Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollment

15 May 2023

Abstract excerpt

PURPOSE: Persistent inequities in genomic medicine and research contribute to health disparities. This analysis uses a context-specific and equity-focused strategy to evaluate enrollment patterns for Genomic Answers for Kids (GA4K), a large, metropolitan-wide genomic study on children. METHODS: Electronic health records for 2247 GA4K study participants were used to evaluate the distribution of individuals by...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to BRCA gene mutations in cancer
Share to Ethics in Clinical Research
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37194653
DOI: 10.1016/j.gim.2023.100895

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollmentPMID 37194653Read ↗

Advancing Understanding of Inequities in Rare Disease GenomicsSemantic proximity Read ↗

A Framework for Promoting Diversity, Equity, and Inclusion in Genetics and Genomics ResearchSemantic proximity Read ↗

Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.Semantic proximity Read ↗

Defining and Achieving Health Equity in Genomic MedicineSemantic proximity Read ↗

Reducing Time to Diagnosis of Rare Genetic Diseases in a Medically Underserved Hispanic Population- Lessons Learned for Meaningful EngagementSemantic proximity Read ↗

Next-Generation Public Health Genomics: A Call to Assess the Equitable Implementation, Population Health Impact, and Sustainability of Precision Public Health ApplicationsSemantic proximity Read ↗

Genomics in Public Health: Perspective from the Office of Public Health Genomics at the Centers for Disease Control and Prevention (CDC)Semantic proximity Read ↗

Landscape of racial and ethnic health disparities in the All of Us Research ProgramSemantic proximity Read ↗

Disparity in Access to Oncology Precision Care: A Geospatial Analysis of Driving Distances to Genetic Counselors in the U.S.Semantic proximity Read ↗

Linking Place-Based Exposures and Genomics to understand Human PhenotypesSemantic proximity Read ↗

Linking Place-Based Exposures and Genomics to understand Human PhenotypesSemantic proximity Read ↗

Beyond race: Recruitment of diverse participants in clinical genomics research for rare diseaseSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.