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Items: 1 to 20 of 94

1.
2.
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Allelic association patterns for a dense SNP map.

Weir BS, Hill WG, Cardon LR; SNP Consortium.

Genet Epidemiol. 2004 Dec;27(4):442-50.

PMID:
15543640
4.

Improved power by use of a weighted score test for linkage disequilibrium mapping.

Wang T, Elston RC.

Am J Hum Genet. 2007 Feb;80(2):353-60. Epub 2006 Dec 21.

5.
6.

Universal false discovery rate estimation methodology for genome-wide association studies.

Forner K, Lamarine M, Guedj M, Dauvillier J, Wojcik J.

Hum Hered. 2008;65(4):183-94. Epub 2007 Dec 11.

PMID:
18073488
7.

Quantification of the power of Hardy-Weinberg equilibrium testing to detect genotyping error.

Cox DG, Kraft P.

Hum Hered. 2006;61(1):10-4. Epub 2006 Mar 1.

PMID:
16514241
8.

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.

9.

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
11.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

12.

The single-nucleotide polymorphism lottery: how useful are a few common SNPs in identifying disease-associated alleles?

Barton A, Chapman P, Myerscough A, Pinel T, Davies N, Worthington J, John S.

Genet Epidemiol. 2001;21 Suppl 1:S384-9.

PMID:
11793704
13.

Challenging false discovery rate: a partition test based on p values in human case-control association studies.

Ott J, Liu Z, Shen Y.

Hum Hered. 2012;74(1):45-50. doi: 10.1159/000343752. Epub 2012 Nov 13.

14.

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.

Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, Stevens JF, Livak KJ, Slotterbeck BD, Slifer SH, Warren LL, Conneally PM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, Vance JM.

Am J Hum Genet. 2000 Aug;67(2):383-94. Epub 2000 Jun 21.

15.

Selecting SNPs in two-stage analysis of disease association data: a model-free approach.

Hoh J, Wille A, Zee R, Cheng S, Reynolds R, Lindpaintner K, Ott J.

Ann Hum Genet. 2000 Sep;64(Pt 5):413-7.

PMID:
11281279
16.

Hidden Markov models for controlling false discovery rate in genome-wide association analysis.

Wei Z.

Methods Mol Biol. 2012;802:337-44. doi: 10.1007/978-1-61779-400-1_22.

PMID:
22130891
17.

Detecting susceptibility genes in case-control studies using set association.

Kim S, Zhang K, Sun F.

BMC Genet. 2003 Dec 31;4 Suppl 1:S9.

18.

Comparative analysis of methods for detecting interacting loci.

Chen L, Yu G, Langefeld CD, Miller DJ, Guy RT, Raghuram J, Yuan X, Herrington DM, Wang Y.

BMC Genomics. 2011 Jul 5;12:344. doi: 10.1186/1471-2164-12-344.

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20.

Testing Hardy-Weinberg disequilibrium using the generalized linear model.

Xu S.

Genet Res (Camb). 2012 Dec;94(6):319-30. doi: 10.1017/S0016672312000511. Epub 2012 Dec 18.

PMID:
23249612

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