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- 2021
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Mark
The genomics of heart failure : design and rationale of the HERMES consortium
(
- Contribution to journal › Article
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Mark
Methodological considerations for identifying multiple plasma proteins associated with all-cause mortality in a population-based prospective cohort
(
- Contribution to journal › Article
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Mark
Amino acids predict prognosis in patients with acute dyspnea
(
- Contribution to journal › Article
- 2020
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Mark
Plasma kidney injury molecule-1 (p-KIM-1) levels and deterioration of kidney function over 16 years
2020) In Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 35(2). p.265-273(
- Contribution to journal › Article
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Mark
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
(
- Contribution to journal › Article
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Mark
Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality : a prospective study
(
- Contribution to journal › Article
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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
- 2019
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Mark
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
(
- Contribution to journal › Article
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Mark
A genetic risk score for hypertension is associated with risk of thoracic aortic aneurysm
(
- Contribution to journal › Article
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Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
(
- Contribution to journal › Article
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Mark
Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
(
- Contribution to journal › Article
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Mark
Dimethylguanidino Valerate : A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality
(
- Contribution to journal › Article
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Mark
Polygenetic risk for coronary artery disease increases hospitalization burden and mortality
(
- Contribution to journal › Article
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Mark
Subsequent Event Risk in Individuals With Established Coronary Heart Disease
(
- Contribution to journal › Article
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Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- Contribution to journal › Article
- 2018
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Mark
Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence
(
- Contribution to journal › Article
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Mark
Plasma levels of the proprotein convertase furin and incidence of diabetes and mortality
(
- Contribution to journal › Article
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Mark
Association between genetic risk variants and glucose intolerance during pregnancy in north Indian women
(
- Contribution to journal › Article
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Mark
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(
- Contribution to journal › Article
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Mark
Plasma concentration of Caspase-8 is associated with short sleep duration and the risk of incident diabetes mellitus
(
- Contribution to journal › Article
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Mark
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(
- Contribution to journal › Article
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Mark
Novel subgroups of adult-onset diabetes and their association with outcomes : A data-driven cluster analysis of six variables
(
- Contribution to journal › Article
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Mark
Genome-wide analysis yields new loci associating with aortic valve stenosis
(
- Contribution to journal › Article
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Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
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Mark
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- Contribution to journal › Article
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Mark
Multi-ethnic genome-wide association study for atrial fibrillation
(
- Contribution to journal › Article
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Mark
N1-methylnicotinamide is a signalling molecule produced in skeletal muscle coordinating energy metabolism
(
- Contribution to journal › Article
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Mark
Incident diabetes mellitus may explain the association between sleep duration and incident coronary heart disease
(
- Contribution to journal › Article
-
Mark
Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study
(
- Contribution to journal › Article
- 2017
-
Mark
Plasma stem cell factor levels are associated with risk of cardiovascular disease and death
(
- Contribution to journal › Article
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Mark
Genetic Risk Prediction of Atrial Fibrillation
(
- Contribution to journal › Article
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Mark
Utilization of genetic data can improve the prediction of type 2 diabetes incidence in a Swedish cohort
(
- Contribution to journal › Article
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Mark
ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis
(
- Contribution to journal › Article
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Mark
Fasting levels of growth hormone are associated with carotid intima media thickness but are not affected by fluvastatin treatment
(
- Contribution to journal › Article
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
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Mark
Elevated Markers of Death Receptor-Activated Apoptosis are Associated with Increased Risk for Development of Diabetes and Cardiovascular Disease
(
- Contribution to journal › Article
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Mark
Genetic determinants of circulating GIP and GLP-1 concentrations
(
- Contribution to journal › Article
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Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
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Mark
Soluble Urokinase-type Plasminogen Activator Receptor (suPAR) and Impaired Kidney Function in the Population-based Malmö Diet and Cancer Study
(
- Contribution to journal › Article
-
Mark
High Level of Fasting Plasma Proenkephalin-A Predicts Deterioration of Kidney Function and Incidence of CKD
(
- Contribution to journal › Article
- 2016
-
Mark
N-terminal prosomatostatin as a risk marker for cardiovascular disease and diabetes in a general population
(
- Contribution to journal › Article
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Mark
Postprandial Levels of Branch Chained and Aromatic Amino Acids Associate with Fasting Glycaemia
(
- Contribution to journal › Article
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Mark
Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.
(
- Contribution to journal › Article
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Mark
Exome array analysis of ischaemic stroke : results from a southern Swedish study
(
- Contribution to journal › Article
- 2015
-
Mark
Cystatin C Is Not Causally Related to Coronary Artery Disease.
(
- Contribution to journal › Article
-
Mark
Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth Hormone.
(
- Contribution to journal › Article
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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
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Mark
Stable Peptide of the Endogenous Opioid Enkephalin Precursor and Breast Cancer Risk.
(
- Contribution to journal › Article
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Mark
GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb.
(
- Contribution to journal › Article
-
Mark
Duffy antigen receptor genetic variant and the association with Interleukin 8 levels.
(
- Contribution to journal › Article
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Mark
The growth hormone receptor exon 3 deleted/full-length polymorphism is associated with central adiposity in the general population.
(
- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
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Mark
Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age.
2015) In International Journal of Obesity(
- Contribution to journal › Article
-
Mark
SNPS in FGF5 and ZNF652 show parent-of-origin specific effects on blood pressure in families from the Botnia study
2015)(
- Contribution to conference › Abstract
- 2014
-
Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
-
Mark
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
(
- Contribution to journal › Article
-
Mark
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease.
(
- Contribution to journal › Article
-
Mark
Fasting levels of high-sensitivity growth hormone predict cardiovascular morbidity and mortality: the malmö diet and cancer study.
(
- Contribution to journal › Article
-
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
-
Mark
Cystatin C identifies cardiovascular risk better than creatinine-based estimates of glomerular filtration in middle-aged individuals without a history of cardiovascular disease.
(
- Contribution to journal › Article
- 2013
-
Mark
Plasma lipid composition and risk of developing cardiovascular disease.
(
- Contribution to journal › Article
-
Mark
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
(
- Contribution to journal › Article
- 2012
-
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
-
Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- 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
Genetic Polymorphisms for Estimating Risk of Atrial Fibrillation in the General Population: A Prospective Study
(
- Contribution to journal › Letter
-
Mark
Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
(
- Contribution to journal › Article
-
Mark
A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
(
- Contribution to journal › Article
-
Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.
2012) In Journal of Internal Medicine(
- Contribution to journal › Article
-
Mark
Vasoactive Peptides with Angiogenesis-Regulating Activity Predict Cancer Risk in Males.
2012) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 21(3). p.513-522(
- Contribution to journal › Article
-
Mark
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
(
- Contribution to journal › Article
-
Mark
Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality.
(
- 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
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
-
Mark
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
- 2010
-
Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
(
- Contribution to journal › Article
-
Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
-
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
A gene score of nine LDL and HDL regulating genes is associated with fluvastatin induced cholesterol changes in women.
(
- Contribution to journal › Article
-
Mark
Plasma copeptin and the risk of diabetes mellitus.
(
- 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
-
Mark
Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation.
(
- Contribution to journal › Article
- 2009
-
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
Novel and conventional biomarkers for prediction of incident cardiovascular events in the community.
(
- Contribution to journal › Article
-
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
-
Mark
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- Contribution to journal › Article
- 2008
-
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
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
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
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
The V433M Variant of the CYP4F2 Is Associated With Ischemic Stroke in Male Swedes Beyond Its Effect on Blood Pressure.
(
- Contribution to journal › Article
- 2007
-
Mark
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes
(
- 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
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
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article