Lucia A. Hindorff

Advancing genomics to improve health equity

The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource

Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods

Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium

US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)

Variant Interpretation for Dilated Cardiomyopathy

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

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

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

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

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

Genetic analyses of diverse populations improves discovery for complex traits

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

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

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

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

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

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

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

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

Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy

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

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

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

Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI

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

Recommendations for the integration of genomics into clinical practice

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

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

Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations