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Items: 1 to 20 of 52

1.

AnoniMME: bringing anonymity to the Matchmaker Exchange platform for rare disease gene discovery.

Oprisanu B, De Cristofaro E.

Bioinformatics. 2018 Jul 1;34(13):i160-i168. doi: 10.1093/bioinformatics/bty269.

2.

Ethical concerns on sharing genomic data including patients' family members.

Takashima K, Maru Y, Mori S, Mano H, Noda T, Muto K.

BMC Med Ethics. 2018 Jun 18;19(1):61. doi: 10.1186/s12910-018-0310-5.

3.

Assessing patient readiness for personalized genomic medicine.

Frost CJ, Andrulis IL, Buys SS, Hopper JL, John EM, Terry MB, Bradbury A, Chung WK, Colbath K, Quintana N, Gamarra E, Egleston B, Galpern N, Bealin L, Glendon G, Miller LP, Daly MB.

J Community Genet. 2018 May 26. doi: 10.1007/s12687-018-0365-5. [Epub ahead of print]

PMID:
29804257
4.

Attitudes of sperm, egg and embryo donors and recipients towards genetic information and screening of donors.

Amor DJ, Kerr A, Somanathan N, McEwen A, Tome M, Hodgson J, Lewis S.

Reprod Health. 2018 Feb 9;15(1):26. doi: 10.1186/s12978-018-0468-9.

5.

BLOOM: BLoom filter based oblivious outsourced matchings.

Ziegeldorf JH, Pennekamp J, Hellmanns D, Schwinger F, Kunze I, Henze M, Hiller J, Matzutt R, Wehrle K.

BMC Med Genomics. 2017 Jul 26;10(Suppl 2):44. doi: 10.1186/s12920-017-0277-y.

6.
7.

Participant views on consent in cancer genetics research: preparing for the precision medicine era.

Edwards KL, Korngiebel DM, Pfeifer L, Goodman D, Renz A, Wenzel L, Bowen DJ, Condit CM.

J Community Genet. 2016 Apr;7(2):133-43. doi: 10.1007/s12687-015-0259-8. Epub 2016 Jan 22.

8.

Privacy in the Genomic Era.

Naveed M, Ayday E, Clayton EW, Fellay J, Gunter CA, Hubaux JP, Malin BA, Wang X.

ACM Comput Surv. 2015 Sep;48(1). pii: 6.

9.

Newborn screening and the era of medical genomics.

Francescatto L, Katsanis N.

Semin Perinatol. 2015 Dec;39(8):617-22. doi: 10.1053/j.semperi.2015.09.010. Epub 2015 Oct 21. Review.

10.

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.

Wolf SM, Branum R, Koenig BA, Petersen GM, Berry SA, Beskow LM, Daly MB, Fernandez CV, Green RC, LeRoy BS, Lindor NM, O'Rourke PP, Breitkopf CR, Rothstein MA, Van Ness B, Wilfond BS.

J Law Med Ethics. 2015 Fall;43(3):440-63. doi: 10.1111/jlme.12288.

11.

[A genetic ID for tomorrow?].

Perbal L.

C R Biol. 2015 Aug-Sep;338(8-9):547-53. doi: 10.1016/j.crvi.2015.06.016. Epub 2015 Jul 26. French.

PMID:
26211982
12.

Getting personal: Head and neck cancer management in the era of genomic medicine.

Birkeland AC, Uhlmann WR, Brenner JC, Shuman AG.

Head Neck. 2016 Apr;38 Suppl 1:E2250-8. doi: 10.1002/hed.24132. Epub 2015 Aug 13. Review.

13.

The growth and gaps of genetic data sharing policies in the United States.

Arias JJ, Pham-Kanter G, Campbell EG.

J Law Biosci. 2014 Dec 20;2(1):56-68. eCollection 2015 Feb.

14.

Following the giant's paces-governance issues and bioethical reflections in China.

Wang Z, Zhang D, Ng VH, Lie R, Zhai X.

BMC Med Ethics. 2014 Oct 31;15:79. doi: 10.1186/1472-6939-15-79.

15.

Protecting posted genes: social networking and the limits of GINA.

Soo-Jin Lee S, Borgelt E.

Am J Bioeth. 2014;14(11):32-44. doi: 10.1080/15265161.2014.957417.

PMID:
25325810
16.

Patient privacy in the genomic era.

Raisaro JL, Ayday E, Hubaux JP.

Praxis (Bern 1994). 2014 May 7;103(10):579-86. doi: 10.1024/1661-8157/a001657. Review.

PMID:
24800770
17.

[Gene mutations; up date].

Nakagawa M.

Rinsho Shinkeigaku. 2013;53(11):903-6. Review. Japanese.

PMID:
24291829
18.

Digital family histories for data mining.

Hoyt R, Linnville S, Chung HM, Hutfless B, Rice C.

Perspect Health Inf Manag. 2013 Oct 1;10:1a. eCollection 2013.

19.

Privacy and protection in the genomic era.

[No authors listed]

Nat Med. 2013 Sep;19(9):1073. doi: 10.1038/nm.3342. No abstract available.

PMID:
24013730
20.

Research ethics in the post-genomic era.

Vähäkangas K.

Environ Mol Mutagen. 2013 Aug;54(7):599-610. doi: 10.1002/em.21804. Epub 2013 Aug 1. Review.

PMID:
23908016

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