Lista de obras -

768Host Gene Polymorphisms and Susceptibility to Viral Enteropathogens in Children Living in The Gambia and Kenya.

artículo científico publicado en 2014

A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease

artículo científico publicado en 2007

Altered Hypoxic-Adenosine Axis and Metabolism in Group III Pulmonary Hypertension

artículo científico publicado en 2015

Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida

artículo científico publicado en 2002

Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study

artículo científico publicado en 2009

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Association of the complement factor H Y402H polymorphism with cardiovascular disease is dependent upon hypertension status: The ARIC study

scientific article published on 21 February 2008

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

artículo científico publicado en 2003

Carbohydrate intake modifies associations between ANGPTL4[E40K] genotype and HDL-cholesterol concentrations in White men from the Atherosclerosis Risk in Communities (ARIC) study

scientific article published on 02 July 2008

Carotid intima-media thickness and presence or absence of plaque improves prediction of coronary heart disease risk: the ARIC (Atherosclerosis Risk In Communities) study

artículo científico publicado en 2010

Causal Role of Alcohol Consumption in an Improved Lipid Profile: The Atherosclerosis Risk in Communities (ARIC) Study

artículo científico publicado en 2016

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease

artículo científico publicado en 2008

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

Deletion of ADORA2B from myeloid cells dampens lung fibrosis and pulmonary hypertension

artículo científico publicado en 2014

Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study

artículo científico publicado en 2010

Differentially regulated gene expression associated with hepatitis C virus clearance

artículo científico publicado en 2012

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?

artículo científico publicado en 2002

Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects

artículo científico publicado en 2003

Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects

artículo científico publicado en 2004

Extracellular adenosine levels are associated with the progression and exacerbation of pulmonary fibrosis

artículo científico publicado en 2015

Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD

artículo científico publicado en 2008

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

artículo científico publicado en 2012

Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites

artículo científico publicado en 2013

Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study

artículo científico publicado en 2010

Genetic variation in the proto-oncogene SKI and risk for orofacial clefting.

artículo científico publicado en 2005

Hypoxia-induced deoxycytidine kinase contributes to epithelial proliferation in pulmonary fibrosis.

artículo científico publicado en 2014

Increased risk of incident stroke associated with the cyclooxygenase 2 (COX-2) G-765C polymorphism in African-Americans: the Atherosclerosis Risk in Communities Study

artículo científico publicado en 2007

Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study.

artículo científico publicado en 2007

Interaction of folate intake and the paraoxonase Q192R polymorphism with risk of incident coronary heart disease and ischemic stroke: the atherosclerosis risk in communities study

artículo científico publicado en 2011

Intercellular adhesion molecule-1 G241R polymorphism predicts risk of incident ischemic stroke: Atherosclerosis Risk in Communities study

artículo científico publicado en 2010

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Longitudinal changes in triglycerides according to ANGPTL4[E40K] genotype and longitudinal body weight change in the atherosclerosis risk in communities study

artículo científico publicado en 2008

MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study

artículo científico publicado en 2009

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project

artículo científico publicado en 2012

P-selectin Thr715Pro polymorphism predicts P-selectin levels but not risk of incident coronary heart disease or ischemic stroke in a cohort of 14595 participants: the Atherosclerosis Risk in Communities Study

artículo científico publicado en 2005

Peroxisome proliferator-activated receptor [alpha] genetic variation interacts with n-6 and long-chain n-3 fatty acid intake to affect total cholesterol and LDL-cholesterol concentrations in the Atherosclerosis Risk in Communities Study

scientific article published on June 2008

Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects

scientific article published on 01 February 2004

Relation of lipid gene scores to longitudinal trends in lipid levels and incidence of abnormal lipid levels among individuals of European ancestry: the Atherosclerosis Risk in Communities (ARIC) study

artículo científico publicado en 2011

Relationship of alcohol consumption and type of alcoholic beverage consumed with plasma lipid levels: differences between Whites and African Americans of the ARIC study

artículo científico publicado en 2007

Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida

artículo científico publicado en 2003

SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study

artículo científico publicado en 2009

Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study

artículo científico publicado en 2007

Suppression of cleavage factor Im 25 promotes the proliferation of lung cancer cells through alternative polyadenylation

scientific article published in 2018

Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations

artículo científico publicado en 2009

Lista de obras de

768Host Gene Polymorphisms and Susceptibility to Viral Enteropathogens in Children Living in The Gambia and Kenya.

A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease

Altered Hypoxic-Adenosine Axis and Metabolism in Group III Pulmonary Hypertension

Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida

Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

Association of the complement factor H Y402H polymorphism with cardiovascular disease is dependent upon hypertension status: The ARIC study

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

Carbohydrate intake modifies associations between ANGPTL4[E40K] genotype and HDL-cholesterol concentrations in White men from the Atherosclerosis Risk in Communities (ARIC) study

Carotid intima-media thickness and presence or absence of plaque improves prediction of coronary heart disease risk: the ARIC (Atherosclerosis Risk In Communities) study

Causal Role of Alcohol Consumption in an Improved Lipid Profile: The Atherosclerosis Risk in Communities (ARIC) Study

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease

Common variants associated with plasma triglycerides and risk for coronary artery disease

Deletion of ADORA2B from myeloid cells dampens lung fibrosis and pulmonary hypertension

Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study

Differentially regulated gene expression associated with hepatitis C virus clearance

Discovery and refinement of loci associated with lipid levels

Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?

Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects

Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects

Extracellular adenosine levels are associated with the progression and exacerbation of pulmonary fibrosis

Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites

Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study

Genetic variation in the proto-oncogene SKI and risk for orofacial clefting.

Hypoxia-induced deoxycytidine kinase contributes to epithelial proliferation in pulmonary fibrosis.

Increased risk of incident stroke associated with the cyclooxygenase 2 (COX-2) G-765C polymorphism in African-Americans: the Atherosclerosis Risk in Communities Study

Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study.

Interaction of folate intake and the paraoxonase Q192R polymorphism with risk of incident coronary heart disease and ischemic stroke: the atherosclerosis risk in communities study

Intercellular adhesion molecule-1 G241R polymorphism predicts risk of incident ischemic stroke: Atherosclerosis Risk in Communities study

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

Longitudinal changes in triglycerides according to ANGPTL4[E40K] genotype and longitudinal body weight change in the atherosclerosis risk in communities study

MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project

P-selectin Thr715Pro polymorphism predicts P-selectin levels but not risk of incident coronary heart disease or ischemic stroke in a cohort of 14595 participants: the Atherosclerosis Risk in Communities Study

Peroxisome proliferator-activated receptor [alpha] genetic variation interacts with n-6 and long-chain n-3 fatty acid intake to affect total cholesterol and LDL-cholesterol concentrations in the Atherosclerosis Risk in Communities Study

Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects

Relation of lipid gene scores to longitudinal trends in lipid levels and incidence of abnormal lipid levels among individuals of European ancestry: the Atherosclerosis Risk in Communities (ARIC) study

Relationship of alcohol consumption and type of alcoholic beverage consumed with plasma lipid levels: differences between Whites and African Americans of the ARIC study

Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida

SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study

Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study

Suppression of cleavage factor Im 25 promotes the proliferation of lung cancer cells through alternative polyadenylation

Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations