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List of works by Michael W Tanck

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy

scientific article published on 01 August 2018

A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi Jews

scientific article published on 23 July 2015

A novel echocardiographic predictor of in-hospital mortality and mid-term haemodynamic improvement after pulmonary endarterectomy for chronic thrombo-embolic pulmonary hypertension.

scientific article

Acute Effects of Morning Light on Plasma Glucose and Triglycerides in Healthy Men and Men with Type 2 Diabetes

scientific article

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

scientific article published on 3 March 2015

Assessment of coagulation and fibrinolysis in families with unexplained thrombophilia.

scientific article published in March 2009

Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings

scientific article

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

scientific article published on 21 March 2019

Association of Connective Tissue Growth Factor With Fibrosis in Vitreoretinal Disorders in the Human Eye

scientific article published on 01 October 2006

Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density

scientific article published on 25 April 2015

Association tests of striatal DAT availability and SNPs that impact a novel splice variant in the DAT gene.

scientific article published on 16 March 2012

Associations between single nucleotide polymorphisms and erythrocyte parameters in humans: A systematic literature review

scientific article published on 01 January 2019

Both paraoxonase-1 genotype and activity do not predict the risk of future coronary artery disease; the EPIC-Norfolk Prospective Population Study

scientific article

CAG repeat length variation in the Androgen Receptor gene is not associated with spermatogenic failure

article

CAG repeat length variation in the polymerase gamma (POLG) gene: effect on semen quality

article

Causes of severe visual impairment and blindness in children in the Republic of Suriname

scientific article

Changes in microbiota during experimental human Rhinovirus infection

scientific article published on 14 August 2015

Chemokine ligand 2 genetic variants, serum monocyte chemoattractant protein-1 levels, and the risk of coronary artery disease

scientific article

Children with hypercholesterolemia of unknown cause: Value of genetic risk scores

scientific article

Clinical Course Long After Atrial Switch: A Novel Risk Score for Major Clinical Events

scientific article published on 22 February 2021

Clonidine increases bone resorption in humans

scientific article published on 6 October 2015

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

scientific article published on 10 December 2021

Common genetic variants do not associate with CAD in familial hypercholesterolemia

scientific article

Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death.

scientific article published on 08 January 2012

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

scientific article published on 16 January 2006

Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels

article

Community-acquired bacterial meningitis in adults in the Netherlands, 2006-14: a prospective cohort study

scientific article

Comparison of Intralesional Corticosteroid and Propranolol Treatment of Periorbital Infantile Hemangiomas: An Outcome Study of 61 Cases

scientific article published on 09 April 2014

Complex inheritance for susceptibility to sudden cardiac death.

scientific article published on January 2013

DC-SIGN Polymorphisms Associated with Risk of Hepatitis C Virus Infection Among Men who Have Sex with Men but not Among Injecting Drug Users

scientific article published on 13 November 2017

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

scientific article

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

article

Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans

scientific article

Efficient ways exist to obtain the optimal sample size in clinical trials in rare diseases.

scientific article published on 21 February 2008

Electrocardiographic evidence of ventricular repolarization remodelling during atrial fibrillation

article

Erratum to: Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

scientific article published on 6 April 2017

Erythrocyte glutathione concentration and production during hyperinsulinemia, hyperglycemia, and endotoxemia in healthy humans ⬇️

scientific article published on September 17, 2010

Estimating effects of rare haplotypes on failure time using a penalized Cox proportional hazards regression model.

scientific article

Estimating haplotype effects on dichotomous outcome for unphased genotype data using a weighted penalized log-likelihood approach.

scientific article

Ethyl pyruvate exerts combined anti-inflammatory and anticoagulant effects on human monocytic cells.

scientific article

Expression and Role of Myeloid-related Protein-14 in Clinical and Experimental Sepsis

scientific article published on 17 September 2009

Ext1 heterozygosity causes a modest effect on postprandial lipid clearance in humans

scientific article

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

scientific article published on 28 August 2006

Family history and inherited thrombophilia

scientific article published on 01 October 2006

Fasting predisposes to hypoglycemia in Surinamese children with severe pneumonia, and young children are more at risk.

scientific article

Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis

scientific article

Functional interaction between -629C/A, -971G/A and -1337C/T polymorphisms in the CETP gene is a major determinant of promoter activity and plasma CETP concentration in the REGRESS Study.

scientific article published on 27 July 2005

Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation

scientific article published on 29 January 2017

Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia

scientific article

Genetic variation in thrombin-activatable fibrinolysis inhibitor (TAFI) is associated with the risk of splanchnic vein thrombosis

scientific article published on 01 February 2007

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

scientific article

Glucose tolerance at age 58 and the decline of glucose tolerance in comparison with age 50 in people prenatally exposed to the Dutch famine.

scientific article published on 10 February 2006

HIV-1 disease progression is associated with bile-salt stimulated lipase (BSSL) gene polymorphism.

