Lista de obras -

A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study

artículo científico publicado en 2008

A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

artículo científico publicado en 2009

A prospective assessment of the Y402H variant in complement factor H, genetic variants in C-reactive protein, and risk of age-related macular degeneration

artículo científico publicado en 2006

A prospective evaluation of the CD14 and CD18 gene polymorphisms and risk of stroke

artículo científico publicado en 2002

A prospective evaluation of the heat shock protein 70 gene polymorphisms and the risk of stroke

scientific article published on 01 April 2002

Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction

artículo científico publicado en 2003

An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study

artículo científico publicado en 2009

Association between polymorphisms in the beta2-adrenergic receptor gene with myocardial infarction and ischaemic stroke in women.

artículo científico publicado en 2009

Association between polymorphisms in the beta2-adrenoceptor gene and migraine in women

artículo científico publicado en 2008

Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study

scientific article published on March 2009

Association of adiponectin gene variations with risk of incident myocardial infarction and ischemic stroke: a nested case-control study

scientific article published on 21 September 2006

Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome Study

artículo científico publicado en 2009

Association of renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study

artículo científico publicado en 2008

Association of shorter mean telomere length with risk of incident myocardial infarction: a prospective, nested case-control approach

scientific article published on 13 February 2009

Biological, clinical and population relevance of 95 loci for blood lipids

artículo científico publicado en 2010

C-reactive protein gene variation and type 2 diabetes mellitus: a case-control study

artículo científico publicado en 2007

Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: dat

artículo científico publicado en 2009

Complement factor H Y402H gene polymorphism, C-reactive protein, and risk of incident myocardial infarction, ischaemic stroke, and venous thromboembolism: a nested case-control study

artículo científico publicado en 2006

Effects of random allocation to vitamin E supplementation on the occurrence of venous thromboembolism: report from the Women's Health Study

artículo científico publicado en 2007

Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women.

artículo científico publicado en 2018

Gene variation of the transient receptor potential cation channel, subfamily M, member 7 (TRPM7), and risk of incident ischemic stroke: prospective, nested, case-control study

artículo científico publicado en 2009

Gene variations of ROCKs and risk of ischaemic stroke: the Women's Genome Health Study

artículo científico publicado en 2014

Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication

artículo científico publicado en 2008

Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach

artículo científico publicado en 2009

Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study ⬇️

artículo científico publicado el 16 de octubre de 2010

Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study

artículo científico publicado en 2011

Genetic variants of arachidonate 5-lipoxygenase-activating protein, and risk of incident myocardial infarction and ischemic stroke: a nested case-control approach

artículo científico publicado en 2006

Genetic variants of tumor necrosis factor superfamily, member 4 (TNFSF4), and risk of incident atherothrombosis and venous thromboembolism.

artículo científico publicado en 2008

Genetic variants within the interleukin-1 gene cluster, and risk of incident myocardial infarction, and ischemic stroke: a nested case-control approach

artículo científico publicado en 2008

Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin

scientific article published on 01 November 2019

Genetic variation in sex-steroid receptors and synthesizing enzymes and colorectal cancer risk in women

artículo científico publicado en 2010

Genetic variation of fifteen folate metabolic pathway associated gene loci and the risk of incident head and neck carcinoma: the Women's Genome Health Study

artículo científico publicado en 2012

Genetic variation of the androgen receptor and risk of myocardial infarction and ischemic stroke in women

artículo científico publicado en 2008

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

artículo científico publicado en 2011

Haplotype analysis of the beta2 adrenergic receptor gene and risk of myocardial infarction in humans

artículo científico publicado en 2004

Homocysteine, 5,10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24,968 initially healthy women

artículo científico publicado en 2007

Interaction between inflammation-related gene polymorphisms and cigarette smoking on the risk of myocardial infarction in the Physician's Health Study

artículo científico publicado en 2005

Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,014 initially healthy white women

artículo científico publicado en 2007

Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study.

artículo científico publicado en 2011

Lack of Association Between Genetic Variation in 9 Innate Immunity Genes and Baseline CRP Levels

article

Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study

artículo científico publicado en 2008

Mean telomere length and risk of incident venous thromboembolism: a prospective, nested case-control approach

artículo científico publicado en 2009

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

artículo científico publicado en 2011

Mitochondrial uncoupling protein gene cluster variation (UCP2–UCP3) and the risk of incident type 2 diabetes mellitus: The Women's Genome Health Study ⬇️

artículo científico publicado el 20 de octubre de 2010

Natriuretic peptide precursor a gene polymorphisms and risk of blood pressure progression and incident hypertension

artículo científico publicado en 2007

Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women

artículo científico publicado en 2008

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

Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study

artículo científico publicado en 2009

Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study

artículo científico publicado en 2009

Polymorphism in the P-selectin and interleukin-4 genes as determinants of stroke: a population-based, prospective genetic analysis

artículo científico publicado en 2003

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy

artículo científico publicado en 2009

Polymorphism in the beta2-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism: a multilocus, population-based, prospective genetic analysis

artículo científico publicado en 2006

Polymorphism in the human C-reactive protein (CRP) gene, plasma concentrations of CRP, and the risk of future arterial thrombosis

artículo científico publicado en 2002

Polymorphisms and haplotypes of the estrogen receptor-beta gene (ESR2) and cardiovascular disease in men and women

artículo científico publicado en 2007

Polymorphisms in the advanced glycosylation end product-specific receptor gene and risk of incident myocardial infarction or ischemic stroke.

