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 *

117 related articles for article (PubMed ID: 19197338)

  • 1. A practical case-control association test for detecting a susceptibility allele at a copy number variation locus.
    Ohashi J
    J Hum Genet; 2009 Mar; 54(3):169-73. PubMed ID: 19197338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [The use of the expectation-maximization (EM) algorithm for maximum likelihood estimation of gametic frequencies of multilocus polymorphic codominant systems based on sampled population data].
    Sergeev AS; Arapova RK
    Genetika; 2002 Mar; 38(3):407-18. PubMed ID: 11963570
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of artificial neural network analysis with other multimarker methods for detecting genetic association.
    Curtis D
    BMC Genet; 2007 Jul; 8():49. PubMed ID: 17640352
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Selecting a contingency table in a population-based association study: allele frequency or positivity?
    Ohashi J; Tokunaga K
    J Hum Genet; 1999; 44(4):246-8. PubMed ID: 10429364
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Issues concerning association studies for fine mapping a susceptibility gene for a complex disease.
    Kaplan N; Morris R
    Genet Epidemiol; 2001 May; 20(4):432-57. PubMed ID: 11319784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.
    Morris RW; Kaplan NL
    Genet Epidemiol; 2002 Oct; 23(3):221-33. PubMed ID: 12384975
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Simple method to analyze SNP-based association studies using DNA pools.
    Visscher PM; Le Hellard S
    Genet Epidemiol; 2003 May; 24(4):291-6. PubMed ID: 12687646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hla-B genotype in Japanese patients with Crohn's disease.
    Kinouchi Y; Matsumoto K; Negoro K; Takagi S; Takahashi S; Hiwatashi N; Shimosegawa T
    Dis Colon Rectum; 2003 Oct; 46(10 Suppl):S10-4. PubMed ID: 14530653
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation.
    Moskvina V; O'Donovan MC
    Hum Hered; 2007; 64(1):63-73. PubMed ID: 17483598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Power estimation of multiple SNP association test of case-control study and application.
    Hao K; Xu X; Laird N; Wang X; Xu X
    Genet Epidemiol; 2004 Jan; 26(1):22-30. PubMed ID: 14691954
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variation of FCGR3A rather than FCGR3B and FCGR2B is associated with susceptibility to anti-GBM disease.
    Zhou XJ; Lv JC; Bu DF; Yu L; Yang YR; Zhao J; Cui Z; Yang R; Zhao MH; Zhang H
    Int Immunol; 2010 Jan; 22(1):45-51. PubMed ID: 19946017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The role of DNA copy number variation in schizophrenia.
    Tam GW; Redon R; Carter NP; Grant SG
    Biol Psychiatry; 2009 Dec; 66(11):1005-12. PubMed ID: 19748074
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus.
    Edberg JC; Langefeld CD; Wu J; Moser KL; Kaufman KM; Kelly J; Bansal V; Brown WM; Salmon JE; Rich SS; Harley JB; Kimberly RP
    Arthritis Rheum; 2002 Aug; 46(8):2132-40. PubMed ID: 12209518
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prospects for association-based fine mapping of a susceptibility gene for a complex disease.
    Kaplan N; Morris R
    Theor Popul Biol; 2001 Nov; 60(3):181-91. PubMed ID: 11855952
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci.
    North BV; Curtis D; Martin ER; Lai EH; Roses AD; Sham PC
    Ann Hum Genet; 2004 May; 68(Pt 3):240-8. PubMed ID: 15180704
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers.
    Ohashi J; Tokunaga K
    J Hum Genet; 2001; 46(8):478-82. PubMed ID: 11501946
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variations in affective disorders and meta-analysis.
    Olsen L; Hansen T; Djurovic S; Haastrup E; Albrecthsen A; Hoeffding LK; Secher A; Gustafsson O; Jakobsen KD; Nielsen FC; Ullum H; Morken G; Agartz I; Melle I; Gether U; Andreassen OA; Werge T
    Psychiatr Genet; 2011 Dec; 21(6):319-22. PubMed ID: 21451435
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
    Weiss LA
    Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Contribution of Fcgamma receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis.
    Thabet MM; Huizinga TW; Marques RB; Stoeken-Rijsbergen G; Bakker AM; Kurreeman FA; White SJ; Toes RE; van der Helm-van Mil AH
    Ann Rheum Dis; 2009 Nov; 68(11):1775-80. PubMed ID: 19019892
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide high-resolution screening in Dupuytren's disease reveals common regions of DNA copy number alterations.
    Shih BB; Tassabehji M; Watson JS; McGrouther AD; Bayat A
    J Hand Surg Am; 2010 Jul; 35(7):1172-1183.e7. PubMed ID: 20561756
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.