Lista de obras - Udo Seedorf - Dominio Público Uruguay

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

ADP-ribosylation factor (ARF)-like 7 (ARL7) is induced by cholesterol loading and participates in apolipoprotein AI-dependent cholesterol export

artículo científico publicado en 2004

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

artículo científico publicado en 2012

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

Branched chain fatty acids induce nitric oxide-dependent apoptosis in vascular smooth muscle cells

artículo científico publicado en 2002

Cell surface localization of ABCG1 does not require LXR activation

artículo científico publicado en 2006

Cholesterol absorption inhibitor Ezetimibe blocks uptake of oxidized LDL in human macrophages

artículo científico publicado en 2004

Chronic oral infection: An emerging risk factor of cerebral small vessel disease

scientific article published on 17 October 2018

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

artículo científico publicado en 2013

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Effects of ezetimibe and/or simvastatin on LDL receptor protein expression and on LDL receptor and HMG-CoA reductase gene expression: a randomized trial in healthy men.

artículo científico publicado en 2007

Expression and functional characterization of ABCG1 splice variant ABCG1(666)

artículo científico publicado en 2006

Gas chromatography-mass spectrometry and molecular genetic studies in families with the Conradi-Hünermann-Happle syndrome.

artículo científico publicado en 2002

Genes, diet and public health.

artículo científico publicado en 2007

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

artículo científico publicado en 2009

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

artículo científico publicado en 2011

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

artículo científico publicado en 2012

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

artículo científico publicado en 2011

Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study

artículo científico publicado en 2009

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

artículo científico publicado en 2012

Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease

artículo científico publicado en 2014

Inflammation in atherosclerosis, not yet time for a paradigm shift?

scientific article published on 01 June 2003

Involvement of Cdc42 signaling in apoA-I-induced cholesterol efflux

artículo científico publicado en 2003

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

Normal platelet reactivity in apolipoprotein E (apo E)-deficient mouse

scientific article published on 01 November 2006

Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study

artículo científico publicado en 2009

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

PROCAM Study: risk prediction for myocardial infarction using microfluidic high-density lipoprotein (HDL) subfractionation is independent of HDL cholesterol

artículo científico publicado en 2008

Periodontitis, dental plaque, and atrial fibrillation in the Hamburg City Health Study

artículo científico publicado en 2021

Phytanic acid accumulation is associated with conduction delay and sudden cardiac death in sterol carrier protein-2/sterol carrier protein-x deficient mice

artículo científico publicado en 2004

Prevalence of cholesteryl ester storage disease

artículo científico publicado en 2007

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

artículo científico publicado en 2007

Lista de obras de Udo Seedorf

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

A genome-wide association search for type 2 diabetes genes in African Americans

ADP-ribosylation factor (ARF)-like 7 (ARL7) is induced by cholesterol loading and participates in apolipoprotein AI-dependent cholesterol export

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

Blood pressure loci identified with a gene-centric array

Branched chain fatty acids induce nitric oxide-dependent apoptosis in vascular smooth muscle cells

Cell surface localization of ABCG1 does not require LXR activation

Cholesterol absorption inhibitor Ezetimibe blocks uptake of oxidized LDL in human macrophages

Chronic oral infection: An emerging risk factor of cerebral small vessel disease

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

Effects of ezetimibe and/or simvastatin on LDL receptor protein expression and on LDL receptor and HMG-CoA reductase gene expression: a randomized trial in healthy men.

Expression and functional characterization of ABCG1 splice variant ABCG1(666)

Gas chromatography-mass spectrometry and molecular genetic studies in families with the Conradi-Hünermann-Happle syndrome.

Genes, diet and public health.

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease

Inflammation in atherosclerosis, not yet time for a paradigm shift?

Involvement of Cdc42 signaling in apoA-I-induced cholesterol efflux

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

Normal platelet reactivity in apolipoprotein E (apo E)-deficient mouse

Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

PROCAM Study: risk prediction for myocardial infarction using microfluidic high-density lipoprotein (HDL) subfractionation is independent of HDL cholesterol

Periodontitis, dental plaque, and atrial fibrillation in the Hamburg City Health Study

Phytanic acid accumulation is associated with conduction delay and sudden cardiac death in sterol carrier protein-2/sterol carrier protein-x deficient mice

Prevalence of cholesteryl ester storage disease

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.