Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practiceSurgical innovation: the ethical agenda: A systematic review.When Children Become Adults: Should Biobanks Re-Contact?Identifiability and privacy in pluripotent stem cell researchConsent procedures in pediatric biobanks.Data sharing in stem cell translational science: policy statement by the International Stem Cell Forum Ethics Working Party.Big Data in medical research and EU data protection law: challenges to the consent or anonymise approachAutonomy and self-esteem of women who donate to an oocyte cryopreservation bank in the Netherlands.Disclosure of individual genetic data to research participants: the debate reconsidered.Stem cell trials for cardiovascular medicine: ethical rationale.Inclusion of residual tissue in biobanks: opt-in or opt-out?The social value of clinical research.Potential conflicts of interest of editorial board members from five leading spine journalsPersonalized assent for pediatric biobanks.Preferences for genetic testing for colorectal cancer within a population-based screening program: a discrete choice experimentSetting Global Standards for Stem Cell Research and Clinical Translation: The 2016 ISSCR Guidelines.Organoid biobanking: identifying the ethics: Organoids revive old and raise new ethical challenges for basic research and therapeutic use.Clarifying assent in pediatric researchEthics of stem cell-derived gametes made in a dish: fertility for everyone?Consent in psychiatric biobanks for pharmacogenetic research.Regenerative medicine interventions for orthopedic disorders: ethical issues in the translation into patients.Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology.Ethical implications of regenerative medicine in orthopedics: an empirical study with surgeons and scientists in the field.Avoid surgery as first line treatment for non-specific low back pain.Reconsidering the ethics of sham interventions in an era of emerging technologies.Postmortem disclosure of genetic information to family members: active or passive?Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered.Participant selection for preventive Regenerative Medicine trials: ethical challenges of selecting individuals at risk.Moral Duties of Genomics Researchers: Why Personalized Medicine Requires a Collective Approach.Human tissues in a dish: The research and ethical implications of organoid technology.Ethical clinical translation of stem cell interventions for neurologic disease.The right to an open future concerning genetic information.Scientific evaluation of spinal implants: an ethical necessity.Next-generation sequencing: does the next generation still have a right to an open future?Avoiding transgenerational risks of mitochondrial DNA disorders: a morally acceptable reason for sex selection?CRISPR germline engineering--the community speaks.Reply to Waligora.A thick opt-out is often sufficient.Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy.
P50
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Anne Lydia Bredenoord
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