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Lista de obras de Abbas Dehghan

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A frequent variant in the ABCA1 gene is associated with increased coronary heart disease risk and a better response to statin treatment in familial hypercholesterolemia patients

article

A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies

artículo científico publicado en 2012

A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease

artículo científico publicado en 2014

A genetic variant inSLC6A20is associated with Type 2 diabetes in white-European and Chinese populations

article

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors

artículo científico publicado en 2017

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

artículo científico publicado en 2015

A meta-analysis of gene expression signatures of blood pressure and hypertension

artículo científico publicado en 2015

A serum 25-hydroxyvitamin D concentration-associated genetic variant in DHCR7 interacts with type 2 diabetes status to influence subclinical atherosclerosis (measured by carotid intima–media thickness)

article

ADAMTS13 activity as a novel risk factor for incident type 2 diabetes mellitus: a population-based cohort study

artículo científico publicado en 2016

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

artículo científico publicado en 2015

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

artículo científico publicado en 2015

An RBP4 promoter polymorphism increases risk of type 2 diabetes

artículo científico publicado en 2008

An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.

artículo científico publicado en 2019

Arterial Stiffness and Decline in Kidney Function

artículo científico publicado en 2015

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

artículo científico publicado en 2014

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

artículo científico publicado en 2011

Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor α.

artículo científico publicado en 2018

Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease

artículo científico publicado en 2015

Association of Uric Acid Genetic Risk Score With Blood Pressure

Association of an APOC3 promoter variant with type 2 diabetes risk and need for insulin treatment in lean persons

artículo científico publicado en 2011

Association of circulating total bilirubin with the metabolic syndrome and type 2 diabetes: A systematic review and meta-analysis of observational evidence.

artículo científico publicado en 2016

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

artículo científico publicado en 2011

Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific journal article

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

artículo científico publicado en 2014

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Association of renal function with vascular stiffness in older adults: the Rotterdam study

scientific article published on 21 August 2014

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

artículo científico publicado en 2008

Association of variation at the ABO locus with circulating levels of soluble intercellular adhesion molecule-1, soluble P-selectin, and soluble E-selectin: a meta-analysis

artículo científico publicado en 2011

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of Steroid Sex Hormones and Sex Hormone-Binding Globulin With the Risk of Type 2 Diabetes in Women: A Population-Based Cohort Study and Meta-analysis

artículo científico publicado en 2016

Associations of genetically determined iron status across the phenome: A mendelian randomization study.

artículo científico publicado en 2019

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation

artículo científico publicado en 2016

Blood pressure parameters and carotid intraplaque hemorrhage as measured by magnetic resonance imaging: The Rotterdam Study

artículo científico publicado en 2012

Circulating Levels of Interleukin 1-Receptor Antagonist and Risk of Cardiovascular Disease: Meta-Analysis of Six Population-Based Cohorts

artículo científico publicado en 2017

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

artículo científico publicado en 2013

Common genetic variants associate with serum phosphorus concentration

artículo científico publicado en 2010

Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling

scientific article published on 03 September 2013

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

artículo científico publicado en 2011

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels

artículo científico publicado en 2010

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

artículo científico publicado en 2017

Comparison of prognosis in unrecognized versus recognized myocardial infarction in men versus women >55 years of age (from the Rotterdam Study).

artículo científico publicado en 2013

Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

Could vitamin D reduce obesity-associated inflammation? Observational and Mendelian randomization study

scientific article published on 31 March 2020

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

artículo científico publicado en 2016

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

artículo científico publicado en 2017

DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis

artículo científico publicado en 2016

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

artículo científico publicado en 2016

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

artículo científico publicado en 2012

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

artículo científico publicado en 2016

Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure

artículo científico publicado en 2016

Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach

article

Dissecting the relationship between high-sensitivity serum C-reactive protein and increased fracture risk: the Rotterdam Study

artículo científico publicado en 2013

Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators

artículo científico publicado en 2009

EN-RAGE: a novel inflammatory marker for incident coronary heart disease

artículo científico publicado en 2014

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

artículo científico publicado en 2014

Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies

artículo científico publicado en 2011

Epigenome-wide association study (EWAS) on lipids: the Rotterdam Study

artículo científico publicado en 2017

Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity

artículo científico publicado en 2016

Erratum: Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms

article

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.