scientific article

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation

scientific article published on 12 March 2009

High levels of protein C are determined byPROCRhaplotype 3

scientific article published on 01 May 2011

Human ATP-binding cassette G1 controls macrophage lipoprotein lipase bioavailability and promotes foam cell formation

scientific article

Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans

scientific article published on 01 June 2006

Hyperglycemia prevents the suppressive effect of hyperinsulinemia on plasma adiponectin levels in healthy humans

scientific article published on 24 June 2008

Impact of an evidence-based guideline on the management of community-acquired bacterial meningitis: a prospective cohort study

scientific article published on 30 July 2016

Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia

scientific article published on 07 November 2006

Integrative genomic approach identifies multiple genes involved in cardiac collagen deposition.

scientific article

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

scientific article published on 04 March 2013

Large genome-wide association study identifies three novel risk variants for restless legs syndrome

scientific article published on 25 November 2020

Lung inflammation induced by lipoteichoic acid or lipopolysaccharide in humans.

scientific article published on 10 April 2008

Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

scientific article published on 3 January 2017

Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration

scientific article published on 17 March 2012

Multiple imputation of missing genotype data for unrelated individuals.

scientific article

Natural history of spheno-orbital meningiomas

scientific article

No linkage for venous thrombosis at a candidate region on chromosome 18 in Dutch thrombophilic families

scientific article published on 24 April 2009

Non-classical FCGR2C haplotype is associated with protection from red blood cell allo-immunization in sickle cell disease

scientific article published on 12 September 2017

Novel method for studying postoperative ileus in mice.

scientific article published on 26 December 2012

Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene

scientific article published on 12 January 2016

Pitfalls in the design and analysis of paediatric clinical trials: a case of a 'failed' multi-centre study, and potential solutions.

scientific article published on 24 September 2008

Plasma lipoprotein(a) levels in patients with homozygous autosomal dominant hypercholesterolemia

scientific article published on 27 February 2017

Platelet and endothelial cell P-selectin are required for host defense against Klebsiella pneumoniae-induced pneumosepsis.

scientific article published on 23 April 2015

Poly(trimethylene carbonate) and poly(D,L-lactic acid) modify human dendritic cell responses to staphylococci but do not affect Th1 and Th2 cell development.

scientific article published on 19 February 2018

Polymorphisms in the Catechol-O-Methyltransferase Gene and Delirium in the Elderly

article

Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention era

article

Pulmonary tuberculosis induces a systemic hypercoagulable state

scientific article published on 29 October 2014

Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse

scientific article published on 18 September 2010

Quantitative trait locus for protein C in a family with thrombophilia

scientific article published on 26 October 2010

Receptor for Advanced Glycation End Products (RAGE) Serves a Protective Role during Klebsiella pneumoniae - Induced Pneumonia

scientific article published on 29 January 2016

Red cell distribution width is associated with physical inactivity and heart failure, independent of established risk factors, inflammation or iron metabolism; the EPIC-Norfolk study

scientific article

Response to letter by Balta et al.

scientific article published on 6 September 2013

Risk scores for outcome in bacterial meningitis: Systematic review and external validation study

scientific article published on 9 August 2016

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

scientific article published on 09 November 2020

SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers

scientific article published on 30 April 2018

SNP rs688 within the low-density lipoprotein receptor (LDL-R) gene associates with HCV susceptibility

scientific article published on 17 October 2018

SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition.

scientific article published on 20 February 2013

Sample size calculations: basic principles and common pitfalls

scientific article published on 12 January 2010

Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure

scientific article published on 26 February 2020

Segregation of microsatellite alleles and residual heterozygosity at single loci in homozygous androgenetic common carp (Cyprinus carpioL.) ⬇️

scientific article published on October 1, 2001

Sequential design with boundaries approach in pediatric intervention research reduces sample size

scientific article published on 27 September 2009

Short-Term Effect of Estrogen on Human Bone Marrow Fat.

scientific article published on 18 May 2015

Simultaneous estimation of gene-gene and gene-environment interactions for numerous loci using double penalized log–likelihood

article

Striatal dopamine transporter availability associated with polymorphisms in the dopamine transporter gene SLC6A3.

scientific article

Study on the protective effect of the KIR3DL1 gene in ankylosing spondylitis

scientific article published on 3 August 2015

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

scientific article published on 21 March 2019

Surgical treatment of sphenoorbital meningiomas

scientific article published on 17 January 2011

Systemic and local high mobility group box 1 concentrations during severe infection

article

The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia A.

scientific article published on 16 July 2014

The angio-fibrotic switch of VEGF and CTGF in proliferative diabetic retinopathy

scientific article

The association between the gene encoding 5-lipoxygenase activating protein and abdominal aortic aneurysms

article

The effect of raloxifene on bone marrow adipose tissue and bone turnover in postmenopausal women with osteoporosis

scientific article published on 11 October 2017

The effects of beta-2 adrenergic agonist and antagonist on human bone metabolism: a randomized controlled trial.

scientific article published on 5 November 2014

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies

scientific article published on 11 November 2008

V-akt murine thymoma viral oncogene homolog 3 (AKT3) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

scientific article

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

scientific article published on 23 December 2011

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