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Items: 1 to 20 of 49

1.

Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.

Jin J, Cerise JE, Kang SJ, Yoon EJ, Yoon S, Mendell NR, Finch SJ.

BMC Proc. 2011 Nov 29;5 Suppl 9:S66. doi: 10.1186/1753-6561-5-S9-S66.

2.

Evaluating methods for the analysis of rare variants in sequence data.

Luedtke A, Powers S, Petersen A, Sitarik A, Bekmetjev A, Tintle NL.

BMC Proc. 2011 Nov 29;5 Suppl 9:S119. doi: 10.1186/1753-6561-5-S9-S119.

3.

Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits.

Zhang Q, Chung D, Kraja A, Borecki II, Province MA.

BMC Proc. 2011 Nov 29;5 Suppl 9:S35. doi: 10.1186/1753-6561-5-S9-S35.

4.

Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence data.

Sung YJ, Rice TK, Rao DC.

BMC Proc. 2011 Nov 29;5 Suppl 9:S121. doi: 10.1186/1753-6561-5-S9-S121.

5.

Design considerations for genetic linkage and association studies.

Nsengimana J, Bishop DT.

Methods Mol Biol. 2012;850:237-62. doi: 10.1007/978-1-61779-555-8_13.

PMID:
22307702
6.

Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data.

Kraja AT, Czajkowski J, Feitosa MF, Borecki IB, Province MA.

BMC Proc. 2011 Nov 29;5 Suppl 9:S96. doi: 10.1186/1753-6561-5-S9-S96.

7.

Power analysis of principal components regression in genetic association studies.

Shen YF, Zhu J.

J Zhejiang Univ Sci B. 2009 Oct;10(10):721-30. doi: 10.1631/jzus.B0830866.

8.

Genetic variation and human longevity.

Soerensen M.

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

PMID:
22549493
9.

Comparison of collapsing methods for the statistical analysis of rare variants.

Dering C, Ziegler A, K├Ânig IR, Hemmelmann C.

BMC Proc. 2011 Nov 29;5 Suppl 9:S115. doi: 10.1186/1753-6561-5-S9-S115.

10.
11.

A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis.

Song YE, Namkung J, Shields RW, Baechle DJ, Song S, Elston RC.

BMC Proc. 2011 Nov 29;5 Suppl 9:S84. doi: 10.1186/1753-6561-5-S9-S84.

13.

Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data.

Ayers KL, Mamasoula C, Cordell HJ.

BMC Proc. 2011 Nov 29;5 Suppl 9:S92. doi: 10.1186/1753-6561-5-S9-S92.

14.

Interrogating population structure and its impact on association tests.

Qin H, Elston RC, Zhu X.

BMC Proc. 2011 Nov 29;5 Suppl 9:S25. doi: 10.1186/1753-6561-5-S9-S25.

15.

Family-based association tests for ordinal traits adjusting for covariates.

Wang X, Ye Y, Zhang H.

Genet Epidemiol. 2006 Dec;30(8):728-36.

PMID:
17086513
16.

A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.

Yang Y, Li SS, Chien JW, Andriesen J, Zhao LP.

BMC Genet. 2008 Dec 22;9:90. doi: 10.1186/1471-2156-9-90.

17.

Predicting quantitative trait levels by modeling SNP interaction.

Fijal BA, Kim LL, Buxbaum SG, Witte JS.

Genet Epidemiol. 2001;21 Suppl 1:S608-13.

PMID:
11793747
18.

Effects of long-term exposure to traffic-related air pollution on respiratory and cardiovascular mortality in the Netherlands: the NLCS-AIR study.

Brunekreef B, Beelen R, Hoek G, Schouten L, Bausch-Goldbohm S, Fischer P, Armstrong B, Hughes E, Jerrett M, van den Brandt P.

Res Rep Health Eff Inst. 2009 Mar;(139):5-71; discussion 73-89.

PMID:
19554969
19.

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.

20.

Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers.

Pugh EW, Papanicolaou GJ, Justice CM, Roy-Gagnon MH, Sorant AJ, Kingman A, Wilson AF.

Genet Epidemiol. 2001;21 Suppl 1:S794-9.

PMID:
11793780
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