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Lista de obras de Lucia A Hindorff

A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans

artículo científico publicado en 2019

A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains

artículo científico publicado en 2011

A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog

artículo científico publicado en 2018

A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.

artículo científico publicado en 2016

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

artículo científico publicado en 2013

A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study.

artículo científico publicado en 2013

Alaska Native genomic research: perspectives from Alaska Native leaders, federal staff, and biomedical researchers

artículo científico publicado en 2020

Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study

artículo científico publicado en 2014

Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

scientific article published on 14 March 2020

Angiotensin II type 1 receptor polymorphisms in the cardiovascular health study: relation to blood pressure, ethnicity, and cardiovascular events

artículo científico publicado en 2002

Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings

artículo científico publicado en 2018

Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study

artículo científico publicado en 2014

Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study

artículo científico publicado en 2011

Association of genetic variations with nonfatal venous thrombosis in postmenopausal women.

artículo científico

Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events

artículo científico publicado en 2006

Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE study

artículo científico publicado en 2013

Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study

scientific article published on 01 February 2008

Associations between incident ischemic stroke events and stroke and cardiovascular disease-related genome-wide association studies single nucleotide polymorphisms in the Population Architecture Using Genomics and Epidemiology study

artículo científico publicado en 2012

Beta2-adrenergic receptor polymorphisms and risk of incident cardiovascular events in the elderly

artículo científico publicado en 2003

CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record

artículo científico publicado en 2015

Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.

artículo científico publicado en 2017

Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke

artículo científico publicado en 2008

Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures

artículo científico publicado en 2020

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

artículo científico publicado en 2016

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

article

Common genetic variation in six lipid-related and statin-related genes, statin use and risk of incident nonfatal myocardial infarction and stroke

scientific article published on August 2008

Common genetic variation in the prothrombin gene, hormone therapy, and incident nonfatal myocardial infarction in postmenopausal women

scientific article published on 08 February 2006

Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: the Cardiovascular Health Study

artículo científico publicado en 2007

Common variation in cytochrome P450 epoxygenase genes and the risk of incident nonfatal myocardial infarction and ischemic stroke.

artículo científico publicado en 2008

Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) Consortium

artículo científico publicado en 2012

Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

artículo científico publicado en 2017

Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

scientific article published on 01 May 2019

Defining and Achieving Health Equity in Genomic Medicine

scientific article published on 21 February 2019

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

artículo científico publicado en 2014

Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study

scientific article published on 01 August 2018

Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study

artículo científico publicado en 2013

Enhancing diversity to reduce health information disparities and build an evidence base for genomic medicine

artículo científico publicado en 2018

Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study

artículo científico publicado en 2012

Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval

artículo científico publicado en 2014

Expression of a Cloned Cyclopropane Fatty Acid Synthase Gene Reduces Solvent Formation in Clostridium acetobutylicum ATCC 824 ⬇️

artículo científico publicado el 1 de mayo de 2003

Family history of diabetes as a potential public health tool.

artículo científico publicado en 2003

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

artículo científico publicado en 2017

Finding the missing heritability of complex diseases

artículo científico publicado en 2009

Fine Mapping and Identification of BMI Loci in African Americans

artículo científico publicado en 2013

Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations

artículo científico publicado en 2016

Fine-mapping and initial characterization of QT interval loci in African Americans

artículo científico publicado en 2012

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

artículo científico publicado en 2016

GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE study

artículo científico publicado en 2018

Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits

Genetic analyses of diverse populations improves discovery for complex traits

scientific article published on 19 June 2019

Genetic architecture of cancer and other complex diseases: lessons learned and future directions

artículo científico publicado en 2011

Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.

artículo científico publicado en 2017

Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study

artículo científico publicado en 2013

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2013

Genetic variants of coagulation factor XIII, postmenopausal estrogen therapy, and risk of nonfatal myocardial infarction

artículo científico publicado en 2002

Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study

artículo científico publicado en 2013

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

artículo científico publicado en 2017

Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

artículo científico publicado en 2017

Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative

artículo científico publicado en 2012

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

artículo científico publicado en 2013

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

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

artículo científico publicado en 2020

Motivating factors for physician ordering of factor V Leiden genetic tests

artículo científico publicado en 2009

Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

artículo científico publicado en 2020

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 clear link between VKORC1 genetic polymorphism and the risk of venous thrombosis or peripheral arterial disease

scholarly article by Marie-Anne Loriot et al published 2008 in Thrombosis and Haemostasis

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

artículo científico publicado en 2013

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

artículo científico publicado en 2013

Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study

artículo científico publicado en 2015

Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia

artículo científico publicado en 2014

Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia

artículo científico publicado en 2013

Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium

artículo científico publicado en 2014

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

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

artículo científico publicado en 2009

Prioritizing diversity in human genomics research.

artículo científico publicado en 2017

Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study

artículo científico publicado en 2014

Recommendations for the integration of genomics into clinical practice

artículo científico

Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.

artículo científico publicado en 2014

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

article

Simple estimates of haplotype relative risks in case-control data

artículo científico publicado en 2006

Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array

artículo científico publicado en 2016

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

artículo científico publicado en 2013

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations

artículo científico publicado en 2018

The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research

scientific article published on 16 May 2019

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

artículo científico publicado en 2014

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019

artículo científico publicado en 2019

The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

artículo científico publicado en 2011

The association of PAI-1 promoter 4G/5G insertion/deletion polymorphism with myocardial infarction and stroke in young women

scientific article published on 01 April 2002

The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics

artículo científico publicado en 2018

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

artículo científico publicado en 2018

The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study

artículo científico publicado en 2013

The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

artículo científico publicado en 2016

Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci

artículo científico publicado en 2017

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained

artículo científico publicado en 2013

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

artículo científico publicado en 2017

Use of Factor V Leiden genetic testing in practice and impact on management

artículo científico publicado en 2009

Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

artículo científico publicado en 2016

Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke

artículo científico publicado en 2007

WikiGWA: an open platform for collecting and using genome-wide association results

artículo científico publicado en 2013

beta(2)-Adrenergic receptor polymorphisms and determinants of cardiovascular risk: the Cardiovascular Health Study

artículo científico publicado en 2005

beta1- and beta2-adrenergic receptor gene variation, beta-blocker use and risk of myocardial infarction and stroke

scientific article published on 24 January 2008

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