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 *

146 related articles for article (PubMed ID: 18814307)

  • 21. Susceptibility of biallelic haplotype and genotype frequencies to genotyping error.
    Moskvina V; Schmidt KM
    Biometrics; 2006 Dec; 62(4):1116-23. PubMed ID: 17156286
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Tests of association between quantitative traits and haplotypes in a reduced-dimensional space.
    Sha Q; Dong J; Jiang R; Zhang S
    Ann Hum Genet; 2005 Nov; 69(Pt 6):715-32. PubMed ID: 16266410
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Efficiency and power in genetic association studies.
    de Bakker PI; Yelensky R; Pe'er I; Gabriel SB; Daly MJ; Altshuler D
    Nat Genet; 2005 Nov; 37(11):1217-23. PubMed ID: 16244653
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Logistic regression model for analyzing extended haplotype data.
    Wallenstein S; Hodge SE; Weston A
    Genet Epidemiol; 1998; 15(2):173-81. PubMed ID: 9554554
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Comparison of the accuracy of methods of computational haplotype inference using a large empirical dataset.
    Adkins RM
    BMC Genet; 2004 Aug; 5():22. PubMed ID: 15291970
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Testing for genetic association: a powerful score test.
    El Galta R; Stijnen T; Houwing-Duistermaat JJ
    Stat Med; 2008 Sep; 27(22):4596-609. PubMed ID: 18551534
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Entropy-supported marker selection and Mantel statistics for haplotype sharing analysis.
    Schulz A; Fischer C; Chang-Claude J; Beckmann L
    Genet Epidemiol; 2010 May; 34(4):354-63. PubMed ID: 20151460
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Comparison of association methods for dense marker data.
    Bacanu SA; Nelson MR; Ehm MG
    Genet Epidemiol; 2008 Dec; 32(8):791-9. PubMed ID: 18551558
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tag SNP selection for association studies.
    Stram DO
    Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Exploring causality via identification of SNPs or haplotypes responsible for a linkage signal.
    Biernacka JM; Cordell HJ
    Genet Epidemiol; 2007 Nov; 31(7):727-40. PubMed ID: 17508343
    [TBL] [Abstract][Full Text] [Related]  

  • 32. CLUMPHAP: a simple tool for performing haplotype-based association analysis.
    Knight J; Curtis D; Sham PC
    Genet Epidemiol; 2008 Sep; 32(6):539-45. PubMed ID: 18395815
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Assessing the power of tag SNPs in the mapping of quantitative trait loci (QTL) with extremal and random samples.
    Zhang K; Sun F
    BMC Genet; 2005 Oct; 6():51. PubMed ID: 16236175
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Optimal selection of SNP markers for disease association studies.
    Halldórsson BV; Istrail S; De La Vega FM
    Hum Hered; 2004; 58(3-4):190-202. PubMed ID: 15812176
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Haplotype sharing analysis using mantel statistics.
    Beckmann L; Thomas DC; Fischer C; Chang-Claude J
    Hum Hered; 2005; 59(2):67-78. PubMed ID: 15838176
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Simple estimates of haplotype relative risks in case-control data.
    French B; Lumley T; Monks SA; Rice KM; Hindorff LA; Reiner AP; Psaty BM
    Genet Epidemiol; 2006 Sep; 30(6):485-94. PubMed ID: 16755519
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Effect of two- and three-locus linkage disequilibrium on the power to detect marker/phenotype associations.
    Nielsen DM; Ehm MG; Zaykin DV; Weir BS
    Genetics; 2004 Oct; 168(2):1029-40. PubMed ID: 15514073
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Use of unphased multilocus genotype data in indirect association studies.
    Clayton D; Chapman J; Cooper J
    Genet Epidemiol; 2004 Dec; 27(4):415-28. PubMed ID: 15481099
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The haplotype runs test: the parent-parent-affected offspring trio design.
    Lange EM; Boehnke M
    Genet Epidemiol; 2004 Sep; 27(2):118-30. PubMed ID: 15305328
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.