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Items: 1 to 20 of 35


A novel bayesian graphical model for genome-wide multi-SNP association mapping.

Zhang Y.

Genet Epidemiol. 2012 Jan;36(1):36-47. doi: 10.1002/gepi.20661.


Stability selection for genome-wide association.

Alexander DH, Lange K.

Genet Epidemiol. 2011 Nov;35(7):722-8. doi: 10.1002/gepi.20623.


Multilocus association testing with penalized regression.

Basu S, Pan W, Shen X, Oetting WS.

Genet Epidemiol. 2011 Dec;35(8):755-65. doi: 10.1002/gepi.20625.


Comparison of statistical tests for disease association with rare variants.

Basu S, Pan W.

Genet Epidemiol. 2011 Nov;35(7):606-19. doi: 10.1002/gepi.20609.


Identification of association between disease and multiple markers via sparse partial least-squares regression.

Chun H, Ballard DH, Cho J, Zhao H.

Genet Epidemiol. 2011 Sep;35(6):479-86. doi: 10.1002/gepi.20596.


Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS.

Shi G, Boerwinkle E, Morrison AC, Gu CC, Chakravarti A, Rao DC.

Genet Epidemiol. 2011 Feb;35(2):111-8. doi: 10.1002/gepi.20556.


A comparison of approaches to account for uncertainty in analysis of imputed genotypes.

Zheng J, Li Y, Abecasis GR, Scheet P.

Genet Epidemiol. 2011 Feb;35(2):102-10. doi: 10.1002/gepi.20552.



Wilson MA, Iversen ES, Clyde MA, Schmidler SC, Schildkraut JM.

Ann Appl Stat. 2010 Sep 1;4(3):1342-1364.


SNP selection in genome-wide and candidate gene studies via penalized logistic regression.

Ayers KL, Cordell HJ.

Genet Epidemiol. 2010 Dec;34(8):879-91. doi: 10.1002/gepi.20543.


MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.

Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR.

Genet Epidemiol. 2010 Dec;34(8):816-34. doi: 10.1002/gepi.20533.


A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2., Strange A, Capon F, Spencer CC, Knight J, Weale ME, Allen MH, Barton A, Band G, Bellenguez C, Bergboer JG, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Cork MJ, Corvin A, Deloukas P, Dilthey A, Duncanson A, Edkins S, Estivill X, Fitzgerald O, Freeman C, Giardina E, Gray E, Hofer A, Hüffmeier U, Hunt SE, Irvine AD, Jankowski J, Kirby B, Langford C, Lascorz J, Leman J, Leslie S, Mallbris L, Markus HS, Mathew CG, McLean WH, McManus R, Mössner R, Moutsianas L, Naluai AT, Nestle FO, Novelli G, Onoufriadis A, Palmer CN, Perricone C, Pirinen M, Plomin R, Potter SC, Pujol RM, Rautanen A, Riveira-Munoz E, Ryan AW, Salmhofer W, Samuelsson L, Sawcer SJ, Schalkwijk J, Smith CH, Ståhle M, Su Z, Tazi-Ahnini R, Traupe H, Viswanathan AC, Warren RB, Weger W, Wolk K, Wood N, Worthington J, Young HS, Zeeuwen PL, Hayday A, Burden AD, Griffiths CE, Kere J, Reis A, McVean G, Evans DM, Brown MA, Barker JN, Peltonen L, Donnelly P, Trembath RC.

Nat Genet. 2010 Nov;42(11):985-90. doi: 10.1038/ng.694.


Regularization Paths for Generalized Linear Models via Coordinate Descent.

Friedman J, Hastie T, Tibshirani R.

J Stat Softw. 2010;33(1):1-22.


Association screening of common and rare genetic variants by penalized regression.

Zhou H, Sehl ME, Sinsheimer JS, Lange K.

Bioinformatics. 2010 Oct 1;26(19):2375-82. doi: 10.1093/bioinformatics/btq448.


New approaches to population stratification in genome-wide association studies.

Price AL, Zaitlen NA, Reich D, Patterson N.

Nat Rev Genet. 2010 Jul;11(7):459-63. doi: 10.1038/nrg2813. Review.


Prioritizing GWAS results: A review of statistical methods and recommendations for their application.

Cantor RM, Lange K, Sinsheimer JS.

Am J Hum Genet. 2010 Jan;86(1):6-22. doi: 10.1016/j.ajhg.2009.11.017. Review.


Finding the missing heritability of complex diseases.

Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark AG, Eichler EE, Gibson G, Haines JL, Mackay TF, McCarroll SA, Visscher PM.

Nature. 2009 Oct 8;461(7265):747-53. doi: 10.1038/nature08494. Review.


Bayesian statistical methods for genetic association studies.

Stephens M, Balding DJ.

Nat Rev Genet. 2009 Oct;10(10):681-90. doi: 10.1038/nrg2615. Review.


Discussion of "Sure Independence Screening for Ultra-High Dimensional Feature Space.

Zhang HH.

J R Stat Soc Series B Stat Methodol. 2008;70(5):849-911. No abstract available.


A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.

Howie BN, Donnelly P, Marchini J.

PLoS Genet. 2009 Jun;5(6):e1000529. doi: 10.1371/journal.pgen.1000529.


Mapping in structured populations by resample model averaging.

Valdar W, Holmes CC, Mott R, Flint J.

Genetics. 2009 Aug;182(4):1263-77. doi: 10.1534/genetics.109.100727.

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