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Items: 1 to 20 of 95

1.

Comparison of statistical tests for association between rare variants and binary traits.

Bacanu SA, Nelson MR, Whittaker JC.

PLoS One. 2012;7(8):e42530. doi: 10.1371/journal.pone.0042530. Epub 2012 Aug 9.

2.

Comparison of methods and sampling designs to test for association between rare variants and quantitative traits.

Bacanu SA, Nelson MR, Whittaker JC.

Genet Epidemiol. 2011 May;35(4):226-35. doi: 10.1002/gepi.20570.

PMID:
21370253
3.

A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.

Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M.

Genet Epidemiol. 2016 Dec;40(8):702-721. doi: 10.1002/gepi.21984. Epub 2016 Jul 4.

4.

Generalized functional linear models for gene-based case-control association studies.

Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M.

Genet Epidemiol. 2014 Nov;38(7):622-637. doi: 10.1002/gepi.21840. Epub 2014 Sep 9.

5.

Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants.

Takeuchi F, Kobayashi S, Ogihara T, Fujioka A, Kato N.

Genome Res. 2011 Jul;21(7):1122-30. doi: 10.1101/gr.115832.110. Epub 2011 Mar 25.

6.

A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.

Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R.

Genet Epidemiol. 2017 Jan;41(1):18-34. doi: 10.1002/gepi.22014. Epub 2016 Dec 5.

PMID:
27917525
7.

An optimum projection and noise reduction approach for detecting rare and common variants associated with complex diseases.

Turkmen A, Lin S.

Hum Hered. 2012;74(1):51-60. doi: 10.1159/000343797. Epub 2012 Nov 13.

8.

Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.

Ma C, Boehnke M, Lee S; GoT2D Investigators.

Genet Epidemiol. 2015 Nov;39(7):499-508. doi: 10.1002/gepi.21935. Epub 2015 Oct 10.

9.

A powerful association test of multiple genetic variants using a random-effects model.

Cheng KF, Lee JY, Zheng W, Li C.

Stat Med. 2014 May 20;33(11):1816-27. doi: 10.1002/sim.6068. Epub 2013 Dec 16.

10.

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.

Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, Nickerson DA; NHLBI GO Exome Sequencing Project—ESP Lung Project Team, Christiani DC, Wurfel MM, Lin X.

Am J Hum Genet. 2012 Aug 10;91(2):224-37. doi: 10.1016/j.ajhg.2012.06.007. Epub 2012 Aug 2.

11.

Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions.

Fan R, Wang Y, Yan Q, Ding Y, Weeks DE, Lu Z, Ren H, Cook RJ, Xiong M, Swaroop A, Chew EY, Chen W.

Genet Epidemiol. 2016 Feb;40(2):133-43. doi: 10.1002/gepi.21947. Epub 2016 Jan 18.

12.

Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.

Dai Y, Jiang R, Dong J.

BMC Genet. 2012 Feb 6;13:7. doi: 10.1186/1471-2156-13-7.

13.

Identifying rare variants associated with complex traits via sequencing.

Li B, Liu DJ, Leal SM.

Curr Protoc Hum Genet. 2013 Jul;Chapter 1:Unit 1.26. doi: 10.1002/0471142905.hg0126s78. Review.

14.

Design considerations for genetic linkage and association studies.

Nsengimana J, Bishop DT.

Methods Mol Biol. 2012;850:237-62. doi: 10.1007/978-1-61779-555-8_13.

PMID:
22307702
15.

A general framework for association tests with multivariate traits in large-scale genomics studies.

He Q, Avery CL, Lin DY.

Genet Epidemiol. 2013 Dec;37(8):759-67. doi: 10.1002/gepi.21759. Epub 2013 Nov 5.

16.

The admixture maximum likelihood test to test for association between rare variants and disease phenotypes.

Tyrer JP, Guo Q, Easton DF, Pharoah PD.

BMC Bioinformatics. 2013 Jun 6;14:177. doi: 10.1186/1471-2105-14-177.

17.

Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits.

Moutsianas L, Morris AP.

Brief Funct Genomics. 2014 Sep;13(5):362-70. doi: 10.1093/bfgp/elu012. Epub 2014 Jun 10.

18.

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.

Zawistowski M, Gopalakrishnan S, Ding J, Li Y, Grimm S, Zöllner S.

Am J Hum Genet. 2010 Nov 12;87(5):604-17. doi: 10.1016/j.ajhg.2010.10.012.

19.

Comparison of three summary statistics for ranking genes in genome-wide association studies.

Freytag S, Bickeböller H.

Stat Med. 2014 May 20;33(11):1828-41. doi: 10.1002/sim.6063. Epub 2013 Dec 9.

PMID:
24323702
20.

Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models.

Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R.

Genet Epidemiol. 2015 May;39(4):259-75. doi: 10.1002/gepi.21895. Epub 2015 Mar 23.

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