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Serum Bilirubin in the Czech Population　― Relationship to the Risk of Myocardial Infarction in Males

Circulation Journal, 2020/09/25, Vol.84(10), pp.1779-1785

2020

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The APOE4 allele is associated with a decreased risk of retinopathy in type 2 diabetics

Molecular biology reports, 2021-08, Vol.48 (8), p.5873-5879

2021

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SLCO1B1 polymorphism is not associated with risk of statin-induced myalgia/myopathy in a Czech population

Medical science monitor, 2015-05, Vol.21, p.1454-1459

2015

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ABCA3 and LZTFL1 Polymorphisms and Risk of COVID-19 in the Czech Population

Physiological research, 2023-08, Vol.72 (4), p.539-543

2023

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Sex-specific effect of APOAV variant (Val153>Met) on plasma levels of high-density lipoprotein cholesterol

Metabolism, clinical and experimental, 2005-12, Vol.54 (12), p.1632-1635

2005

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The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case–Control Study

Molecular diagnosis & therapy, 2019-08, Vol.23 (4), p.555-562

2019

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The FTO gene polymorphism is associated with end-stage renal disease: two large independent case―control studies in a general population

Nephrology, dialysis, transplantation, 2012-03, Vol.27 (3), p.1030-1035

2012

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Polymorphisms in the Lipopolysaccharide-Binding Protein and Bactericidal/Permeability-Increasing Protein in Patients with Myocardial Infarction

Clinical chemistry and laboratory medicine, 2002-12, Vol.40 (11), p.1097-1100

2002

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Rare Alleles within the CYP2E1 (MEOS System) Could be Associated with Better Short‐Term Health Outcome after Acute Methanol Poisoning

Basic & clinical pharmacology & toxicology, 2015-02, Vol.116 (2), p.168-172

2015

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Possible gene-gender interaction between the SLCO1B1 polymorphism and statin treatment efficacy

Neuro-endocrinology letters, 2012, Vol.33 Suppl 2, p.22-25

2012

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Lack of an Association Between Three Tagging SNPs Within The FTO Gene And Smoking Behavior

Nicotine & tobacco research, 2012-08, Vol.14 (8), p.998-1002

2012

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Impact of apolipoprotein A5 variants on statin treatment efficacy

Pharmacogenomics, 2009-06, Vol.10 (6), p.945-950

2009

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MLXIPL variant in individuals with low and high triglyceridemia in white population in Central Europe

Human genetics, 2008-12, Vol.124 (5), p.553-555

2008

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Rare variants in known and novel candidate genes predisposing to statin-associated myopathy

Pharmacogenomics, 2016-08, Vol.17 (13), p.1405-1414

2016

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Distribution of ADH1B genotypes predisposed to enhanced alcohol consumption in the Czech Roma/Gypsy population

Central European journal of public health, 2018-12, Vol.26 (4), p.284-288

2018

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Smoking impairs and circulating stem cells favour the protective effect of the T allele of the connexin37 gene in ischemic heart disease – A multinational study

Atherosclerosis, 2016-01, Vol.244, p.73-78

2016

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No significant association between A-501C single nucleotide polymorphism in preproghrelin and body mass index or waist-to-hip ratio in central European population

Metabolism, clinical and experimental, 2008-07, Vol.57 (7), p.1016-1017

2008

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Sex-specific interaction between APOE and APOA5 variants and determination of plasma lipid levels

European journal of human genetics : EJHG, 2008-01, Vol.16 (1), p.135-138

2008

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Variants within HNF1α and ANGPTL4 genes and acute coronary syndrome in Czech population. The GENDEMIP study

Neuro-endocrinology letters, 2012, Vol.33 Suppl 2, p.13-16

2012

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No associations between genetic polymorphisms of TGF-beta, PAI-1, and COL1A1, and bone mineral density in Caucasian females

Endocrine regulations (Bratislava), 2006-12, Vol.40 (4), p.107

2006

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APOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levels

Clinical chemistry and laboratory medicine, 2008-01, Vol.46 (6), p.773-777

2008

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Insertion/deletion polymorphism in the angiotensin-converting enzyme gene in myocardial infarction survivors

Medical science monitor, 2000-05, Vol.6 (3), p.503-506

2000

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Serum Bilirubin in the Czech Population　― Relationship to the Risk of Myocardial Infarction in Males

The APOE4 allele is associated with a decreased risk of retinopathy in type 2 diabetics

SLCO1B1 polymorphism is not associated with risk of statin-induced myalgia/myopathy in a Czech population

ABCA3 and LZTFL1 Polymorphisms and Risk of COVID-19 in the Czech Population

Sex-specific effect of APOAV variant (Val153>Met) on plasma levels of high-density lipoprotein cholesterol

The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case–Control Study

The FTO gene polymorphism is associated with end-stage renal disease: two large independent case―control studies in a general population

Polymorphisms in the Lipopolysaccharide-Binding Protein and Bactericidal/Permeability-Increasing Protein in Patients with Myocardial Infarction

Rare Alleles within the CYP2E1 (MEOS System) Could be Associated with Better Short‐Term Health Outcome after Acute Methanol Poisoning

A systematic review and meta-analysis of 130,000 individuals shows smoking does not modify the association of APOE genotype on risk of coronary heart disease

Possible gene-gender interaction between the SLCO1B1 polymorphism and statin treatment efficacy

Lack of an Association Between Three Tagging SNPs Within The FTO Gene And Smoking Behavior

Impact of apolipoprotein A5 variants on statin treatment efficacy

MLXIPL variant in individuals with low and high triglyceridemia in white population in Central Europe

Rare variants in known and novel candidate genes predisposing to statin-associated myopathy

Distribution of ADH1B genotypes predisposed to enhanced alcohol consumption in the Czech Roma/Gypsy population

Smoking impairs and circulating stem cells favour the protective effect of the T allele of the connexin37 gene in ischemic heart disease – A multinational study

No significant association between A-501C single nucleotide polymorphism in preproghrelin and body mass index or waist-to-hip ratio in central European population

Sex-specific interaction between APOE and APOA5 variants and determination of plasma lipid levels

Variants within HNF1α and ANGPTL4 genes and acute coronary syndrome in Czech population. The GENDEMIP study

No associations between genetic polymorphisms of TGF-beta, PAI-1, and COL1A1, and bone mineral density in Caucasian females

APOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levels

Insertion/deletion polymorphism in the angiotensin-converting enzyme gene in myocardial infarction survivors

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