| Analysis of 60 Reported Glioma Risk <scp>SNP</scp>s Replicates Published <scp>GWAS</scp> Findings but Fails to Replicate Associations From Published Candidate‐Gene Studies |
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✓ |
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| Sequence Kernel Association Test for Quantitative Traits in Family Samples |
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| <scp>SNP</scp> Prioritization Using a <scp>B</scp>ayesian Probability of Association |
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| Detecting Rare Variant Effects Using Extreme Phenotype Sampling in Sequencing Association Studies |
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| A Multi‐Locus Likelihood Method for Assessing Parent‐of‐Origin Effects Using Case‐Control Mother‐Child Pairs |
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| Performance and Robustness of Penalized and Unpenalized Methods for Genetic Prediction of Complex Human Disease |
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| Simulating Realistic Genomic Data With Rare Variants |
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| Incorporating Network Structure in Integrative Analysis of Cancer Prognosis Data |
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| Multiway Admixture Deconvolution Using Phased or Unphased Ancestral Panels |
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✓ |
✓ |
✓ |
"European and West African ancestry"; "European, West African and Native American ancestry"; "West African"; "Native American" |
| Trees Assembling Mann‐Whitney Approach for Detecting Genome‐Wide Joint Association Among Low‐Marginal‐Effect Loci |
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| Exploring the Genetic Architecture of Circulating 25‐Hydroxyvitamin D |
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| A Conversation With Professor Newton Ennis Morton |
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| MaCH‐Admix: Genotype Imputation for Admixed Populations |
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✓ |
✓ |
African Americans; Hispanic Americans; admixed populations |
| Adjustment for Population Stratification via Principal Components in Association Analysis of Rare Variants |
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✓ |
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European |
| Maximum Likelihood Pedigree Reconstruction Using Integer Linear Programming |
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| Genetic Association Test for Multiple Traits at Gene Level |
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| Robust and Powerful Tests for Rare Variants Using Fisher's Method to Combine Evidence of Association From Two or More Complementary Tests |
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| Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin |
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✓ |
✓ |
Hispanic; African American; ethnicity-specific; ethnic group |
| Testing Genetic Association With Rare Variants in Admixed Populations |
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✓ |
✓ |
African Americans; Hispanic Americans |
| Empirical Bayes Correction for the Winner's Curse in Genetic Association Studies |
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| Joint Analysis of Binary and Quantitative Traits With Data Sharing and Outcome‐Dependent Sampling |
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| Utilizing Graph Theory to Select the Largest Set of Unrelated Individuals for Genetic Analysis |
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| Extracting Actionable Information From Genome Scans |
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| Power of IRT in GWAS: Successful QTL Mapping of Sum Score Phenotypes Depends on Interplay Between Risk Allele Frequency, Variance Explained by the Risk Allele, and Test Characteristics |
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| Longitudinal Association Analysis of Quantitative Traits |
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| Validity of the Family‐Based Association Test for Copy Number Variant Data in the Case of Non‐Linear Intensity‐Genotype Relationship |
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| SNP Set Association Analysis for Familial Data |
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| Analysis and Optimal Design for Association Studies Using Next‐Generation Sequencing With Case‐Control Pools |
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| Genome‐Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases |
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| ABSTRACTS FROM THE ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY |
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| IGES 2012 Abstracts: Author‐Abstract Index |
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| IGES 2012 Abstracts: Keyword Index |
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| Loss of Power in Two‐Stage Residual‐Outcome Regression Analysis in Genetic Association Studies |
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| SVM‐Based Generalized Multifactor Dimensionality Reduction Approaches for Detecting Gene‐Gene Interactions in Family Studies |
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| IGES 2011 Abstracts: Keyword Index |
