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 *

120 related articles for article (PubMed ID: 20642358)

  • 1. Chromosomal distribution of disease genes in the human genome.
    Cooper DN; Ball EV; Mort M
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):441-6. PubMed ID: 20642358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural variants: changing the landscape of chromosomes and design of disease studies.
    Feuk L; Marshall CR; Wintle RF; Scherer SW
    Hum Mol Genet; 2006 Apr; 15 Spec No 1():R57-66. PubMed ID: 16651370
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The morbid anatomy of the human genome: chromosomal location of mutations causing disease (update 1 December 1993).
    McKusick VA; Amberger JS
    J Med Genet; 1994 Apr; 31(4):265-79. PubMed ID: 8071951
    [No Abstract]   [Full Text] [Related]  

  • 4. A similarity-based method for genome-wide prediction of disease-relevant human genes.
    Freudenberg J; Propping P
    Bioinformatics; 2002; 18 Suppl 2():S110-5. PubMed ID: 12385992
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of genes to genetically inherited diseases using data mining.
    Perez-Iratxeta C; Bork P; Andrade MA
    Nat Genet; 2002 Jul; 31(3):316-9. PubMed ID: 12006977
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Joe Doupe Young Investigators Award. The Human Genome Project: tools for the identification of disease genes.
    Hudson TJ
    Clin Invest Med; 1998 Dec; 21(6):267-76. PubMed ID: 9885761
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
    Abeysinghe SS; Chuzhanova N; Krawczak M; Ball EV; Cooper DN
    Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic rearrangements in inherited disease and cancer.
    Chen JM; Cooper DN; Férec C; Kehrer-Sawatzki H; Patrinos GP
    Semin Cancer Biol; 2010 Aug; 20(4):222-33. PubMed ID: 20541013
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome.
    Lock LF; Gilbert DJ; Street VA; Migeon MB; Jenkins NA; Copeland NG; Tempel BL
    Genomics; 1994 Apr; 20(3):354-62. PubMed ID: 8034307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disease genes and chromosomes: disease maps of the human genome. Chromosome 4.
    Goldfrank D; Schoenberger E; Gilbert F
    Genet Test; 2003; 7(4):351-72. PubMed ID: 15000816
    [No Abstract]   [Full Text] [Related]  

  • 11. Structure of chromosomal duplicons and their role in mediating human genomic disorders.
    Ji Y; Eichler EE; Schwartz S; Nicholls RD
    Genome Res; 2000 May; 10(5):597-610. PubMed ID: 10810082
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microdissection and microcloning of human chromosome regions in genome and genetic disease analysis.
    Kao FT
    Bioessays; 1993 Feb; 15(2):141-6. PubMed ID: 8471059
    [No Abstract]   [Full Text] [Related]  

  • 13. Discovering disease-genes by topological features in human protein-protein interaction network.
    Xu J; Li Y
    Bioinformatics; 2006 Nov; 22(22):2800-5. PubMed ID: 16954137
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Chromosomal abnormalities and genomic disorders].
    Inoue K
    Nihon Rinsho; 2005 Dec; 63 Suppl 12():64-9. PubMed ID: 16416772
    [No Abstract]   [Full Text] [Related]  

  • 15. The allelic spectra of common diseases may resemble the allelic spectrum of the full genome.
    Wang WY; Pike N
    Med Hypotheses; 2004; 63(4):748-51. PubMed ID: 15325027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
    Chuzhanova N; Abeysinghe SS; Krawczak M; Cooper DN
    Hum Mutat; 2003 Sep; 22(3):245-51. PubMed ID: 12938089
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factors influencing the identification of major genes in a complex disease genome scan.
    Yang H; Wang Y; Goldstein DR; Li Z; Vora H; Cantor RM
    Genet Epidemiol; 1997; 14(6):933-8. PubMed ID: 9433603
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The application of DNA recombinant technology to the analysis of the human genome and genetic disease.
    Davies KE
    Hum Genet; 1981; 58(4):351-7. PubMed ID: 7035333
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Report of the committee on clinical disorders and chromosomal deletion syndromes.
    Harper PS; Frézal J; Ferguson-Smith MA; Schinzel A
    Cytogenet Cell Genet; 1989; 51(1-4):563-611. PubMed ID: 2676384
    [No Abstract]   [Full Text] [Related]  

  • 20. Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes.
    Handyside AH; Harton GL; Mariani B; Thornhill AR; Affara N; Shaw MA; Griffin DK
    J Med Genet; 2010 Oct; 47(10):651-8. PubMed ID: 19858130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.