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 *

136 related articles for article (PubMed ID: 23046882)

  • 1. Opportunities and challenges for genome sequencing in the clinic.
    Cavalleri GL; Delanty N
    Adv Protein Chem Struct Biol; 2012; 89():65-83. PubMed ID: 23046882
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epilepsy pharmacogenetics.
    Kasperaviciūte D; Sisodiya SM
    Pharmacogenomics; 2009 May; 10(5):817-36. PubMed ID: 19450130
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. 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]  

  • 5. Whole-genome sequencing in pharmacogenetics.
    Urban TJ
    Pharmacogenomics; 2013 Mar; 14(4):345-8. PubMed ID: 23438878
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Genome sequencing and assembly.
    Grabherr MG; Mauceli E; Ma LJ
    Methods Mol Biol; 2011; 722():1-9. PubMed ID: 21590409
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing.
    Teare MD; Santibañez Koref MF
    Brief Funct Genomics; 2014 Sep; 13(5):378-83. PubMed ID: 25024279
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. QTL mapping using high-throughput sequencing.
    Jamann TM; Balint-Kurti PJ; Holland JB
    Methods Mol Biol; 2015; 1284():257-85. PubMed ID: 25757777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of EMS-induced causal mutations in a non-reference Arabidopsis thaliana accession by whole genome sequencing.
    Uchida N; Sakamoto T; Kurata T; Tasaka M
    Plant Cell Physiol; 2011 Apr; 52(4):716-22. PubMed ID: 21398646
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.
    Li MJ; Yan B; Sham PC; Wang J
    Brief Bioinform; 2015 May; 16(3):393-412. PubMed ID: 24916300
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cancer genomics: technology, discovery, and translation.
    Tran B; Dancey JE; Kamel-Reid S; McPherson JD; Bedard PL; Brown AM; Zhang T; Shaw P; Onetto N; Stein L; Hudson TJ; Neel BG; Siu LL
    J Clin Oncol; 2012 Feb; 30(6):647-60. PubMed ID: 22271477
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Next generation sequencing in the clinical domain: clinical advantages, practical, and ethical challenges.
    Thompson R; Drew CJ; Thomas RH
    Adv Protein Chem Struct Biol; 2012; 89():27-63. PubMed ID: 23046881
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare-disease genetics in the era of next-generation sequencing: discovery to translation.
    Boycott KM; Vanstone MR; Bulman DE; MacKenzie AE
    Nat Rev Genet; 2013 Oct; 14(10):681-91. PubMed ID: 23999272
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole genome sequencing and the transformation of C. elegans forward genetics.
    Hu PJ
    Methods; 2014 Aug; 68(3):437-40. PubMed ID: 24874788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impact of next generation sequencing on diagnostics in a genetic skin disease clinic.
    Takeichi T; Nanda A; Liu L; Salam A; Campbell P; Fong K; Akiyama M; Ozoemena L; Stone KL; Al-Ajmi H; Simpson MA; McGrath JA
    Exp Dermatol; 2013 Dec; 22(12):825-31. PubMed ID: 24279917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Developing genome and exome sequencing for candidate gene identification in inherited disorders: an integrated technical and bioinformatics approach.
    Coonrod EM; Durtschi JD; Margraf RL; Voelkerding KV
    Arch Pathol Lab Med; 2013 Mar; 137(3):415-33. PubMed ID: 22770468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Challenges and opportunities for next-generation sequencing in companion diagnostics.
    Lin E; Chien J; Ong FS; Fan JB
    Expert Rev Mol Diagn; 2015 Feb; 15(2):193-209. PubMed ID: 25249308
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.