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| Genotype Imputation of <scp>M</scp>etabochip<scp>SNPs</scp> Using a Study‐Specific Reference Panel of ∼4,000 Haplotypes in <scp>A</scp>frican <scp>A</scp>mericans From the Women's Health Initiative |
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✓ |
✓ |
non-European individuals; African Americans |
| ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY |
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| IGES 2011 Abstracts: Author‐Abstract Index |
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| Translational Genomics is Not a Spectator Sport: A Call to Action |
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| Bootstrap Aggregating of Alternating Decision Trees to Detect Sets of <scp>SNP</scp>s That Associate With Disease |
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| Multivariate Phenotype Association Analysis by Marker‐Set Kernel Machine Regression |
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| A Comparison of <scp>B</scp>ayesian and Frequentist Approaches to Incorporating External Information for the Prediction of Prostate Cancer Risk |
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| New Editor and New Directions for <i>Genetic Epidemiology</i> |
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| Unveiling Case‐Control Relationships in Designing a Simple and Powerful Method for Detecting Gene‐Gene Interactions |
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| Comparative Power of Family‐Based Association Strategies to Detect Disease‐Causing Variants Under Two‐Locus Models |
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| A Fast and Noise‐Resilient Approach to Detect Rare‐Variant Associations With Deep Sequencing Data for Complex Disorders |
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| Identifying Plausible Genetic Models Based on Association and Linkage Results: Application to Type 2 Diabetes |
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| A Sample Selection Strategy for Next‐Generation Sequencing |
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| Exploring Data From Genetic Association Studies Using Bayesian Variable Selection and the Dirichlet Process: Application to Searching for Gene × Gene Patterns |
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| Combining Family and Twin Data in Association Studies to Estimate the Noninherited Maternal Antigens Effect |
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| Integrative Analysis of Cancer Prognosis Data With Multiple Subtypes Using Regularized Gradient Descent |
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| Prospective Calculation of Identification Power for Individual Genes in Analyses Controlling the False Discovery Rate |
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| Direct Genetic Effects and Their Estimation From Matched Case‐Control Data |
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| Joint Genotype Calling With Array and Sequence Data |
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| Using Maximal Segmental Score in Genome‐Wide Association Studies |
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| Joint Association Testing of Common and Rare Genetic Variants Using Hierarchical Modeling |
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| Projection Regression Models for Multivariate Imaging Phenotype |
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| Multivariate Detection of Gene‐Gene Interactions |
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| A Likelihood Ratio‐Based Mann‐Whitney Approach Finds Novel Replicable Joint Gene Action for Type 2 Diabetes |
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| Analysis of Genetic Interactions Involving Maternal and Offspring Genotypes at Different Loci: Power Simulation and Application to Testicular Cancer |
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| Computationally Efficient Multipoint Linkage Analysis on Extended Pedigrees for Trait Models With Two Contributing Major Loci |
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| Haplotype‐Based Methods for Detecting Uncommon Causal Variants With Common SNPs |
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| Detecting Association of Rare and Common Variants by Testing an Optimally Weighted Combination of Variants |
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| Power and Sample Size Calculations for SNP Association Studies With Censored Time‐to‐Event Outcomes |
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| Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 |
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✓ |
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✓ |
|
European Ancestry; Asian; African American |
| Two Adaptive Weighting Methods to Test for Rare Variant Associations in Family‐Based Designs |
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| Biases and Errors on Allele Frequency Estimation and Disease Association Tests of Next‐Generation Sequencing of Pooled Samples |
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| Power of Single‐ vs. Multi‐Marker Tests of Association |
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| Genotype Imputation for <scp>A</scp>frican <scp>A</scp>mericans Using Data From <scp>H</scp>ap<scp>M</scp>ap Phase <scp>II</scp> Versus 1000 <scp>G</scp>enomes <scp>P</scp>rojects |
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|
✓ |
✓ |
African Americans; CEU; YRI |
| Unidentified Genetic Variants Influence Pancreatic Cancer Risk: An Analysis of Polygenic Susceptibility in the <scp>P</scp>an<scp>S</scp>can Study |
