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 *

394 related articles for article (PubMed ID: 18654633)

  • 21. SNPs, haplotypes, and model selection in a candidate gene region: the SIMPle analysis for multilocus data.
    Conti DV; Gauderman WJ
    Genet Epidemiol; 2004 Dec; 27(4):429-41. PubMed ID: 15543635
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel bayesian graphical model for genome-wide multi-SNP association mapping.
    Zhang Y
    Genet Epidemiol; 2012 Jan; 36(1):36-47. PubMed ID: 22127647
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hierarchical Naive Bayes for genetic association studies.
    Malovini A; Barbarini N; Bellazzi R; de Michelis F
    BMC Bioinformatics; 2012; 13 Suppl 14(Suppl 14):S6. PubMed ID: 23095471
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fine mapping by linkage and association in nuclear family and case-control designs.
    Bull SB; John S; Briollais L
    Genet Epidemiol; 2005; 29 Suppl 1():S48-58. PubMed ID: 16342184
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Selecting Closely-Linked SNPs Based on Local Epistatic Effects for Haplotype Construction Improves Power of Association Mapping.
    Liu F; Schmidt RH; Reif JC; Jiang Y
    G3 (Bethesda); 2019 Dec; 9(12):4115-4126. PubMed ID: 31604824
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exploiting genome structure in association analysis.
    Kim S; Xing EP
    J Comput Biol; 2014 Apr; 21(4):345-60. PubMed ID: 21548809
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A custom correlation coefficient (CCC) approach for fast identification of multi-SNP association patterns in genome-wide SNPs data.
    Climer S; Yang W; de las Fuentes L; Dávila-Román VG; Gu CC
    Genet Epidemiol; 2014 Nov; 38(7):610-21. PubMed ID: 25168954
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations.
    Goodin DS; Khankhanian P
    PLoS One; 2014; 9(4):e90034. PubMed ID: 24727690
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bivariate association analysis for quantitative traits using generalized estimation equation.
    Yang F; Tang Z; Deng H
    J Genet Genomics; 2009 Dec; 36(12):733-43. PubMed ID: 20129400
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
    Huang J; Ellinghaus D; Franke A; Howie B; Li Y
    Eur J Hum Genet; 2012 Jul; 20(7):801-5. PubMed ID: 22293688
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Accuracy of prediction of simulated polygenic phenotypes and their underlying quantitative trait loci genotypes using real or imputed whole-genome markers in cattle.
    Hassani S; Saatchi M; Fernando RL; Garrick DJ
    Genet Sel Evol; 2015 Dec; 47():99. PubMed ID: 26698091
    [TBL] [Abstract][Full Text] [Related]  

  • 32. SNP-PRAGE: SNP-based parametric robust analysis of gene set enrichment.
    Lee J; Ahn S; Oh S; Weir B; Park T
    BMC Syst Biol; 2011; 5 Suppl 2(Suppl 2):S11. PubMed ID: 22784568
    [TBL] [Abstract][Full Text] [Related]  

  • 33. SNP-VISTA: an interactive SNP visualization tool.
    Shah N; Teplitsky MV; Minovitsky S; Pennacchio LA; Hugenholtz P; Hamann B; Dubchak IL
    BMC Bioinformatics; 2005 Dec; 6():292. PubMed ID: 16336665
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Weighted single-step genomic best linear unbiased prediction integrating variants selected from sequencing data by association and bioinformatics analyses.
    Liu A; Lund MS; Boichard D; Karaman E; Guldbrandtsen B; Fritz S; Aamand GP; Nielsen US; Sahana G; Wang Y; Su G
    Genet Sel Evol; 2020 Aug; 52(1):48. PubMed ID: 32799816
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
    Wallace C; Cutler AJ; Pontikos N; Pekalski ML; Burren OS; Cooper JD; García AR; Ferreira RC; Guo H; Walker NM; Smyth DJ; Rich SS; Onengut-Gumuscu S; Sawcer SJ; Ban M; Richardson S; Todd JA; Wicker LS
    PLoS Genet; 2015 Jun; 11(6):e1005272. PubMed ID: 26106896
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
    Maniatis N; Collins A; Morton NE
    Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multi-SNP Haplotype Analysis Methods for Association Analysis.
    Stram DO
    Methods Mol Biol; 2017; 1666():485-504. PubMed ID: 28980261
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Genomic screening and replication using the same data set in family-based association testing.
    Van Steen K; McQueen MB; Herbert A; Raby B; Lyon H; Demeo DL; Murphy A; Su J; Datta S; Rosenow C; Christman M; Silverman EK; Laird NM; Weiss ST; Lange C
    Nat Genet; 2005 Jul; 37(7):683-91. PubMed ID: 15937480
    [TBL] [Abstract][Full Text] [Related]  

  • 40. RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method.
    Hamazaki K; Iwata H
    PLoS Comput Biol; 2020 Feb; 16(2):e1007663. PubMed ID: 32059004
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.