Search Results - "Harst, P van der"
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1
The single-cell eQTLGen consortium
Published in eLife (09-03-2020)“…In recent years, functional genomics approaches combining genetic information with bulk RNA-sequencing data have identified the downstream expression effects…”
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2
The fibrosis marker galectin-3 and outcome in the general population
Published in Journal of internal medicine (01-07-2012)“… de Boer RA, van Veldhuisen DJ, Gansevoort RT, Muller Kobold AC, van Gilst WH, Hillege HL, Bakker SJL, van der Harst P (University of Groningen). The…”
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3
Telomere length loss due to smoking and metabolic traits
Published in Journal of internal medicine (01-02-2014)“…Objectives Human age‐dependent telomere attrition and telomere shortening are associated with several age‐associated diseases and poorer overall survival. The…”
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Association between anxiety but not depressive disorders and leukocyte telomere length after 2 years of follow-up in a population-based sample
Published in Psychological medicine (01-04-2013)“…Telomere length is considered an emerging marker of biological aging. Depression and anxiety are associated with excess mortality risk but the mechanisms…”
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5
Genetically-determined body mass index and the risk of atrial fibrillation progression in men and women
Published in PloS one (18-02-2021)“…Limited causal evidence is available on the relationship between body mass index (BMI) and atrial fibrillation (AF) progression. Sex differences have been…”
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6
Diagnostic performance of semi-quantitative and quantitative stress CMR perfusion analysis: a meta-analysis
Published in Journal of cardiovascular magnetic resonance (27-11-2017)“…Stress cardiovascular magnetic resonance (CMR) perfusion imaging is a promising modality for the evaluation of coronary artery disease (CAD) due to high…”
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7
Vitamin D biology in heart failure: molecular mechanisms and systematic review
Published in Current drug targets (01-01-2011)“…Vitamin D has recently been suggested as an important mediator of blood pressure and cardiovascular disease, including heart failure. In patient with heart…”
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Novel endotypes in heart failure: effects on guideline-directed medical therapy
Published in European heart journal (21-12-2018)Get full text
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Recurrent and founder mutations in the Netherlands—Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy
Published in Netherlands heart journal (01-06-2013)“…Background Recently, we showed that the c.40_42delAGA (p.Arg14del) mutation in the phospholamban (PLN) gene can be identified in 10–15 % of Dutch patients with…”
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10
Angiotensin II Type 2 Receptor Vasoactivity in Internal Mammary Arteries of Patients With Coronary Artery Disease
Published in Journal of cardiovascular pharmacology (01-10-2007)“…BACKGROUND:Several animal studies suggested that the angiotensin II type 2 (AT2) receptor subtype mediates vasodilation, yet the results in human arteries are…”
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11
Determinants and clinical outcome of uptitration of ACE-inhibitors and beta-blockers in patients with heart failure: a prospective European study
Published in European heart journal (21-06-2017)“…Despite clear guidelines recommendations, most patients with heart failure and reduced ejection-fraction (HFrEF) do not attain guideline-recommended target…”
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12
Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration—Brief Report
Published in Arteriosclerosis, thrombosis, and vascular biology (05-05-2021)“…[Figure: see text]…”
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13
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
Published in European heart journal (21-05-2022)“…Abstract This document describes the contribution of clinical criteria to the interpretation of genetic variants using heritable Mendelian cardiomyopathies as…”
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14
A primer in artificial intelligence in cardiovascular medicine
Published in Netherlands heart journal (01-09-2019)“…Driven by recent developments in computational power, algorithms and web-based storage resources, machine learning (ML)-based artificial intelligence (AI) has…”
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15
Association of recognized and unrecognized myocardial infarction with depressive and anxiety disorders in 125,988 individuals: A report of the LifeLines cohort study
Published in Journal of psychosomatic research (01-06-2022)“…Background No previous study examined the role of recognition of myocardial infarction (MI) and the presence of affective disorders in a large population…”
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16
Novel endotypes in heart failure: effects on guideline-directed medical therapy
Published in European heart journal (21-12-2018)“…We sought to determine subtypes of patients with heart failure (HF) with a distinct clinical profile and treatment response, using a wide range of biomarkers…”
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Routine reporting of grey-white matter differentiation in early brain computed tomography in comatose patients after cardiac arrest: A substudy of the COACT trial
Published in Resuscitation (01-06-2022)“…A multimodal approach is advised for neurological prognostication in comatose patients after out-of-hospital cardiac arrest (OHCA). Grey-white matter…”
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Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease
Published in Journal of human genetics (01-06-2021)“…The stress hormone cortisol modulates fuel metabolism, cardiovascular homoeostasis, mood, inflammation and cognition. The CORtisol NETwork (CORNET) consortium…”
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Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium
Published in PloS one (20-05-2022)“…Both elevated and low resting heart rates are associated with atrial fibrillation (AF), suggesting a U-shaped relationship. However, evidence for a U-shaped…”
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Genetic loci influencing kidney function and chronic kidney disease
Published in Nature genetics (01-05-2010)“…Using genome-wide association, we identify common variants at 2p12-p13, 6q26, 17q23 and 19q13 associated with serum creatinine, a marker of kidney function (P…”
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