205 related articles for article (PubMed ID: 11731502)
1. Trimming, weighting, and grouping SNPs in human case-control association studies.
Hoh J; Wille A; Ott J
Genome Res; 2001 Dec; 11(12):2115-9. PubMed ID: 11731502
[TBL] [Abstract][Full Text] [Related]
2. Quantification of the power of Hardy-Weinberg equilibrium testing to detect genotyping error.
Cox DG; Kraft P
Hum Hered; 2006; 61(1):10-4. PubMed ID: 16514241
[TBL] [Abstract][Full Text] [Related]
3. Detecting susceptibility genes in case-control studies using set association.
Kim S; Zhang K; Sun F
BMC Genet; 2003 Dec; 4 Suppl 1(Suppl 1):S9. PubMed ID: 14975077
[TBL] [Abstract][Full Text] [Related]
4. Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium.
Leal SM
Genet Epidemiol; 2005 Nov; 29(3):204-14. PubMed ID: 16080207
[TBL] [Abstract][Full Text] [Related]
5. Statistical multilocus methods for disequilibrium analysis in complex traits.
Ott J; Hoh J
Hum Mutat; 2001 Apr; 17(4):285-8. PubMed ID: 11295826
[TBL] [Abstract][Full Text] [Related]
6. Testing Hardy-Weinberg disequilibrium using the generalized linear model.
Xu S
Genet Res (Camb); 2012 Dec; 94(6):319-30. PubMed ID: 23249612
[TBL] [Abstract][Full Text] [Related]
7. The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers.
Ohashi J; Tokunaga K
J Hum Genet; 2001; 46(8):478-82. PubMed ID: 11501946
[TBL] [Abstract][Full Text] [Related]
8. Detection of genotyping errors by Hardy-Weinberg equilibrium testing.
Hosking L; Lumsden S; Lewis K; Yeo A; McCarthy L; Bansal A; Riley J; Purvis I; Xu CF
Eur J Hum Genet; 2004 May; 12(5):395-9. PubMed ID: 14872201
[TBL] [Abstract][Full Text] [Related]
9. Physiology and Endocrinology Symposium: How single nucleotide polymorphism chips will advance our knowledge of factors controlling puberty and aid in selecting replacement beef females.
Snelling WM; Cushman RA; Fortes MR; Reverter A; Bennett GL; Keele JW; Kuehn LA; McDaneld TG; Thallman RM; Thomas MG
J Anim Sci; 2012 Apr; 90(4):1152-65. PubMed ID: 22038989
[TBL] [Abstract][Full Text] [Related]
10. The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.
Liu W; Zhao W; Chase GA
Hum Hered; 2006; 61(1):31-44. PubMed ID: 16557026
[TBL] [Abstract][Full Text] [Related]
11. The relative power of SNPs and haplotype as genetic markers for association tests.
Bader JS
Pharmacogenomics; 2001 Feb; 2(1):11-24. PubMed ID: 11258193
[TBL] [Abstract][Full Text] [Related]
12. Construction of the model for the Genetic Analysis Workshop 14 simulated data: genotype-phenotype relationships, gene interaction, linkage, association, disequilibrium, and ascertainment effects for a complex phenotype.
Greenberg DA; Zhang J; Shmulewitz D; Strug LJ; Zimmerman R; Singh V; Marathe S
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S3. PubMed ID: 16451639
[TBL] [Abstract][Full Text] [Related]
13. Bivariate association analysis for quantitative traits using generalized estimation equation.
Yang F; Tang Z; Deng H
J Genet Genomics; 2009 Dec; 36(12):733-43. PubMed ID: 20129400
[TBL] [Abstract][Full Text] [Related]
14. Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers.
Wille A; Hoh J; Ott J
Genet Epidemiol; 2003 Dec; 25(4):350-9. PubMed ID: 14639704
[TBL] [Abstract][Full Text] [Related]
15. A POWERFUL METHOD FOR INCLUDING GENOTYPE UNCERTAINTY IN TESTS OF HARDY-WEINBERG EQUILIBRIUM.
Beck A; Luedtke A; Liu K; Tintle N
Pac Symp Biocomput; 2017; 22():368-379. PubMed ID: 27896990
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. What SNP genotyping errors are most costly for genetic association studies?
Kang SJ; Gordon D; Finch SJ
Genet Epidemiol; 2004 Feb; 26(2):132-41. PubMed ID: 14748013
[TBL] [Abstract][Full Text] [Related]
18. Tag SNP selection for association studies.
Stram DO
Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
[TBL] [Abstract][Full Text] [Related]
19. A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms.
Gao X; Starmer J; Martin ER
Genet Epidemiol; 2008 May; 32(4):361-9. PubMed ID: 18271029
[TBL] [Abstract][Full Text] [Related]
20. Testing for association with a case-parents design in the presence of genotyping errors.
Morris RW; Kaplan NL
Genet Epidemiol; 2004 Feb; 26(2):142-54. PubMed ID: 14748014
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
