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- 2024
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Mark
The Gly82Ser polymorphism in the receptor for advanced glycation endproducts increases the risk for coronary events in the general population
(
- Contribution to journal › Article
- 2020
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Mark
Orthostatic hypotension and novel blood pressure associated gene variants in older adults : data from the TILDA Study
2020) In Journals of Gerontology. Series A: Biological Sciences & Medical Sciences 75(11). p.2074-2080(
- 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
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Mark
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
(
- Contribution to journal › Article
- 2019
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Mark
Polygenetic risk for coronary artery disease increases hospitalization burden and mortality
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- Contribution to journal › Article
- 2018
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
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- Contribution to journal › Article
- 2017
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Mark
Elevated ambulatory systolic-diastolic pressure regression index is genetically determined in hypertensive patients with coronary heart disease
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- Contribution to journal › Article
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Mark
Relationship between selected DNA polymorphisms and coronary artery disease complications
(
- Contribution to journal › Article
- 2016
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Mark
Genetic vasopressin 1b receptor variance in overweight and diabetes mellitus.
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- Contribution to journal › Article
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Mark
Gene variance in the nicotinic receptor cluster (CHRNA5-CHRNA3-CHRNB4) predicts death from cardiopulmonary disease and cancer in smokers.
(
- Contribution to journal › Article
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Mark
The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease
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- Contribution to journal › Article
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Mark
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure
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- 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
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Mark
A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study.
(
- Contribution to journal › Article
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Mark
1A.10: ASSOCIATION BETWEEN GENE POLYMORPHISMS AND RISK OF CARDIOVASCULAR EVENTS IN PATIENTS WITH CORONARY HEART DISEASE.
(
- Contribution to journal › Article
- 2014
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Mark
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
(
- Contribution to journal › Article
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Mark
ASSOCIATION OF BTG2, CYR61, ZFP36, AND SCD GENE POLYMORPHISMS WITH GRAVES' DISEASE AND OPHTHALMOPATHY.
(
- Contribution to journal › Article
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Mark
Twelve-Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke.
(
- Contribution to journal › Article
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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
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Mark
Genetic variation in NEDD4L, an epithelial sodium channel regulator, is associated with cardiovascular disease and cardiovascular death.
(
- Contribution to journal › Article
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Mark
Ceruloplasmin and atrial fibrillation: evidence of causality from a population-based Mendelian randomization study.
(
- Contribution to journal › Article
- 2013
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Mark
Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?
(
- Contribution to journal › Article
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Mark
Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study.
(
- Contribution to journal › Article
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Mark
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
(
- Contribution to journal › Article
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Mark
Smoking and obesity associated BDNF gene variance predicts total and cardiovascular mortality in smokers.
(
- Contribution to journal › Article
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Mark
Genetic Associations with Valvular Calcification and Aortic Stenosis
(
- Contribution to journal › Article
- 2012
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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
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Mark
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
(
- Contribution to journal › Article
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Mark
Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke
(
- Contribution to journal › Article
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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
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Mark
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
(
- Contribution to journal › Article
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Mark
A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
(
- Contribution to journal › Article
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Mark
Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
(
- Contribution to journal › Article
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Mark
A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
(
- Contribution to journal › Article
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Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
- 2011
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Mark
Genetic Variant on Chromosome 12p13 Does Not Show Association to Ischemic Stroke in 3 Swedish Case-Control Studies
(
- Contribution to journal › Article
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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
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Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
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Mark
Lack of association between genetic variations in the KALRN region and ischemic stroke
(
- Contribution to journal › Article
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Mark
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
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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
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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
Genetic loci influencing kidney function and chronic kidney disease
(
- Contribution to journal › Article
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Mark
Stk39 Is A Candidate Gene For Primary Hypertension Especially In Women: Results From 2 Cohort Studies In Swedes
2010) 20th Annual Meeting of the European-Society-of-Hypertension In Journal of Hypertension 28. p.238-238(
- 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
- 2008
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Mark
Genetics of Type 2 Diabetes and Metabolic Syndrome: From Genome Wide Linkage Scan and Candidate Genes to Genome Wide Association Studies
(
- Thesis › Doctoral thesis (compilation)
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Mark
Is there a unifying genetic factor predisposing to the metabolic syndrome?
2008) 44th EASD Annual Meeting of the European Association for the Study of Diabetes In Diabetologia 51(S1). p.32-33(
- Contribution to journal › Published meeting abstract
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Mark
A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population
(
- Contribution to journal › Article
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Mark
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
(
- Contribution to journal › Article
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Mark
The search for putative unifying genetic factors for components of the metabolic syndrome.
(
- Contribution to journal › Article