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 *

890 related articles for article (PubMed ID: 21730106)

  • 1. What can exome sequencing do for you?
    Majewski J; Schwartzentruber J; Lalonde E; Montpetit A; Jabado N
    J Med Genet; 2011 Sep; 48(9):580-9. PubMed ID: 21730106
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Whole exome and whole genome sequencing.
    Bick D; Dimmock D
    Curr Opin Pediatr; 2011 Dec; 23(6):594-600. PubMed ID: 21881504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Revealing the human mutome.
    Chen JM; Férec C; Cooper DN
    Clin Genet; 2010 Oct; 78(4):310-20. PubMed ID: 20569258
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis.
    Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
    Expert Rev Mol Diagn; 2012 Mar; 12(2):159-73. PubMed ID: 22369376
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Cancer genome analysis through next-generation sequencing].
    Aburatani H
    Gan To Kagaku Ryoho; 2011 Jan; 38(1):1-6. PubMed ID: 21368453
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Genome sequencing and personalized medicine: perspectives and limitations].
    Le Gall JY; Debré P;
    Bull Acad Natl Med; 2014 Jan; 198(1):101-17. PubMed ID: 26259290
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Next generation sequencing and rare genetic variants: from human population studies to medical genetics.
    Matullo G; Di Gaetano C; Guarrera S
    Environ Mol Mutagen; 2013 Aug; 54(7):518-32. PubMed ID: 23922201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.
    Chou J; Ohsumi TK; Geha RS
    Curr Opin Allergy Clin Immunol; 2012 Dec; 12(6):623-8. PubMed ID: 23095910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing.
    Lalonde E; Albrecht S; Ha KC; Jacob K; Bolduc N; Polychronakos C; Dechelotte P; Majewski J; Jabado N
    Hum Mutat; 2010 Aug; 31(8):918-23. PubMed ID: 20518025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Exome sequencing: an efficient strategy for identifying the causative genes of monogenic disorders].
    Rebiya N; Patamu M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):525-7. PubMed ID: 21983726
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2012 Mar; 33(3):586-90. PubMed ID: 22213110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expanding DNA diagnostic panel testing: is more better?
    Klee EW; Hoppman-Chaney NL; Ferber MJ
    Expert Rev Mol Diagn; 2011 Sep; 11(7):703-9. PubMed ID: 21902532
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Present efforts in the medical genome center at the University of Tokyo Hospital].
    Mitsui J; Ishiura H; Tsuji S
    Brain Nerve; 2013 Mar; 65(3):247-55. PubMed ID: 23475516
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
    Rudan I
    Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole cancer genome sequencing by next-generation methods.
    Ross JS; Cronin M
    Am J Clin Pathol; 2011 Oct; 136(4):527-39. PubMed ID: 21917674
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing analysis: a guide to disease variant detection.
    Isakov O; Perrone M; Shomron N
    Methods Mol Biol; 2013; 1038():137-58. PubMed ID: 23872973
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 45.