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 *

141 related articles for article (PubMed ID: 24905468)

  • 1. FFBSKAT: fast family-based sequence kernel association test.
    Svishcheva GR; Belonogova NM; Axenovich TI
    PLoS One; 2014; 9(6):e99407. PubMed ID: 24905468
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FREGAT: an R package for region-based association analysis.
    Belonogova NM; Svishcheva GR; Axenovich TI
    Bioinformatics; 2016 Aug; 32(15):2392-3. PubMed ID: 27153598
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare variant association test in family-based sequencing studies.
    Wang X; Zhang Z; Morris N; Cai T; Lee S; Wang C; Yu TW; Walsh CA; Lin X
    Brief Bioinform; 2017 Nov; 18(6):954-961. PubMed ID: 27677958
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Region-based association analysis of human quantitative traits in related individuals.
    Belonogova NM; Svishcheva GR; van Duijn CM; Aulchenko YS; Axenovich TI
    PLoS One; 2013; 8(6):e65395. PubMed ID: 23799013
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family-based gene-environment interaction using sequence kernel association test (FGE-SKAT) for complex quantitative traits.
    Guo CY; Wang RH; Yang HC
    Sci Rep; 2021 Apr; 11(1):7431. PubMed ID: 33795796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction.
    Marceau R; Lu W; Holloway S; Sale MM; Worrall BB; Williams SR; Hsu FC; Tzeng JY
    Genet Epidemiol; 2015 Sep; 39(6):456-68. PubMed ID: 26139508
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model.
    Yan Q; Tiwari HK; Yi N; Gao G; Zhang K; Lin WY; Lou XY; Cui X; Liu N
    Hum Hered; 2015; 79(2):60-8. PubMed ID: 25791389
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data.
    Zhang D; Zhao L; Li B; He Z; Wang GT; Liu DJ; Leal SM
    Am J Hum Genet; 2017 Jul; 101(1):115-122. PubMed ID: 28669402
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adjusted sequence kernel association test for rare variants controlling for cryptic and family relatedness.
    Oualkacha K; Dastani Z; Li R; Cingolani PE; Spector TD; Hammond CJ; Richards JB; Ciampi A; Greenwood CM
    Genet Epidemiol; 2013 May; 37(4):366-76. PubMed ID: 23529756
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.
    Yan Q; Tiwari HK; Yi N; Lin WY; Gao G; Lou XY; Cui X; Liu N
    Genet Epidemiol; 2014 Jul; 38(5):447-56. PubMed ID: 24849109
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare variants detection with kernel machine learning based on likelihood ratio test.
    Zeng P; Zhao Y; Zhang L; Huang S; Chen F
    PLoS One; 2014; 9(3):e93355. PubMed ID: 24675868
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MQScore_SNP software for multipoint parametric linkage analysis of quantitative traits in large pedigrees.
    Axenovich TI; Aulchenko YS
    Ann Hum Genet; 2010 May; 74(3):286-9. PubMed ID: 20529018
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sequence kernel association tests for the combined effect of rare and common variants.
    Ionita-Laza I; Lee S; Makarov V; Buxbaum JD; Lin X
    Am J Hum Genet; 2013 Jun; 92(6):841-53. PubMed ID: 23684009
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Region-based association tests for sequencing data on survival traits.
    Chien LC; Bowden DW; Chiu YF
    Genet Epidemiol; 2017 Sep; 41(6):511-522. PubMed ID: 28580640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Boosting Gene Mapping Power and Efficiency with Efficient Exact Variance Component Tests of Single Nucleotide Polymorphism Sets.
    Zhou JJ; Hu T; Qiao D; Cho MH; Zhou H
    Genetics; 2016 Nov; 204(3):921-931. PubMed ID: 27646141
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare-variant association testing for sequencing data with the sequence kernel association test.
    Wu MC; Lee S; Cai T; Li Y; Boehnke M; Lin X
    Am J Hum Genet; 2011 Jul; 89(1):82-93. PubMed ID: 21737059
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sequence Kernel Association Test of Multiple Continuous Phenotypes.
    Wu B; Pankow JS
    Genet Epidemiol; 2016 Feb; 40(2):91-100. PubMed ID: 26782911
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Region-Based Association Test for Familial Data under Functional Linear Models.
    Svishcheva GR; Belonogova NM; Axenovich TI
    PLoS One; 2015; 10(6):e0128999. PubMed ID: 26111046
    [TBL] [Abstract][Full Text] [Related]  

  • 19. On Robust Association Testing for Quantitative Traits and Rare Variants.
    Wei P; Cao Y; Zhang Y; Xu Z; Kwak IY; Boerwinkle E; Pan W
    G3 (Bethesda); 2016 Dec; 6(12):3941-3950. PubMed ID: 27678522
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits.
    Oualkacha K; Lakhal-Chaieb L; Greenwood CM
    Int J Epidemiol; 2016 Apr; 45(2):402-7. PubMed ID: 27085080
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.