167 related articles for article (PubMed ID: 15937480)
21. Bivariate association analysis for quantitative traits using generalized estimation equation.
Yang F; Tang Z; Deng H
J Genet Genomics; 2009 Dec; 36(12):733-43. PubMed ID: 20129400
[TBL] [Abstract][Full Text] [Related]
22. Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies.
Hoggart CJ; Whittaker JC; De Iorio M; Balding DJ
PLoS Genet; 2008 Jul; 4(7):e1000130. PubMed ID: 18654633
[TBL] [Abstract][Full Text] [Related]
23. ADAM33 polymorphisms are associated with asthma susceptibility in a Japanese population.
Noguchi E; Ohtsuki Y; Tokunaga K; Yamaoka-Sageshima M; Ichikawa K; Aoki T; Shibasaki M; Arinami T
Clin Exp Allergy; 2006 May; 36(5):602-8. PubMed ID: 16650044
[TBL] [Abstract][Full Text] [Related]
24. On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.
Morris RW; Kaplan NL
Genet Epidemiol; 2002 Oct; 23(3):221-33. PubMed ID: 12384975
[TBL] [Abstract][Full Text] [Related]
25. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
Maniatis N; Collins A; Morton NE
Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621
[TBL] [Abstract][Full Text] [Related]
26. [Analysis and application of SNP and haplotype in the human genome].
Li J; Pan YC; Li YX; Shi TL
Yi Chuan Xue Bao; 2005 Aug; 32(8):879-89. PubMed ID: 16231744
[TBL] [Abstract][Full Text] [Related]
27. Linkage and haplotype analysis for chemokine receptors clustered on chromosome 3p21.3 and transmitted in family pedigrees with asthma and atopy.
Al-Abdulhadi SA; Al-Rabia MW
Ann Saudi Med; 2010; 30(2):115-22. PubMed ID: 20220260
[TBL] [Abstract][Full Text] [Related]
28. Prioritize and select SNPs for association studies with multi-stage designs.
Li J
J Comput Biol; 2008 Apr; 15(3):241-57. PubMed ID: 18352819
[TBL] [Abstract][Full Text] [Related]
29. Assessing the power of tag SNPs in the mapping of quantitative trait loci (QTL) with extremal and random samples.
Zhang K; Sun F
BMC Genet; 2005 Oct; 6():51. PubMed ID: 16236175
[TBL] [Abstract][Full Text] [Related]
30. Haplotype block partitioning as a tool for dimensionality reduction in SNP association studies.
Pattaro C; Ruczinski I; Fallin DM; Parmigiani G
BMC Genomics; 2008 Aug; 9():405. PubMed ID: 18759977
[TBL] [Abstract][Full Text] [Related]
31. Computing the minimum recombinant haplotype configuration from incomplete genotype data on a pedigree by integer linear programming.
Li J; Jiang T
J Comput Biol; 2005; 12(6):719-39. PubMed ID: 16108713
[TBL] [Abstract][Full Text] [Related]
32. Two-Stage sampling designs for gene association studies.
Thomas D; Xie R; Gebregziabher M
Genet Epidemiol; 2004 Dec; 27(4):401-14. PubMed ID: 15543639
[TBL] [Abstract][Full Text] [Related]
33. A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.
Conrad DF; Jakobsson M; Coop G; Wen X; Wall JD; Rosenberg NA; Pritchard JK
Nat Genet; 2006 Nov; 38(11):1251-60. PubMed ID: 17057719
[TBL] [Abstract][Full Text] [Related]
34. Using tree-based recursive partitioning methods to group haplotypes for increased power in association studies.
Yu K; Xu J; Rao DC; Province M
Ann Hum Genet; 2005 Sep; 69(Pt 5):577-89. PubMed ID: 16138916
[TBL] [Abstract][Full Text] [Related]
35. Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population.
Hamada D; Takata Y; Osabe D; Nomura K; Shinohara S; Egawa H; Nakano S; Shinomiya F; Scafe CR; Reeve VM; Miyamoto T; Moritani M; Kunika K; Inoue H; Yasui N; Itakura M
Arthritis Rheum; 2005 May; 52(5):1371-80. PubMed ID: 15880602
[TBL] [Abstract][Full Text] [Related]
36. Missing data in haplotype analysis: a study on the MILC method.
Bourgain C; Genin E; Ober C; Clerget-Darpoux F
Ann Hum Genet; 2002 Jan; 66(Pt 1):99-108. PubMed ID: 12022148
[TBL] [Abstract][Full Text] [Related]
37. Powerful testing via hierarchical linkage disequilibrium in haplotype association studies.
Balliu B; Houwing-Duistermaat JJ; Böhringer S
Biom J; 2019 May; 61(3):747-768. PubMed ID: 30693553
[TBL] [Abstract][Full Text] [Related]
38. Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power.
Becker T; Herold C
Eur J Hum Genet; 2009 Aug; 17(8):1043-9. PubMed ID: 19223937
[TBL] [Abstract][Full Text] [Related]
39. An omnibus test for family-based association studies with multiple SNPs and multiple phenotypes.
Lasky-Su J; Murphy A; McQueen MB; Weiss S; Lange C
Eur J Hum Genet; 2010 Jun; 18(6):720-5. PubMed ID: 20087406
[TBL] [Abstract][Full Text] [Related]
40. Association mapping and significance estimation via the coalescent.
Kimmel G; Karp RM; Jordan MI; Halperin E
Am J Hum Genet; 2008 Dec; 83(6):675-83. PubMed ID: 19026399
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]