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 2021-11-01 to 2025-11-01.)
ArticleCitations
Age-Based Genomic Screening: Pediatric Providers’ Perspectives on Implementation11
Effect of Trust in Science on Parental Reactions to Messaging about Children’s Epigenetics-Related Obesity Risk9
Understanding Social, Cultural, and Religious Factors Influencing Medical Decision-Making on BRCA1/2 Genetic Testing in the Orthodox Jewish Community9
Just Dissemination of Genomics-Informed Public Health Applications: Time to Deepen Our Public Engagement Approaches9
Next-Generation Public Health Genomics: A Call to Assess the Equitable Implementation, Population Health Impact, and Sustainability of Precision Public Health Applications8
Development, Evaluation, and User Testing of a Decision-Making Toolkit to Promote Organizations to Implement Universal Tumor Screening for Lynch Syndrome7
Workplace Genomic Testing: What Do Company Websites Say about Federal Privacy and Anti-Discrimination Laws?7
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis7
Your Family Connects: A Theory-Based Intervention to Encourage Communication about Possible Inherited Cancer Risk among Ovarian Cancer Survivors and Close Relatives7
Facilitating Equitable Access to Genomic Testing for Advanced Cancer: A Combined Intuition and Theory-Informed Approach to Intervention Development and Deployment7
Associations of GST Gene Polymorphisms and GST Enzyme Activity with the Development of Noise-Induced Hearing Loss in Chinese Han Males6
Impact of <i>PD-L1</i> Gene Polymorphisms and Interactions with Cooking with Solid Fuel Exposure on Tuberculosis6
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members6
A Genetic Counselor’s Reflections on Lessons Learned, Challenges, and Successes Experienced during a One-Year Pilot Integration in a Primary Care Clinic5
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice5
Acknowledgement to Reviewers5
Associations between <b><i>TNFAIP3</i></b> Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis5
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study5
Results from the Delivery of a Community Health Worker Training to Advance Competencies in Cancer Genomics5
Evaluating Rural Ethiopian Youths’ Willingness and Competency to Promote Literacy Regarding G × E Influences on Podoconiosis5
Psychometric Properties of a Culturally Adapted Spanish Version of the Attitudes toward Genomics and Precision Medicine Instrument5
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study4
Financial Advisers’ and Key Informants’ Perspectives on the Australian Industry-Led Moratorium on Genetic Tests in Life Insurance3
Screening of Serum miRNAs as Diagnostic Biomarkers for Lung Cancer Using the Minimal-Redundancy-Maximal-Relevance Algorithm and Random Forest Classifier Based on a Public Database3
Who’s on Your Genomics Research Team? Consumer Experiences from Australia3
Community Collaboration in Public Health Genetic Literacy: Methods for Co-Designing Educational Resources for Equitable Genomics Research and Practice3
Knowledge and Attitudes about Privacy and Secondary Data Use among African-Americans Using Direct-to-Consumer Genetic Testing3
Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research3
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions3
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
Exploring Dutch citizens’ perspectives, expectations, and decision-making regarding health-related direct-to-consumer genetic testing (DTC-GT)3
Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study2
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
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic2
Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort2
“Should I Let Them Know I Have This?”: Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes2
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects1
Integrating Genomics into the Care of People with Palliative Needs: A Global Scoping Review of Policy Recommendations1
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
Informational, Support, and Educational Needs of Parents of Children with Sickle Cell Trait1
The Biggest Struggle: Navigating Trust and Uncertainty in Genetic Variant Interpretation1
Call to Action for Advancing Equitable Genomic Newborn Screening1
Adopting Public Health Genomics when the House Is on Fire: How Will We Navigate to 2030?1
Public Opinions and Attitudes toward Non-invasive Prenatal Testing on Reddit: Content and Sentiment Analysis1
Genetic Variants in <b><i>MIR3142HG</i></b> Contribute to the Predisposition of IgA Nephropathy in a Chinese Han Population1
‘If I knew more… I would feel less worried’: Filipino Americans’ Attitudes and Knowledge of Genetic Disease, Counseling, and Testing1
Evaluating the Applied Knowledge of BRCA Testing among Spanish-Preferring Latino Americans: The Influence of Acculturation and Literacy1
Pediatric DTC Genetic Testing for Adult-Onset Inherited Cancer Risk: The Perspectives of High-Risk Parents1
“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation1
An Electronic Health Record Tool Increases Genetic Counseling Referral of Individuals at Hereditary Cancer Risk: An Intervention Study1
Acknowledgement to Reviewers1
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study1
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