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 2021-08-01 to 2025-08-01.)
ArticleCitations
Age-Based Genomic Screening: Pediatric Providers’ Perspectives on Implementation11
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research10
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 Community8
Just Dissemination of Genomics-Informed Public Health Applications: Time to Deepen Our Public Engagement Approaches8
Facilitating Equitable Access to Genomic Testing for Advanced Cancer: A Combined Intuition and Theory-Informed Approach to Intervention Development and Deployment6
Next-Generation Public Health Genomics: A Call to Assess the Equitable Implementation, Population Health Impact, and Sustainability of Precision Public Health Applications6
Your Family Connects: A Theory-Based Intervention to Encourage Communication about Possible Inherited Cancer Risk among Ovarian Cancer Survivors and Close Relatives5
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members5
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis5
Workplace Genomic Testing: What Do Company Websites Say about Federal Privacy and Anti-Discrimination Laws?5
Impact of <i>PD-L1</i> Gene Polymorphisms and Interactions with Cooking with Solid Fuel Exposure on Tuberculosis5
Development, Evaluation, and User Testing of a Decision-Making Toolkit to Promote Organizations to Implement Universal Tumor Screening for Lynch Syndrome5
Associations of GST Gene Polymorphisms and GST Enzyme Activity with the Development of Noise-Induced Hearing Loss in Chinese Han Males5
Associations between <b><i>TNFAIP3</i></b> Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis4
A Genetic Counselor’s Reflections on Lessons Learned, Challenges, and Successes Experienced during a One-Year Pilot Integration in a Primary Care Clinic4
Evaluating Rural Ethiopian Youths’ Willingness and Competency to Promote Literacy Regarding G × E Influences on Podoconiosis4
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice4
Acknowledgement to Reviewers4
Results from the Delivery of a Community Health Worker Training to Advance Competencies in Cancer Genomics4
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study3
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
Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research3
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study3
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
Financial Advisers’ and Key Informants’ Perspectives on the Australian Industry-Led Moratorium on Genetic Tests in Life Insurance2
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic2
Community Collaboration in Public Health Genetic Literacy: Methods for Co-Designing Educational Resources for Equitable Genomics Research and Practice2
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations2
Exploring Dutch citizens’ perspectives, expectations, and decision-making regarding health-related direct-to-consumer genetic testing (DTC-GT)2
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions2
Behavioral Changes after Psychiatric Genetic Counseling: An Exploratory Study2
Knowledge and Attitudes about Privacy and Secondary Data Use among African-Americans Using Direct-to-Consumer Genetic Testing2
Adopting Public Health Genomics when the House Is on Fire: How Will We Navigate to 2030?1
Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort1
Integrating Genomics into the Care of People with Palliative Needs: A Global Scoping Review of Policy Recommendations1
An Electronic Health Record Tool Increases Genetic Counseling Referral of Individuals at Hereditary Cancer Risk: An Intervention Study1
“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation1
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects1
Pediatric DTC Genetic Testing for Adult-Onset Inherited Cancer Risk: The Perspectives of High-Risk Parents1
ConnectMyVariant: An Innovative Use of Technology and Social Networks to Realize the Benefits of Cascade Screening1
“Should I Let Them Know I Have This?”: Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes1
Identification of Candidate Genes in Early-Stage Invasive Ductal Carcinoma Patients with High-Risk Mortality Using Genes Commonly Involved in Breast Cancer: A Retrospective Study1
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
Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study1
Co-Creating the Experience of Consent for Newborn Genome Sequencing: The Generation Study1
Public Opinions and Attitudes toward Non-invasive Prenatal Testing on Reddit: Content and Sentiment Analysis1
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
Call to Action for Advancing Equitable Genomic Newborn Screening1
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