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5861 - 5870 of 5927 Topics
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Publication
Consumer-driven health care: Implications for providers, payers, and policymakers
WileyDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Risk, culture, and health inequality: Shifting perceptions of danger and blame
Greenwood Publishing GroupDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Plain talk about the Human Genome Project: A Tuskegee University conference on its promise and perils...and matters of race
Tuskegee UniversityDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Textbook of ethics in pediatric research
KriegerDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
The commercialization of human stem cells: Ethical and policy issues
Health Care Analysis: An International Journal of Health Care Philosophy and PolicyDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Grant Abstract
Comparing Game Facilitated Interactivity to Genetic Counseling for Prenatal Screening Education
PROJECT NARRATIVE Advancements in prenatal genetic screening have significantly improved the identification of chromosomal abnormalities and heritable conditions during pregnancy, yet current…- Address
- Age
- American
- American College of Obstetricians and Gynecologists
- Appointment
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Grant Abstract
Utility of Genomic Sequencing in Community Care Contexts
PROJECT NARRATIVE Families with children who have identified deficits in speech and/or sensory or musculoskeletal impairments without a known cause may be referred for genetic testing to find out…- Address
- Advisory Committees
- Area
- base
- Behavior
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Grant Abstract
Human Geneticists' Practices Preferences and Beliefs about Biobanks and Large Cohort Studies
Biobanks that collect and store participants' clinical and genetic information have become important tools in genomic research, disseminating data to a large number of investigators conducting…- American
- Area
- Attitude
- Authorization documentation
- base
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Grant Abstract
The Electronic Medical Records and Genomics (eMERGE) Network Phase III - Coordinating Center
The eMERGE project brings together researchers with a wide range of expertise in genomics, statistics, ethics, informatics, and clinical medicine from leading medical research institutions across…- Agreement
- Algorithms
- Arbitration
- biobank
- clinical implementation
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Publication
Genetic testing: Care, consent, and liability
WileyDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National…