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jasonbobe research [17 articles]

最近 jasonbobe さんのライブラリに追加された論文の中から タグ research. You can also see everyone's research.
  • WHAT SHOULD RESEARCH PARTICIPANTS UNDERSTAND TO UNDERSTAND THEY ARE PARTICIPANTS IN RESEARCH?
    Bioethics (2008)
    by David Wendler, Christine Grady
    posted to consent informed-consent participatory-research research by jasonbobe on 2008-02-26 17:51:09 as **
  • Why most published research findings are false.
    PLoS Med, Vol. 2, No. 8. (August 2005)
    by JP Ioannidis
    posted to research statistics study-design by jasonbobe on 2008-01-23 14:23:33 as read along with 38 people and 4 groups shoshin achinerarias austin rklancer jyuh phnk sebpaquet incites garyfeng monod Borelli jmeppley chad_davis Najamuddin irinas indigoviolet mwyarbro ddahlem dullhunk madhadron balabu jiyu msierk Imat lmi_swap chenlc03 biblio24 pratap OriginalLurch cjeans feipan arne suizan lonettma buggle dnugent Malc elsbury ReadingLab EisenLab Sciences_communication_societe dIEMoSIRIS
  • Certificates of confidentiality.
    Genet Test, Vol. 8, No. 2. (2004), pp. 77-78.
    by PR Reilly
    posted to coc elsi irb policy privacy research by jasonbobe on 2007-12-13 02:30:41 as ****
  • betrayed by my shadow
    Journal of Privacy Technology (2006)
    by Malin
    posted to anonymity genomics privacy reidentification research trail by jasonbobe on 2007-08-08 14:00:13 as read
  • The Application Of Business Models To Medical Research: Interviews With Two Founders Of Directed-Philanthropy Foundations
    Health Aff, Vol. 26, No. 4. (1 July 2007), pp. 1181-1185.
    by Kathryn A Phillips
    posted to business canaryfoundation philanthropy research science by jasonbobe on 2007-07-16 14:45:44 as ****
  • The rights of patients in research
    BMJ, Vol. 310, No. 6990. (20 May 1995), pp. 1277-1278.
    by Heather Goodare, Richard Smith
    posted to citizenscience patients research researchmodels by jasonbobe on 2007-07-11 23:16:24 as read
  • Consumer involvement in research is essential.
    BMJ, Vol. 320, No. 7231. (5 February 2000), pp. 380-381.
    by D Tallon, J Chard, P Dieppe
    posted to citizenscience patients research researchmodels by jasonbobe on 2007-07-11 23:15:48 as read
  • What does involving consumers in research mean?
    QJM, Vol. 94, No. 12. (1 December 2001), pp. 661-664.
    by Charlotte Williamson
    posted to citizenscience patients research researchmodels by jasonbobe on 2007-07-11 23:10:14 as *****
  • Advocacy groups as research organizations: the PXE International example
    Nature Reviews Genetics, Vol. 8, No. 2., pp. 157-164.
    by Sharon F Terry, Patrick F Terry, Katherine A Rauen, Jouni Uitto, Lionel G Bercovitch
    posted to advocacy organizations patients research translational by jasonbobe on 2007-07-11 23:06:58 as read
  • Ethics of Population-Based Research
    The Journal of Law, Medicine & Ethics, Vol. 35, No. 2. (2007), pp. 295-299.
    by Holly A Taylor, Summer Johnson
    posted to design populationstudies publichealth research review studydesign by jasonbobe on 2007-07-11 21:57:38 as ** along with 2 people jahughes PredictER
  • The emergence of an ethical duty to disclose genetic research results: international perspectives
    European Journal of Human Genetics, Vol. aop, No. current.
    by Bartha M Knoppers, Yann Joly, Jacques Simard, Francine Durocher,
    posted to disclosure duty_to_warn ethics genetics research by jasonbobe on 2007-07-04 09:10:47 as *****
  • Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database
    Nature Genetics, Vol. 39, No. 1., pp. 17-23.
    by Lars Bertram, Matthew B Mcqueen, Kristina Mullin, Deborah Blacker, Rudolph E Tanzi
    posted to alzgene alzheimers curation evidencegrading metaanalysis research by jasonbobe on 2007-07-04 05:13:35 as read along with 3 people and 1 group applebyb giovanni jeremymiller GeschwindLab
  • The advocates
    Nat Genet, Vol. 38, No. 4. (April 2006), pp. 391-391.
    posted to advocacy disease empowerment genetic research by jasonbobe on 2007-07-04 05:08:10 as read
  • GENETICS: No Longer De-Identified
    Science, Vol. 312, No. 5772. (21 April 2006), pp. 370-371.
    by Amy L Mcguire, Richard A Gibbs
    posted to anonymity confidentiality genetics identifiability privacy research by jasonbobe on 2007-07-01 06:02:30 as read along with 2 people and 1 group cgreal brixtonmc CGREL
  • A vision for the future of genomics research
    Nature, Vol. 422, No. 6934. (24 April 2003), pp. 835-847.
    by Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer
    posted to futurism genomics research by jasonbobe on 2007-05-31 20:40:24 as read along with 2 people kaarsinogen massivemayhem
  • Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization.
    Am J Med Genet A, Vol. 143, No. 6. (15 March 2007), pp. 564-569.
    by B Diergaarde, DJ Bowen, EJ Ludman, JO Culver, N Press, W Burke
    posted to genetic genomics opinion research testing by jasonbobe on 2007-05-23 00:47:15 as ** along with 1 person PredictER
  • Obligations and responsibilities of epidemiologists to research subjects.
    J Clin Epidemiol, Vol. 44 Suppl 1 (1991)
    by JM Last
    posted to design epidemiology ethics research study subjects by jasonbobe on 2007-05-13 05:43:56 as *****
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