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Items: 1 to 20 of 310

1.

Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms.

Niu T, Qin ZS, Xu X, Liu JS.

Am J Hum Genet. 2002 Jan;70(1):157-69. Epub 2001 Nov 26. Erratum in: Am J Hum Genet. 2006 Jan;78(1):174.

2.
4.

Bayesian analysis of multilocus association in quantitative and qualitative traits.

Kilpikari R, Sillanpää MJ.

Genet Epidemiol. 2003 Sep;25(2):122-35.

PMID:
12916021
5.

Haplotype reconstruction for diploid populations.

Zhang J, Vingron M, Hoehe MR.

Hum Hered. 2005;59(3):144-56. Epub 2005 May 26.

PMID:
15925893
6.

Inference of missing SNPs and information quantity measurements for haplotype blocks.

Su SC, Kuo CC, Chen T.

Bioinformatics. 2005 May 1;21(9):2001-7. Epub 2005 Feb 4.

PMID:
15699029
7.

Power-based, phase-informed selection of single nucleotide polymorphisms for disease association screens.

Saccone SF, Rice JP, Saccone NL.

Genet Epidemiol. 2006 Sep;30(6):459-70.

PMID:
16685721
8.

[Construction of haplotype and haplotype block based on tag single nucleotide polymorphisms and their applications in association studies].

Gu ML, Chu JY.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Dec;24(6):660-5. Review. Chinese.

PMID:
18067078
9.

Efficiency and power in genetic association studies.

de Bakker PI, Yelensky R, Pe'er I, Gabriel SB, Daly MJ, Altshuler D.

Nat Genet. 2005 Nov;37(11):1217-23. Epub 2005 Oct 23.

PMID:
16244653
10.

Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal.

Li M, Boehnke M, Abecasis GR.

Am J Hum Genet. 2005 Jun;76(6):934-49. Epub 2005 Apr 5.

11.

Haplotype analysis in the presence of informatively missing genotype data.

Liu N, Beerman I, Lifton R, Zhao H.

Genet Epidemiol. 2006 May;30(4):290-300.

PMID:
16528706
12.

A Markov chain model for haplotype assembly from SNP fragments.

Wang RS, Wu LY, Zhang XS, Chen L.

Genome Inform. 2006;17(2):162-71.

PMID:
17503389
13.

Constrained hidden Markov models for population-based haplotyping.

Landwehr N, Mielikäinen T, Eronen L, Toivonen H, Mannila H.

BMC Bioinformatics. 2007 May 3;8 Suppl 2:S9.

14.

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.

PMID:
17285621
15.

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.

Excoffier L, Slatkin M.

Mol Biol Evol. 1995 Sep;12(5):921-7.

PMID:
7476138
16.

Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.

Zhang K, Qin ZS, Liu JS, Chen T, Waterman MS, Sun F.

Genome Res. 2004 May;14(5):908-16. Epub 2004 Apr 12.

17.

Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies.

Morris AP, Whittaker JC, Balding DJ.

Am J Hum Genet. 2002 Mar;70(3):686-707. Epub 2002 Feb 8.

18.

Haplotype block structure and its applications to association studies: power and study designs.

Zhang K, Calabrese P, Nordborg M, Sun F.

Am J Hum Genet. 2002 Dec;71(6):1386-94. Epub 2002 Nov 18.

20.

HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.

Zhang K, Sun F, Zhao H.

Bioinformatics. 2005 Jan 1;21(1):90-103. Epub 2004 Jul 1.

PMID:
15231536

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