Lista de obras -

A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro

artículo científico publicado en 2010

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection

artículo científico publicado en 2008

Aspirin Resistance in healthy drug-naive men versus women (from the Heredity and Phenotype Intervention Heart Study).

artículo científico publicado en 2009

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

artículo científico publicado en 2010

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

artículo científico publicado en 2010

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

artículo científico publicado en 2007

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

artículo científico publicado en 2013

Common variants in the GDF5-UQCC region are associated with variation in human height

artículo científico publicado en 2008

Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100.

artículo científico publicado en 2013

Determinants of coronary artery and aortic calcification in the Old Order Amish

artículo científico publicado en 2007

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Extent and distribution of linkage disequilibrium in the Old Order Amish

artículo científico publicado en 2010

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

artículo científico publicado en 2010

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

artículo científico publicado en 2008

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels

artículo científico publicado en 2009

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

artículo científico publicado en 2011

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

artículo científico publicado en 2009

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

artículo científico publicado en 2007

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

artículo científico publicado en 2008

Physical activity and the association of common FTO gene variants with body mass index and obesity

artículo científico publicado en 2008

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance

artículo científico publicado en 2006

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

artículo científico publicado en 2008

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

artículo científico publicado en 2008

Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women

artículo científico publicado en 2007

Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels

artículo científico publicado en 2008

Lista de obras de

A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection

Aspirin Resistance in healthy drug-naive men versus women (from the Heredity and Phenotype Intervention Heart Study).

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

Common variants in the GDF5-UQCC region are associated with variation in human height

Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100.

Determinants of coronary artery and aortic calcification in the Old Order Amish

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Extent and distribution of linkage disequilibrium in the Old Order Amish

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Loci influencing blood pressure identified using a cardiovascular gene-centric array

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Physical activity and the association of common FTO gene variants with body mass index and obesity

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women

Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels