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 *

133 related articles for article (PubMed ID: 18941524)

  • 21. Copy-number polymorphisms: mining the tip of an iceberg.
    Buckley PG; Mantripragada KK; Piotrowski A; Diaz de Ståhl T; Dumanski JP
    Trends Genet; 2005 Jun; 21(6):315-7. PubMed ID: 15922827
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies.
    Edwards BJ; Haynes C; Levenstien MA; Finch SJ; Gordon D
    BMC Genet; 2005 Apr; 6():18. PubMed ID: 15819990
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Likelihood ratio tests in behavioral genetics: problems and solutions.
    Dominicus A; Skrondal A; Gjessing HK; Pedersen NL; Palmgren J
    Behav Genet; 2006 Mar; 36(2):331-40. PubMed ID: 16474914
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Empirical likelihood-based confidence intervals for the sensitivity of a continuous-scale diagnostic test at a fixed level of specificity.
    Gengsheng Qin ; Davis AE; Jing BY
    Stat Methods Med Res; 2011 Jun; 20(3):217-31. PubMed ID: 19654172
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A revisit to sample size and power calculations for testing odds ratio in two independent binomials.
    Liu F
    Biometrics; 2013 Jun; 69(2):530-6. PubMed ID: 23724826
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Incorporating individual error rate into association test of unmatched case-control design.
    Hao K; Wang X
    Hum Hered; 2004; 58(3-4):154-63. PubMed ID: 15812172
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Methods for flexible sample-size design in clinical trials: Likelihood, weighted, dual test, and promising zone approaches.
    Shih WJ; Li G; Wang Y
    Contemp Clin Trials; 2016 Mar; 47():40-8. PubMed ID: 26674739
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sample size and optimal design for logistic regression with binary interaction.
    Demidenko E
    Stat Med; 2008 Jan; 27(1):36-46. PubMed ID: 17634969
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Bayesian approach to copy-number-polymorphism analysis in nuclear pedigrees.
    Kosta K; Sabroe I; Goke J; Nibbs RJ; Tsanakas J; Whyte MK; Teare MD
    Am J Hum Genet; 2007 Oct; 81(4):808-12. PubMed ID: 17847005
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Comparison of one-sample two-sided sequential t-tests for application in epidemiological studies.
    van der Tweel I; Kaaks R; van Noord PA
    Stat Med; 1996 Dec; 15(24):2781-95. PubMed ID: 8981686
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection of copy number variation and single nucleotide polymorphisms in genes involved in drug resistance and other phenotypic traits in P. falciparum clinical isolates collected from Uganda.
    Kiwuwa MS; Byarugaba J; Wahlgren M; Kironde F
    Acta Trop; 2013 Mar; 125(3):269-75. PubMed ID: 23220229
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A comparison of statistical selection strategies for univariate and bivariate log-linear models.
    Moses T; Holland PW
    Br J Math Stat Psychol; 2010 Nov; 63(Pt 3):557-74. PubMed ID: 20030964
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genotypic relative risks under ordered restriction.
    Chiano MN; Clayton DG
    Genet Epidemiol; 1998; 15(2):135-46. PubMed ID: 9554552
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chi-Squared Test of Fit and Sample Size-A Comparison between a Random Sample Approach and a Chi-Square Value Adjustment Method.
    Bergh D
    J Appl Meas; 2015; 16(2):204-17. PubMed ID: 26075668
    [TBL] [Abstract][Full Text] [Related]  

  • 35. PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.
    Kumasaka N; Fujisawa H; Hosono N; Okada Y; Takahashi A; Nakamura Y; Kubo M; Kamatani N
    Genet Epidemiol; 2011 Dec; 35(8):831-44. PubMed ID: 22125222
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Statistical tests of genetic association for case-control study designs.
    Wang K
    Biostatistics; 2012 Sep; 13(4):724-33. PubMed ID: 22389176
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Xeroderma pigmentosum group D polymorphisms and esophageal cancer susceptibility: a meta-analysis based on case-control studies.
    Yang R; Zhang C; Malik A; Shen ZD; Hu J; Wu YH
    World J Gastroenterol; 2014 Nov; 20(44):16765-73. PubMed ID: 25469049
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association between HRH4 polymorphisms and ankylosing spondylitis susceptibility.
    Ran B; Wang Y; Zhang Y; Mao K; Wang Y
    Int J Clin Exp Pathol; 2015; 8(11):15265-9. PubMed ID: 26823878
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note.
    Zou GY; Donner A
    Ann Hum Genet; 2006 Nov; 70(Pt 6):923-33. PubMed ID: 17044866
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The use of imputed sibling genotypes in sibship-based association analysis: on modeling alternatives, power and model misspecification.
    Minică CC; Dolan CV; Hottenga JJ; Willemsen G; Vink JM; Boomsma DI
    Behav Genet; 2013 May; 43(3):254-66. PubMed ID: 23519635
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.