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Roberto Corrocher

University of Verona

335

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12089

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A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist

2017 European Journal of Internal Medicine
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Global DNA methylation and hydroxymethylation differ in hepatocellular carcinoma and cholangiocarcinoma and relate to survival rate

2015 Hepatology
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DNA methylation and gene expression profiles show novel regulatory pathways in hepatocellular carcinoma

2015 Clinical Epigenetics
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Genomics of coronary artery disease and myocardial infarction.From Genome Wide Association Studies to the Next-Generation-Sequencing era

2014
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Paraoxonases: ancient substrate hunters and their evolving role in ischemic heart disease.

2013 Advances in Clinical Chemistry
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Global DNA Hypomethylation in Peripheral Blood Mononuclear Cells as a Biomarker of Cancer Risk

2013 Cancer Epidemiology, Biomarkers & Prevention
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Promoter methylation in coagulation F7 gene influences plasma FVII concentrations and relates to coronary artery disease

2012 Journal of Medical Genetics
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Low Levels of Serum Paraoxonase Activities are Characteristic of Metabolic Syndrome and May Influence the Metabolic-Syndrome-Related Risk of Coronary Artery Disease

2012 Experimental Diabetes Research
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Polymorphisms of cyclo-oxygenases and5-lipo-oxygenase-activating protein are associated with chronic spontaneousurticaria and urinary leukotriene E4

2011 Default journal
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Serum uric acid, but not rs7442295 polymorphism of SCL2A9 gene, predicts total and cardiovascular mortality in severe coronary artery disease.

2011
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