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| Inheritance Model Introduces Differential Bias in <scp>CNV</scp> Calls Between Parents and Offspring |
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| Optimized Selection of Unrelated Subjects for Whole‐Genome Sequencing Studies of Rare High‐Penetrance Alleles |
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✓ |
✓ |
Anabaptist (Anabaptist genealogy) |
| Using Family Data as a Verification Standard to Evaluate Copy Number Variation Calling Strategies for Genetic Association Studies |
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| Evaluation of Association Methods for Analysing Modifiers of Disease Risk in Carriers of High‐Risk Mutations |
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| Genome‐Wide Association Mapping With Longitudinal Data |
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| Association Testing for Next‐Generation Sequencing Data Using Score Statistics |
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| Is It Rare or Common? |
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✓ |
✓ |
German |
| Reprioritizing Genetic Associations in Hit Regions Using LASSO‐Based Resample Model Averaging |
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| XM: Association Testing on the X‐Chromosome in Case‐Control Samples With Related Individuals |
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| Smoking and Genetic Risk Variation Across Populations of <scp>E</scp>uropean, <scp>A</scp>sian, and <scp>A</scp>frican <scp>A</scp>merican Ancestry—A Meta‐Analysis of Chromosome 15q25 |
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✓ |
✓ |
European ancestry; Asian; African American |
| <i>h<scp>TERT</scp></i> Cancer Risk Genotypes Are Associated With Telomere Length |
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| An Integrative Segmentation Method for Detecting Germline Copy Number Variations in SNP Arrays |
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| Incorporating Genotype Uncertainties Into the Genotypic TDT for Main Effects and Gene‐Environment Interactions |
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| Incorporating Biological Information into Association Studies of Sequencing Data |
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| On Optimal Gene‐Based Analysis of Genome Scans |
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| Sparse Principal Component Analysis for Identifying Ancestry‐Informative Markers in Genome‐Wide Association Studies |
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| Link Functions in Multi‐Locus Genetic Models: Implications for Testing, Prediction, and Interpretation |
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| DIVERGENOME: A Bioinformatics Platform to Assist Population Genetics and Genetic Epidemiology Studies |
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| Fasting Glucose <scp>GWAS</scp> Candidate Region Analysis Across Ethnic Groups in the Multiethnic Study of Atherosclerosis (<scp>MESA</scp>) |
|
✓ |
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|
|
European ancestry populations |
| A Two‐Platform Design for Next Generation Genome‐Wide Association Studies |
|
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| Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between <scp>A</scp>sians and <scp>E</scp>uropeans |
|
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✓ |
✓ |
European ancestry; Asians; Asian ancestry; Europeans; Asians/Asians ancestry |
| A Better Coefficient of Determination for Genetic Profile Analysis |
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| Powerful Cocktail Methods for Detecting Genome‐Wide Gene‐Environment Interaction |
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| Stratification‐Score Matching Improves Correction for Confounding by Population Stratification in Case‐Control Association Studies |
|
|
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|
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|
✓ |
✓ |
African‐American |
| <scp>PSEA</scp>: Phenotype Set Enrichment Analysis—A New Method for Analysis of Multiple Phenotypes |
|
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|
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| Power Comparison of Admixture Mapping and Direct Association Analysis in Genome‐Wide Association Studies |
|
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| A Comparison of Methods Sensitive to Interactions With Small Main Effects |
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| Two‐Phase Stratified Sampling Designs for Regional Sequencing |
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| Joint Analysis of Binary and Quantitative Traits With Data Sharing and Outcome‐Dependent Sampling |
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| Accurate Imputation of Rare and Common Variants in a Founder Population From a Small Number of Sequenced Individuals |
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|
European populations |
| A <scp>B</scp>ayesian Integrative Genomic Model for Pathway Analysis of Complex Traits |
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| Gene–Environment Interactions on Growth Trajectories |
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| Genetic Epidemiology with a Capital E: Where Will We Be in Another 10 Years? |
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