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

Bioinformatics, 2010-05, Vol.26 (9), p.1205-1210

2010

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

American journal of human genetics, 2010-04, Vol.86 (4), p.560-572

2010

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Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations

American journal of epidemiology, 2013-05, Vol.177 (9), p.923-932

2013

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Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

Neurobiology of aging, 2016-02, Vol.38, p.141-150

2016

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Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations The PAGE Study

American journal of epidemiology, 2013-05, Vol.177 (9), p.923-932

2013

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

PloS one, 2010-12, Vol.5 (12), p.e15088

2010

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

PloS one, 2011-01, Vol.6 (1), p.e16604-e16604

2011

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Genetic variation in recipient B-cell activating factor modulates phenotype of GVHD

Blood, 2011-07, Vol.118 (4), p.1140-1144

2011

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

The American heart journal, 2014, Vol.167 (1), p.101-108.e1

2014

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Evidence for Age As a Modifier of Genetic Associations for Lipid Levels

Annals of human genetics, 2011-09, Vol.75 (5), p.589-597

2011

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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

Human genetics, 2012-11, Vol.131 (11), p.1699-1708

2012

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Defining the role of common variation in the genomic and biological architecture of adult human height

Nature genetics, 2014-11, Vol.46 (11), p.1173-1186

2014

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CRP Polymorphisms and Progression of Chronic Kidney Disease in African Americans

Clinical journal of the American Society of Nephrology, 2010-01, Vol.5 (1), p.24-33

2010

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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

Annals of human genetics, 2013-09, Vol.77 (5), p.416-425

2013

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Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study

PLoS biology, 2013-09, Vol.11 (9), p.e1001661-e1001661

2013

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

Genetics in medicine, 2010-10, Vol.12 (10), p.648-650

2010

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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

Thrombosis and haemostasis, 2012-03, Vol.107 (3), p.458

2012

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

Human genetics, 2014-07, Vol.133 (7), p.861-868

2014

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Genetic Variation in Donor CTLA-4 Regulatory Region is a Strong Predictor of Outcome after Allogeneic Hematopoietic Cell Transplantation for Hematologic Malignancies

Biology of blood and marrow transplantation, 2012-07, Vol.18 (7), p.1069-1075

2012

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

PLoS genetics, 2011-06, Vol.7 (6), p.e1002138-e1002138

2011

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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 (NHANES)

Frontiers in genetics, 2015-10, Vol.6, p.317-317

2015

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Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) study

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

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

Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations The 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

Genetic variation in recipient B-cell activating factor modulates phenotype of GVHD

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

Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four U.S. populations: The Population Architecture using Genomics and Epidemiology (PAGE) study

Evidence for Age As a Modifier of Genetic Associations for Lipid Levels

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

Defining the role of common variation in the genomic and biological architecture of adult human height

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

CRP Polymorphisms and Progression of Chronic Kidney Disease in African Americans

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

Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study

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

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

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

Genetic Variation in Donor CTLA-4 Regulatory Region is a Strong Predictor of Outcome after Allogeneic Hematopoietic Cell Transplantation for Hematologic Malignancies

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

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

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 (NHANES)

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