1.
Expanding Access to Large-Scale Genomic Data While Promoting Privacy: A Game Theoretic Approach
by Wan, Zhiyu
American journal of human genetics, 2017-02-02, Vol.100 (2), p.316-322
2.
The legal risks of returning results of genomics research
by Clayton, Ellen Wright
Genetics in medicine, 2012-04, Vol.14 (4), p.473-477
3.
Recommendations for returning genomic incidental findings? We need to talk
by Burke, Wylie
Genetics in medicine, 2013-11, Vol.15 (11), p.854-859
4.
Experimental Arrest of Cerebral Blood Flow in Human Subjects: The Red Wing Studies Revisited
by Smith, Brian A
Perspectives in biology and medicine, 2011, Vol.54 (2), p.121-131
5.
Premature guidance about whole-genome sequencing
by Ross, Lainie Friedman
Personalized medicine, 2013-08-01, Vol.10 (6), p.523-526
6.
Managing incidental genomic findings: legal obligations of clinicians
by Clayton, Ellen Wright
Genetics in medicine, 2013-08, Vol.15 (8), p.624-629
7.
Patient awareness and approval for an opt-out genomic biorepository
by Brothers, Kyle B
Personalized medicine, 2013-06-01, Vol.10 (4), p.349-359
8.
Return of research results from genomic biobanks: cost matters
by Bledsoe, Marianna J
Genetics in medicine, 2013-02, Vol.15 (2), p.103-105
9.
In support of mitochondrial replacement therapy
by Adashi, Eli Y
Nature medicine, 2019-06, Vol.25 (6), p.870-871
10.
Stakeholder engagement: a key component of integrating genomic information into electronic health records
by Hartzler, Andrea
Genetics in medicine, 2013-10, Vol.15 (10), p.792-801
11.
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network
by Fullerton, Stephanie M
Genetics in medicine, 2012-04, Vol.14 (4), p.424-431
12.
Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testing
by Westbrook, Matthew J
Genetics in medicine, 2013-05, Vol.15 (5), p.325-331
13.
It’s all in the timing: calibrating temporal penalties for biomedical data sharing
by Xia, Weiyi Weiyi
Journal of the American Medical Informatics Association : JAMIA, 2017-09-26, Vol.25 (1), p.25-31
14.
Confronting Real Time Ethical, Legal, and Social Issues in the eMERGE (Electronic Medical Records and Genomics) Consortium
by Clayton, Ellen Wright Ellen Wright
Genetics in medicine, 2010-10-01, Vol.12 (10), p.616-620
15.
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US
by Sanderson, Saskia C
American journal of human genetics, 2017-03-02, Vol.100 (3), p.414-427
16.
Openness of patients' reporting with use of electronic records: psychiatric clinicians' views
by Salomon, Ronald M
Journal of the American Medical Informatics Association : JAMIA, 2010-01, Vol.17 (1), p.54-60
17.
Let us ask better questions
by Clayton, Ellen Wright
Genetics in medicine, 2013-11, Vol.15 (11), p.871-872
18.
Ethical and practical challenges to studying patients who opt out of large-scale biorepository research
by Rosenbloom, S Trent
Journal of the American Medical Informatics Association : JAMIA, 2013-12, Vol.20 (e2), p.e221-e225
19.
Recontacting Pediatric Research Participants for Consent When They Reach the Age of Majority
by Knoppers, Bartha Maria
IRB, 2016-12-01, Vol.38 (6), p.1-9
20.
Return of research results from genomic biobanks: a call for data
by Bledsoe, Marianna J
Genetics in medicine, 2013-02, Vol.15 (2), p.159-160
