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 *

198 related articles for article (PubMed ID: 29522190)

  • 1. Society and personal genome data.
    Middleton A
    Hum Mol Genet; 2018 May; 27(R1):R8-R13. PubMed ID: 29522190
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomics: data sharing needs an international code of conduct.
    Phillips M; Molnár-Gábor F; Korbel JO; Thorogood A; Joly Y; Chalmers D; Townend D; Knoppers BM
    Nature; 2020 Feb; 578(7793):31-33. PubMed ID: 32025008
    [No Abstract]   [Full Text] [Related]  

  • 3. Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
    Murtagh MJ; Blell MT; Butters OW; Cowley L; Dove ES; Goodman A; Griggs RL; Hall A; Hallowell N; Kumari M; Mangino M; Maughan B; Mills MC; Minion JT; Murphy T; Prior G; Suderman M; Ring SM; Rogers NT; Roberts SJ; Van der Straeten C; Viney W; Wiltshire D; Wong A; Walker N; Burton PR
    Hum Genomics; 2018 Apr; 12(1):24. PubMed ID: 29695297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 19(1):61. PubMed ID: 29914459
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnostic genomic laboratories should share their data.
    Poon KS; Koay ES
    Nature; 2021 Jun; 594(7862):177. PubMed ID: 34103719
    [No Abstract]   [Full Text] [Related]  

  • 6. Public variant databases: liability?
    Thorogood A; Cook-Deegan R; Knoppers BM
    Genet Med; 2017 Jul; 19(7):838-841. PubMed ID: 27977006
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The future of Cochrane Neonatal.
    Soll RF; Ovelman C; McGuire W
    Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Informed consent and ethical re-use of African genomic data.
    Wright GE; Adeyemo AA; Tiffin N
    Hum Genomics; 2014 Oct; 8(1):18. PubMed ID: 25339190
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Statement on bioinformatics and capturing the benefits of genome sequencing for society.
    Capps B; Chadwick R; Joly Y; Lysaght T; Mills C; Mulvihill JJ; Zwart H
    Hum Genomics; 2019 May; 13(1):24. PubMed ID: 31142362
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Oversight of Genomic Data Sharing: What Roles for Ethics and Data Access Committees?
    Shabani M; Dove ES; Murtagh M; Knoppers BM; Borry P
    Biopreserv Biobank; 2017 Oct; 15(5):469-474. PubMed ID: 28836815
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GenoShare: Supporting Privacy-Informed Decisions for Sharing Individual-Level Genetic Data.
    Raisaro JL; Troncoso-Pastoriza JR; El-Zein Y; Humbert M; Troncoso C; Fellay J; Hubaux JP
    Stud Health Technol Inform; 2020 Jun; 270():238-241. PubMed ID: 32570382
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The next 20 years of human genomics must be more equitable and more open.
    Nature; 2021 Feb; 590(7845):183-184. PubMed ID: 33568832
    [No Abstract]   [Full Text] [Related]  

  • 13. Genomic sovereignty and the African promise: mining the African genome for the benefit of Africa.
    de Vries J; Pepper M
    J Med Ethics; 2012 Aug; 38(8):474-8. PubMed ID: 22493187
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Emerging technologies towards enhancing privacy in genomic data sharing.
    Berger B; Cho H
    Genome Biol; 2019 Jul; 20(1):128. PubMed ID: 31262363
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ClinGen advancing genomic data-sharing standards as a GA4GH driver project.
    Dolman L; Page A; Babb L; Freimuth RR; Arachchi H; Bizon C; Brush M; Fiume M; Haendel M; Hansen DP; Milosavljevic A; Patel RY; Pawliczek P; Yates AD; Rehm HL
    Hum Mutat; 2018 Nov; 39(11):1686-1689. PubMed ID: 30311379
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 21(6):377-384. PubMed ID: 32251390
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO).
    Joly Y; Dove ES; Knoppers BM; Bobrow M; Chalmers D
    PLoS Comput Biol; 2012; 8(7):e1002549. PubMed ID: 22807659
    [No Abstract]   [Full Text] [Related]  

  • 18. Shared genomics: high performance computing for distributed insights in genomic medical research.
    Hoyle DC; Delderfield M; Kitching L; Smith G; Buchan I
    Stud Health Technol Inform; 2009; 147():232-41. PubMed ID: 19593061
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience.
    McGuire AL; Basford M; Dressler LG; Fullerton SM; Koenig BA; Li R; McCarty CA; Ramos E; Smith ME; Somkin CP; Waudby C; Wolf WA; Clayton EW
    Genome Res; 2011 Jul; 21(7):1001-7. PubMed ID: 21632745
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ClinGen's GenomeConnect registry enables patient-centered data sharing.
    Savatt JM; Azzariti DR; Faucett WA; Harrison S; Hart J; Kattman B; Landrum MJ; Ledbetter DH; Miller VR; Palen E; Rehm HL; Rhode J; Turner S; Vidal JA; Wain KE; Riggs ER; Martin CL
    Hum Mutat; 2018 Nov; 39(11):1668-1676. PubMed ID: 30311371
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.