BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 23982363)

  • 1. Revealing the incidentalome when targeting the tumor genome.
    Bombard Y; Robson M; Offit K
    JAMA; 2013 Aug; 310(8):795-6. PubMed ID: 23982363
    [No Abstract]   [Full Text] [Related]  

  • 2. Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making.
    Ross LF; Rothstein MA; Clayton EW
    JAMA; 2013 Jul; 310(4):367-8. PubMed ID: 23917281
    [No Abstract]   [Full Text] [Related]  

  • 3. Tumor profiling and the incidentalome: patient decisions and risks.
    Hofstatter E; Mehra K; Yushak M; Pusztai L
    Future Oncol; 2015; 11(24):3299-305. PubMed ID: 26562094
    [TBL] [Abstract][Full Text] [Related]  

  • 4. "Somatic" Tumor Genomic Profiling and Potential Germline Implications: Ethical Considerations for Children with Cancer.
    Knapp E
    J Law Med Ethics; 2020 Dec; 48(4):778-783. PubMed ID: 33404327
    [No Abstract]   [Full Text] [Related]  

  • 5. Genomic test validation for incidental findings.
    Park JY; Fortina P; Kricka LJ
    Clin Chem; 2014 Feb; 60(2):292-3. PubMed ID: 23818443
    [No Abstract]   [Full Text] [Related]  

  • 6. Tumor-Only Sequencing Has Limitations.
    Cancer Discov; 2015 Jul; 5(7):OF17. PubMed ID: 25929850
    [No Abstract]   [Full Text] [Related]  

  • 7. Reporting genomic sequencing results to ordering clinicians: incidental, but not exceptional.
    Green RC; Lupski JR; Biesecker LG
    JAMA; 2013 Jul; 310(4):365-6. PubMed ID: 23917280
    [No Abstract]   [Full Text] [Related]  

  • 8. [The genome and cancer treatment].
    Nielsen FC; Lassen U
    Ugeskr Laeger; 2014 Nov; 176(46):. PubMed ID: 25394934
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disclosure of Misattributed Paternity.
    Prero MY; Strenk M; Garrett J; Kessler A; Fanaroff JM; Lantos JD
    Pediatrics; 2019 Jun; 143(6):. PubMed ID: 31097466
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.
    Daack-Hirsch S; Driessnack M; Hanish A; Johnson VA; Shah LL; Simon CM; Williams JK
    Clin Genet; 2013 Jul; 84(1):11-8. PubMed ID: 23590238
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Generating a taxonomy for genetic conditions relevant to reproductive planning.
    Korngiebel DM; McMullen CK; Amendola LM; Berg JS; Davis JV; Gilmore MJ; Harding CO; Himes P; Jarvik GP; Kauffman TL; Kennedy KA; Simpson DK; Leo MC; Lynch FL; Quigley DI; Reiss JA; Richards CS; Rope AF; Schneider JL; Goddard KA; Wilfond BS
    Am J Med Genet A; 2016 Mar; 170(3):565-73. PubMed ID: 26889673
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic testing: a struggle for oncologists.
    Hede K
    J Natl Cancer Inst; 2014 Jun; 106(6):dju172. PubMed ID: 24907388
    [No Abstract]   [Full Text] [Related]  

  • 13. That tumor you're going to get tomorrow … maybe: making an informed decision.
    Aitini E; Adami F; Barni S; Zaniboni A
    Tumori; 2015 Jul; 101(4):e113-4. PubMed ID: 26045122
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Understanding variations in secondary findings reporting practices across U.S. genome sequencing laboratories.
    Ackerman SL; Koenig BA
    AJOB Empir Bioeth; 2018; 9(1):48-57. PubMed ID: 29131714
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome sequencing and cancer.
    Mardis ER
    Curr Opin Genet Dev; 2012 Jun; 22(3):245-50. PubMed ID: 22534183
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Germline, hematopoietic, mosaic, and somatic variation: interplay between inherited and acquired genetic alterations in disease assessment.
    Konnick EQ; Pritchard CC
    Genome Med; 2016 Oct; 8(1):100. PubMed ID: 27716394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. From next-generation sequencing to nanopore sequencing technology: paving the way to personalized genomic medicine.
    Ku CS; Roukos DH
    Expert Rev Med Devices; 2013 Jan; 10(1):1-6. PubMed ID: 23278216
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetic counseling and testing for germline p16 mutations in two pancreatic cancer-prone families.
    Lynch HT; Brand RE; Lynch JF; Fusaro RM; Smyrk TC; Goggins M; Kern SE
    Gastroenterology; 2000 Dec; 119(6):1756-60. PubMed ID: 11113097
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Medicine. Personalized cancer diagnostics.
    Corless CL
    Science; 2011 Dec; 334(6060):1217-8. PubMed ID: 22144608
    [No Abstract]   [Full Text] [Related]  

  • 20. Germline Testing for Men With Prostate Cancer: Navigating an Expanding New World of Genetic Evaluation for Precision Therapy and Precision Management.
    Giri VN; Hyatt C; Gomella LG
    J Clin Oncol; 2019 Jun; 37(17):1455-1459. PubMed ID: 30978156
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.