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 *

169 related articles for article (PubMed ID: 25119605)

  • 1. Genotype-phenotype correlation--promiscuity in the era of next-generation sequencing.
    Lu JT; Campeau PM; Lee BH
    N Engl J Med; 2014 Aug; 371(7):593-6. PubMed ID: 25119605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The contribution of next generation sequencing to epilepsy genetics.
    Møller RS; Dahl HA; Helbig I
    Expert Rev Mol Diagn; 2015; 15(12):1531-8. PubMed ID: 26565596
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
    Wagner MJ
    Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studies.
    Cao H; Wang Y; Zhang W; Chai X; Zhang X; Chen S; Yang F; Zhang C; Guo Y; Liu Y; Tang Z; Chen C; Xue Y; Zhen H; Xu Y; Rao B; Liu T; Zhao M; Zhang W; Li Y; Zhang X; Tellier LC; Krogh A; Kristiansen K; Wang J; Li J
    Hum Mutat; 2013 Dec; 34(12):1715-20. PubMed ID: 24014314
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Resequencing rice genomes: an emerging new era of rice genomics.
    Huang X; Lu T; Han B
    Trends Genet; 2013 Apr; 29(4):225-32. PubMed ID: 23295340
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-exome sequencing reveals recurrent somatic mutation networks in cancer.
    Liu X; Wang J; Chen L
    Cancer Lett; 2013 Nov; 340(2):270-6. PubMed ID: 23153794
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling.
    Marroni F; Pinosio S; Di Centa E; Jurman I; Boerjan W; Felice N; Cattonaro F; Morgante M
    Plant J; 2011 Aug; 67(4):736-45. PubMed ID: 21554453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Next generation diagnostics of heritable connective tissue disorders.
    Salam A; Simpson MA; Stone KL; Takeichi T; Nanda A; Akiyama M; McGrath JA
    Matrix Biol; 2014 Jan; 33():35-40. PubMed ID: 23896220
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The challenges of developing a 'medical-grade' genome.
    van der Straaten T; Guchelaar HJ; Swen JJ
    Pharmacogenomics; 2012 Mar; 13(4):369-72. PubMed ID: 22379992
    [No Abstract]   [Full Text] [Related]  

  • 11. Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.
    Nijman IJ; van Montfrans JM; Hoogstraat M; Boes ML; van de Corput L; Renner ED; van Zon P; van Lieshout S; Elferink MG; van der Burg M; Vermont CL; van der Zwaag B; Janson E; Cuppen E; Ploos van Amstel JK; van Gijn ME
    J Allergy Clin Immunol; 2014 Feb; 133(2):529-34. PubMed ID: 24139496
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations.
    Londin E; Yadav P; Surrey S; Kricka LJ; Fortina P
    Methods Mol Biol; 2013; 1015():127-46. PubMed ID: 23824853
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Progress in detecting genetic alterations and their association with human disease.
    Schwartz CE; Chen CF
    J Mol Biol; 2013 Nov; 425(21):3914-8. PubMed ID: 23876707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next generation sequencing is here now.
    Erickson RP
    Lymphology; 2014 Dec; 47(4):196-7. PubMed ID: 25915980
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions.
    Fang M; Abolhassani H; Lim CK; Zhang J; Hammarström L
    J Clin Immunol; 2016 May; 36 Suppl 1():68-75. PubMed ID: 26993986
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Somatic point mutations occurring early in development: a monozygotic twin study.
    Li R; Montpetit A; Rousseau M; Wu SY; Greenwood CM; Spector TD; Pollak M; Polychronakos C; Richards JB
    J Med Genet; 2014 Jan; 51(1):28-34. PubMed ID: 24123875
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hepatitis C Virus Genotyping Using Next-Generation Sequencing: An Efficient Alternative to Sanger Sequencing.
    Wales C; Corpus G; Chang C
    Arch Pathol Lab Med; 2017 Mar; 141(3):323-324. PubMed ID: 28234569
    [No Abstract]   [Full Text] [Related]  

  • 19. Exome sequencing identifies RDH12 compound heterozygous mutations in a family with severe retinitis pigmentosa.
    Chacon-Camacho OF; Jitskii S; Buentello-Volante B; Quevedo-Martinez J; Zenteno JC
    Gene; 2013 Oct; 528(2):178-82. PubMed ID: 23900199
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Implementing genomic medicine in pathology.
    Williams ES; Hegde M
    Adv Anat Pathol; 2013 Jul; 20(4):238-44. PubMed ID: 23752086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.