224 related articles for article (PubMed ID: 21252078)
1. Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.
Heron EA; O'Dushlaine C; Segurado R; Gallagher L; Gill M
Biostatistics; 2011 Jul; 12(3):445-61. PubMed ID: 21252078
[TBL] [Abstract][Full Text] [Related]
2. Identifying disease related sub-pathways for analysis of genome-wide association studies.
Li C; Han J; Shang D; Li J; Wang Y; Wang Y; Zhang Y; Yao Q; Zhang C; Li K; Li X
Gene; 2012 Jul; 503(1):101-9. PubMed ID: 22565193
[TBL] [Abstract][Full Text] [Related]
3. A pathway analysis method for genome-wide association studies.
Shahbaba B; Shachaf CM; Yu Z
Stat Med; 2012 May; 31(10):988-1000. PubMed ID: 22302470
[TBL] [Abstract][Full Text] [Related]
4. Performance and robustness of penalized and unpenalized methods for genetic prediction of complex human disease.
Abraham G; Kowalczyk A; Zobel J; Inouye M
Genet Epidemiol; 2013 Feb; 37(2):184-95. PubMed ID: 23203348
[TBL] [Abstract][Full Text] [Related]
5. Using genome-wide pathway analysis to unravel the etiology of complex diseases.
Elbers CC; van Eijk KR; Franke L; Mulder F; van der Schouw YT; Wijmenga C; Onland-Moret NC
Genet Epidemiol; 2009 Jul; 33(5):419-31. PubMed ID: 19235186
[TBL] [Abstract][Full Text] [Related]
6. IndOR: a new statistical procedure to test for SNP-SNP epistasis in genome-wide association studies.
Emily M
Stat Med; 2012 Sep; 31(21):2359-73. PubMed ID: 22711278
[TBL] [Abstract][Full Text] [Related]
7. SNPs, haplotypes, and model selection in a candidate gene region: the SIMPle analysis for multilocus data.
Conti DV; Gauderman WJ
Genet Epidemiol; 2004 Dec; 27(4):429-41. PubMed ID: 15543635
[TBL] [Abstract][Full Text] [Related]
8. Hierarchical modeling in association studies of multiple phenotypes.
Liu X; Jorgenson E; Witte JS
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S104. PubMed ID: 16451560
[TBL] [Abstract][Full Text] [Related]
9. Detecting SNP-expression associations: a comparison of mutual information and median test with standard statistical approaches.
Szymczak S; Igl BW; Ziegler A
Stat Med; 2009 Dec; 28(29):3581-96. PubMed ID: 19691035
[TBL] [Abstract][Full Text] [Related]
10. Using biological knowledge to discover higher order interactions in genetic association studies.
Chen GK; Thomas DC
Genet Epidemiol; 2010 Dec; 34(8):863-78. PubMed ID: 21104889
[TBL] [Abstract][Full Text] [Related]
11. A two-stage mixed-effects model approach for gene-set analyses in candidate gene studies.
Tsonaka R; van der Helm-van Mil AH; Houwing-Duistermaat JJ
Stat Med; 2012 May; 31(11-12):1190-202. PubMed ID: 21997511
[TBL] [Abstract][Full Text] [Related]
12. Modeling interactions with known risk loci-a Bayesian model averaging approach.
Ferreira T; Marchini J
Ann Hum Genet; 2011 Jan; 75(1):1-9. PubMed ID: 21118191
[TBL] [Abstract][Full Text] [Related]
13. Comparison of association mapping methods in a complex pedigreed population.
Sahana G; Guldbrandtsen B; Janss L; Lund MS
Genet Epidemiol; 2010 Jul; 34(5):455-62. PubMed ID: 20568276
[TBL] [Abstract][Full Text] [Related]
14. Increasing power of genome-wide association studies by collecting additional single-nucleotide polymorphisms.
Kostem E; Lozano JA; Eskin E
Genetics; 2011 Jun; 188(2):449-60. PubMed ID: 21467568
[TBL] [Abstract][Full Text] [Related]
15. How to link call rate and p-values for Hardy-Weinberg equilibrium as measures of genome-wide SNP data quality.
Finner H; Strassburger K; Heid IM; Herder C; Rathmann W; Giani G; Dickhaus T; Lichtner P; Meitinger T; Wichmann HE; Illig T; Gieger C
Stat Med; 2010 Sep; 29(22):2347-58. PubMed ID: 20641143
[TBL] [Abstract][Full Text] [Related]
16. Alternative methods for H1 simulations in genome-wide association studies.
Perduca V; Sinoquet C; Mourad R; Nuel G
Hum Hered; 2012; 73(2):95-104. PubMed ID: 22472690
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide association studies using haplotype clustering with a new haplotype similarity.
Jin L; Zhu W; Guo J
Genet Epidemiol; 2010 Sep; 34(6):633-41. PubMed ID: 20718046
[TBL] [Abstract][Full Text] [Related]
18. Evaluating rare variants under two-stage design.
Li Q; Pan D; Yue W; Gao Y; Yu K
J Hum Genet; 2012 Jun; 57(6):352-7. PubMed ID: 22572736
[TBL] [Abstract][Full Text] [Related]
19. SNP selection and classification of genome-wide SNP data using stratified sampling random forests.
Wu Q; Ye Y; Liu Y; Ng MK
IEEE Trans Nanobioscience; 2012 Sep; 11(3):216-27. PubMed ID: 22987127
[TBL] [Abstract][Full Text] [Related]
20. The optimal discovery procedure in multiple significance testing: an empirical Bayes approach.
Noma H; Matsui S
Stat Med; 2012 Jan; 31(2):165-76. PubMed ID: 21969277
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
