Lista de obras -

Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records

artículo científico publicado en 2010

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

artículo científico publicado en 2011

CRP polymorphisms and progression of chronic kidney disease in African Americans

artículo científico publicado en 2009

Characterization of mitochondrial haplogroups in a large population-based sample from the United States

artículo científico publicado en 2014

Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project

artículo científico publicado en 2013

Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANE

artículo científico publicado en 2015

Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2013

Evidence for age as a modifier of genetic associations for lipid levels

artículo científico publicado en 2011

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

artículo científico publicado en 2011

Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium

artículo científico publicado en 2012

Genetic variation in the β1-adrenergic receptor is associated with the risk of atrial fibrillation after cardiac surgery.

artículo científico publicado en 2013

Identification of gene-gene and gene-environment interactions within the fibrinogen gene cluster for fibrinogen levels in three ethnically diverse populations

artículo científico publicado en 2015

Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study

artículo científico publicado en 2013

KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE.

artículo científico publicado en 2016

Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).

artículo científico publicado en 2013

Measures of exposure impact genetic association studies: an example in vitamin K levels and VKORC1.

artículo científico publicado en 2015

Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study

artículo científico publicado en 2014

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population

artículo científico publicado en 2013

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations

artículo científico publicado en 2010

Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network

artículo científico publicado en 2013

Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data

artículo científico publicado en 2016

Population differences in genetic risk for age-related macular degeneration and implications for genetic testing

artículo científico publicado en 2012

Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2013

Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study

artículo científico publicado en 2014

Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey

artículo científico publicado en 2012

Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies

article

Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record

artículo científico publicado en 2010

SCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study.

artículo científico publicado en 2011

Serum vitamins A and E as modifiers of lipid trait genetics in the National Health and Nutrition Examination Surveys as part of the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2012

VKORC1 common variation and bone mineral density in the Third National Health and Nutrition Examination Survey

artículo científico publicado en 2010

Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey

artículo científico publicado en 2011

Lista de obras de

Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

CRP polymorphisms and progression of chronic kidney disease in African Americans

Characterization of mitochondrial haplogroups in a large population-based sample from the United States

Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project

Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANE

Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study

Evidence for age as a modifier of genetic associations for lipid levels

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium

Genetic variation in the β1-adrenergic receptor is associated with the risk of atrial fibrillation after cardiac surgery.

Identification of gene-gene and gene-environment interactions within the fibrinogen gene cluster for fibrinogen levels in three ethnically diverse populations

Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study

KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE.

Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).

Measures of exposure impact genetic association studies: an example in vitamin K levels and VKORC1.

Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations

Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network

Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data

Population differences in genetic risk for age-related macular degeneration and implications for genetic testing

Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study

Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study

Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey

Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies

Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record

SCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study.

Serum vitamins A and E as modifiers of lipid trait genetics in the National Health and Nutrition Examination Surveys as part of the Population Architecture using Genomics and Epidemiology (PAGE) study

VKORC1 common variation and bone mineral density in the Third National Health and Nutrition Examination Survey

Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey