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 *

93 related articles for article (PubMed ID: 22373382)

  • 1. Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates.
    Kazma R; Hoffmann TJ; Witte JS
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S29. PubMed ID: 22373382
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Gene-based multiple trait analysis for exome sequencing data.
    Zhao J; Thalamuthu A
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S75. PubMed ID: 22373189
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Utilizing mutual information for detecting rare and common variants associated with a categorical trait.
    Sun L; Wang C; Hu YQ
    PeerJ; 2016; 4():e2139. PubMed ID: 27350900
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Improved power by collapsing rare and common variants based on a data-adaptive forward selection strategy.
    Dai Y; Guo L; Dong J; Jiang R
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S114. PubMed ID: 22373230
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling.
    Nock N; Zhang L
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S47. PubMed ID: 22373404
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.
    Dai Y; Jiang R; Dong J
    BMC Genet; 2012 Feb; 13():7. PubMed ID: 22309429
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association tests for rare and common variants based on genotypic and phenotypic measures of similarity between individuals.
    Thalamuthu A; Zhao J; Keong GT; Kondragunta V; Mukhopadhyay I
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S89. PubMed ID: 22373048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits.
    Zhang Q; Chung D; Kraja A; Borecki II; Province MA
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S35. PubMed ID: 22373066
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association studies for next-generation sequencing.
    Luo L; Boerwinkle E; Xiong M
    Genome Res; 2011 Jul; 21(7):1099-108. PubMed ID: 21521787
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Family-based association studies for next-generation sequencing.
    Zhu Y; Xiong M
    Am J Hum Genet; 2012 Jun; 90(6):1028-45. PubMed ID: 22682329
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide case-control study in GAW17 using coalesced rare variants.
    Wang L; Pungpapong V; Lin Y; Zhang M; Zhang D
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S110. PubMed ID: 22373135
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of multiple rare variants associated with a disease.
    Jung J; Dantzer J; Liu Y
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S103. PubMed ID: 22373445
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19.
    Ho YY; Guan W; O'Connell M; Basu S
    BMC Proc; 2016; 10(Suppl 7):251-255. PubMed ID: 27980645
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adjustment of familial relatedness in association test for rare variants.
    Li C; Yang C; Chen M; Chen X; Hou L; Zhao H
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S39. PubMed ID: 25519384
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Comparison of statistical tests for association between rare variants and binary traits.
    Bacanu SA; Nelson MR; Whittaker JC
    PLoS One; 2012; 7(8):e42530. PubMed ID: 22912707
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A robust GWSS method to simultaneously detect rare and common variants for complex disease.
    Kao CF; Liu JR; Hung H; Kuo PH
    PLoS One; 2015; 10(4):e0120873. PubMed ID: 25880329
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparison of genetic association strategies in the presence of rare alleles.
    Mahachie John JM; Cattaert T; De Lobel L; Van Lishout F; Empain A; Van Steen K
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S32. PubMed ID: 22373505
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data.
    Saad M; Pierre AS; Bohossian N; Macé M; Martinez M
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S33. PubMed ID: 22373523
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.