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 2020-03-01 to 2024-03-01.)
ArticleCitations
Impact of Previous Genetic Counseling and Objective Numeracy on Accurate Interpretation of a Pharmacogenetics Test Report11
Identifying Aspects of Public Attitudes Toward Whole Genome Sequencing to Inform the Integration of Genomics into Care10
Genetic Variation and Evolution of the 2019 Novel Coronavirus9
Stakeholders’ Interest and Attitudes toward Genomic Medicine and Pharmacogenomics Implementation in the United Arab Emirates: A Qualitative Study8
p53 Mutation at Serine 249 and Its Gain of Function Are Highly Related to Hepatocellular Carcinoma after Smoking Exposure7
“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
The Perception of Premarital Genetic Screening within Young Jordanian Individuals5
Oncologists’ Perceptions of Tumor Genomic Profiling and the Communication of Test Results and Risks5
Comparative Genome-Wide Characterization of Microsatellites in <b><i>Candida albicans</i></b> and <b><i>Candida dubliniensis</i></b> Leading to the Deve5
Practices and Attitudes toward Returning Genomic Research Results to Low-Resource Research Participants5
Ethical Aspects of Genotype Disclosure: Perceptions of Participants in a Nutrigenetic Study in Finland5
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects4
The Belgian DNA Debate: An Online Deliberative Platform on the Ethical, Legal, and Social Issues of Genomics4
A Case-Control Study of the Luteinizing Hormone Level in Luteinizing Hormone Receptor Gene (rs2293275) Polymorphism in Polycystic Ovarian Syndrome Females4
“Integrating China in the International Consortium for Personalized Medicine”: The Coordination and Support Action to Foster Collaboration in Personalized Medicine Development between Europe and China4
Development and Validation of a Comprehensive Genomics Knowledge Scale4
Experiences of Latino Participants Receiving Neutral Genomic Screening Results: A Qualitative Study3
Teenagers and Precision Psychiatry: A Window of Opportunity3
Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India3
Development of an Implementation Framework for Overcoming Underdiagnoses of Familial Hypercholesterolemia in the USA3
Investigation of the Association between 45 Tag SNPs and Type 2 Diabetes Mellitus in Han Chinese Adults: A Prospective Cohort 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
Secondary Data Usage in Direct-to-Consumer Genetic Testing: To What Extent Are Customers Aware and Concerned?2
Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study2
Contribution of XPD and XPF Polymorphisms to Susceptibility of Non-Small Cell Lung Cancer in High-Altitude Areas2
Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing2
Role of Metabolic Risk Factors, Family History, and Genetic Polymorphisms (PPARγ and TCF7L2) on Type 2 Diabetes Mellitus Risk in an Asian Indian Population2
Meta-Analyses of Multiple Gene Expression Profiles to Screen Hub Genes Related to Osteoarthritis2
Factors Influencing Discussion of Cancer Genetic Testing with Health-Care Providers in a Population-Based Survey2
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations2
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions2
Comparison of a Cancer Family History Collection and Risk Assessment Tool – ItRunsInMyFamily – with Risk Assessment by Health-Care Professionals2
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities2
Behavioral Changes after Psychiatric Genetic Counseling: An Exploratory Study2
Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by <b><i>TMEM43</i></b> p.S358L1
Financial Advisers’ and Key Informants’ Perspectives on the Australian Industry-Led Moratorium on Genetic Tests in Life Insurance1
Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A <b><i>BRCA</i></b> Pilot Study1
“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation1
Genotype-Phenotype Analysis of 8q24.3 Duplication and 21q22.3 Deletion in a Chinese Patient and Literature Review1
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research1
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
Call to Action for Advancing Equitable Genomic Newborn Screening1
Altruism as an Explanation for Human Consanguinity1
Genetic Testing in Natural History Studies: A Review of the Regulatory and Legal Landscape1
Genetic Testing and Other Healthcare Use by Black and White Individuals in a Genomic Sequencing Study1
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic1
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
Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research1
<i>MTNR1B</i> rs1387153 Polymorphism and Risk of Gestational Diabetes Mellitus: Meta-Analysis and Trial Sequential Analysis1
Motivating and Discouraging Factors for Bipolar Patient Participation in Genomic Research1
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