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Items: 1 to 20 of 192

1.

Sequenced from the start.

[No authors listed]

Nature. 2013 Sep 12;501(7466):135. No abstract available.

PMID:
24032129
2.

The ethical hazards and programmatic challenges of genomic newborn screening.

Goldenberg AJ, Sharp RR.

JAMA. 2012 Feb 1;307(5):461-2. doi: 10.1001/jama.2012.68. No abstract available.

3.

Getting personal.

[No authors listed]

Nature. 2008 Oct 23;455(7216):1007. doi: 10.1038/4551007a. No abstract available.

PMID:
18948899
4.

Response to open peer commentaries on "Research 2.0: social networking and direct-to-consumer personal genomics".

Lee SS, Crawley L.

Am J Bioeth. 2009;9(6-7):W1-3. doi: 10.1080/15265160902967009. No abstract available.

PMID:
19998097
5.

Ethical, legal, and social implications of genomic medicine.

Clayton EW.

N Engl J Med. 2003 Aug 7;349(6):562-9. Review. No abstract available.

6.

Currents in contemporary ethics. State run newborn screening in the genomic era, or how to avoid drowning when drinking from a fire hose.

Clayton EW.

J Law Med Ethics. 2010 Fall;38(3):697-700. doi: 10.1111/j.1748-720X.2010.00522.x. No abstract available.

PMID:
20880251
7.

A clinical perspective on ethical issues in genetic testing.

Sijmons RH, Van Langen IM, Sijmons JG.

Account Res. 2011 May;18(3):148-62. doi: 10.1080/08989621.2011.575033. Review.

PMID:
21574071
8.

Personal genomes: Misdirected precaution.

Prainsack B, Reardon J, Hindmarsh R, Gottweis H, Naue U, Lunshof JE.

Nature. 2008 Nov 6;456(7218):34-5. doi: 10.1038/456034a. No abstract available.

PMID:
18987720
9.

Recreational genomics? Dreams and fears on genetic susceptibility screening.

van Ommen GB, Cornel MC.

Eur J Hum Genet. 2008 Apr;16(4):403-4. doi: 10.1038/ejhg.2008.32. No abstract available.

10.

Neonatal genetic testing is more than screening.

Kenner C, Lewis JA, Pressler JL, Little CM.

Crit Care Nurs Clin North Am. 2008 Jun;20(2):233-7, vii. doi: 10.1016/j.ccell.2008.01.005. Review.

PMID:
18424352
11.
12.

Worth waiting for.

[No authors listed]

Nature. 2010 Nov 11;468(7321):134. doi: 10.1038/468134a. No abstract available.

PMID:
21068784
13.

Guthrie cards: legal and ethical issues.

Elkin K, Jones DG.

N Z Bioeth J. 2000 Oct;1(2):22-6. No abstract available.

PMID:
15586976
14.

Voting with their mice: personal genome testing and the "participatory turn" in disease research.

Prainsack B.

Account Res. 2011 May;18(3):132-47. doi: 10.1080/08989621.2011.575032. Review.

PMID:
21574070
15.

Genetic testing.

Wexler B.

Genet Genet Eng. 2004:71-83. No abstract available.

PMID:
16562354
16.

The new genetics and informed consent: differentiating choice to preserve autonomy.

Bunnik EM, de Jong A, Nijsingh N, de Wert GM.

Bioethics. 2013 Jul;27(6):348-55. doi: 10.1111/bioe.12030. Epub 2013 May 30.

PMID:
23718722
17.

Genetic profiling of newborns: ethical and social issues.

Almond B.

Nat Rev Genet. 2006 Jan;7(1):67-71. doi: 10.1038/nrg1745. Review.

PMID:
16369573
18.

[The real « personal genome » ?].

Jordan B.

Med Sci (Paris). 2011 May;27(5):553-6. doi: 10.1051/medsci/2011275023. Epub 2011 May 25. French. No abstract available.

19.

Genetic screening and public health.

Holtzman NA.

Am J Public Health. 1997 Aug;87(8):1275-7. No abstract available.

20.

Ethical issues with newborn screening in the genomics era.

Tarini BA, Goldenberg AJ.

Annu Rev Genomics Hum Genet. 2012;13:381-93. doi: 10.1146/annurev-genom-090711-163741. Epub 2012 May 1. Review.

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