about
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populationsPredicting phenotype from genotype: normal pigmentationCarnitine palmitoyltransferase 1A P479L and infant death: policy implications of emerging data.Return of results in the genomic medicine projects of the eMERGE networkA systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.Impact of Psychiatric Information on Potential Jurors in Evaluating High-Functioning Autism Spectrum Disorder (hfASD).Awareness and Acceptable Practices: IRB and Researcher Reflections on the Havasupai LawsuitCustomers or research participants? Guidance for research practices in commercialization of personal genomicsStress across generations: A qualitative study of stress, coping, and caregiving among Mexican immigrant mothers.Forensic familial searching: scientific and social implications.Relationships matter: ethical considerations for returning results to family members of deceased subjects.Beyond the recommendation: discerning achievable goals in clinical ethics consultation.Response to Patryn and Zagaja.The instrumental role of hospital ethics committees in policy work.Direct-to-consumer genomics companies should provide guidance to their customers on (not) sharing personal genomic information.Trust, Precision Medicine Research, and Equitable Participation of Underserved Populations.New Words and Old Stories: Indigenous Teachings in Health Care and BioethicsNaming Indigenous Concerns, Framing Considerations for Stored BiospecimensA framework for enhancing ethical genomic research with Indigenous communitiesGenomics in the clinic: ethical and policy challenges in clinical next-generation sequencing programs at early adopter USA institutionsMeningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinismAn Ethical Case for Dual-Role Consent: Increasing Research Diversity as a Matter of Respect and JusticeGenomic Contextualism: Shifting the Rhetoric of Genetic ExceptionalismRights, interests and expectations: Indigenous perspectives on unrestricted access to genomic dataParents' attitudes toward consent and data sharing in biobanks: A multisite experimental surveyUnderstanding as an Ethical Aspiration in an Era of Digital Technology-Based Communication: An Analysis of Informed Consent Functions
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description
researcher ORCID ID = 0000-0002-6228-3216
@en
wetenschapper
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name
Nanibaa' A Garrison
@ast
Nanibaa' A Garrison
@en
Nanibaa' A Garrison
@nl
type
label
Nanibaa' A Garrison
@ast
Nanibaa' A Garrison
@en
Nanibaa' A Garrison
@nl
prefLabel
Nanibaa' A Garrison
@ast
Nanibaa' A Garrison
@en
Nanibaa' A Garrison
@nl
P106
P31
P496
0000-0002-6228-3216