artículo científico publicado en 2016

Fetuin-A and risk of coronary heart disease: A Mendelian randomization analysis and a pooled analysis of AHSG genetic variants in 7 prospective studies

artículo científico publicado en 2015

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

artículo científico publicado en 2018

Gait characteristics in older adults with diabetes and impaired fasting glucose: The Rotterdam Study

artículo científico publicado en 2015

Gait patterns associated with thyroid function: The Rotterdam Study

scientific article published on 14 December 2016

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

artículo científico publicado en 2014

Genetic Variants in MicroRNAs and Their Binding Sites Are Associated with the Risk of Parkinson Disease

artículo científico publicado en 2015

Genetic Variations in MicroRNA-Binding Sites Affect MicroRNA-Mediated Regulation of Several Genes Associated With Cardio-metabolic Phenotypes

article

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles

artículo científico publicado en 2016

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

artículo científico publicado en 2020

Genetic predictors of fibrin D-dimer levels in healthy adults

artículo científico publicado en 2011

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

artículo científico publicado en 2009

Genetic variants in microRNAs and their binding sites within gene 3'UTRs associate with susceptibility to age-related macular degeneration.

artículo científico publicado en 2017

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity

article

Genetic variation associated with circulating monocyte count in the eMERGE Network

artículo científico publicado en 2013

Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis

artículo científico publicado en 2010

Genetic variation, C-reactive protein levels, and incidence of diabetes.

artículo científico publicado en 2007

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

artículo científico publicado en 2016

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

artículo científico publicado en 2016

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci

artículo científico publicado en 2011

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

scientific article published on 09 January 2020

Genome-wide association and functional follow-up reveals new loci for kidney function

artículo científico publicado en 2012

Genome-wide association meta-analysis for total serum bilirubin levels

artículo científico publicado en 2009

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

artículo científico publicado en 2015

Genome-wide association studies identify genetic loci for low von Willebrand factor levels

artículo científico publicado en 2016

Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels

artículo científico publicado en 2010

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

artículo científico publicado en 2012

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

artículo científico publicado en 2014

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

artículo científico publicado en 2011

Genome-wide association study of blood pressure and hypertension

scientific journal article

Genome-wide association study of kidney function decline in individuals of European descent

artículo científico publicado en 2014

Genome-wide identification of microRNA-related variants associated with risk of Alzheimer's disease

artículo científico publicado en 2016

Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk

artículo científico publicado en 2017

Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium

artículo científico publicado en 2010

Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval

artículo científico publicado en 2015

High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam Study

artículo científico publicado en 2013

High serum uric acid as a novel risk factor for type 2 diabetes

artículo científico publicado en 2007

Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation

artículo científico publicado en 2017

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

artículo científico publicado en 2011

Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors

artículo científico publicado en 2015

Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach

artículo científico publicado en 2014

Incremental predictive value of 152 single nucleotide polymorphisms in the 10-year risk prediction of incident coronary heart disease: the Rotterdam Study

artículo científico publicado en 2015

Intake of different types of dairy and its prospective association with risk of type 2 diabetes: The Rotterdam Study

artículo científico publicado en 2016

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

artículo científico publicado en 2012

Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

artículo científico publicado en 2016

Kidney Function and Cerebral Blood Flow: The Rotterdam Study

artículo científico publicado en 2015

Kidney function and microstructural integrity of brain white matter

artículo científico publicado en 2015

LDL cholesterol still a problem in old age? A Mendelian randomization study

LOng-term follow-up after liVE kidney donation (LOVE) study: a longitudinal comparison study protocol.

artículo científico publicado en 2016

Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study

artículo científico publicado en 2008

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

artículo científico publicado en 2016

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels

artículo científico publicado en 2010

Lifetime risk of developing impaired glucose metabolism and eventual progression from prediabetes to type 2 diabetes: a prospective cohort study

artículo científico publicado en 2015

Long-term prognosis after kidney donation: a propensity score matched comparison of living donors and non-donors from two population cohorts

artículo científico publicado en 2020

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

artículo científico publicado en 2017

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

Low-risk susceptibility alleles in 40 human breast cancer cell lines

artículo científico publicado en 2009

Lower microstructural integrity of brain white matter is related to higher mortality

artículo científico publicado en 2016

Mass spectrometry in epidemiological studies: What are the key considerations?