artículo científico publicado en 2006

Polymorphisms of the phosphodiesterase 4D, cAMP-specific (PDE4D) gene and risk of ischemic stroke: a prospective, nested case-control evaluation

artículo científico publicado en 2006

Prospective evaluation of the alcohol dehydrogenase gamma1/gamma2 gene polymorphism and risk of stroke

artículo científico publicado en 2004

Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism

artículo científico publicado en 2007

Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women

artículo científico publicado en 2007

Relation of polymorphism within the C-reactive protein gene and plasma CRP levels

artículo científico publicado en 2005

Relative leukocyte telomere length and risk of incident ischemic stroke in men: a prospective, nested case-control approach

artículo científico publicado en 2010

Threonine for alanine substitution in the eotaxin (CCL11) gene and the risk of incident myocardial infarction

artículo científico publicado en 2004

Toll-like receptor 4 Asp299Gly gene polymorphism and risk of atherothrombosis

artículo científico publicado en 2004

Tree and spline based association analysis of gene-gene interaction models for ischemic stroke

artículo científico publicado en 2004

Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarction

scientific article published on 17 February 2005

Two common gene variants on chromosome 9 and risk of atherothrombosis

scientific article published on 23 August 2007

Lista de obras de

A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study

A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

A prospective assessment of the Y402H variant in complement factor H, genetic variants in C-reactive protein, and risk of age-related macular degeneration

A prospective evaluation of the CD14 and CD18 gene polymorphisms and risk of stroke

A prospective evaluation of the heat shock protein 70 gene polymorphisms and the risk of stroke

Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction

An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study

Association between polymorphisms in the beta2-adrenergic receptor gene with myocardial infarction and ischaemic stroke in women.

Association between polymorphisms in the beta2-adrenoceptor gene and migraine in women

Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study

Association of adiponectin gene variations with risk of incident myocardial infarction and ischemic stroke: a nested case-control study

Association of genetic variants with the metabolic syndrome in 20,806 white women: The Women's Health Genome Study

Association of renin-angiotensin and endothelial nitric oxide synthase gene polymorphisms with blood pressure progression and incident hypertension: prospective cohort study

Association of shorter mean telomere length with risk of incident myocardial infarction: a prospective, nested case-control approach

Biological, clinical and population relevance of 95 loci for blood lipids

C-reactive protein gene variation and type 2 diabetes mellitus: a case-control study

Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: dat

Complement factor H Y402H gene polymorphism, C-reactive protein, and risk of incident myocardial infarction, ischaemic stroke, and venous thromboembolism: a nested case-control study

Effects of random allocation to vitamin E supplementation on the occurrence of venous thromboembolism: report from the Women's Health Study

Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women.

Gene variation of the transient receptor potential cation channel, subfamily M, member 7 (TRPM7), and risk of incident ischemic stroke: prospective, nested, case-control study

Gene variations of ROCKs and risk of ischaemic stroke: the Women's Genome Health Study

Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication

Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach

Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study ⬇️

Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study

Genetic variants of arachidonate 5-lipoxygenase-activating protein, and risk of incident myocardial infarction and ischemic stroke: a nested case-control approach

Genetic variants of tumor necrosis factor superfamily, member 4 (TNFSF4), and risk of incident atherothrombosis and venous thromboembolism.

Genetic variants within the interleukin-1 gene cluster, and risk of incident myocardial infarction, and ischemic stroke: a nested case-control approach

Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin

Genetic variation in sex-steroid receptors and synthesizing enzymes and colorectal cancer risk in women

Genetic variation of fifteen folate metabolic pathway associated gene loci and the risk of incident head and neck carcinoma: the Women's Genome Health Study

Genetic variation of the androgen receptor and risk of myocardial infarction and ischemic stroke in women

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

Haplotype analysis of the beta2 adrenergic receptor gene and risk of myocardial infarction in humans

Homocysteine, 5,10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24,968 initially healthy women

Interaction between inflammation-related gene polymorphisms and cigarette smoking on the risk of myocardial infarction in the Physician's Health Study

Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,014 initially healthy white women

Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study.

Lack of Association Between Genetic Variation in 9 Innate Immunity Genes and Baseline CRP Levels

Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study

Mean telomere length and risk of incident venous thromboembolism: a prospective, nested case-control approach

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

Mitochondrial uncoupling protein gene cluster variation (UCP2–UCP3) and the risk of incident type 2 diabetes mellitus: The Women's Genome Health Study ⬇️

Natriuretic peptide precursor a gene polymorphisms and risk of blood pressure progression and incident hypertension

Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women

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

Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study

Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study

Polymorphism in the P-selectin and interleukin-4 genes as determinants of stroke: a population-based, prospective genetic analysis

Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy

Polymorphism in the beta2-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism: a multilocus, population-based, prospective genetic analysis

Polymorphism in the human C-reactive protein (CRP) gene, plasma concentrations of CRP, and the risk of future arterial thrombosis

Polymorphisms and haplotypes of the estrogen receptor-beta gene (ESR2) and cardiovascular disease in men and women

Polymorphisms in the advanced glycosylation end product-specific receptor gene and risk of incident myocardial infarction or ischemic stroke.

Polymorphisms of the phosphodiesterase 4D, cAMP-specific (PDE4D) gene and risk of ischemic stroke: a prospective, nested case-control evaluation

Prospective evaluation of the alcohol dehydrogenase gamma1/gamma2 gene polymorphism and risk of stroke

Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism

Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women

Relation of polymorphism within the C-reactive protein gene and plasma CRP levels

Relative leukocyte telomere length and risk of incident ischemic stroke in men: a prospective, nested case-control approach

Threonine for alanine substitution in the eotaxin (CCL11) gene and the risk of incident myocardial infarction

Toll-like receptor 4 Asp299Gly gene polymorphism and risk of atherothrombosis

Tree and spline based association analysis of gene-gene interaction models for ischemic stroke

Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarction

Two common gene variants on chromosome 9 and risk of atherothrombosis