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Items: 1 to 20 of 113

1.

SHARE: an adaptive algorithm to select the most informative set of SNPs for candidate genetic association.

Dai JY, Leblanc M, Smith NL, Psaty B, Kooperberg C.

Biostatistics. 2009 Oct;10(4):680-93. doi: 10.1093/biostatistics/kxp023. Epub 2009 Jul 15.

2.

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. Epub 2006 Mar 23.

PMID:
16557026
3.

Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia.

Wason JM, Dudbridge F.

BMC Genet. 2010 Sep 9;11:80. doi: 10.1186/1471-2156-11-80.

4.

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis.

Knüppel S, Esparza-Gordillo J, Marenholz I, Holzhütter HG, Bauerfeind A, Ruether A, Weidinger S, Lee YA, Rohde K.

BMC Med Genet. 2012 Jan 27;13:8. doi: 10.1186/1471-2350-13-8.

5.

Genome-wide association data classification and SNPs selection using two-stage quality-based Random Forests.

Nguyen TT, Huang J, Wu Q, Nguyen T, Li M.

BMC Genomics. 2015;16 Suppl 2:S5. doi: 10.1186/1471-2164-16-S2-S5. Epub 2015 Jan 21.

6.

Efficient haplotype block partitioning and tag SNP selection algorithms under various constraints.

Chen WP, Hung CL, Lin YL.

Biomed Res Int. 2013;2013:984014. doi: 10.1155/2013/984014. Epub 2013 Nov 11.

7.

A hidden Markov random field model for genome-wide association studies.

Li H, Wei Z, Maris J.

Biostatistics. 2010 Jan;11(1):139-50. doi: 10.1093/biostatistics/kxp043. Epub 2009 Oct 12.

8.

A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.

Yang Y, Li SS, Chien JW, Andriesen J, Zhao LP.

BMC Genet. 2008 Dec 22;9:90. doi: 10.1186/1471-2156-9-90.

9.
10.

[Analysis and application of SNP and haplotype in the human genome].

Li J, Pan YC, Li YX, Shi TL.

Yi Chuan Xue Bao. 2005 Aug;32(8):879-89. Review. Chinese.

PMID:
16231744
11.

Informative SNP selection methods based on SNP prediction.

He J, Zelikovsky A.

IEEE Trans Nanobioscience. 2007 Mar;6(1):60-7.

PMID:
17393851
12.

Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.

Lee MH, Tzeng JY, Huang SY, Hsiao CK.

BMC Genet. 2011 May 19;12:48. doi: 10.1186/1471-2156-12-48.

13.

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.

14.

HapBoost: a fast approach to boosting haplotype association analyses in genome-wide association studies.

Wan X, Yang C, Yang Q, Zhao H, Yu W.

IEEE/ACM Trans Comput Biol Bioinform. 2013 Jan-Feb;10(1):207-12. doi: 10.1109/TCBB.2013.6.

PMID:
23702557
15.

Sequential haplotype scan methods for association analysis.

Yu Z, Schaid DJ.

Genet Epidemiol. 2007 Sep;31(6):553-64.

PMID:
17487883
16.

Haplotype block partitioning as a tool for dimensionality reduction in SNP association studies.

Pattaro C, Ruczinski I, Fallin DM, Parmigiani G.

BMC Genomics. 2008 Aug 29;9:405. doi: 10.1186/1471-2164-9-405.

17.

Association mapping by generalized linear regression with density-based haplotype clustering.

Igo RP Jr, Li J, Goddard KA.

Genet Epidemiol. 2009 Jan;33(1):16-26. doi: 10.1002/gepi.20352.

18.

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
19.
20.

Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test.

Abad-Grau MM, Medina-Medina N, Montes-Soldado R, Moreno-Ortega J, Matesanz F.

Hum Genet. 2010 Sep;128(3):325-44. doi: 10.1007/s00439-010-0854-z. Epub 2010 Jul 6.

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