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Results: 1 to 20 of 105

Similar articles for PubMed (Select 25060534)

1.

Incorporating gene-environment interaction in testing for association with rare genetic variants.

Chen H, Meigs JB, Dupuis J.

Hum Hered. 2014;78(2):81-90. doi: 10.1159/000363347. Epub 2014 Jul 18.

2.

A robust model-free approach for rare variants association studies incorporating gene-gene and gene-environmental interactions.

Fan R, Lo SH.

PLoS One. 2013 Dec 17;8(12):e83057. doi: 10.1371/journal.pone.0083057. eCollection 2013. Erratum in: PLoS One. 2014;9(5):e98083.

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.

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.

Tzeng JY, Zhang D, Pongpanich M, Smith C, McCarthy MI, Sale MM, Worrall BB, Hsu FC, Thomas DC, Sullivan PF.

Am J Hum Genet. 2011 Aug 12;89(2):277-88. doi: 10.1016/j.ajhg.2011.07.007.

5.
6.

Does accounting for gene-environment interactions help uncover association between rare variants and complex diseases?

Kazma R, Cardin NJ, Witte JS.

Hum Hered. 2012;74(3-4):205-14. doi: 10.1159/000346825. Epub 2013 Apr 11.

PMID:
23594498
7.

Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.

Kinnamon DD, Hershberger RE, Martin ER.

PLoS One. 2012;7(2):e30238. doi: 10.1371/journal.pone.0030238. Epub 2012 Feb 17.

8.

Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants.

Ma C, Blackwell T, Boehnke M, Scott LJ; GoT2D investigators.

Genet Epidemiol. 2013 Sep;37(6):539-50. doi: 10.1002/gepi.21742. Epub 2013 Jun 20.

9.

Assessing gene-environment interactions for common and rare variants with binary traits using gene-trait similarity regression.

Zhao G, Marceau R, Zhang D, Tzeng JY.

Genetics. 2015 Mar;199(3):695-710. doi: 10.1534/genetics.114.171686. Epub 2015 Jan 12.

PMID:
25585620
10.

Association studies including genotype by environment interactions: prospects and limits.

Saïdou AA, Thuillet AC, Couderc M, Mariac C, Vigouroux Y.

BMC Genet. 2014 Jan 6;15:3. doi: 10.1186/1471-2156-15-3.

11.

Genome-wide meta-analysis of joint tests for genetic and gene-environment interaction effects.

Aschard H, Hancock DB, London SJ, Kraft P.

Hum Hered. 2010;70(4):292-300. doi: 10.1159/000323318. Epub 2011 Feb 3.

12.

Meta-analysis of gene-level associations for rare variants based on single-variant statistics.

Hu YJ, Berndt SI, Gustafsson S, Ganna A; Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Hirschhorn J, North KE, Ingelsson E, Lin DY.

Am J Hum Genet. 2013 Aug 8;93(2):236-48. doi: 10.1016/j.ajhg.2013.06.011. Epub 2013 Jul 25.

13.

Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.

Lin WY, Yi N, Lou XY, Zhi D, Zhang K, Gao G, Tiwari HK, Liu N.

Genet Epidemiol. 2013 Sep;37(6):560-70. doi: 10.1002/gepi.21740. Epub 2013 Jun 5.

14.

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.

15.

Natural and orthogonal interaction framework for modeling gene-environment interactions with application to lung cancer.

Ma J, Xiao F, Xiong M, Andrew AS, Brenner H, Duell EJ, Haugen A, Hoggart C, Hung RJ, Lazarus P, Liu C, Matsuo K, Mayordomo JI, Schwartz AG, Staratschek-Jox A, Wichmann E, Yang P, Amos CI.

Hum Hered. 2012;73(4):185-94. doi: 10.1159/000339906. Epub 2012 Aug 9.

16.

Sequence kernel association tests for the combined effect of rare and common variants.

Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X.

Am J Hum Genet. 2013 Jun 6;92(6):841-53. doi: 10.1016/j.ajhg.2013.04.015. Epub 2013 May 16.

17.

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.

18.

Gene-environment interaction tests for dichotomous traits in trios and sibships.

Hoffmann TJ, Lange C, Vansteelandt S, Laird NM.

Genet Epidemiol. 2009 Dec;33(8):691-9. doi: 10.1002/gepi.20421.

19.

Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients.

Manning AK, LaValley M, Liu CT, Rice K, An P, Liu Y, Miljkovic I, Rasmussen-Torvik L, Harris TB, Province MA, Borecki IB, Florez JC, Meigs JB, Cupples LA, Dupuis J.

Genet Epidemiol. 2011 Jan;35(1):11-8. doi: 10.1002/gepi.20546.

20.

SBERIA: set-based gene-environment interaction test for rare and common variants in complex diseases.

Jiao S, Hsu L, Bézieau S, Brenner H, Chan AT, Chang-Claude J, Le Marchand L, Lemire M, Newcomb PA, Slattery ML, Peters U.

Genet Epidemiol. 2013 Jul;37(5):452-64. doi: 10.1002/gepi.21735. Epub 2013 May 29.

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