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by Caulfield, Timothy
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The legal risks of returning results of genomics research
by Clayton, Ellen Wright
Genetics in medicine, 2012-04, Vol.14 (4), p.473-477
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Informed consent in genomics and genetic research
by McGuire, Amy L
Annual review of genomics and human genetics, 2010, Vol.11 (1), p.361-381
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Clarify the HIPAA right of access to individuals' research data
by Guerrini, Christi J
Nature biotechnology, 2019-08, Vol.37 (8), p.850-852
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Should you profit from your genome?
by Roberts, Jessica L
Nature biotechnology, 2017-01-10, Vol.35 (1), p.18-20
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Development of the clinical next-generation sequencing industry in a shifting policy climate
by Curnutte, Margaret A
Nature biotechnology, 2014-10, Vol.32 (10), p.980-982
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Exploring concordance and discordance for return of incidental findings from clinical sequencing
by Green, Robert C
Genetics in medicine, 2012-04, Vol.14 (4), p.405-410
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Persistent confusion and controversy surrounding gene patents
by Guerrini, Christi J
Nature biotechnology, 2016-02, Vol.34 (2), p.145-147
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Health System Implications of Direct-to-Consumer Personal Genome Testing
by McGuire, Amy L
Community genetics, 2011-01-01, Vol.14 (1), p.53-58
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A One-Page Summary Report of Genome Sequencing for the Healthy Adult
by Vassy, Jason L
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To share or not to share: a randomized trial of consent for data sharing in genome research
by McGuire, Amy L
Genetics in medicine, 2011-11, Vol.13 (11), p.948-955
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Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group
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In support of mitochondrial replacement therapy
by Adashi, Eli Y
Nature medicine, 2019-06, Vol.25 (6), p.870-871
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Return of research results from genomic biobanks: cost matters
by Bledsoe, Marianna J
Genetics in medicine, 2013-02, Vol.15 (2), p.103-105
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by Ramoni, Rachel B.
Genetics in medicine, 2013-11, Vol.15 (11), p.882-887
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Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network
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Developing context-specific next-generation sequencing policy
by Curnutte, Margaret Ann
Nature biotechnology, 2016-05-06, Vol.34 (5), p.466-470
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DNA data sharing: research participants' perspectives
by McGuire, Amy L.
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Adult Genetic Risk Screening
by Caskey, C. Thomas
Annual review of medicine, 2014-01-14, Vol.65 (1), p.1-17
