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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 19, 2024
. (Total: 63627 Documents since 2012)
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A qualitative feasibility study of a prototype patient-centered video intervention to increase uptake of cancer genetic testing among Black Americans.
Katherine Clegg Smith et al. Pilot Feasibility Stud 2024 10(1) 62
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Contextual factors influencing the equitable implementation of precision medicine in routine cancer care in Belgium.
Tugce Schmitt et al. Eur J Public Health 2024
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What Legal Frameworks Should Govern Use of Genetic Test Results by Private Health Insurers in New Zealand?
Hanne Janes et al. J Law Med 2024 30(4) 862-883
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A systematic literature review of the 'commercialisation effect' on public attitudes towards biobank and genomic data repositories.
Jarrod Walshe et al. Public Underst Sci 2024 9636625241230864
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Direct-to-Consumer Genetic Tests and Canadian Genetic Counselors: A Pilot Exploration of Professional Roles in Response to Novel Biotechnologies.
Cassandra E Haley et al. Genes (Basel) 2024 15(2)
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Walk a mile in my shoes: perspectives towards sharing of health and experience data among individuals living with sickle cell disorder.
Simon Leigh et al. Mhealth 2024 104
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The importance, challenges, and possible solutions for sharing proteomics data while safeguarding individuals' privacy.
Mahasish Shome et al. Mol Cell Proteomics 2024 100731
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Sharing of Genomic Data: Exploring the Privacy Implications of the Changing Status of Genomic Data.
Margaret Otlowski et al. J Law Med 2024 30(2) 326-344
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Relatives' Right to Know Genetic Information in Aotearoa New Zealand.
Christian Poland et al. J Law Med 2024 30(2) 410-429
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Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies.
Harriet T Rothschild et al. Prenat Diagn 2023
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Release of reclassified VUS results of now deceased patients to family members: Practices and opinions.
Seth Lascurain et al. J Genet Couns 2024
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Implementing pharmacogenetics in clinical trials: considerations about current methodological, ethical, and regulatory challenges.
Irene García et al. Expert Rev Clin Pharmacol 2023
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Returning Genetic Information About Risk for Alcohol Use Disorder to Adolescents: Findings of a Preliminary Qualitative Study of Precision Prevention.
Elissa R Weitzman et al. AJPM Focus 2023 3(1) 100153
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A systematic review of knowledge, attitude and practice of pharmacogenomics in pediatric oncology patients.
Claire Moore et al. Pharmacol Res Perspect 2023 11(6) e01150
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The Impact of Artificial Intelligence on Optimizing Diagnosis and Treatment Plans for Rare Genetic Disorders.
Shenouda Abdallah et al. Cureus 2023 15(10) e46860
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British South Asian ancestry participants views of pharmacogenomics clinical implementation and research: a thematic analysis.
Emma F Magavern et al. Pharmacogenomics J 2023
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Call to Action for Advancing Equitable Genomic Newborn Screening.
Anne L Ersig et al. Public Health Genomics 2023
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Research participants' perception of ethical issues in stroke genomics and neurobiobanking research in Africa.
Ayodele Jegede et al. medRxiv 2023
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"There should be one spot that you can go:" BRCA mutation carriers' perspectives on cancer risk management and a hereditary cancer registry.
J Hynes et al. J Community Genet 2023
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PRScalc, a privacy-preserving calculation of raw polygenic risk scores from direct-to-consumer genomics data.
Lorena Sandoval et al. Bioinform Adv 2023 3(1) vbad145
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The Genetic Information Privacy Act: Drawbacks and Limitations.
Anya E R Prince et al. JAMA 2023
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Public attitudes towards genomic data sharing: results from a provincial online survey in Canada.
Holly Etchegary et al. BMC Med Ethics 2023 24(1) 81
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Ethics of artificial intelligence in prenatal and pediatric genomic medicine.
Simon Coghlan et al. J Community Genet 2023
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Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients.
Nandana D Rao et al. Eur J Hum Genet 2023
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Ethical Aspects of Pediatric Genetic Care: Testing and Treatment.
Kelly E Ormond et al. Pediatr Clin North Am 2023 70(5) 1029-1046
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Direct-to-Consumer Genomic Testing Through an Ethics Lens: Oncology Nursing Considerations.
Cheryl Ann VerStrate et al. Clin J Oncol Nurs 2023 27(4) 380-388
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Public and Healthcare Provider Receptivity toward the Retention of Dried Blood Spot Cards and Their Usage for Extended Genetic Testing in Hong Kong.
Kiran Moti Belaramani et al. Int J Neonatal Screen 2023 9(3)
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Parents' Perspectives on Secondary Genetic Ancestry Findings in Pediatric Genomic Medicine.
Jaimie L Richards et al. Clin Ther 2023
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Direct-to-Consumer Genetic Testing: A Comprehensive Review.
Sharon Jiang et al. Ther Innov Regul Sci 2023
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Federated Analysis for Privacy-Preserving Data Sharing: A Technical and Legal Primer.
James Casaletto et al. Annu Rev Genomics Hum Genet 2023
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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