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 *

212 related articles for article (PubMed ID: 22319458)

  • 1. The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.
    Ladouceur M; Dastani Z; Aulchenko YS; Greenwood CM; Richards JB
    PLoS Genet; 2012 Feb; 8(2):e1002496. PubMed ID: 22319458
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals.
    Ladouceur M; Zheng HF; Greenwood CM; Richards JB
    Eur J Hum Genet; 2013 Sep; 21(9):1027-30. PubMed ID: 23321613
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of methods and sampling designs to test for association between rare variants and quantitative traits.
    Bacanu SA; Nelson MR; Whittaker JC
    Genet Epidemiol; 2011 May; 35(4):226-35. PubMed ID: 21370253
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An evaluation of statistical approaches to rare variant analysis in genetic association studies.
    Morris AP; Zeggini E
    Genet Epidemiol; 2010 Feb; 34(2):188-93. PubMed ID: 19810025
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants.
    Guey LT; Kravic J; Melander O; Burtt NP; Laramie JM; Lyssenko V; Jonsson A; Lindholm E; Tuomi T; Isomaa B; Nilsson P; Almgren P; Kathiresan S; Groop L; Seymour AB; Altshuler D; Voight BF
    Genet Epidemiol; 2011 May; 35(4):236-46. PubMed ID: 21308769
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare variant association testing for next-generation sequencing data via hierarchical clustering.
    Tachmazidou I; Morris A; Zeggini E
    Hum Hered; 2012; 74(3-4):165-71. PubMed ID: 23594494
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two adaptive weighting methods to test for rare variant associations in family-based designs.
    Fang S; Sha Q; Zhang S
    Genet Epidemiol; 2012 Jul; 36(5):499-507. PubMed ID: 22674630
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Resequencing of pooled DNA for detecting disease associations with rare variants.
    Wang T; Lin CY; Rohan TE; Ye K
    Genet Epidemiol; 2010 Jul; 34(5):492-501. PubMed ID: 20578089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions.
    Liu DJ; Leal SM
    PLoS Genet; 2010 Oct; 6(10):e1001156. PubMed ID: 20976247
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.
    Cheung YH; Wang G; Leal SM; Wang S
    Genet Epidemiol; 2012 Nov; 36(7):675-85. PubMed ID: 22865616
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A power set-based statistical selection procedure to locate susceptible rare variants associated with complex traits with sequencing data.
    Sun H; Wang S
    Bioinformatics; 2014 Aug; 30(16):2317-23. PubMed ID: 24755303
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data.
    Wang P; Rahman M; Jin L; Xiong M
    BMC Genomics; 2016 Nov; 17(1):881. PubMed ID: 27821073
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Robust and Powerful Affected Sibpair Test for Rare Variant Association.
    Lin KH; Zöllner S
    Genet Epidemiol; 2015 Jul; 39(5):325-33. PubMed ID: 25966809
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.
    Moutsianas L; Agarwala V; Fuchsberger C; Flannick J; Rivas MA; Gaulton KJ; Albers PK; ; McVean G; Boehnke M; Altshuler D; McCarthy MI
    PLoS Genet; 2015 Apr; 11(4):e1005165. PubMed ID: 25906071
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare variant association test with multiple phenotypes.
    Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
    Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Discovery of rare variants for complex phenotypes.
    Kosmicki JA; Churchhouse CL; Rivas MA; Neale BM
    Hum Genet; 2016 Jun; 135(6):625-34. PubMed ID: 27221085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
    DE LA Vega FM; Bustamante CD; Leal SM
    Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
    [TBL] [Abstract][Full Text] [Related]  

  • 20. KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBIN.
    Basile AO; Wallace JR; Peissig P; McCarty CA; Brilliant M; Ritchie MD
    Pac Symp Biocomput; 2016; 21():249-60. PubMed ID: 26776191
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.