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 *

134 related articles for article (PubMed ID: 33343192)

  • 1. Use of broad consent and related procedures in genomics research: Perspectives from research participants in the Genetics of Rheumatic Heart Disease (RHDGen) study in a University Teaching Hospital in Zambia.
    Mweemba O; Musuku J; Mayosi BM; Parker M; Rutakumwa R; Seeley J; Tindana P; De Vries J
    Glob Bioeth; 2019 Mar; 31(1):184-199. PubMed ID: 33343192
    [TBL] [Abstract][Full Text] [Related]  

  • 2. "I passed the test!" Evidence of diagnostic misconception in the recruitment of population controls for an H3Africa genomic study in Cape Town, South Africa.
    Masiye F; Mayosi B; de Vries J
    BMC Med Ethics; 2017 Feb; 18(1):12. PubMed ID: 28202021
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evolving perspectives on broad consent for genomics research and biobanking in Africa. Report of the Second H3Africa Ethics Consultation Meeting, 11 May 2015.
    de Vries J; Littler K; Matimba A; McCurdy S; Ouwe Missi Oukem-Boyer O; Seeley J; Tindana P
    Glob Health Epidemiol Genom; 2016; 1():e13. PubMed ID: 29868205
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Informed consent in genomic research and biobanking: taking feedback of findings seriously.
    Tindana P; Depuur C; de Vries J; Seeley J; Parker M
    Glob Bioeth; 2020 Feb; 31(1):200-215. PubMed ID: 33343193
    [TBL] [Abstract][Full Text] [Related]  

  • 5. "It's for a good cause, isn't it?" - Exploring views of South African TB research participants on sample storage and re-use.
    van Schalkwyk G; de Vries J; Moodley K
    BMC Med Ethics; 2012 Jul; 13():19. PubMed ID: 22831568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Consent Issues in Genetic Research: Views of Research Participants.
    Goodman D; Johnson CO; Wenzel L; Bowen D; Condit C; Edwards KL
    Public Health Genomics; 2016; 19(4):220-8. PubMed ID: 27376949
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries.
    de Vries J; Munung SN; Matimba A; McCurdy S; Ouwe Missi Oukem-Boyer O; Staunton C; Yakubu A; Tindana P;
    BMC Med Ethics; 2017 Feb; 18(1):8. PubMed ID: 28153006
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perspectives and ethical considerations for return of genetics and genomics research results: a qualitative study of genomics researchers in Uganda.
    Ochieng J; Kwagala B; Barugahare J; Mwaka E; Ekusai-Sebatta D; Ali J; Sewankambo NK
    BMC Med Ethics; 2021 Nov; 22(1):154. PubMed ID: 34798900
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 'It is an entrustment': Broad consent for genomic research and biobanks in sub-Saharan Africa.
    Tindana P; Molyneux S; Bull S; Parker M
    Dev World Bioeth; 2019 Mar; 19(1):9-17. PubMed ID: 29063669
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.
    Cheah PY; Jatupornpimol N; Hanboonkunupakarn B; Khirikoekkong N; Jittamala P; Pukrittayakamee S; Day NPJ; Parker M; Bull S
    BMC Med Ethics; 2018 Nov; 19(1):86. PubMed ID: 30404642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A qualitative study exploring stakeholder perspectives on the use of biological samples for future unspecified research in Malawi.
    Matandika L; Ngóngóla RT; Mita K; Manda-Taylor L; Gooding K; Mwale D; Masiye F; Mfutso-Bengo J
    BMC Med Ethics; 2020 Jul; 21(1):61. PubMed ID: 32689995
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parental perspectives on consent for participation in large-scale, non-biological data repositories.
    Manhas KP; Page S; Dodd SX; Letourneau N; Ambrose A; Cui X; Tough SC
    Life Sci Soc Policy; 2016; 12():1. PubMed ID: 26790860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. "It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.
    Moodley K; Sibanda N; February K; Rossouw T
    BMC Med Ethics; 2014 Jan; 15():4. PubMed ID: 24447822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. "It's all about trust": reflections of researchers on the complexity and controversy surrounding biobanking in South Africa.
    Moodley K; Singh S
    BMC Med Ethics; 2016 Oct; 17(1):57. PubMed ID: 27724893
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.
    Traore K; Bull S; Niare A; Konate S; Thera MA; Kwiatkowski D; Parker M; Doumbo OK
    BMC Med Ethics; 2015 Jun; 16():42. PubMed ID: 26077875
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A qualitative study on aspects of consent for genomic research in communities with low literacy.
    Bukini D; Mbekenga C; Nkya S; Purvis L; McCurdy S; Parker M; Makani J
    BMC Med Ethics; 2020 Jun; 21(1):48. PubMed ID: 32532327
    [TBL] [Abstract][Full Text] [Related]  

  • 17. "Still Rather Hazy at Present": Citizens' and Physicians' Views on Returning Results from Biobank Research Using Broad Consent.
    Barazzetti G; Cavalli S; Benaroyo L; Kaufmann A
    Genet Test Mol Biomarkers; 2017 Mar; 21(3):159-165. PubMed ID: 28177781
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Secondary Use of Patient Tissue in Cancer Biobanks.
    Mathews DJH; Rabin JT; Quain K; Campbell E; Collyar D; Hlubocky FJ; Isakoff S; Peppercorn J
    Oncologist; 2019 Dec; 24(12):1577-1583. PubMed ID: 31182655
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An evaluation of the process of informed consent: views from research participants and staff.
    O' Sullivan L; Feeney L; Crowley RK; Sukumar P; McAuliffe E; Doran P
    Trials; 2021 Aug; 22(1):544. PubMed ID: 34407858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Webinar report: stakeholder perspectives on informed consent for the use of genomic data by commercial entities.
    Schultz B; Agamah FE; Ewuoso C; Madden EB; Troyer J; Skelton M; Mwaka E;
    J Med Ethics; 2023 Dec; 50(1):57-61. PubMed ID: 36941048
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.