artículo científico publicado en 2016

Maternal plasma folate impacts differential DNA methylation in an epigenome-wide meta-analysis of newborns

artículo científico publicado en 2016

Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

artículo científico publicado en 2019

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

artículo científico publicado en 2011

Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

artículo científico publicado en 2011

Metabolic syndrome is related to polyneuropathy and impaired peripheral nerve function: a prospective population-based cohort study

artículo científico publicado en 2016

Mining the human phenome using allelic scores that index biological intermediates

artículo científico publicado en 2013

Modulation of genetic associations with serum urate levels by body-mass-index in humans

artículo científico publicado en 2015

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

artículo científico publicado en 2010

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

Multiple loci associated with indices of renal function and chronic kidney disease

scientific journal article

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

artículo científico publicado en 2009

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

artículo científico publicado en 2022

NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality

artículo científico

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ⬇️

artículo científico publicado en 2016

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

Normal Thyroid Function and the Risk of Atrial Fibrillation: the Rotterdam Study

artículo científico publicado en 2015

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

artículo científico publicado en 2010

Novel inflammatory markers for incident pre-diabetes and type 2 diabetes: the Rotterdam Study

artículo científico publicado en 2017

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Obesity and Life Expectancy with and without Diabetes in Adults Aged 55 Years and Older in the Netherlands: A Prospective Cohort Study

artículo científico publicado en 2016

Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium

artículo científico publicado en 2013

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

Partner's smoking status and acute coronary syndrome: population-based case-control study in Tirana, Albania

artículo científico publicado en 2008

Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations

artículo científico publicado en 2016

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

Phosphodiesterase 1 regulation is a key mechanism in vascular aging

artículo científico publicado en 2015

Plasma lipids and risk of aortic valve stenosis: a Mendelian randomization study

artículo científico publicado en 2020

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

artículo científico publicado en 2016

Pleiotropic genes for metabolic syndrome and inflammation

artículo científico publicado en 2014

Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

artículo científico publicado en 2015

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

artículo científico publicado en 2015

Polygenic dissection of major depression clinical heterogeneity

artículo científico publicado en 2015

Polyunsaturated fatty acids and serum C-reactive protein: the Rotterdam study

artículo científico publicado en 2015

Practice patterns and outcomes after stroke across countries at different economic levels (INTERSTROKE): an international observational study

artículo científico publicado en 2018

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

artículo científico publicado en 2014

Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study

artículo científico publicado en 2008

Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study

artículo científico publicado en 2014

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

artículo científico publicado en 2015

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

artículo científico publicado en 2018

Relation of antioxidant capacity of diet and markers of oxidative status with C-reactive protein and adipocytokines: a prospective study

artículo científico publicado en 2017

Renal function is related to severity of coronary artery calcification in elderly persons: the Rotterdam study

artículo científico publicado en 2011

Resting heart rate and the risk of heart failure in healthy adults: the Rotterdam Study

artículo científico publicado en 2013

Risk of Type 2 Diabetes Attributable to C-Reactive Protein and Other Risk Factors

scientific article published on 10 July 2007

Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart disease

artículo científico publicado en 2013

SIRT1 genetic variation and mortality in type 2 diabetes: interaction with smoking and dietary niacin

artículo científico publicado en 2009

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

scientific article published on 31 July 2013

Serum Levels of Apolipoproteins and Incident Type 2 Diabetes: A Prospective Cohort Study

artículo científico publicado en 2016

Serum dehydroepiandrosterone levels are associated with lower risk of type 2 diabetes: the Rotterdam Study.

artículo científico publicado en 2016

Serum magnesium and the risk of prediabetes: a population-based cohort study

artículo científico publicado en 2017

Serum uric acid and chronic kidney disease: the role of hypertension

artículo científico publicado en 2013

Sex-specific differences in the effects of local androgen metabolism in the heart as an indicator for the risk of myocardial infarction

Sex-specific effects of naturally occurring variants in the dopamine receptor D2 locus on insulin secretion and type 2 diabetes susceptibility.

