523 related articles for article (PubMed ID: 21467568)
1. 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]
2. Efficient association study design via power-optimized tag SNP selection.
Han B; Kang HM; Seo MS; Zaitlen N; Eskin E
Ann Hum Genet; 2008 Nov; 72(Pt 6):834-47. PubMed ID: 18702637
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 16685721
[TBL] [Abstract][Full Text] [Related]
4. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium.
Pasaniuc B; Zaitlen N; Lettre G; Chen GK; Tandon A; Kao WH; Ruczinski I; Fornage M; Siscovick DS; Zhu X; Larkin E; Lange LA; Cupples LA; Yang Q; Akylbekova EL; Musani SK; Divers J; Mychaleckyj J; Li M; Papanicolaou GJ; Millikan RC; Ambrosone CB; John EM; Bernstein L; Zheng W; Hu JJ; Ziegler RG; Nyante SJ; Bandera EV; Ingles SA; Press MF; Chanock SJ; Deming SL; Rodriguez-Gil JL; Palmer CD; Buxbaum S; Ekunwe L; Hirschhorn JN; Henderson BE; Myers S; Haiman CA; Reich D; Patterson N; Wilson JG; Price AL
PLoS Genet; 2011 Apr; 7(4):e1001371. PubMed ID: 21541012
[TBL] [Abstract][Full Text] [Related]
5. Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.
Pal LR; Moult J
J Mol Biol; 2015 Jul; 427(13):2271-89. PubMed ID: 25937569
[TBL] [Abstract][Full Text] [Related]
6. ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
Wang Z; McPeek MS
Am J Hum Genet; 2009 Nov; 85(5):667-78. PubMed ID: 19913122
[TBL] [Abstract][Full Text] [Related]
7. Analysis of untyped SNPs: maximum likelihood and imputation methods.
Hu YJ; Lin DY
Genet Epidemiol; 2010 Dec; 34(8):803-15. PubMed ID: 21104886
[TBL] [Abstract][Full Text] [Related]
8. An efficient weighted tag SNP-set analytical method in genome-wide association studies.
Yan B; Wang S; Jia H; Liu X; Wang X
BMC Genet; 2015 Mar; 16():25. PubMed ID: 25879733
[TBL] [Abstract][Full Text] [Related]
9. Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data.
Kang C; Yu H; Yi GS
BMC Med Inform Decis Mak; 2013; 13 Suppl 1(Suppl 1):S3. PubMed ID: 23566118
[TBL] [Abstract][Full Text] [Related]
10. Tagging SNP-set selection with maximum information based on linkage disequilibrium structure in genome-wide association studies.
Wang S; He S; Yuan F; Zhu X
Bioinformatics; 2017 Jul; 33(14):2078-2081. PubMed ID: 28334342
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Fast and robust association tests for untyped SNPs in case-control studies.
Allen AS; Satten GA; Bray SL; Dudbridge F; Epstein MP
Hum Hered; 2010; 70(3):167-76. PubMed ID: 20689309
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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(Suppl 2):S5. PubMed ID: 25708662
[TBL] [Abstract][Full Text] [Related]
15. Pathway analysis of seven common diseases assessed by genome-wide association.
Torkamani A; Topol EJ; Schork NJ
Genomics; 2008 Nov; 92(5):265-72. PubMed ID: 18722519
[TBL] [Abstract][Full Text] [Related]
16. Tag SNP selection for association studies.
Stram DO
Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
[TBL] [Abstract][Full Text] [Related]
17. Haplotype-based quantitative trait mapping using a clustering algorithm.
Li J; Zhou Y; Elston RC
BMC Bioinformatics; 2006 May; 7():258. PubMed ID: 16709248
[TBL] [Abstract][Full Text] [Related]
18. Power analysis for genome-wide association studies.
Klein RJ
BMC Genet; 2007 Aug; 8():58. PubMed ID: 17725844
[TBL] [Abstract][Full Text] [Related]
19. RS-SNP: a random-set method for genome-wide association studies.
D'Addabbo A; Palmieri O; Latiano A; Annese V; Mukherjee S; Ancona N
BMC Genomics; 2011 Mar; 12():166. PubMed ID: 21450072
[TBL] [Abstract][Full Text] [Related]
20. Improved heritability estimation from genome-wide SNPs.
Speed D; Hemani G; Johnson MR; Balding DJ
Am J Hum Genet; 2012 Dec; 91(6):1011-21. PubMed ID: 23217325
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
