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Pubmed for Handhelds

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Journal Abstract Search

240 related items for PubMed ID: 29400986

  • 21. 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. PubMed ID: 25361573
    [Abstract] [Full Text] [Related]

  • 22. Public attitudes towards genomic data sharing: results from a provincial online survey in Canada.
    Etchegary H, Darmonkov G, Simmonds C, Pullman D, Rahman P.
    BMC Med Ethics; 2023 Oct 07; 24(1):81. PubMed ID: 37805493
    [Abstract] [Full Text] [Related]

  • 23. Moving beyond Bermuda: sharing data to build a medical information commons.
    Cook-Deegan R, McGuire AL.
    Genome Res; 2017 Jun 07; 27(6):897-901. PubMed ID: 28373484
    [Abstract] [Full Text] [Related]

  • 24. On the future of genomic data.
    Kahn SD.
    Science; 2011 Feb 11; 331(6018):728-9. PubMed ID: 21311016
    [Abstract] [Full Text] [Related]

  • 25. Genomic Privacy.
    Schwab AP, Luu HS, Wang J, Park JY.
    Clin Chem; 2018 Dec 11; 64(12):1696-1703. PubMed ID: 29991478
    [Abstract] [Full Text] [Related]

  • 26. Expanding Access to Large-Scale Genomic Data While Promoting Privacy: A Game Theoretic Approach.
    Wan Z, Vorobeychik Y, Xia W, Clayton EW, Kantarcioglu M, Malin B.
    Am J Hum Genet; 2017 Feb 02; 100(2):316-322. PubMed ID: 28065469
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  • 29. Research ethics. The complexities of genomic identifiability.
    Rodriguez LL, Brooks LD, Greenberg JH, Green ED.
    Science; 2013 Jan 18; 339(6117):275-6. PubMed ID: 23329035
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  • 32. Genomic Data-Sharing Practices.
    Villanueva AG, Cook-Deegan R, Robinson JO, McGuire AL, Majumder MA.
    J Law Med Ethics; 2019 Mar 18; 47(1):31-40. PubMed ID: 30994063
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  • 33. Enabling responsible public genomics.
    Conley JM, Doerr AK, Vorhaus DB.
    Health Matrix Clevel; 2010 Mar 18; 20(2):325-85. PubMed ID: 21243847
    [Abstract] [Full Text] [Related]

  • 34. Ethical, legal and social issues in the context of the planning stages of the Southern African Human Genome Programme.
    de Vries J, Slabbert M, Pepper MS.
    Med Law; 2012 Mar 18; 31(1):119-52. PubMed ID: 22908741
    [Abstract] [Full Text] [Related]

  • 35. Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience.
    Peppercorn J, Shapira I, Deshields T, Kroetz D, Friedman P, Spears P, Collyar DE, Shulman LN, Dressler L, Bertagnolli MM.
    Cancer; 2012 Oct 15; 118(20):5060-8. PubMed ID: 22415847
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  • 37. Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data.
    Hudson M, Garrison NA, Sterling R, Caron NR, Fox K, Yracheta J, Anderson J, Wilcox P, Arbour L, Brown A, Taualii M, Kukutai T, Haring R, Te Aika B, Baynam GS, Dearden PK, Chagné D, Malhi RS, Garba I, Tiffin N, Bolnick D, Stott M, Rolleston AK, Ballantyne LL, Lovett R, David-Chavez D, Martinez A, Sporle A, Walter M, Reading J, Carroll SR.
    Nat Rev Genet; 2020 Jun 15; 21(6):377-384. PubMed ID: 32251390
    [Abstract] [Full Text] [Related]

  • 38. Data Lakes, Clouds, and Commons: A Review of Platforms for Analyzing and Sharing Genomic Data.
    Grossman RL.
    Trends Genet; 2019 Mar 15; 35(3):223-234. PubMed ID: 30691868
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  • 39. 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. PubMed ID: 29914459
    [Abstract] [Full Text] [Related]

  • 40. Proxy consent and a national DNA databank: an unethical and discriminatory combination.
    Baumann TK.
    Iowa Law Rev; 2001 Jan 18; 86(2):667-701. PubMed ID: 16184651
    [No Abstract] [Full Text] [Related]

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