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 2020-11-01 to 2024-11-01.)
ArticleCitations
Identifying Aspects of Public Attitudes Toward Whole Genome Sequencing to Inform the Integration of Genomics into Care12
Impact of Previous Genetic Counseling and Objective Numeracy on Accurate Interpretation of a Pharmacogenetics Test Report11
Stakeholders’ Interest and Attitudes toward Genomic Medicine and Pharmacogenomics Implementation in the United Arab Emirates: A Qualitative Study11
Genetic Variation and Evolution of the 2019 Novel Coronavirus9
Oncologists’ Perceptions of Tumor Genomic Profiling and the Communication of Test Results and Risks9
p53 Mutation at Serine 249 and Its Gain of Function Are Highly Related to Hepatocellular Carcinoma after Smoking Exposure8
Development and Validation of a Comprehensive Genomics Knowledge Scale7
Comparative Genome-Wide Characterization of Microsatellites in <b><i>Candida albicans</i></b> and <b><i>Candida dubliniensis</i></b> Leading to the Deve7
“We-Diseases” and Dyadic Decision-Making Processes: A Critical Perspective7
Formative Evaluation of the Families SHARE Disease Risk Tool among Low-Income African Americans6
Genetic Variation of Glutathione S-Transferase M1 Is Associated with Patients with Ovarian Endometriosis and Endometriosis-Related Primary Infertility6
“Integrating China in the International Consortium for Personalized Medicine”: The Coordination and Support Action to Foster Collaboration in Personalized Medicine Development between Europe and China6
Practices and Attitudes toward Returning Genomic Research Results to Low-Resource Research Participants6
Call to Action for Advancing Equitable Genomic Newborn Screening5
Ethical Aspects of Genotype Disclosure: Perceptions of Participants in a Nutrigenetic Study in Finland5
The Belgian DNA Debate: An Online Deliberative Platform on the Ethical, Legal, and Social Issues of Genomics5
The Perception of Premarital Genetic Screening within Young Jordanian Individuals5
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects4
Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India4
A Case-Control Study of the Luteinizing Hormone Level in Luteinizing Hormone Receptor Gene (rs2293275) Polymorphism in Polycystic Ovarian Syndrome Females4
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations4
Investigation of the Association between 45 Tag SNPs and Type 2 Diabetes Mellitus in Han Chinese Adults: A Prospective Cohort Study4
Meta-Analyses of Multiple Gene Expression Profiles to Screen Hub Genes Related to Osteoarthritis4
Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing4
Experiences of Latino Participants Receiving Neutral Genomic Screening Results: A Qualitative Study3
Challenges and Opportunities for Communication about the Role of Genomics in Public Health3
Gene Hunting Approaches through the Combination of Linkage Analysis with Whole-Exome Sequencing in Mendelian Diseases: From Darwin to the Present Day3
Contribution of XPD and XPF Polymorphisms to Susceptibility of Non-Small Cell Lung Cancer in High-Altitude Areas3
Associations between <b><i>TNFAIP3</i></b> Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis3
Teenagers and Precision Psychiatry: A Window of Opportunity3
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions3
Human-Centered Design Study to Inform Traceback Cascade Genetic Testing Programs at Three Integrated Health Systems3
Development of an Implementation Framework for Overcoming Underdiagnoses of Familial Hypercholesterolemia in the USA3
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities2
Factors Influencing Discussion of Cancer Genetic Testing with Health-Care Providers in a Population-Based Survey2
Behavioral Changes after Psychiatric Genetic Counseling: An Exploratory Study2
Financial Advisers’ and Key Informants’ Perspectives on the Australian Industry-Led Moratorium on Genetic Tests in Life Insurance2
Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study2
Next-Generation Public Health Genomics: A Call to Assess the Equitable Implementation, Population Health Impact, and Sustainability of Precision Public Health Applications2
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study2
Future Forecasting for Research and Practice in Genetic Literacy2
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research2
Digital Health Tools in Genomics: Advancing Diversity, Equity, and Inclusion2
Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research2
Integrating China in the International Consortium for Personalized Medicine: A Position Paper on Personalized Medicine in Sustainable Healthcare2
Genotype-Phenotype Analysis of 8q24.3 Duplication and 21q22.3 Deletion in a Chinese Patient and Literature Review2
Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by <b><i>TMEM43</i></b> p.S358L2
Role of Metabolic Risk Factors, Family History, and Genetic Polymorphisms (PPARγ and TCF7L2) on Type 2 Diabetes Mellitus Risk in an Asian Indian Population2
Comparison of a Cancer Family History Collection and Risk Assessment Tool – ItRunsInMyFamily – with Risk Assessment by Health-Care Professionals2
Your Family Connects: A Theory-Based Intervention to Encourage Communication about Possible Inherited Cancer Risk among Ovarian Cancer Survivors and Close Relatives2
Secondary Data Usage in Direct-to-Consumer Genetic Testing: To What Extent Are Customers Aware and Concerned?1
Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A <b><i>BRCA</i></b> Pilot Study1
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 Database1
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis1
Evaluating Rural Ethiopian Youths’ Willingness and Competency to Promote Literacy Regarding G × E Influences on Podoconiosis1
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic1
Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network1
Genetic Variants in <b><i>MIR3142HG</i></b> Contribute to the Predisposition of IgA Nephropathy in a Chinese Han Population1
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
Understanding Social, Cultural, and Religious Factors Influencing Medical Decision-Making on BRCA1/2 Genetic Testing in the Orthodox Jewish Community1
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice1
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 China1
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members1
Altruism as an Explanation for Human Consanguinity1
Genetic Testing in Natural History Studies: A Review of the Regulatory and Legal Landscape1
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results1
Motivating and Discouraging Factors for Bipolar Patient Participation in Genomic Research1
ConnectMyVariant: An Innovative Use of Technology and Social Networks to Realize the Benefits of Cascade Screening1
0.022974967956543