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Results: 1 to 20 of 83

1.

Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach.

Ding L, Baye TM, He H, Zhang X, Kurowski BG, Martin LJ.

BMC Proc. 2011 Nov 29;5 Suppl 9:S10. doi: 10.1186/1753-6561-5-S9-S10.

PMID:
22373351
[PubMed]
Free PMC Article
2.

GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm.

Bottolo L, Chadeau-Hyam M, Hastie DI, Zeller T, Liquet B, Newcombe P, Yengo L, Wild PS, Schillert A, Ziegler A, Nielsen SF, Butterworth AS, Ho WK, Castagné R, Munzel T, Tregouet D, Falchi M, Cambien F, Nordestgaard BG, Fumeron F, Tybjærg-Hansen A, Froguel P, Danesh J, Petretto E, Blankenberg S, Tiret L, Richardson S.

PLoS Genet. 2013;9(8):e1003657. doi: 10.1371/journal.pgen.1003657. Epub 2013 Aug 8.

PMID:
23950726
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A non-parametric mixture model for genome-enabled prediction of genetic value for a quantitative trait.

Gianola D, Wu XL, Manfredi E, Simianer H.

Genetica. 2010 Oct;138(9-10):959-77. doi: 10.1007/s10709-010-9478-4. Epub 2010 Aug 25.

PMID:
20737196
[PubMed - indexed for MEDLINE]
4.

Resequencing of IRS2 reveals rare variants for obesity but not fasting glucose homeostasis in Hispanic children.

Butte NF, Voruganti VS, Cole SA, Haack K, Comuzzie AG, Muzny DM, Wheeler DA, Chang K, Hawes A, Gibbs RA.

Physiol Genomics. 2011 Sep 22;43(18):1029-37. doi: 10.1152/physiolgenomics.00019.2011. Epub 2011 Jul 19.

PMID:
21771880
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Gene-based partial least-squares approaches for detecting rare variant associations with complex traits.

Turkmen AS, Lin S.

BMC Proc. 2011 Nov 29;5 Suppl 9:S19. doi: 10.1186/1753-6561-5-S9-S19.

PMID:
22373126
[PubMed]
Free PMC Article
6.

A unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms.

Chen Q, Sun F.

BMC Genomics. 2013;14 Suppl 1:S1. doi: 10.1186/1471-2164-14-S1-S1. Epub 2013 Jan 21.

PMID:
23369070
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations.

Gupta M, Cheung CL, Hsu YH, Demissie S, Cupples LA, Kiel DP, Karasik D.

J Bone Miner Res. 2011 Jun;26(6):1261-71. doi: 10.1002/jbmr.333.

PMID:
21611967
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Effect of population stratification analysis on false-positive rates for common and rare variants.

He H, Zhang X, Ding L, Baye TM, Kurowski BG, Martin LJ.

BMC Proc. 2011 Nov 29;5 Suppl 9:S116. doi: 10.1186/1753-6561-5-S9-S116.

PMID:
22373282
[PubMed]
Free PMC Article
9.

Improved power by collapsing rare and common variants based on a data-adaptive forward selection strategy.

Dai Y, Guo L, Dong J, Jiang R.

BMC Proc. 2011 Nov 29;5 Suppl 9:S114. doi: 10.1186/1753-6561-5-S9-S114.

PMID:
22373230
[PubMed]
Free PMC Article
10.

Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis.

Yoo YJ, Sun L, Bull SB.

Front Genet. 2013 Nov 12;4:233. doi: 10.3389/fgene.2013.00233. eCollection 2013.

PMID:
24273553
[PubMed]
Free PMC Article
11.

Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17.

Guo W, Elston RC, Zhu X.

BMC Proc. 2011 Nov 29;5 Suppl 9:S12. doi: 10.1186/1753-6561-5-S9-S12.

PMID:
22373385
[PubMed]
Free PMC Article
12.

DNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding (GNAS) genomic imprinting domain are associated with performance traits.

Sikora KM, Magee DA, Berkowicz EW, Berry DP, Howard DJ, Mullen MP, Evans RD, Machugh DE, Spillane C.

BMC Genet. 2011 Jan 7;12:4. doi: 10.1186/1471-2156-12-4.

PMID:
21214909
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.

PMID:
22549493
[PubMed - indexed for MEDLINE]
14.

Comparison of tagging single-nucleotide polymorphism methods in association analyses.

Goode EL, Fridley BL, Sun Z, Atkinson EJ, Nord AS, McDonnell SK, Jarvik GP, de Andrade M, Slager SL.

BMC Proc. 2007;1 Suppl 1:S6. Epub 2007 Dec 18.

PMID:
18466560
[PubMed]
Free PMC Article
15.

Approaches for evaluating rare polymorphisms in genetic association studies.

Li Q, Zhang H, Yu K.

Hum Hered. 2010;69(4):219-28. doi: 10.1159/000291927. Epub 2010 Mar 24.

PMID:
20332646
[PubMed - indexed for MEDLINE]
Free PMC Article
16.
17.

Association screening for genes with multiple potentially rare variants: an inverse-probability weighted clustering approach.

Liu Y, Huang CH, Hu I, Lo SH, Zheng T.

BMC Proc. 2011 Nov 29;5 Suppl 9:S106. doi: 10.1186/1753-6561-5-S9-S106.

PMID:
22373536
[PubMed]
Free PMC Article
18.

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.

PMID:
22309429
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Genome-wide association with diabetes-related traits in the Framingham Heart Study.

Meigs JB, Manning AK, Fox CS, Florez JC, Liu C, Cupples LA, Dupuis J.

BMC Med Genet. 2007 Sep 19;8 Suppl 1:S16.

PMID:
17903298
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

A novel support vector machine-based approach for rare variant detection.

Fang YH, Chiu YF.

PLoS One. 2013 Aug 7;8(8):e71114. doi: 10.1371/journal.pone.0071114. Print 2013.

PMID:
23940698
[PubMed - indexed for MEDLINE]
Free PMC Article
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