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Publication
Physician duty to warn a patient's offspring of hereditary genetic defects: Balancing the patient's right to confidentiality against the family member's right to know -- can or should Tarasoff apply
Quinnipiac Health Law JournalDigital 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 double-edge helix: Social implications of genetics in a diverse society, edited by Joseph S. Alper, Catherine Ard, Adrienne Asch, Jon Beckwith, Peter Conrad and Lisa N. Geller
New Genetics and SocietyDigital 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
European opposition to exclusive control over predictive breast cancer testing and the inherent implications for U.S. patent law and public policy: A case study of the myriad genetics' BRCA patent controversy
Food and Drug Law JournalDigital 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… -
News
Engaging Underrepresented Communities in Research
Attention to the unique inclusion and engagement needs of understudied populations is of critical importance to the advancement of genomic and precision medicine research, the elimination of health… -
Publication
How can the genetic risks of embryo donation be minimized? Proposed guidelines of the French Federation of CECOS (Centre d'Etude et de Conservation des Oeufs et du Sperme)
Human ReproductionDigital 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… -
News
ELSI in Review • May 2022
About this listing ELSI in Review is a listing of recently published, systematic reviews of the literature on key ELSI topics curated by CERA staff. Our May 2022 set explores person-centered… -
Research Tool
CSER Phase 1: Parental Consent for Child to Participate in a Research Study, Minor Subjects- Relatives of Study Subject - NCGENES: A Next-Generation Sequencing Platform for Genetic Diagnosis and Research
This parental consent form from the NCGENES: A Next-Generation Sequencing Platform for Genetic Diagnosis study is designed for the minor relatives of NCGENES study participants that received a… -
Publication
Best quality vs. sex selection - an analysis of embryo selection preferences for patients undergoing preimplantation genetic testing for aneuploidy over a 10-year period
Journal of Assisted Reproduction and Genetics -
Publication
Human heredity and politics: A comparative institutional study of the Eugenics Record Office at Cold Spring Harbor, the Kaiser Wilhelm Institute for Anthropology, Human Heredity, and Eugenics, and the Maxim Gorky Medical Genetics Institute
OsirisDigital 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…