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 *

182 related articles for article (PubMed ID: 19595370)

  • 41. Public's attitudes on participation in a biobank for research: an Italian survey.
    Porteri C; Pasqualetti P; Togni E; Parker M
    BMC Med Ethics; 2014 Nov; 15():81. PubMed ID: 25425352
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The moral concerns of biobank donors: the effect of non-welfare interests on willingness to donate.
    De Vries RG; Tomlinson T; Kim HM; Krenz CD; Ryan KA; Lehpamer N; Kim SY
    Life Sci Soc Policy; 2016; 12():3. PubMed ID: 26968989
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Willingness to participate in a personalized health cohort - insights from the swiss health study pilot phase.
    Bühler N; Frahsa A; Jaramillo NG; Bourqui RM; Nusslé SG; Zuppinger C; Bochud M; von Goetz N
    BMC Public Health; 2024 Aug; 24(1):2140. PubMed ID: 39112992
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Attitudes of emergency department patients and visitors regarding emergency exception from informed consent in resuscitation research, community consultation, and public notification.
    McClure KB; DeIorio NM; Gunnels MD; Ochsner MJ; Biros MH; Schmidt TA
    Acad Emerg Med; 2003 Apr; 10(4):352-9. PubMed ID: 12670849
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Trust and Expectations of Researchers and Public Health Departments for the Use of HIV Molecular Epidemiology.
    Schairer CE; Mehta SR; Vinterbo SA; Hoenigl M; Kalichman M; Little SJ
    AJOB Empir Bioeth; 2019; 10(3):201-213. PubMed ID: 31050604
    [No Abstract]   [Full Text] [Related]  

  • 46. 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]  

  • 47. Children, biobanks and the scope of parental consent.
    Hens K; Cassiman JJ; Nys H; Dierickx K
    Eur J Hum Genet; 2011 Jul; 19(7):735-9. PubMed ID: 21386873
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Informed consent, biobank research, and locality: perceptions of breast cancer patients in three European countries.
    Petersen I; Desmedt C; Harris A; Buffa F; Kollek R
    J Empir Res Hum Res Ethics; 2014 Jul; 9(3):48-55. PubMed ID: 25746784
    [TBL] [Abstract][Full Text] [Related]  

  • 49. European biobanks forge cross-border ties.
    Keogh B
    J Natl Cancer Inst; 2011 Oct; 103(19):1429-31. PubMed ID: 21934073
    [No Abstract]   [Full Text] [Related]  

  • 50. Biobank research, informed consent and society. Towards a new alliance?
    D'Abramo F
    J Epidemiol Community Health; 2015 Nov; 69(11):1125-8. PubMed ID: 25669218
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Intentions to donate to a biobank in a national sample of African Americans.
    McDonald JA; Vadaparampil S; Bowen D; Magwood G; Obeid JS; Jefferson M; Drake R; Gebregziabher M; Hughes Halbert C
    Public Health Genomics; 2014; 17(3):173-82. PubMed ID: 24942180
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Australian Attitudes Towards Waivers of Consent Within the Context of Genomic Data Sharing.
    Newett L; McWhirter R; Eckstein L; Warren V; Nicol D
    J Empir Res Hum Res Ethics; 2024 Jul; 19(3):113-123. PubMed ID: 39096208
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Ethical considerations in biobanks: how a public health ethics perspective sheds new light on old controversies.
    Virani AH; Longstaff H
    J Genet Couns; 2015 Jun; 24(3):428-32. PubMed ID: 25348083
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Biobanks and the Moral Concerns of Donors: A Democratic Deliberation.
    De Vries RG; Ryan KA; Gordon L; Krenz CD; Tomlinson T; Jewell S; Kim SYH
    Qual Health Res; 2019 Nov; 29(13):1942-1953. PubMed ID: 30095038
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Perspectives on Electronic Informed Consent From Patients Underrepresented in Research in the United States: A Focus Group Study.
    Simon CM; Schartz HA; Rosenthal GE; Eisenstein EL; Klein DW
    J Empir Res Hum Res Ethics; 2018 Oct; 13(4):338-348. PubMed ID: 29790410
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Paediatric biobanks: what makes them so unique?
    Samuël J; Knoppers BM; Avard D
    J Paediatr Child Health; 2012 Feb; 48(2):E1-3. PubMed ID: 21535284
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Beliefs and attitudes towards participating in genetic research - a population based cross-sectional study.
    Kerath SM; Klein G; Kern M; Shapira I; Witthuhn J; Norohna N; Kline M; Baksh F; Gregersen P; Taioli E
    BMC Public Health; 2013 Feb; 13():114. PubMed ID: 23388465
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
    Tupasela A; Sihvo S; Snell K; Jallinoja P; Aro AR; Hemminki E
    Scand J Public Health; 2010 Feb; 38(1):46-52. PubMed ID: 19906772
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Opinions of Young Adults on Re-Consenting for Biobanking.
    Rush A; Battisti R; Barton B; Catchpoole D
    J Pediatr; 2015 Oct; 167(4):925-30. PubMed ID: 26235663
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Public perceptions of biobanks in China: a focus group study.
    Chen H; Gottweis H; Starkbaum J
    Biopreserv Biobank; 2013 Oct; 11(5):267-71. PubMed ID: 24835257
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.