BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 25487853)

  • 1. [Concepts for the return of secondary genetic findings in medical diagnostics and research].
    Fisher E; Achilles S; Tönnies H; Schmidtke J
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2015 Feb; 58(2):166-73. PubMed ID: 25487853
    [TBL] [Abstract][Full Text] [Related]  

  • 2. On the ethics of clinical whole genome sequencing of children.
    May T; Zusevics KL; Strong KA
    Pediatrics; 2013 Aug; 132(2):207-9. PubMed ID: 23837175
    [No Abstract]   [Full Text] [Related]  

  • 3. Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
    Hegde M; Santani A; Mao R; Ferreira-Gonzalez A; Weck KE; Voelkerding KV
    Arch Pathol Lab Med; 2017 Jun; 141(6):798-805. PubMed ID: 28362156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Challenge of Analyzing the Results of Next-Generation Sequencing in Children.
    Thiffault I; Lantos J
    Pediatrics; 2016 Jan; 137 Suppl 1():S3-7. PubMed ID: 26729700
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling.
    O'Daniel JM; Lee K
    Cancer J; 2012; 18(4):287-92. PubMed ID: 22846728
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-exome/genome sequencing and genomics.
    Grody WW; Thompson BH; Hudgins L
    Pediatrics; 2013 Dec; 132(Suppl 3):S211-5. PubMed ID: 24298129
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome versus transcriptome sequencing in identifying coding region variants.
    Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
    Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
    Hollegaard MV; Grauholm J; Nielsen R; Grove J; Mandrup S; Hougaard DM
    Mol Genet Metab; 2013; 110(1-2):65-72. PubMed ID: 23830478
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues.
    Hallowell N; Hall A; Alberg C; Zimmern R
    J Med Ethics; 2015 Apr; 41(4):317-21. PubMed ID: 25038088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Making headway with genetic diagnostics of intellectual disabilities.
    Willemsen MH; Kleefstra T
    Clin Genet; 2014 Feb; 85(2):101-10. PubMed ID: 23895455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Who's on first in exome and whole genome sequencing? Is it the patient or the incidental findings?
    Rosenblatt DS
    Mol Genet Metab; 2013; 110(1-2):1-2. PubMed ID: 23809103
    [No Abstract]   [Full Text] [Related]  

  • 12. Exome sequencing: a transient technology for molecular diagnostics?
    Ku CS; Cooper DN
    Expert Rev Mol Diagn; 2012 Apr; 12(3):211-4. PubMed ID: 22468808
    [No Abstract]   [Full Text] [Related]  

  • 13. An automatic and efficient pipeline for disease gene identification through utilizing family-based sequencing data.
    Song D; Li N; Liao L
    Biomed Mater Eng; 2015; 26 Suppl 1():S1797-803. PubMed ID: 26405949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A commentary on the promise of whole-exome sequencing in medical genetics.
    Kaname T; Yanagi K; Naritomi K
    J Hum Genet; 2014 Mar; 59(3):117-8. PubMed ID: 24500682
    [No Abstract]   [Full Text] [Related]  

  • 15. Next-generation diagnostics: gene panel, exome, or whole genome?
    Sun Y; Ruivenkamp CA; Hoffer MJ; Vrijenhoek T; Kriek M; van Asperen CJ; den Dunnen JT; Santen GW
    Hum Mutat; 2015 Jun; 36(6):648-55. PubMed ID: 25772376
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome sequencing: dual role as a discovery and diagnostic tool.
    Ku CS; Cooper DN; Polychronakos C; Naidoo N; Wu M; Soong R
    Ann Neurol; 2012 Jan; 71(1):5-14. PubMed ID: 22275248
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
    Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
    Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?
    Zawati MH; Parry D; Thorogood A; Nguyen MT; Boycott KM; Rosenblatt D; Knoppers BM
    J Med Genet; 2014 Jan; 51(1):68-70. PubMed ID: 24078715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel bioinformatic developments for exome sequencing.
    Lelieveld SH; Veltman JA; Gilissen C
    Hum Genet; 2016 Jun; 135(6):603-14. PubMed ID: 27075447
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Challenges of using next generation sequencing in newborn screening.
    Reinstein E
    Genet Res (Camb); 2015 Nov; 97():e21. PubMed ID: 26521961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.