Lista de obras -

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

artículo científico publicado en 2019

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data

artículo científico publicado en 2012

A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT.

artículo científico publicado en 2010

A multi-stage genome-wide association study of uterine fibroids in African Americans

artículo científico publicado en 2017

ASAP: an environment for automated preprocessing of sequencing data

artículo científico publicado en 2013

African genetic ancestry interacts with body mass index to modify risk for uterine fibroids.

artículo científico publicado en 2017

Association between First Trimester Antidepressant Use and Risk of Spontaneous Abortion

artículo científico publicado en 2019

Association of uterine fibroids with birthweight and gestational age

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.

artículo científico publicado en 2014

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

Epidemiology of Functional Seizures Among Adults Treated at a University Hospital

artículo científico publicado en 2020

Erratum to: A multi-stage genome-wide association study of uterine fibroids in African Americans

artículo científico publicado en 2017

Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids

scientific article published on 03 September 2019

Evaluating power and type 1 error in large pedigree analyses of binary traits

artículo científico publicado en 2013

Evaluating risk factors for differences in fibroid size and number using a large electronic health record population

artículo científico publicado en 2018

Evidence of selection as a cause for racial disparities in fibroproliferative disease.

artículo científico publicado en 2017

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

Exploring epistasis in candidate genes for rheumatoid arthritis

artículo científico publicado en 2007

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.

artículo científico publicado en 2018

Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data

artículo científico publicado en 2010

Genetic analysis of biological pathway data through genomic randomization

artículo científico publicado en 2011

Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network

artículo científico publicado en 2019

Interpregnancy Interval After Pregnancy Loss and Risk of Repeat Miscarriage.

artículo científico publicado en 2017

LD-spline: mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium

artículo científico publicado en 2009

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

artículo científico publicado en 2016

Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program

scientific article published on 26 August 2019

Nonsteroidal Anti-inflammatory Drug Interaction with Prostacyclin Synthase Protects from Miscarriage

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

artículo científico publicado en 2016

Recurrent tissue-specific mtDNA mutations are common in humans

artículo científico publicado en 2013

The effects of linkage disequilibrium in large scale SNP datasets for MDR ⬇️

artículo científico publicado el 5 de mayo de 2011

The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery

artículo científico publicado en 2011

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women

Use of biological knowledge to inform the analysis of gene-gene interactions involved in modulating virologic failure with efavirenz-containing treatment regimens in ART-naïve ACTG clinical trials participants ⬇️

artículo científico publicado el 1 de enero de 2011

Validation of maternal recall of early pregnancy medication exposure using prospective diary data

artículo científico publicado en 2016

Week-by-week alcohol consumption in early pregnancy and spontaneous abortion risk: A prospective cohort study

scientific article published on 13 July 2020

Lista de obras de

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data

A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT.

A multi-stage genome-wide association study of uterine fibroids in African Americans

ASAP: an environment for automated preprocessing of sequencing data

African genetic ancestry interacts with body mass index to modify risk for uterine fibroids.

Association between First Trimester Antidepressant Use and Risk of Spontaneous Abortion

Association of uterine fibroids with birthweight and gestational age

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

Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.

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

Epidemiology of Functional Seizures Among Adults Treated at a University Hospital

Erratum to: A multi-stage genome-wide association study of uterine fibroids in African Americans

Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids

Evaluating power and type 1 error in large pedigree analyses of binary traits

Evaluating risk factors for differences in fibroid size and number using a large electronic health record population

Evidence of selection as a cause for racial disparities in fibroproliferative disease.

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

Exploring epistasis in candidate genes for rheumatoid arthritis

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.

Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data

Genetic analysis of biological pathway data through genomic randomization

Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network

Interpregnancy Interval After Pregnancy Loss and Risk of Repeat Miscarriage.

LD-spline: mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program

Nonsteroidal Anti-inflammatory Drug Interaction with Prostacyclin Synthase Protects from Miscarriage

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

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

Recurrent tissue-specific mtDNA mutations are common in humans

The effects of linkage disequilibrium in large scale SNP datasets for MDR ⬇️

The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women

Use of biological knowledge to inform the analysis of gene-gene interactions involved in modulating virologic failure with efavirenz-containing treatment regimens in ART-naïve ACTG clinical trials participants ⬇️

Validation of maternal recall of early pregnancy medication exposure using prospective diary data

Week-by-week alcohol consumption in early pregnancy and spontaneous abortion risk: A prospective cohort study