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Items: 1 to 20 of 187

1.

Broadening research consent in the era of genome-informed medicine.

Kronenthal C, Delaney SK, Christman MF.

Genet Med. 2012 Apr;14(4):432-6. doi: 10.1038/gim.2011.76.

PMID:
22422050
3.

International normative perspectives on the return of individual research results and incidental findings in genomic biobanks.

Zawati MH, Knoppers BM.

Genet Med. 2012 Apr;14(4):484-9. doi: 10.1038/gim.2012.13.

PMID:
22344229
4.

Return of research results from genomic biobanks: cost matters.

Bledsoe MJ, Clayton EW, McGuire AL, Grizzle WE, O'Rourke PP, Zeps N.

Genet Med. 2013 Feb;15(2):103-5. doi: 10.1038/gim.2012.105. No abstract available.

5.

Using biointelligence to search the cancer genome: an epistemological perspective on knowledge recovery strategies to enable precision medical genomics.

Mousses S, Kiefer J, Von Hoff D, Trent J.

Oncogene. 2008 Dec;27 Suppl 2:S58-66. doi: 10.1038/onc.2009.354. Review.

PMID:
19956181
6.

An empirical examination of the management of return of individual research results and incidental findings in genomic biobanks.

Johnson G, Lawrenz F, Thao M.

Genet Med. 2012 Apr;14(4):444-50. doi: 10.1038/gim.2012.20.

PMID:
22361899
7.

Ethical and legal implications of whole genome and whole exome sequencing in African populations.

Wright GE, Koornhof PG, Adeyemo AA, Tiffin N.

BMC Med Ethics. 2013 May 28;14:21. doi: 10.1186/1472-6939-14-21.

8.

Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small.

Sharp RR.

Genet Med. 2011 Mar;13(3):191-4. doi: 10.1097/GIM.0b013e31820f603f.

PMID:
21311340
9.

A closer look revisited: are we subjects or are we donors?

Fisher R.

Genet Med. 2012 Apr;14(4):458-60. doi: 10.1038/gim.2012.6.

PMID:
22361901
10.

Models of consent to return of incidental findings in genomic research.

Appelbaum PS, Parens E, Waldman CR, Klitzman R, Fyer A, Martinez J, Price WN 2nd, Chung WK.

Hastings Cent Rep. 2014 Jul-Aug;44(4):22-32. doi: 10.1002/hast.328.

12.
13.

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.

Wolf SM, Crock BN, Van Ness B, Lawrenz F, Kahn JP, Beskow LM, Cho MK, Christman MF, Green RC, Hall R, Illes J, Keane M, Knoppers BM, Koenig BA, Kohane IS, Leroy B, Maschke KJ, McGeveran W, Ossorio P, Parker LS, Petersen GM, Richardson HS, Scott JA, Terry SF, Wilfond BS, Wolf WA.

Genet Med. 2012 Apr;14(4):361-84. doi: 10.1038/gim.2012.23.

14.
15.

Ethical issues raised by whole genome sequencing.

Pinxten W, Howard HC.

Best Pract Res Clin Gastroenterol. 2014 Apr;28(2):269-79. doi: 10.1016/j.bpg.2014.02.004. Review.

PMID:
24810188
16.

Intersection of biobanking and clinical care: should discrepant diagnoses and pathological findings be returned to research participants?

Lockhart NC, Yassin R, Weil CJ, Compton CC.

Genet Med. 2012 Apr;14(4):417-23. doi: 10.1038/gim.2012.11.

PMID:
22344228
17.

Emerging DNA sequencing technologies for human genomic medicine.

Strausberg RL, Levy S, Rogers YH.

Drug Discov Today. 2008 Jul;13(13-14):569-77. doi: 10.1016/j.drudis.2008.03.025. Review.

PMID:
18598911
18.

The ethical use of existing samples for genome research.

Bathe OF, McGuire AL.

Genet Med. 2009 Oct;11(10):712-5. doi: 10.1097/GIM.0b013e3181b2e168. Review.

PMID:
19745750
19.

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.

Fullerton SM, Wolf WA, Brothers KB, Clayton EW, Crawford DC, Denny JC, Greenland P, Koenig BA, Leppig KA, Lindor NM, McCarty CA, McGuire AL, McPeek Hinz ER, Mirel DB, Ramos EM, Ritchie MD, Smith ME, Waudby CJ, Burke W, Jarvik GP.

Genet Med. 2012 Apr;14(4):424-31. doi: 10.1038/gim.2012.15.

20.

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