BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 9728890)

  • 1. Parental genotype reconstruction: applications of haplotype relative risk to incomplete parental data.
    Martin RB; Alda M; MacLean CJ
    Genet Epidemiol; 1998; 15(5):471-90. PubMed ID: 9728890
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype relative-risks and association tests for nuclear families with missing parental data.
    Schaid DJ; Li H
    Genet Epidemiol; 1997; 14(6):1113-8. PubMed ID: 9433633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haplotype association analysis for late onset diseases using nuclear family data.
    Li C; Boehnke M
    Genet Epidemiol; 2006 Apr; 30(3):220-30. PubMed ID: 16470533
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Quantifying the amount of missing information in genetic association studies.
    Nicolae DL
    Genet Epidemiol; 2006 Dec; 30(8):703-17. PubMed ID: 16986163
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.
    Zhang K; Sun F; Zhao H
    Bioinformatics; 2005 Jan; 21(1):90-103. PubMed ID: 15231536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Statistical properties of the haplotype relative risk.
    Ott J
    Genet Epidemiol; 1989; 6(1):127-30. PubMed ID: 2731704
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype construction of sires with progeny genotypes based on an exact likelihood.
    Du FX; Woodward BW; Denise SK
    J Dairy Sci; 1998 May; 81(5):1462-8. PubMed ID: 9621250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reconstructing parental genotypes when testing for linkage in the presence of association.
    Knapp M
    Theor Popul Biol; 2001 Nov; 60(3):141-8. PubMed ID: 11855948
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High resolution T association tests of complex diseases based on family data.
    Fan R; Knapp M; Wjst M; Zhao C; Xiong M
    Ann Hum Genet; 2005 Mar; 69(Pt 2):187-208. PubMed ID: 15720300
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Maximum-likelihood estimation of haplotype frequencies in nuclear families.
    Becker T; Knapp M
    Genet Epidemiol; 2004 Jul; 27(1):21-32. PubMed ID: 15185400
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment.
    Carayol J; Philippi A; Tores F
    Genet Epidemiol; 2006 Dec; 30(8):666-76. PubMed ID: 16917928
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Power of direct vs. indirect haplotyping in association studies.
    Thomas S; Porteous D; Visscher PM
    Genet Epidemiol; 2004 Feb; 26(2):116-24. PubMed ID: 14748011
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Use of siblings as controls in case-control association studies.
    Curtis D
    Ann Hum Genet; 1997 Jul; 61(Pt 4):319-33. PubMed ID: 9365785
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tests for genetic association using family data.
    Shih MC; Whittemore AS
    Genet Epidemiol; 2002 Feb; 22(2):128-45. PubMed ID: 11788959
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design.
    Zhang L; Martin ER; Chung RH; Li YJ; Morris RW
    Genet Epidemiol; 2008 May; 32(4):370-80. PubMed ID: 18278816
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multipoint linkage disequilibrium mapping using multilocus allele frequency data.
    Johnson T
    Ann Hum Genet; 2005 Jul; 69(Pt 4):474-97. PubMed ID: 15996175
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Susceptibility of biallelic haplotype and genotype frequencies to genotyping error.
    Moskvina V; Schmidt KM
    Biometrics; 2006 Dec; 62(4):1116-23. PubMed ID: 17156286
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The haplotype runs test: the parent-parent-affected offspring trio design.
    Lange EM; Boehnke M
    Genet Epidemiol; 2004 Sep; 27(2):118-30. PubMed ID: 15305328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.
    Morris RW; Kaplan NL
    Genet Epidemiol; 2002 Oct; 23(3):221-33. PubMed ID: 12384975
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haplotype sharing transmission/disequilibrium tests that allow for genotyping errors.
    Sha Q; Dong J; Jiang R; Chen HS; Zhang S
    Genet Epidemiol; 2005 May; 28(4):341-51. PubMed ID: 15662724
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.