| Health Data in Dentistry: An Attempt to Master the Digital Challenge |
8 |
| Developing a Process for Returning Medically Actionable Genomic Variant to Latino Patient in a Federally Qualified Health Center |
5 |
| Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland: Findings from an International Workshop |
4 |
| Personalised Nutrition Technologies and Innovations: A Cross-National Survey of Registered Dietitians |
3 |
| Do Women who Receive a Negative BRCA1/2 Risk Result Understand the Implications for Breast Cancer Risk? |
3 |
| Genetic Knowledge within a National Australian Sample: Comparisons with Other Diverse Populations |
3 |
| Optimising SME Potential in Modern Healthcare Systems: Challenges, Opportunities and Policy Recommendations |
3 |
| Beyond Public Health Genomics: Can Big Data and Predictive Analytics Deliver Precision Public Health? |
3 |
| Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines |
3 |
| Lifestyle Interventions for Weight Control Modified by Genetic Variation: A Review of the Evidence |
3 |
| Generic Cost-Effectiveness Models: A Proof of Concept of a Tool for Informed Decision-Making for Public Health Precision Medicine |
3 |
| Identifying Perceptions and Preferences of the General Public Concerning Universal Screening of Children for Familial Hypercholesterolaemia |
2 |
| The Value of Diagnostic Information in Personalised Healthcare: A Comprehensive Concept to Facilitate Bringing This Technology into Healthcare Systems |
2 |
| Epigenetic Risk Assessment of Female Cancers: Women's Information Needs and Attitudes |
2 |
| Ethical, Legal, and Regulatory Issues for the Implementation of Omics-Based Risk Prediction of Women's Cancer: Points to Consider |
2 |
| Factors Associated with Acceptability, Consideration and Intention of Uptake of Direct-To-Consumer Genetic Testing: A Survey Study |
2 |
| Use and Impact of the 21-Gene Recurrence Score in Relation to Clinical Risk of Developing Metastases in Early Breast Cancer Patient in the Netherlands |
2 |
| Current Social Media Conversations about Genetics and Genomics in Health: A Twitter-Based Analysis |
2 |
| Southeast Asian Pharmacogenomics Research Network (SEAPharm): Current Status and Perspectives |
2 |
| Factors Influencing Not Perceiving Family Health History Assessments as Important: Opportunities to Improve Dissemination of Evidence-Based Population Screening for Cancer |
1 |
| Family History Taking in Pediatric Practice: A Qualitative Interview Study |
1 |
| Psychosocial and Cultural Determinants of Interest and Uptake of Skin Cancer Genetic Testing in Diverse Primary Care |
1 |
| Syndromic Oral Clefts: Challenges of Genetic Assessment in Brazil and Suggestions to Improve Health Policies |
1 |
| Access to Cancer Precision Medicines in Switzerland: A Comparative Analysis (USA and EU) and Health Policy Implications |
1 |
| Recall and Retention of Consent Procedure Contents and Decisions: Results of a Randomized Controlled Trial |
1 |
| Implementation of a Carrier Screening Program in a High-Risk Undergraduate Student Population Using Digital Marketing, Online Education, and Telehealth |
1 |
| Multiple Stakeholder Views on Data Sharing in a Biobank in an Integrated Healthcare Delivery System: Implications for Biobank Governance |
1 |
| Understanding Factors Associated with Uptake of BRCA1/2 Genetic Testing among Orthodox Jewish Women in the USA Using a Mixed-Methods Approach |
0 |
| The Creation and Management of Innovations in Healthcare and ICT: The European and African Experience |
0 |
| How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family HealthLink |
0 |
| Controversies among Cancer Registry Participants, Genomic Researchers, and Institutional Review Boards about Returning Participants' Genomic Results |
0 |
| Public Understanding and Opinions regarding Genetic Research on Alzheimer's Disease |
0 |
| Personal Genetic Information about HIV: Research Participants' Views of Ethical, Social, and Behavioral Implications |
0 |
| Psychological Impact of Learning CDKN2A Variant Status as a Genetic Research Result |
0 |
| Making the Most of Innovation in Personalised Medicine: An EU Strategy for a Faster Bench to Bedside and Beyond Process |
0 |
| Healthcare System-Funded Preventive Genomic Screening: Challenges for Australia and Other Single-Payer Systems |
0 |
