BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1018 related articles for article (PubMed ID: 22863193)

  • 1. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
    Lee S; Emond MJ; Bamshad MJ; Barnes KC; Rieder MJ; Nickerson DA; ; Christiani DC; Wurfel MM; Lin X
    Am J Hum Genet; 2012 Aug; 91(2):224-37. PubMed ID: 22863193
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Optimal tests for rare variant effects in sequencing association studies.
    Lee S; Wu MC; Lin X
    Biostatistics; 2012 Sep; 13(4):762-75. PubMed ID: 22699862
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Likelihood ratio tests in rare variant detection for continuous phenotypes.
    Zeng P; Zhao Y; Liu J; Liu L; Zhang L; Wang T; Huang S; Chen F
    Ann Hum Genet; 2014 Sep; 78(5):320-32. PubMed ID: 25117149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Generalized functional linear models for gene-based case-control association studies.
    Fan R; Wang Y; Mills JL; Carter TC; Lobach I; Wilson AF; Bailey-Wilson JE; Weeks DE; Xiong M
    Genet Epidemiol; 2014 Nov; 38(7):622-637. PubMed ID: 25203683
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.
    Fan R; Chiu CY; Jung J; Weeks DE; Wilson AF; Bailey-Wilson JE; Amos CI; Chen Z; Mills JL; Xiong M
    Genet Epidemiol; 2016 Dec; 40(8):702-721. PubMed ID: 27374056
    [TBL] [Abstract][Full Text] [Related]  

  • 7. On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set.
    Wu B; Guan W; Pankow JS
    Ann Hum Genet; 2016 Mar; 80(2):123-35. PubMed ID: 26757198
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A Zoom-Focus algorithm (ZFA) to locate the optimal testing region for rare variant association tests.
    Wang MH; Weng H; Sun R; Lee J; Wu WKK; Chong KC; Zee BC
    Bioinformatics; 2017 Aug; 33(15):2330-2336. PubMed ID: 28334355
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies.
    Liu Y; Chen S; Li Z; Morrison AC; Boerwinkle E; Lin X
    Am J Hum Genet; 2019 Mar; 104(3):410-421. PubMed ID: 30849328
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.
    Dutta D; Scott L; Boehnke M; Lee S
    Genet Epidemiol; 2019 Feb; 43(1):4-23. PubMed ID: 30298564
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A powerful association test of multiple genetic variants using a random-effects model.
    Cheng KF; Lee JY; Zheng W; Li C
    Stat Med; 2014 May; 33(11):1816-27. PubMed ID: 24338936
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A variational Bayes discrete mixture test for rare variant association.
    Logsdon BA; Dai JY; Auer PL; Johnsen JM; Ganesh SK; Smith NL; Wilson JG; Tracy RP; Lange LA; Jiao S; Rich SS; Lettre G; Carlson CS; Jackson RD; O'Donnell CJ; Wurfel MM; Nickerson DA; Tang H; Reiner AP; Kooperberg C;
    Genet Epidemiol; 2014 Jan; 38(1):21-30. PubMed ID: 24482836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.
    Ma C; Boehnke M; Lee S;
    Genet Epidemiol; 2015 Nov; 39(7):499-508. PubMed ID: 26454253
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Functional linear models for association analysis of quantitative traits.
    Fan R; Wang Y; Mills JL; Wilson AF; Bailey-Wilson JE; Xiong M
    Genet Epidemiol; 2013 Nov; 37(7):726-42. PubMed ID: 24130119
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions.
    Fan R; Wang Y; Yan Q; Ding Y; Weeks DE; Lu Z; Ren H; Cook RJ; Xiong M; Swaroop A; Chew EY; Chen W
    Genet Epidemiol; 2016 Feb; 40(2):133-43. PubMed ID: 26782979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. AP-SKAT: highly-efficient genome-wide rare variant association test.
    Hasegawa T; Kojima K; Kawai Y; Misawa K; Mimori T; Nagasaki M
    BMC Genomics; 2016 Sep; 17(1):745. PubMed ID: 27654840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico.
    Zhang X; Basile AO; Pendergrass SA; Ritchie MD
    BMC Bioinformatics; 2019 Jan; 20(1):46. PubMed ID: 30669967
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 51.