Lista de obras - Michael W Tanck - Dominio Público Uruguay

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

artículo científico publicado en 2018

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

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Assessment of coagulation and fibrinolysis in families with unexplained thrombophilia.

artículo científico publicado en 2009

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

artículo científico publicado en 2007

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 2019

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

artículo científico publicado en 2009

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

artículo científico publicado en 2013

Changes in microbiota during experimental human Rhinovirus infection

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

artículo científico publicado en 2016

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

artículo científico publicado en 2021

Clonidine increases bone resorption in humans

artículo científico publicado en 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

artículo científico publicado en 2013

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

artículo científico

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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Complex inheritance for susceptibility to sudden cardiac death.

artículo científico publicado en 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

artículo científico publicado en 2017

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

artículo científico publicado en 2006

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

artículo científico publicado en 2008

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

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado el 17 de septiembre de 2010

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

artículo científico publicado en 2008

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

artículo científico publicado en 2006

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

artículo científico publicado en 2006

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 2006

Family history and inherited thrombophilia

artículo científico publicado en 2006

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

artículo científico publicado en 2012

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

artículo científico publicado en 2016

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.

artículo científico publicado en 2005

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

artículo científico publicado en 2017

Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia

artículo científico publicado en 2005

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

artículo científico publicado en 2010

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

artículo científico

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

artículo científico publicado en 2012

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

artículo científico publicado en 2011

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

artículo científico publicado en 2012

Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans

artículo científico publicado en 2006

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

artículo científico publicado en 2008

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

artículo científico publicado en 2016

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

artículo científico publicado en 2006

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

artículo científico publicado en 2014

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

artículo científico publicado en 2020

Lung inflammation induced by lipoteichoic acid or lipopolysaccharide in humans.

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

Multiple imputation of missing genotype data for unrelated individuals.

artículo científico publicado en 2006

Natural history of spheno-orbital meningiomas

artículo científico publicado en 2010

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

artículo científico publicado en 2009

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

artículo científico publicado en 2017

Novel method for studying postoperative ileus in mice.

artículo científico publicado en 2012

Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado en 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.

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 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

artículo científico publicado en 2013

Response to letter by Balta et al.

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

artículo científico publicado en 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.

artículo científico publicado en 2013

Sample size calculations: basic principles and common pitfalls

artículo científico publicado en 2010

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

artículo científico publicado en 2020

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.

artículo científico publicado en 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.

artículo científico publicado en 2008

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

artículo científico publicado en 2015

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 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.

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Lista de obras de 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

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

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

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

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

Assessment of coagulation and fibrinolysis in families with unexplained thrombophilia.

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

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

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

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

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

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

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

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

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

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

Changes in microbiota during experimental human Rhinovirus infection

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

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

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

Clonidine increases bone resorption in humans

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

Common genetic variants do not associate with CAD in familial hypercholesterolemia

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

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

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

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

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

Complex inheritance for susceptibility to sudden cardiac death.

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

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing

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

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

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

Electrocardiographic evidence of ventricular repolarization remodelling during atrial fibrillation

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

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

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

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

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

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

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

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

Family history and inherited thrombophilia

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

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

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.

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

Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia

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

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

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

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

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

High levels of protein C are determined byPROCRhaplotype 3

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

Hyperglycemia Stimulates Coagulation, Whereas Hyperinsulinemia Impairs Fibrinolysis in Healthy Humans

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

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

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

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

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

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

Lung inflammation induced by lipoteichoic acid or lipopolysaccharide in humans.

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

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

Multiple imputation of missing genotype data for unrelated individuals.

Natural history of spheno-orbital meningiomas

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

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

Novel method for studying postoperative ileus in mice.

Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene

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

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

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

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.

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

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