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- 2024
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Mark
A genomic mutational constraint map using variation in 76,156 human genomes
(
- Contribution to journal › Article
- 2023
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Mark
Endogenous incretin levels and risk of first incident cancer: a prospective cohort study
(
- Contribution to journal › Article
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Mark
Identification of biomarkers for glycaemic deterioration in type 2 diabetes
(
- Contribution to journal › Article
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Genetic insights into resting heart rate and its role in cardiovascular disease
(
- Contribution to journal › Article
- 2022
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
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Mark
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes
(
- Contribution to journal › Article
- 2021
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Elevated circulating follistatin associates with an increased risk of type 2 diabetes
(
- Contribution to journal › Article
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Mark
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
(
- Contribution to journal › Article
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Mark
Glucose-Dependent Insulinotropic Peptide in the High-Normal Range Is Associated With Increased Carotid Intima-Media Thickness
(
- Contribution to journal › Article
- 2020
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Mark
Circulating protein biomarkers predict incident hypertensive heart failure independently of N-terminal pro-B-type natriuretic peptide levels
(
- Contribution to journal › Article
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Mark
The effect of LRRK2 loss-of-function variants in humans
(
- Contribution to journal › Article
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Mark
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC
(
- 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
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Mark
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals
(
- Contribution to journal › Article
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Mark
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes
(
- Contribution to journal › Article
- 2019
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Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- 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
The associations of self-rated health with cardiovascular risk proteins : A proteomics approach
(
- Contribution to journal › Article
- 2018
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Mark
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
(
- 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
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- Contribution to journal › Article
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
(
- 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
- 2017
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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
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Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
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Mark
Genetic Risk Prediction of Atrial Fibrillation
(
- Contribution to journal › Article
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- 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
Exome-wide association study of plasma lipids in >300,000 individuals
(
- Contribution to journal › Article
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Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
(
- Contribution to journal › Article
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Mark
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
(
- 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
- 2016
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Mark
Glucose-Dependent Insulinotropic Polypeptide (GIP) Stimulates Osteopontin Expression in the Vasculature via Endothelin-1 and CREB.
(
- 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
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
Atrial Natriuretic Peptide in the high normal range is associated with lower prevalence of insulin resistance.
(
- 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
Exome array analysis of ischaemic stroke : results from a southern Swedish study
(
- Contribution to journal › Article
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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
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
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Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
(
- Contribution to journal › Article
- 2015
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Mark
Cystatin C Is Not Causally Related to Coronary Artery Disease.
(
- Contribution to journal › Article
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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
Duffy antigen receptor genetic variant and the association with Interleukin 8 levels.
(
- 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
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
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
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Mark
C-peptide concentration, mortality and vascular complications in people with Type 2 diabetes. The Skaraborg Diabetes Register.
(
- 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
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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
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease.
(
- Contribution to journal › Article
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Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
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Mark
Fasting levels of high-sensitivity growth hormone predict cardiovascular morbidity and mortality: the malmö diet and cancer study.
(
- 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
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
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Mark
Plasma lipid composition and risk of developing cardiovascular disease.
(
- 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
- 2012
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Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
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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
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
From circulating biomarkers to genomics and imaging in the prediction of cardiovascular events in the general population.
(
- Contribution to journal › Article
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Mark
Genetic Polymorphisms for Estimating Risk of Atrial Fibrillation in the General Population: A Prospective Study
(
- Contribution to journal › Letter
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Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
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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
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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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Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
(
- Contribution to journal › Article
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Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
(
- Contribution to journal › Article
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Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.
2012) In Journal of Internal Medicine(
- Contribution to journal › Article
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Mark
Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality.
(
- Contribution to journal › Article
- 2011
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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
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FTO, Type 2 Diabetes, and Weight Gain Throughout Adult Life A Meta-Analysis of 41,504 Subjects From the Scandinavian HUNT, MDC, and MPP Studies
(
- Contribution to journal › Article
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Mark
Power in the Phenotypic Extremes: A Simulation Study of Power in Discovery and Replication of Rare Variants
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
(
- Contribution to journal › Article
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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
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Uromodulin gene variant is associated with type 2 diabetic nephropathy.
(
- Contribution to journal › Article
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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
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Mark
Pleiotropic Effects of GIP on Islet Function Involve Osteopontin
(
- Contribution to journal › Article
- 2010
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Mark
Brain natriuretic peptide is related to diastolic dysfunction whereas urinary albumin excretion rate is related to left ventricular mass in asymptomatic type 2 diabetes patients
(
- Contribution to journal › Article
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Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
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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
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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 › Article
-
Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
(
- Contribution to journal › Article
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Mark
Genetic loci influencing kidney function and chronic kidney disease
(
- 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
-
Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
-
Mark
Niemann-Pick C1 Modulates Hepatic Triglyceride Metabolism and Its Genetic Variation Contributes to Serum Triglyceride Levels
(
- 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
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
(
- Contribution to journal › Article
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Mark
Genetic susceptibility for obesity increases the risk of type 2 diabetes and is modified by macronutrient intakes
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.50-50(
- Contribution to journal › Published meeting abstract
-
Mark
Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation.
(
- Contribution to journal › Article
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Mark
Plasma copeptin and the risk of diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Polymorphisms in α- And β-adrenergic receptor genes, hypertension, and obstructive sleep apnea : The skaraborg sleep study
(
- Contribution to journal › Article
- 2009
-
Mark
ION Mobility Analysis Of Lipoprotein Subfractions Suggests Three Independent Mechanisms Of Cardiovascular Risk
(
- Contribution to journal › Published meeting abstract
-
Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
-
Mark
Overexpression of cytochrome P450 4F2 in mice increases 20-hydroxyeicosatetraenoic acid production and arterial blood pressure
(
- Contribution to journal › Letter
-
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
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- 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
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
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- 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
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- 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
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
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
(
- 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
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
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
Determinants of kidney function in Swedish families: role of heritable factors.
(
- Contribution to journal › Article
-
Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
-
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
- 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
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- 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
Interaction between the angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea as a mechanism for hypertension.
(
- Contribution to journal › Article
-
Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- 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
- 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
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
- 2005
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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
Nt-proANP in plasma, a marker of salt sensitivity, is reduced in type 2 diabetes patients.
(
- Contribution to journal › Article
- 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
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- Contribution to journal › Article
-
Mark
A Functional Variant in the {alpha}2B Adrenoceptor Gene, a Positional Candidate on Chromosome 2, Associates With Hypertension.
(
- Contribution to journal › Article
- 2003
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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
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
-
Mark
No evidence of a relation between 11beta-hydroxysteroid dehydrogenasetype 2 activity and salt sensitivity.
(
- 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
- 2002
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
Plasma ProANP(1-30) reflects salt sensitivity in subjects with heredity for hypertension
(
- 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
Polymorphism in the beta(1)-adrenergic receptor gene and hypertension
(
- Contribution to journal › Article
- 2000
-
Mark
Angiotensin converting enzyme (ACE) gene polymorphism in sarcoidosis in relation to associated autoimmune diseases
(
- 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
Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension
(
- Contribution to journal › Article
-
Mark
Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians
(
- 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