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 *

87 related articles for article (PubMed ID: 30255768)

  • 1. Indirect effect inference and application to GAW20 data.
    Li L; Wang C; Lu T; Lin S; Hu YQ
    BMC Genet; 2018 Sep; 19(Suppl 1):67. PubMed ID: 30255768
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.
    Sarnowski C; Lent S; Dupuis J
    BMC Genet; 2018 Sep; 19(Suppl 1):83. PubMed ID: 30255771
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20.
    Fuady AM; Lent S; Sarnowski C; Tintle NL
    BMC Genet; 2018 Sep; 19(Suppl 1):72. PubMed ID: 30255777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Causal modeling in a multi-omic setting: insights from GAW20.
    Auerbach J; Howey R; Jiang L; Justice A; Li L; Oualkacha K; Sayols-Baixeras S; Aslibekyan SW
    BMC Genet; 2018 Sep; 19(Suppl 1):74. PubMed ID: 30255779
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The challenge of detecting genotype-by-methylation interaction: GAW20.
    de Andrade M; Warwick Daw E; Kraja AT; Fisher V; Wang L; Hu K; Li J; Romanescu R; Veenstra J; Sun R; Weng H; Zhou W
    BMC Genet; 2018 Sep; 19(Suppl 1):81. PubMed ID: 30255819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Joint analysis of genetic and epigenetic data using a conditional autoregressive model.
    Shen X; Lu Q
    BMC Genet; 2018 Sep; 19(Suppl 1):71. PubMed ID: 30255769
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quality control for Illumina 450K methylation data in the absence of iDat files using correlation structure in pedigrees and repeated measures.
    LeBlanc M; Nustad HE; Zucknick M; Page CM
    BMC Genet; 2018 Sep; 19(Suppl 1):66. PubMed ID: 30255766
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparison of novel and existing methods for detecting differentially methylated regions.
    Lent S; Xu H; Wang L; Wang Z; Sarnowski C; Hivert MF; Dupuis J
    BMC Genet; 2018 Sep; 19(Suppl 1):84. PubMed ID: 30255775
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Methods and results from the genome-wide association group at GAW20.
    Wang X; Boekstegers F; Brinster R
    BMC Genet; 2018 Sep; 19(Suppl 1):79. PubMed ID: 30255814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association analyses of repeated measures on triglyceride and high-density lipoprotein levels: insights from GAW20.
    Ghosh S; Fardo DW
    BMC Genet; 2018 Sep; 19(Suppl 1):73. PubMed ID: 30255818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An integrative association method for omics data based on a modified Fisher's method with application to childhood asthma.
    Yan Q; Liu N; Forno E; Canino G; Celedón JC; Chen W
    PLoS Genet; 2019 May; 15(5):e1008142. PubMed ID: 31063461
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Incorporating methylation genome information improves prediction accuracy for drug treatment responses.
    Xia X; Weng H; Men R; Sun R; Zee BCY; Chong KC; Wang MH
    BMC Genet; 2018 Sep; 19(Suppl 1):78. PubMed ID: 30255773
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An adaptive gene-level association test for pedigree data.
    Park JY; Wu C; Pan W
    BMC Genet; 2018 Sep; 19(Suppl 1):68. PubMed ID: 30255770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Do changes in DNA methylation mediate or interact with SNP variation? A pharmacoepigenetic analysis.
    Fisher VA; Wang L; Deng X; Sarnowski C; Cupples LA; Liu CT
    BMC Genet; 2018 Sep; 19(Suppl 1):70. PubMed ID: 30255765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A retrospective likelihood approach for efficient integration of multiple omics factors in case-control association studies.
    Balliu B; Tsonaka R; Boehringer S; Houwing-Duistermaat J
    Genet Epidemiol; 2015 Mar; 39(3):156-65. PubMed ID: 25620726
    [TBL] [Abstract][Full Text] [Related]  

  • 16. BioVLAB-mCpG-SNP-EXPRESS: A system for multi-level and multi-perspective analysis and exploration of DNA methylation, sequence variation (SNPs), and gene expression from multi-omics data.
    Chae H; Lee S; Seo S; Jung D; Chang H; Nephew KP; Kim S
    Methods; 2016 Dec; 111():64-71. PubMed ID: 27477210
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel Markov Blanket-based repeated-fishing strategy for capturing phenotype-related biomarkers in big omics data.
    Li H; Yuan Z; Ji J; Xu J; Zhang T; Zhang X; Xue F
    BMC Genet; 2016 Mar; 17():51. PubMed ID: 26957081
    [TBL] [Abstract][Full Text] [Related]  

  • 18. iGWAS: Integrative Genome-Wide Association Studies of Genetic and Genomic Data for Disease Susceptibility Using Mediation Analysis.
    Huang YT; Liang L; Moffatt MF; Cookson WO; Lin X
    Genet Epidemiol; 2015 Jul; 39(5):347-56. PubMed ID: 25997986
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype distribution-based inference of collective effects in genome-wide association studies: insights to age-related macular degeneration disease mechanism.
    Woo HJ; Yu C; Kumar K; Gold B; Reifman J
    BMC Genomics; 2016 Aug; 17(1):695. PubMed ID: 27576376
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Using recursive feature elimination in random forest to account for correlated variables in high dimensional data.
    Darst BF; Malecki KC; Engelman CD
    BMC Genet; 2018 Sep; 19(Suppl 1):65. PubMed ID: 30255764
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.