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 2021-04-01 to 2025-04-01.)
ArticleCitations
ConnectMyVariant: An Innovative Use of Technology and Social Networks to Realize the Benefits of Cascade Screening7
A new agenda for implementing population genomic screening7
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice6
Results from the Delivery of a Community Health Worker Training to Advance Competencies in Cancer Genomics5
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research4
Association between Genetic Polymorphisms of <b><i>MIR3142HG</i></b> and the Risk of Steroid-Induced Osteonecrosis of the Femoral Head in the Population of Northern China4
Acknowledgement to Reviewers4
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic4
A Genetic Counselor’s Reflections on Lessons Learned, Challenges, and Successes Experienced during a One-Year Pilot Integration in a Primary Care Clinic4
Associations between <b><i>TNFAIP3</i></b> Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis4
‘If I knew more… I would feel less worried’: Filipino Americans’ Attitudes and Knowledge of Genetic Disease, Counseling, and Testing4
“We-Diseases” and Dyadic Decision-Making Processes: A Critical Perspective4
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations3
“Should I Let Them Know I Have This?”: Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes3
Co-Creating the Experience of Consent for Newborn Genome Sequencing: The Generation Study3
Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing2
The Biggest Struggle: Navigating Trust and Uncertainty in Genetic Variant Interpretation2
Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort2
Evaluating Rural Ethiopian Youths’ Willingness and Competency to Promote Literacy Regarding G × E Influences on Podoconiosis2
Future Forecasting for Research and Practice in Genetic Literacy2
Development and Pilot Testing of Evidence-Based Interventions to Improve Adherence after Receiving a Genetic Result2
Just Dissemination of Genomics-Informed Public Health Applications: Time to Deepen Our Public Engagement Approaches2
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study2
Behavioral Changes after Psychiatric Genetic Counseling: An Exploratory Study2
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study2
Placing Publics in Public Health Genomics1
Pediatric DTC Genetic Testing for Adult-Onset Inherited Cancer Risk: The Perspectives of High-Risk Parents1
Integrating Genomics into the Care of People with Palliative Needs: A Global Scoping Review of Policy Recommendations1
Mapping Users’ Experience of a Family History and Genetic Risk Algorithm Tool in Primary Care1
Understanding Social, Cultural, and Religious Factors Influencing Medical Decision-Making on BRCA1/2 Genetic Testing in the Orthodox Jewish Community1
“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 China in the International Consortium for Personalized Medicine: A Position Paper on Personalized Medicine in Sustainable Healthcare1
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study1
Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India1
Effect of Trust in Science on Parental Reactions to Messaging about Children’s Epigenetics-Related Obesity Risk1
Acknowledgement to Reviewers1
We Need to Stand Together on the Shoulders of Giants: Consolidating Effective Approaches for Translating Genomics into Practice with Implementation Science1
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities1
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis1
Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study1
Receiving a Pathogenic Variant in a Population Breast Cancer Screening Trial: A Mixed Method Study1
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