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Items: 1 to 20 of 136

1.

Classifying disease chromosomes arising from multiple founders, with application to fine-scale haplotype mapping.

Yu K, Martin RB, Whittemore AS.

Genet Epidemiol. 2004 Nov;27(3):173-81.

PMID:
15389930
2.

Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes.

Yu K, Gu CC, Province M, Xiong CJ, Rao DC.

Genet Epidemiol. 2004 Nov;27(3):182-91.

PMID:
15389925
3.

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.

4.

A haplotype similarity based transmission/disequilibrium test under founder heterogeneity.

Yu K, Zhang S, Borecki I, Kraja A, Xiong C, Myers R, Province M.

Ann Hum Genet. 2005 Jul;69(Pt 4):455-67.

5.

Fine scale association mapping of disease loci using simplex families.

Morris AP, Whittaker JC.

Ann Hum Genet. 2000 May;64(Pt 3):223-37.

6.

High density linkage disequilibrium mapping using models of haplotype block variation.

Greenspan G, Geiger D.

Bioinformatics. 2004 Aug 4;20 Suppl 1:i137-44.

PMID:
15262792
7.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, Morris AP.

Am J Hum Genet. 2004 Jul;75(1):35-43. Epub 2004 May 13.

8.

Linkage disequilibrium mapping with genotype data.

Zhang S, Zhao H.

Genet Epidemiol. 2002 Jan;22(1):66-77.

PMID:
11754474
10.

Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations.

Service SK, Lang DW, Freimer NB, Sandkuijl LA.

Am J Hum Genet. 1999 Jun;64(6):1728-38.

11.

Bayesian fine-scale mapping of disease loci, by hidden Markov models.

Morris AP, Whittaker JC, Balding DJ.

Am J Hum Genet. 2000 Jul;67(1):155-69. Epub 2000 Jun 1.

12.
13.

Haplotype analysis to determine the position of a mutation among closely linked DNA markers.

Ramsay M, Williamson R, Estivill X, Wainwright BJ, Ho MF, Halford S, Kere J, Savilahti E, de la Chapelle A, Schwartz M, et al.

Hum Mol Genet. 1993 Jul;2(7):1007-14. Erratum in: Hum Mol Genet 1993 Sep;2(9):1523.

PMID:
8364537
15.

A spatial probit model for fine-scale mapping of disease genes.

De Iorio M, Verzilli CJ.

Genet Epidemiol. 2007 Apr;31(3):252-60.

PMID:
17266116
16.

Linkage disequilibrium mapping: the role of population history, size, and structure.

Chapman NH, Thompson EA.

Adv Genet. 2001;42:413-37. Review.

PMID:
11037333
17.

Fine mapping of disease genes using tagging SNPs.

Sjölander A, Hössjer O, Hartman LW, Humphreys K.

Ann Hum Genet. 2007 Nov;71(Pt 6):815-27. Epub 2007 Jun 22.

18.

Disease association tests by inferring ancestral haplotypes using a hidden markov model.

Su SY, Balding DJ, Coin LJ.

Bioinformatics. 2008 Apr 1;24(7):972-8. doi: 10.1093/bioinformatics/btn071. Epub 2008 Feb 23.

PMID:
18296746
19.

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.

20.

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.

Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E.

Nat Genet. 1992 Nov;2(3):204-11. Erratum in: Nat Genet 1992 Dec;2(4):343.

PMID:
1345170

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