artículo científico publicado en 2014

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

artículo científico publicado en 2018

Subclinical Hypothyroidism and the Risk of Stroke Events and Fatal Stroke: An Individual Participant Data Analysis

artículo científico publicado en 2015

Subclinical thyroid dysfunction and the risk of stroke: a systematic review and meta-analysis

artículo científico

Systematic evaluation of the causal relationship between DNA methylation and C-reactive protein

The Association between Metabolic Syndrome, Bone Mineral Density, Hip Bone Geometry and Fracture Risk: The Rotterdam Study

artículo científico publicado en 2015

The Influence of Serum Uric Acid on Bone Mineral Density, Hip Geometry, and Fracture Risk: The Rotterdam Study

artículo científico publicado en 2015

The Role of DNA Methylation and Histone Modifications in Neurodegenerative Diseases: A Systematic Review

artículo científico publicado en 2016

The association between serum uric acid and the incidence of prediabetes and type 2 diabetes mellitus: The Rotterdam Study

artículo científico publicado en 2017

The association of common polymorphisms in miR-196a2 with waist to hip ratio and miR-1908 with serum lipid and glucose

artículo científico publicado en 2014

The association of thyroid function and the risk of kidney function decline: a population-based cohort study

artículo científico publicado en 2016

The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study

artículo científico publicado en 2016

The long-term risk of recognized and unrecognized myocardial infarction for depression in older men.

artículo científico publicado en 2016

The presumed increased bleeding tendency in red-haired individuals is not associated with von Willebrand factor antigen levels in older individuals

artículo científico publicado en 2011

The relation of uric acid to brain atrophy and cognition: the Rotterdam Scan Study

artículo científico publicado en 2013

The role of DNA methylation in dyslipidaemia: A systematic review

artículo científico publicado en 2016

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

artículo científico publicado en 2013

The role of epigenetic modifications in cardiovascular disease: A systematic review

artículo científico publicado en 2016

The role of global and regional DNA methylation and histone modifications in glycemic traits and type 2 diabetes: A systematic review.

artículo científico publicado en 2016

Thyroid Function Characteristics and Determinants: The Rotterdam Study

artículo científico publicado en 2016

Thyroid Function and Cancer Risk: The Rotterdam Study

artículo científico publicado en 2016

Thyroid Function and Sudden Cardiac Death: A Prospective Population-Based Cohort Study

artículo científico publicado en 2016

Thyroid Function and the Risk of Nonalcoholic Fatty Liver Disease: The Rotterdam Study

artículo científico publicado en 2016

Thyroid function and age-related macular degeneration: a prospective population-based cohort study--the Rotterdam Study

artículo científico publicado en 2015

Thyroid function and risk of type 2 diabetes: a population-based prospective cohort study

artículo científico publicado en 2016

Thyroid function and the risk of dementia: The Rotterdam Study

artículo científico publicado en 2016

Tobacco smoking is associated with DNA methylation of diabetes susceptibility genes

artículo científico publicado en 2016

Tobacco smoking is associated with methylation of genes related to coronary artery disease

artículo científico publicado en 2015

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

artículo científico publicado en 2015

Trans-ethnic meta-analysis of white blood cell phenotypes

artículo científico publicado en 2014

Understanding the consequences of education inequality on cardiovascular disease: mendelian randomisation study.

artículo científico publicado en 2019

Uromodulin levels associate with a common UMOD variant and risk for incident CKD.

artículo científico publicado en 2009

Variance heterogeneity analysis for detection of potentially interacting genetic loci: method and its limitations

artículo científico publicado en 2010

Variants in MTNR1B influence fasting glucose levels

artículo científico publicado en 2008

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

scientific article published on 13 July 2009

Vitamin D and C-Reactive Protein: A Mendelian Randomization Study

artículo científico publicado en 2015

What explains the effect of education on cardiovascular disease? Applying Mendelian randomization to identify the consequences of education inequality:

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

artículo científico publicado en 2016

Workflow for Integrated Processing of Multicohort Untargeted 1H NMR Metabolomics Data in Large-Scale Metabolic Epidemiology

artículo científico publicado en 2016

von Willebrand Factor, ADAMTS13 Activity, and Decline in Kidney Function: A Population-Based Cohort Study

artículo científico publicado en 2016

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