BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 24500682)

  • 1. 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]  

  • 2. 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]  

  • 3. The promise of whole-exome sequencing in medical genetics.
    Rabbani B; Tekin M; Mahdieh N
    J Hum Genet; 2014 Jan; 59(1):5-15. PubMed ID: 24196381
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Technology: Read the instructions.
    Scott AR
    Nature; 2016 Sep; 537(7619):S54-6. PubMed ID: 27602740
    [No Abstract]   [Full Text] [Related]  

  • 6. Refining the structure and content of clinical genomic reports.
    Dorschner MO; Amendola LM; Shirts BH; Kiedrowski L; Salama J; Gordon AS; Fullerton SM; Tarczy-Hornoch P; Byers PH; Jarvik GP
    Am J Med Genet C Semin Med Genet; 2014 Mar; 166C(1):85-92. PubMed ID: 24616401
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [New generation sequencing in medical genetics].
    Stoppa-Lyonnet D; Houdayer C
    Med Sci (Paris); 2012 Feb; 28(2):123-4. PubMed ID: 22377291
    [No Abstract]   [Full Text] [Related]  

  • 8. Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data.
    Khateb S; Hanany M; Khalaileh A; Beryozkin A; Meyer S; Abu-Diab A; Abu Turky F; Mizrahi-Meissonnier L; Lieberman S; Ben-Yosef T; Banin E; Sharon D
    J Med Genet; 2016 Sep; 53(9):600-7. PubMed ID: 27208209
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Implementing individualized medicine into the medical practice.
    Lazaridis KN; McAllister TM; Babovic-Vuksanovic D; Beck SA; Borad MJ; Bryce AH; Chanan-Khan AA; Ferber MJ; Fonseca R; Johnson KJ; Klee EW; Lindor NM; McCormick JB; McWilliams RR; Parker AS; Riegert-Johnson DL; Rohrer Vitek CR; Schahl KA; Schultz C; Stewart K; Then GC; Wieben ED; Farrugia G
    Am J Med Genet C Semin Med Genet; 2014 Mar; 166C(1):15-23. PubMed ID: 24616301
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The DNA of a nation.
    Marx V
    Nature; 2015 Aug; 524(7566):503-5. PubMed ID: 26310768
    [No Abstract]   [Full Text] [Related]  

  • 14. Living laboratory: whole-genome sequencing as a learning healthcare enterprise.
    Angrist M; Jamal L
    Clin Genet; 2015 Apr; 87(4):311-8. PubMed ID: 25045831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The challenge for the next generation of medical geneticists.
    Frebourg T
    Hum Mutat; 2014 Aug; 35(8):909-11. PubMed ID: 24838402
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Using population data for assessing next-generation sequencing performance.
    Houniet DT; Rahman TJ; Al Turki S; Hurles ME; Xu Y; Goodship J; Keavney B; Santibanez Koref M
    Bioinformatics; 2015 Jan; 31(1):56-61. PubMed ID: 25236458
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Medical implications of technical accuracy in genome sequencing.
    Goldfeder RL; Priest JR; Zook JM; Grove ME; Waggott D; Wheeler MT; Salit M; Ashley EA
    Genome Med; 2016 Mar; 8(1):24. PubMed ID: 26932475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype-Based Criteria Increases Diagnostic Impact of Exome Sequencing in Neonates.
    Am J Med Genet A; 2020 Mar; 182(3):422-423. PubMed ID: 32052580
    [No Abstract]   [Full Text] [Related]  

  • 20. The next phase in human genetics.
    Bansal V; Tewhey R; Topol EJ; Schork NJ
    Nat Biotechnol; 2011 Jan; 29(1):38-9. PubMed ID: 21221098
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.