Genomics is failing on diversity

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Effective recruitment and retention of minority research participants.

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Genetic Misdiagnoses and the Potential for Health Disparities

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Comprehensive Evaluation of Tamoxifen Sequential Biotransformation by the Human Cytochrome P450 System in Vitro: Prominent Roles for CYP3A and CYP2D6

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Genomics for the world

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Greenlandic Inuit show genetic signatures of diet and climate adaptation

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Next generation disparities in human genomics: concerns and remedies

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Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study

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Genome-wide association studies in pharmacogenomics

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Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine

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Clinical use of current polygenic risk scores may exacerbate health disparities

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The “All of Us” Research Program

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Genome-wide association studies

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The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource

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The Missing Diversity in Human Genetic Studies

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Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

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2025 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association

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Analysis of polygenic risk score usage and performance in diverse human populations

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Genetic analyses of diverse populations improves discovery for complex traits

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Cancer health disparities in racial/ethnic minorities in the United States

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Addressing bias in big data and AI for health care: A call for open science

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The “All of Us” Research Program

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A catalog of genetic loci associated with kidney function from analyses of a million individuals

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Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations

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Improving polygenic prediction in ancestrally diverse populations

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Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

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Paediatric genomics: diagnosing rare disease in children

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Applications of machine learning to diagnosis and treatment of neurodegenerative diseases

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Gender equality in science, medicine, and global health: where are we at and why does it matter?

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15 years of GWAS discovery: Realizing the promise

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Discovery of common and rare genetic risk variants for colorectal cancer

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Enabling Technologies for Personalized and Precision Medicine

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Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

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The Human Pangenome Project: a global resource to map genomic diversity

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A framework for enhancing ethical genomic research with Indigenous communities

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Variable prediction accuracy of polygenic scores within an ancestry group

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The GenomeAsia 100K Project enables genetic discoveries across Asia

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A scientometric review of genome-wide association studies

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Prioritizing diversity in human genomics research

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Axes of a revolution: challenges and promises of big data in healthcare

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Genetics of Parkinson's disease: An introspection of its journey towards precision medicine

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Assembly of a pan-genome from deep sequencing of 910 humans of African descent

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Diversity and inclusion in genomic research: why the uneven progress?

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Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

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Personalized Medicine and the Power of Electronic Health Records

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Lack of diversity in genomic databases is a barrier to translating precision medicine research into practice

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Stress-Related Biosocial Mechanisms of Discrimination and African American Health Inequities

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Multi-omic measurements of heterogeneity in HeLa cells across laboratories

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Strategic vision for improving human health at The Forefront of Genomics

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Challenges and opportunities to meet the mental health needs of underserved and disenfranchised populations in the United States

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The Missing Diversity in Human Genetic Studies

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2026 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association

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The gut microbiome and hypertension

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Predicting Polygenic Risk of Psychiatric Disorders

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The influence of evolutionary history on human health and disease

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Comprehensive omic characterization of breast cancer in Mexican-Hispanic women

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Multiethnic polygenic risk scores improve risk prediction in diverse populations

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Diversity and inclusion for the All of Us research program: A scoping review

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Enrollment of Racial Minorities in Clinical Trials: Old Problem Assumes New Urgency in the Age of Immunotherapy

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Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese

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H3Africa: current perspectives

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Genetics of Common, Complex Coronary Artery Disease

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Treating health disparities with artificial intelligence

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Precision Medicine from a Public Health Perspective

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Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

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Severe hypertriglyceridemia is primarily polygenic

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Genomic Research Through an Indigenous Lens: Understanding the Expectations

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From target discovery to clinical drug development with human genetics

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Public human microbiome data are dominated by highly developed countries

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

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Association of Neighborhood-Level Disadvantage With Alzheimer Disease Neuropathology

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Genetic disease risks can be misestimated across global populations

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The Challenge of Genetic Variants of Uncertain Clinical Significance

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Genotyping Array Design and Data Quality Control in the Million Veteran Program

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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

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Rare disease emerging as a global public health priority

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Revolutionizing clinical trials: the role of AI in accelerating medical breakthroughs

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The road ahead in genetics and genomics

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African genetic diversity and adaptation inform a precision medicine agenda

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Examining How Race, Ethnicity, and Ancestry Data Are Used in Biomedical Research

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Latin Americans show wide-spread Converso ancestry and imprint of local Native ancestry on physical appearance

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

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Demographics of physics education research

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