-
Mark
Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians
(
- Contribution to journal › Article
-
Mark
Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension
(
- Contribution to journal › Article
-
Mark
Association between a variant in the 11 beta-hydroxysteroid dehydrogenase type 2 gene and primary hypertension
(
- Contribution to journal › Article
-
Mark
Angiotensin converting enzyme (ACE) gene polymorphism in sarcoidosis in relation to associated autoimmune diseases
(
- Contribution to journal › Article
-
Mark
Genetic factors in primary hypertension- with emphasis on renal sodium reabsorption
2000)(
- Thesis › Doctoral thesis (compilation)
- 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