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Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction.
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- Genetic Epidemiology, 2011, v. 35, p. S35, doi. 10.1002/gepi.20647
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Identification of genetic association of multiple rare variants using collapsing methods.
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- Genetic Epidemiology, 2011, v. 35, p. S101, doi. 10.1002/gepi.20658
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Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience.
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- Genetic Epidemiology, 2011, v. 35, p. S5, doi. 10.1002/gepi.20642
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Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data.
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- Genetic Epidemiology, 2011, v. 35, p. S67, doi. 10.1002/gepi.20653
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Effect of linkage disequilibrium on the identification of functional variants.
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- Genetic Epidemiology, 2011, v. 35, p. S115, doi. 10.1002/gepi.20660
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Incorporating biological information into association studies of sequencing data.
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- Genetic Epidemiology, 2011, v. 35, p. S29, doi. 10.1002/gepi.20646
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Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data.
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- Genetic Epidemiology, 2011, v. 35, p. S92, doi. 10.1002/gepi.20657
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Quality control issues and the identification of rare functional variants with next-generation sequencing data.
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- Genetic Epidemiology, 2011, v. 35, p. S22, doi. 10.1002/gepi.20645
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Analysis of exome sequences with and without incorporating prior biological knowledge.
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- Genetic Epidemiology, 2011, v. 35, p. S48, doi. 10.1002/gepi.20649
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Introduction to genetic analysis workshop 17 summaries.
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- Genetic Epidemiology, 2011, v. 35, p. S1, doi. 10.1002/gepi.20641
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Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes.
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- Genetic Epidemiology, 2011, v. 35, p. S85, doi. 10.1002/gepi.20656
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Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17.
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- Genetic Epidemiology, 2011, v. 35, p. S61, doi. 10.1002/gepi.20651
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Detecting multiple causal rare variants in exome sequence data.
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- Genetic Epidemiology, 2011, v. 35, p. S18, doi. 10.1002/gepi.20644
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Rare variants, common markers: synthetic association and beyond.
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- Genetic Epidemiology, 2011, v. 35, p. S80, doi. 10.1002/gepi.20655
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Population-based and family-based designs to analyze rare variants in complex diseases.
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- Genetic Epidemiology, 2011, v. 35, p. S41, doi. 10.1002/gepi.20648
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Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis.
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- Genetic Epidemiology, 2011, v. 35, p. S107, doi. 10.1002/gepi.20659
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Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17.
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- Genetic Epidemiology, 2011, v. 35, p. S56, doi. 10.1002/gepi.20650
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Statistical analysis of rare sequence variants: an overview of collapsing methods.
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- Genetic Epidemiology, 2011, v. 35, p. S12, doi. 10.1002/gepi.20643
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Incorporating linkage information into a common disease/rare variant framework.
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- Genetic Epidemiology, 2011, v. 35, p. S74, doi. 10.1002/gepi.20654
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Multilocus association testing with penalized regression.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 755, doi. 10.1002/gepi.20625
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Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 861, doi. 10.1002/gepi.20636
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Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 800, doi. 10.1002/gepi.20629
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Robust Mantel-Haenszel test under genetic model uncertainty allowing for covariates in case-control association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 695, doi. 10.1002/gepi.20620
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Improving power and robustness for detecting genetic association with extreme-value sampling design.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 823, doi. 10.1002/gepi.20631
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Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 790, doi. 10.1002/gepi.20628
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Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 887, doi. 10.1002/gepi.20639
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A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 729, doi. 10.1002/gepi.20624
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To stratify or not to stratify: power considerations for population-based genome-wide association studies of quantitative traits.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 867, doi. 10.1002/gepi.20637
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Identity-by-descent-based phasing and imputation in founder populations using graphical models.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 853, doi. 10.1002/gepi.20635
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Genetic epidemiology with a Capital E, ten years after.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 845, doi. 10.1002/gepi.20634
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Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 638, doi. 10.1002/gepi.20613
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Transethnic meta-analysis of genomewide association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 809, doi. 10.1002/gepi.20630
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Defining the power limits of genome-wide association scan meta-analyses.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 781, doi. 10.1002/gepi.20627
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A test of Hardy-Weinberg equilibrium in structured populations.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 671, doi. 10.1002/gepi.20617
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On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 880, doi. 10.1002/gepi.20638
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Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 745, doi. 10.1002/gepi.20622
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PlatinumCNV: A Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 831, doi. 10.1002/gepi.20633
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Haplotype variation and genotype imputation in African populations.
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- Genetic Epidemiology, 2011, v. 35, n. 8, p. 766, doi. 10.1002/gepi.20626
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Approximate and exact tests of Hardy-Weinberg equilibrium using uncertain genotypes.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 632, doi. 10.1002/gepi.20612
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Stability selection for genome-wide association.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 722, doi. 10.1002/gepi.20623
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X chromosome association testing in genome wide association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 664, doi. 10.1002/gepi.20616
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Comparison of statistical tests for disease association with rare variants.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 606, doi. 10.1002/gepi.20609
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Power and type I error results for a bias-correction approach recently shown to provide accurate odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 739, doi. 10.1002/gepi.20611
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Optimal methods for meta-analysis of genome-wide association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 581, doi. 10.1002/gepi.20603
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A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 650, doi. 10.1002/gepi.20614
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Bias due to two-stage residual-outcome regression analysis in genetic association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 592, doi. 10.1002/gepi.20607
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A data-driven method for identifying rare variants with heterogeneous trait effects.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 679, doi. 10.1002/gepi.20618
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A new association test based on Chi-square partition for case-control GWA studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 658, doi. 10.1002/gepi.20615
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Evaluation of methods accounting for population structure with pedigree data and continuous outcomes.
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- Genetic Epidemiology, 2011, v. 35, n. 6, p. 427, doi. 10.1002/gepi.20590
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The use of imputed values in the meta-analysis of genome-wide association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 7, p. 597, doi. 10.1002/gepi.20608
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