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Items: 1 to 20 of 71

1.

Pathway analysis by adaptive combination of P-values.

Yu K, Li Q, Bergen AW, Pfeiffer RM, Rosenberg PS, Caporaso N, Kraft P, Chatterjee N.

Genet Epidemiol. 2009 Dec;33(8):700-9. doi: 10.1002/gepi.20422.

2.

Association tests using kernel-based measures of multi-locus genotype similarity between individuals.

Mukhopadhyay I, Feingold E, Weeks DE, Thalamuthu A.

Genet Epidemiol. 2010 Apr;34(3):213-21. doi: 10.1002/gepi.20451.

3.

Detecting genetic interactions for quantitative traits with U-statistics.

Li M, Ye C, Fu W, Elston RC, Lu Q.

Genet Epidemiol. 2011 Sep;35(6):457-68. doi: 10.1002/gepi.20594. Epub 2011 May 26.

4.

MAX-rank: a simple and robust genome-wide scan for case-control association studies.

Li Q, Yu K, Li Z, Zheng G.

Hum Genet. 2008 Jul;123(6):617-23. doi: 10.1007/s00439-008-0514-8. Epub 2008 May 20.

PMID:
18491142
5.

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families.

Wang YT, Sung PY, Lin PL, Yu YW, Chung RH.

BMC Genomics. 2015 May 15;16:381. doi: 10.1186/s12864-015-1620-3.

6.

SNP-based pathway enrichment analysis for genome-wide association studies.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.

BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99.

7.

Bootstrap aggregating of alternating decision trees to detect sets of SNPs that associate with disease.

Guy RT, Santago P, Langefeld CD.

Genet Epidemiol. 2012 Feb;36(2):99-106. doi: 10.1002/gepi.21608.

8.

A system-level pathway-phenotype association analysis using synthetic feature random forest.

Pan Q, Hu T, Malley JD, Andrew AS, Karagas MR, Moore JH.

Genet Epidemiol. 2014 Apr;38(3):209-19. doi: 10.1002/gepi.21794. Epub 2014 Feb 17.

9.

Comparison of methods for competitive tests of pathway analysis.

Evangelou M, Rendon A, Ouwehand WH, Wernisch L, Dudbridge F.

PLoS One. 2012;7(7):e41018. doi: 10.1371/journal.pone.0041018. Epub 2012 Jul 31.

11.

Gene, region and pathway level analyses in whole-genome studies.

De la Cruz O, Wen X, Ke B, Song M, Nicolae DL.

Genet Epidemiol. 2010 Apr;34(3):222-31. doi: 10.1002/gepi.20452.

12.

The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke.

Pedneault M, Labbe A, Roy-Gagnon MH, Low NC, Dugas E, Engert JC, O'Loughlin J.

Addict Behav. 2014 Jan;39(1):316-20. doi: 10.1016/j.addbeh.2013.08.033. Epub 2013 Sep 7.

PMID:
24119711
13.

Resampling-based multiple hypothesis testing procedures for genetic case-control association studies.

Chen BE, Sakoda LC, Hsing AW, Rosenberg PS.

Genet Epidemiol. 2006 Sep;30(6):495-507.

PMID:
16755536
14.

A fast multilocus test with adaptive SNP selection for large-scale genetic-association studies.

Zhang H, Shi J, Liang F, Wheeler W, Stolzenberg-Solomon R, Yu K.

Eur J Hum Genet. 2014 May;22(5):696-702. doi: 10.1038/ejhg.2013.201. Epub 2013 Sep 11.

15.

Use of the gamma method for self-contained gene-set analysis of SNP data.

Biernacka JM, Jenkins GD, Wang L, Moyer AM, Fridley BL.

Eur J Hum Genet. 2012 May;20(5):565-71. doi: 10.1038/ejhg.2011.236. Epub 2011 Dec 14.

16.
17.

Test for interactions between a genetic marker set and environment in generalized linear models.

Lin X, Lee S, Christiani DC, Lin X.

Biostatistics. 2013 Sep;14(4):667-81. doi: 10.1093/biostatistics/kxt006. Epub 2013 Mar 5.

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.

Genetic association analysis of complex diseases incorporating intermediate phenotype information.

Li Y, Huang J, Amos CI.

PLoS One. 2012;7(10):e46612. doi: 10.1371/journal.pone.0046612. Epub 2012 Oct 19.

20.

A powerful and robust test in genetic association studies.

Cheng KF, Lee JY.

Hum Hered. 2014;78(1):38-46. doi: 10.1159/000360987. Epub 2014 Jun 21.

PMID:
24969671

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