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Publication
Health system-led early consent and direct contact of at-risk relatives: Pilot study results
Public Health Genomics -
Publication
Scientists’ and policy professionals’ views on the translational pipeline of human gene editing
The American Journal of Bioethics -
Publication
AI and data surveillance: Embedding a human rights-based approach
Journal of Law, Medicine & Ethics -
Publication
Nonadherence to guidelines for genetic testing in families with ovarian cancer shows racial bias
Genetics in Medicine -
Publication
A qualitative approach to life with neurofibromatosis type 1 based on Mishel's Uncertainty in Illness Theory: “My body is a ticking time bomb”
Journal of Genetic Counseling -
Publication
A qualitative study of the experiences of patients with prostate cancer when receiving negative genetic results: “I still don't have a grasp of what it all means”
Journal of Genetic Counseling -
Publication
Reproductive decision-making experiences of Australian adults with neurofibromatosis type 1 and schwannomatosis
Journal of Genetic Counseling -
Publication
Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions
Journal of Genetic Counseling -
Publication
Exploring preferences and support needs for disclosing 47, XXY status: A qualitative study of adults with XXY
Journal of Genetic Counseling -
Publication
Patient understanding of fetal sex versus gender in the context of routine cell-free DNA screening
Journal of Genetic Counseling