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Items: 8


Privacy and confidentiality in pragmatic clinical trials.

McGraw D, Greene SM, Miner CS, Staman KL, Welch MJ, Rubel A.

Clin Trials. 2015 Oct;12(5):520-9. doi: 10.1177/1740774515597677. Epub 2015 Sep 15.


Instrumenting the health care enterprise for discovery research in the genomic era.

Murphy S, Churchill S, Bry L, Chueh H, Weiss S, Lazarus R, Zeng Q, Dubey A, Gainer V, Mendis M, Glaser J, Kohane I.

Genome Res. 2009 Sep;19(9):1675-81. doi: 10.1101/gr.094615.109. Epub 2009 Jul 14.


A globally optimal k-anonymity method for the de-identification of health data.

El Emam K, Dankar FK, Issa R, Jonker E, Amyot D, Cogo E, Corriveau JP, Walker M, Chowdhury S, Vaillancourt R, Roffey T, Bottomley J.

J Am Med Inform Assoc. 2009 Sep-Oct;16(5):670-82. doi: 10.1197/jamia.M3144. Epub 2009 Jun 30.


Written informed consent and selection bias in observational studies using medical records: systematic review.

Kho ME, Duffett M, Willison DJ, Cook DJ, Brouwers MC.

BMJ. 2009 Mar 12;338:b866. doi: 10.1136/bmj.b866. Review.


Impact of the Health Insurance Portability and Accountability Act on participant recruitment and retention.

Wipke-Tevis DD, Pickett MA.

West J Nurs Res. 2008 Feb;30(1):39-53. Epub 2007 Jun 5. Review.


Passive consent for clinical research in the age of HIPAA.

Littenberg B, MacLean CD.

J Gen Intern Med. 2006 Mar;21(3):207-11.


The new research ethic: will oversight requirements sink forensic research?

Candilis PJ, Arikan R, Noone SB, Holzer JC.

J Am Acad Psychiatry Law. 2005;33(3):361-7.


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