These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 32160204)

  • 1. Evolving public views on the value of one's DNA and expectations for genomic database governance: Results from a national survey.
    Briscoe F; Ajunwa I; Gaddis A; McCormick J
    PLoS One; 2020; 15(3):e0229044. PubMed ID: 32160204
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Public willingness to participate in personalized health research and biobanking: A large-scale Swiss survey.
    Brall C; Berlin C; Zwahlen M; Ormond KE; Egger M; Vayena E
    PLoS One; 2021; 16(4):e0249141. PubMed ID: 33793624
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A survey of U.S. public perspectives on facial recognition technology and facial imaging data practices in health and research contexts.
    Katsanis SH; Claes P; Doerr M; Cook-Deegan R; Tenenbaum JD; Evans BJ; Lee MK; Anderton J; Weinberg SM; Wagner JK
    PLoS One; 2021; 16(10):e0257923. PubMed ID: 34648520
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Health research participants' preferences for receiving research results.
    Long CR; Stewart MK; Cunningham TV; Warmack TS; McElfish PA
    Clin Trials; 2016 Dec; 13(6):582-591. PubMed ID: 27562368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fair Shares and Sharing Fairly: A Survey of Public Views on Open Science, Informed Consent and Participatory Research in Biobanking.
    Joly Y; Dalpé G; So D; Birko S
    PLoS One; 2015; 10(7):e0129893. PubMed ID: 26154134
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The benefits, risks and costs of privacy: patient preferences and willingness to pay.
    Trachtenbarg DE; Asche C; Ramsahai S; Duling J; Ren J
    Curr Med Res Opin; 2017 May; 33(5):845-851. PubMed ID: 28166481
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
    Middleton A; Milne R; Almarri MA; Anwer S; Atutornu J; Baranova EE; Bevan P; Cerezo M; Cong Y; Critchley C; Fernow J; Goodhand P; Hasan Q; Hibino A; Houeland G; Howard HC; Hussain SZ; Malmgren CI; Izhevskaya VL; Jędrzejak A; Jinhong C; Kimura M; Kleiderman E; Leach B; Liu K; Mascalzoni D; Mendes Á; Minari J; Wang N; Nicol D; Niemiec E; Patch C; Pollard J; Prainsack B; Rivière M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefànsdóttir V; Tandre C; Thorogood A; Voigt TH; West AV; Yoshizawa G; Morley KI
    Am J Hum Genet; 2020 Oct; 107(4):743-752. PubMed ID: 32946764
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Patient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UK.
    Riordan F; Papoutsi C; Reed JE; Marston C; Bell D; Majeed A
    Int J Med Inform; 2015 Apr; 84(4):237-47. PubMed ID: 25649841
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Views of US Voters on Compensating Living Kidney Donors.
    Peters TG; Fisher JS; Gish RG; Howard RJ
    JAMA Surg; 2016 Aug; 151(8):710-6. PubMed ID: 27007405
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Public preferences for electronic health data storage, access, and sharing - evidence from a pan-European survey.
    Patil S; Lu H; Saunders CL; Potoglou D; Robinson N
    J Am Med Inform Assoc; 2016 Nov; 23(6):1096-1106. PubMed ID: 27107445
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Context matters in genomic data sharing: a qualitative investigation into responses from the Australian public.
    Warren V; Critchley C; McWhirter R; Walshe J; Nicol D
    BMC Med Genomics; 2023 Apr; 15(Suppl 3):275. PubMed ID: 37005651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Limitations on the compensation of gamete donors: a public opinion survey.
    Lee MS; Farland LV; Missmer SA; Ginsburg ES
    Fertil Steril; 2017 Jun; 107(6):1355-1363.e4. PubMed ID: 28390693
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Data sharing, management, use, and reuse: Practices and perceptions of scientists worldwide.
    Tenopir C; Rice NM; Allard S; Baird L; Borycz J; Christian L; Grant B; Olendorf R; Sandusky RJ
    PLoS One; 2020; 15(3):e0229003. PubMed ID: 32160189
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Attitudes regarding the national forensic DNA database: Survey data from the general public, prison inmates and prosecutors' offices in the Republic of Serbia.
    Teodorović S; Mijović D; Radovanović Nenadić U; Savić M
    Forensic Sci Int Genet; 2017 May; 28():44-51. PubMed ID: 28171783
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sharing longitudinal, non-biological birth cohort data: a cross-sectional analysis of parent consent preferences.
    Manhas KP; Dodd SX; Page S; Letourneau N; Adair CE; Cui X; Tough SC
    BMC Med Inform Decis Mak; 2018 Nov; 18(1):97. PubMed ID: 30419910
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Public Opinion on Organ Donation After Death and Its Influence on Attitudes Toward Organ Donation.
    Aijing L; Wenzhao X; Wei W; Qiquan W; Xuantong D
    Ann Transplant; 2016 Aug; 21():516-24. PubMed ID: 27535587
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods.
    Middleton A; Niemiec E; Prainsack B; Bobe J; Farley L; Steed C; Smith J; Bevan P; Bonhomme N; Kleiderman E; Thorogood A; Schickhardt C; Garattini C; Vears D; Littler K; Banner N; Scott E; Kovalevskaya NV; Levin E; Morley KI; Howard HC
    Per Med; 2018 Jul; 15(4):311-318. PubMed ID: 29856292
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Perspectives of Australian adults about protecting the privacy of their health information in statistical databases.
    King T; Brankovic L; Gillard P
    Int J Med Inform; 2012 Apr; 81(4):279-89. PubMed ID: 22306206
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Should Researchers Offer Results to Family Members of Cancer Biobank Participants? A Mixed-Methods Study of Proband and Family Preferences.
    Gordon DR; Radecki Breitkopf C; Robinson M; Petersen WO; Egginton JS; Chaffee KG; Petersen GM; Wolf SM; Koenig BA
    AJOB Empir Bioeth; 2019; 10(1):1-22. PubMed ID: 30596322
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Public Views on Models for Accessing Genomic and Health Data for Research: Mixed Methods Study.
    Jones KH; Daniels H; Squires E; Ford DV
    J Med Internet Res; 2019 Aug; 21(8):e14384. PubMed ID: 31436163
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.