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- 2024
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Mark
Long-Term Cardiovascular Effects of Medications for Attention-Deficit/ Hyperactivity Disorder—Balancing Benefits and Risks of Treatment
(
- Contribution to journal › Debate/Note/Editorial
- 2022
-
Mark
Cardiovascular risk factors in attention-deficit/hyperactivity disorder : A family design study of Swedish conscripts
(
- Contribution to journal › Article
-
Mark
Calcium, Its Regulatory Hormones, and Their Causal Role on Blood Pressure : A Two-Sample Mendelian Randomization Study
(
- Contribution to journal › Article
- 2021
-
Mark
Relationship between Blood Pressure and Incident Cardiovascular Disease : Linear and Nonlinear Mendelian Randomization Analyses
(
- Contribution to journal › Article
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Mark
Causal effect of adiposity measures on blood pressure traits in 2 urban swedish cohorts : A mendelian randomization study
(
- Contribution to journal › Article
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Mark
Association of thyroid function with blood pressure and cardiovascular disease : A mendelian randomization
(
- Contribution to journal › Article
- 2020
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Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
(
- Contribution to journal › Article
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Mark
Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting
(
- Contribution to journal › Article
- 2019
-
Mark
A genetic risk score for hypertension is associated with risk of thoracic aortic aneurysm
(
- Contribution to journal › Article
- 2018
-
Mark
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
2018) In Nature Communications(
- Contribution to journal › Article
- 2017
-
Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
(
- Contribution to journal › Article
- 2016
-
Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
(
- Contribution to journal › Article
-
Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
(
- Contribution to journal › Article
-
Mark
Ischemic Stroke and Six Genetic Variants in CRP, EPHX2, FGA, and NOTCH3 Genes : A Meta-Analysis
(
- Contribution to journal › Article
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Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
- 2015
-
Mark
Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease.
(
- Contribution to journal › Article
-
Mark
Intakes of omega-3 polyunsaturated fatty acids and blood pressure change over time: Possible interaction with genes involved in 20-HETE and EETs metabolism.
(
- Contribution to journal › Article
-
Mark
A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study.
(
- Contribution to journal › Article
- 2014
-
Mark
Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö Diet and Cancer.
(
- Contribution to journal › Article
- 2012
-
Mark
Hypertension, cardiovascular risk and polymorphisms in genes controlling the cytochrome P450 pathway of arachidonic acid: A sex-specific relation?
(
- Contribution to journal › Article
-
Mark
Prediction of Blood Pressure Changes Over Time and Incidence of Hypertension by a Genetic Risk Score in Swedes.
2012) In Hypertension(
- Contribution to journal › Article
-
Mark
From circulating biomarkers to genomics and imaging in the prediction of cardiovascular events in the general population.
(
- Contribution to journal › Article
-
Mark
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk
(
- Contribution to journal › Article
-
Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Impact of the CYP4F2 p.V433M Polymorphism on Coumarin Dose Requirement: Systematic Review and Meta-Analysis
(
- Contribution to journal › Scientific review
-
Mark
The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
(
- Contribution to journal › Article
- 2011
-
Mark
A functional variant of the NEDD4L gene is associated with beneficial treatment response with β-blockers and diuretics in hypertensive patients.
(
- Contribution to journal › Article
-
Mark
Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
2011) In Nutrition Metabolism and Cardiovascular Diseases(
- Contribution to journal › Article
-
Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
-
Mark
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.
(
- Contribution to journal › Article
- 2010
-
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
-
Mark
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension
(
- Contribution to journal › Article
-
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
-
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
-
Mark
Overexpression of cytochrome P450 4F2 in mice increases 20-hydroxyeicosatetraenoic acid production and arterial blood pressure
(
- Contribution to journal › Letter
-
Mark
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- Contribution to journal › Article
-
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
- 2008
-
Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
(
- Contribution to journal › Article
-
Mark
Determinants of kidney function in Swedish families: role of heritable factors.
(
- Contribution to journal › Article
-
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
Heritability of the ambulatory arterial stiffness index in Swedish families.
(
- 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
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
- 2007
-
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
Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes
(
- Contribution to journal › Article
-
Mark
Heritability of blood pressure: monogenes and polygenes
(
- Thesis › Doctoral thesis (compilation)
-
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
Determinants of diastolic dysfunction: a geometric matter?
(
- Contribution to journal › Letter
- 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
-
Mark
In the name of the father... and the mother.
(
- Contribution to journal › Letter
- 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
- 2004
-
Mark
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- Contribution to journal › Article