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Items: 1 to 20 of 48


Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk.

Hsu FC, Sides EG, Mychaleckyj JC, Worrall BB, Elias GA, Liu Y, Chen WM, Coull BM, Toole JF, Rich SS, Furie KL, Sale MM.

Neurology. 2011 Oct 18;77(16):1543-50. doi: 10.1212/WNL.0b013e318233b1f9.


Testing for an unusual distribution of rare variants.

Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ.

PLoS Genet. 2011 Mar;7(3):e1001322. doi: 10.1371/journal.pgen.1001322.


Self-contained gene-set analysis of expression data: an evaluation of existing and novel methods.

Fridley BL, Jenkins GD, Biernacka JM.

PLoS One. 2010 Sep 17;5(9). pii: e12693. doi: 10.1371/journal.pone.0012693.


Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations.

Schaid DJ.

Hum Hered. 2010;70(2):109-31. doi: 10.1159/000312641. Review.


Genomic similarity and kernel methods II: methods for genomic information.

Schaid DJ.

Hum Hered. 2010;70(2):132-40. doi: 10.1159/000312643. Review.


Powerful SNP-set analysis for case-control genome-wide association studies.

Wu MC, Kraft P, Epstein MP, Taylor DM, Chanock SJ, Hunter DJ, Lin X.

Am J Hum Genet. 2010 Jun 11;86(6):929-42. doi: 10.1016/j.ajhg.2010.05.002.


Pooled association tests for rare variants in exon-resequencing studies.

Price AL, Kryukov GV, de Bakker PI, Purcell SM, Staples J, Wei LJ, Sunyaev SR.

Am J Hum Genet. 2010 Jun 11;86(6):832-8. doi: 10.1016/j.ajhg.2010.04.005. Erratum in: Am J Hum Genet. 2010 Jun 11;86(6):982.


Gene--environment-wide association studies: emerging approaches.

Thomas D.

Nat Rev Genet. 2010 Apr;11(4):259-72. doi: 10.1038/nrg2764. Review.


Methods for investigating gene-environment interactions in candidate pathway and genome-wide association studies.

Thomas D.

Annu Rev Public Health. 2010;31:21-36. doi: 10.1146/annurev.publhealth.012809.103619. Review.


Gene, region and pathway level analyses in whole-genome studies.

De la Cruz O, Wen X, Ke B, Song M, Nicolae DL.

Genet Epidemiol. 2010 Apr;34(3):222-31. doi: 10.1002/gepi.20452.


Comparisons of multi-marker association methods to detect association between a candidate region and disease.

Ballard DH, Cho J, Zhao H.

Genet Epidemiol. 2010 Apr;34(3):201-12. doi: 10.1002/gepi.20448.


Association tests using kernel-based measures of multi-locus genotype similarity between individuals.

Mukhopadhyay I, Feingold E, Weeks DE, Thalamuthu A.

Genet Epidemiol. 2010 Apr;34(3):213-21. doi: 10.1002/gepi.20451.


A groupwise association test for rare mutations using a weighted sum statistic.

Madsen BE, Browning SR.

PLoS Genet. 2009 Feb;5(2):e1000384. doi: 10.1371/journal.pgen.1000384.


Gene-trait similarity regression for multimarker-based association analysis.

Tzeng JY, Zhang D, Chang SM, Thomas DC, Davidian M.

Biometrics. 2009 Sep;65(3):822-32. doi: 10.1111/j.1541-0420.2008.01176.x.


ATOM: a powerful gene-based association test by combining optimally weighted markers.

Li M, Wang K, Grant SF, Hakonarson H, Li C.

Bioinformatics. 2009 Feb 15;25(4):497-503. doi: 10.1093/bioinformatics/btn641.


Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

Li B, Leal SM.

Am J Hum Genet. 2008 Sep;83(3):311-21. doi: 10.1016/j.ajhg.2008.06.024.


U-statistics-based tests for multiple genes in genetic association studies.

Wei Z, Li M, Rebbeck T, Li H.

Ann Hum Genet. 2008 Nov;72(Pt 6):821-33. doi: 10.1111/j.1469-1809.2008.00473.x.


Gene-environment interactions for complex traits: definitions, methodological requirements and challenges.

Dempfle A, Scherag A, Hein R, Beckmann L, Chang-Claude J, Schäfer H.

Eur J Hum Genet. 2008 Oct;16(10):1164-72. doi: 10.1038/ejhg.2008.106. Review.

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