276 related articles for article (PubMed ID: 16451556)
1. Linkage disequilibrium mapping via cladistic analysis of phase-unknown genotypes and inferred haplotypes in the Genetic Analysis Workshop 14 simulated data.
Durrant C; Morris AP
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S100. PubMed ID: 16451556
[TBL] [Abstract][Full Text] [Related]
2. Linkage disequilibrium assessment via log-linear modeling of SNP haplotype frequencies.
Morris A; Pedder A; Ayres K
Genet Epidemiol; 2003 Sep; 25(2):106-14. PubMed ID: 12916019
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data.
Morris AP; Whittaker JC; Balding DJ
Am J Hum Genet; 2004 May; 74(5):945-53. PubMed ID: 15077198
[TBL] [Abstract][Full Text] [Related]
5. High density linkage disequilibrium mapping using models of haplotype block variation.
Greenspan G; Geiger D
Bioinformatics; 2004 Aug; 20 Suppl 1():i137-44. PubMed ID: 15262792
[TBL] [Abstract][Full Text] [Related]
6. Accounting for haplotype phase uncertainty in linkage disequilibrium estimation.
Kulle B; Frigessi A; Edvardsen H; Kristensen V; Wojnowski L
Genet Epidemiol; 2008 Feb; 32(2):168-78. PubMed ID: 17968987
[TBL] [Abstract][Full Text] [Related]
7. Linkage disequilibrium mapping with genotype data.
Zhang S; Zhao H
Genet Epidemiol; 2002 Jan; 22(1):66-77. PubMed ID: 11754474
[TBL] [Abstract][Full Text] [Related]
8. Haplotype frequency estimation in patient populations: the effect of departures from Hardy-Weinberg proportions and collapsing over a locus in the HLA region.
Single RM; Meyer D; Hollenbach JA; Nelson MP; Noble JA; Erlich HA; Thomson G
Genet Epidemiol; 2002 Feb; 22(2):186-95. PubMed ID: 11788963
[TBL] [Abstract][Full Text] [Related]
9. Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages.
Marroni F; Toni C; Pennato B; Tsai YY; Duggal P; Bailey-Wilson JE; Presciuttini S
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S77. PubMed ID: 16451691
[TBL] [Abstract][Full Text] [Related]
10. Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.
Rohde K; Fuerst R
Hum Mutat; 2001 Apr; 17(4):289-95. PubMed ID: 11295827
[TBL] [Abstract][Full Text] [Related]
11. Use of unphased multilocus genotype data in indirect association studies.
Clayton D; Chapman J; Cooper J
Genet Epidemiol; 2004 Dec; 27(4):415-28. PubMed ID: 15481099
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes.
Morris AP
Genet Epidemiol; 2005 Sep; 29(2):91-107. PubMed ID: 15940704
[TBL] [Abstract][Full Text] [Related]
14. Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.
Cheng R; Ma JZ; Elston RC; Li MD
Ann Hum Genet; 2005 Jan; 69(Pt 1):102-12. PubMed ID: 15638831
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits.
Klein AP; Tsai YY; Duggal P; Gillanders EM; Barnhart M; Mathias RA; Dusenberry IP; Turiff A; Chines PS; Goldstein J; Wojciechowski R; Hening W; Pugh EW; Bailey-Wilson JE
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S20. PubMed ID: 16451629
[TBL] [Abstract][Full Text] [Related]
17. SNPs, haplotypes, and model selection in a candidate gene region: the SIMPle analysis for multilocus data.
Conti DV; Gauderman WJ
Genet Epidemiol; 2004 Dec; 27(4):429-41. PubMed ID: 15543635
[TBL] [Abstract][Full Text] [Related]
18. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
Maniatis N; Collins A; Morton NE
Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621
[TBL] [Abstract][Full Text] [Related]
19. On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.
Garner C; Slatkin M
Genet Epidemiol; 2003 Jan; 24(1):57-67. PubMed ID: 12508256
[TBL] [Abstract][Full Text] [Related]
20. The effect of missing data on linkage disequilibrium mapping and haplotype association analysis in the GAW14 simulated datasets.
McCaskie PA; Carter KW; McCaskie SR; Palmer LJ
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S151. PubMed ID: 16451612
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
