Public Health Genomics

Papers
(The median citation count of Public Health Genomics is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
Age-Based Genomic Screening: Pediatric Providers’ Perspectives on Implementation14
Understanding Social, Cultural, and Religious Factors Influencing Medical Decision-Making on BRCA1/2 Genetic Testing in the Orthodox Jewish Community12
Effect of Trust in Science on Parental Reactions to Messaging about Children’s Epigenetics-Related Obesity Risk11
Just Dissemination of Genomics-Informed Public Health Applications: Time to Deepen Our Public Engagement Approaches11
Health Literacy and Awareness of Family Health History in the All of Us Research Program10
Charting the Future of Clinical Genomics: An Implementation Science Lens10
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis8
Facilitating Equitable Access to Genomic Testing for Advanced Cancer: A Combined Intuition and Theory-Informed Approach to Intervention Development and Deployment8
Next-Generation Public Health Genomics: A Call to Assess the Equitable Implementation, Population Health Impact, and Sustainability of Precision Public Health Applications8
Your Family Connects: A Theory-Based Intervention to Encourage Communication about Possible Inherited Cancer Risk among Ovarian Cancer Survivors and Close Relatives6
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members6
Development, Evaluation, and User Testing of a Decision-Making Toolkit to Promote Organizations to Implement Universal Tumor Screening for Lynch Syndrome6
Workplace Genomic Testing: What Do Company Websites Say about Federal Privacy and Anti-Discrimination Laws?6
Implementing Genomic Medicine in a Federally Qualified Health Center: Assessing Readiness through a Mixed-Methods Approach6
Public Perspectives on Sharing Profits with Biospecimen Donors5
Associations of GST Gene Polymorphisms and GST Enzyme Activity with the Development of Noise-Induced Hearing Loss in Chinese Han Males5
Results from the Delivery of a Community Health Worker Training to Advance Competencies in Cancer Genomics5
Impact of <i>PD-L1</i> Gene Polymorphisms and Interactions with Cooking with Solid Fuel Exposure on Tuberculosis5
Evaluating Rural Ethiopian Youths’ Willingness and Competency to Promote Literacy Regarding G × E Influences on Podoconiosis4
A Genetic Counselor’s Reflections on Lessons Learned, Challenges, and Successes Experienced during a One-Year Pilot Integration in a Primary Care Clinic4
Acknowledgement to Reviewers3
Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research3
Psychometric Properties of a Culturally Adapted Spanish Version of the Attitudes toward Genomics and Precision Medicine Instrument3
Sociodemographic and Clinical Characteristics Associated with Genetic Testing among Cancer Survivors: Evidence from Three Cancer Registries3
Variation Exists in Service Delivery: Similarities and Differences in the Provision of a Whole Genome Sequencing Service for Paediatric Rare Disease Patients in the National Health Service in England3
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study3
Who’s on Your Genomics Research Team? Consumer Experiences from Australia2
Exploring Dutch Citizens’ Perspectives, Expectations, and Decision-Making Regarding Health-Related Direct-to-Consumer Genetic Testing2
Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study2
Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort2
Financial Advisers’ and Key Informants’ Perspectives on the Australian Industry-Led Moratorium on Genetic Tests in Life Insurance2
Single Nucleotide Polymorphisms in Orexin-1 and BDNF Receptor Genes are Associated with Increased Risk of Developing Postpartum Depression among Women with Gestational Diabetes Mellitus2
“Should I Let Them Know I Have This?”: Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes2
Democratizing Education for Sickle Cell Disease Gene Therapy: A Community-Based Model for Creating Patient Education Materials2
What Makes Families SHARE: The Family Communication Environments of Disseminators and Non-Disseminators of Family Cancer History2
Community Collaboration in Public Health Genetic Literacy: Methods for Co-Designing Educational Resources for Equitable Genomics Research and Practice2
ConnectMyVariant: An Innovative Use of Technology and Social Networks to Realize the Benefits of Cascade Screening2
Co-Creating the Experience of Consent for Newborn Genome Sequencing: The Generation Study2
Behavioral Changes after Psychiatric Genetic Counseling: An Exploratory Study2
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study1
Pediatric DTC Genetic Testing for Adult-Onset Inherited Cancer Risk: The Perspectives of High-Risk Parents1
Public Opinions and Attitudes toward Non-invasive Prenatal Testing on Reddit: Content and Sentiment Analysis1
Informational, Support, and Educational Needs of Parents of Children with Sickle Cell Trait1
Imagining Genomics and Population Health in 2050: Anticipating Future Research, Policy, and Governance Needs1
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study1
Streamlined Genetic Education and Cascade Testing in Men from Hereditary Breast Ovarian Cancer Families: A Randomized Trial1
Evaluating the Applied Knowledge of BRCA Testing among Spanish-Preferring Latino Americans: The Influence of Acculturation and Literacy1
Acknowledgement to Reviewers1
Employee Perspectives on Genetic Testing in the Workplace: Results from a National Survey1
The Path to Screening US Newborns for Severe Combined Immunodeficiency, 1968–2018: A Narrative Review of a Successful Biomedical Research and Public Health Partnership1
‘If I knew more… I would feel less worried’: Filipino Americans’ Attitudes and Knowledge of Genetic Disease, Counseling, and Testing1
Beyond the Flush: Reframing ALDH2 Deficiency as a Public Health Risk1
Human-Centered Design Study to Inform Traceback Cascade Genetic Testing Programs at Three Integrated Health Systems1
“I Didn't Have to Worry about It”: Patient and Family Experiences with Health System Involvement in Notifying Relatives of Genetic Test Results1
Adopting Public Health Genomics when the House Is on Fire: How Will We Navigate to 2030?1
Integrating Genomics into the Care of People with Palliative Needs: A Global Scoping Review of Policy Recommendations1
Call to Action for Advancing Equitable Genomic Newborn Screening1
Is Habitual Dietary Intake of Fats Associated with Apelin Gene Expression in Visceral and Subcutaneous Adipose Tissues and Its Serum Levels in Obese Adults?1
Advancing Implementation Science in Cancer Genomics: Progressing from Discovery to Population Health Benefit1
The Biggest Struggle: Navigating Trust and Uncertainty in Genetic Variant Interpretation1
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