Confidence intervals for candidate gene effects and environmental factors in population-based association studies of families
A Bidirectional Corridor in the Sahel-Sudan Belt and the Distinctive Features of the Chad Basin Populations
Common Adiponectin Gene Variants Show Different Effects on Risk of Cardiovascular Disease and Type 2 Diabetes in European Subjects
Accounting for Genotyping Errors in Tagging SNP Selection
Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms
The Missing ApoE Allele
Structured Incorporation of Prior Information in Relationship Identification Problems
Evidence for Association of Polymorphisms in CYP2J2 and Susceptibility to Essential Hypertension
Correlation Between Genetic Variations in Hox Clusters and Hirschsprung's Disease
Regularized Least Squares Classifiers may Predict Crohn's Disease from Profiles of Single Nucleotide Polymorphisms
Identifying Common QTLs for a Bivariate Phen- otype
A New Test to Detect a Possible Gene-Environment Interaction without Genotyping!
Robust testing for genetic linkage taking into account age at onset
Using a 500K SNP map for linkage analysis in a large and highly inbred pedigree
Gene Prioritization by Genomic Data Fusion
A Game-Theoretic Model of the Evolution of Chick Killing by Brood Parasitic Offspring
A Model of Brood Parasitism Using Extensive Form Games
Temporal Behaviour of the Stepwise Mutation Model
The Interplay Between Recombination and Selection Can Confound Their Inference from Population Data - But Suggests a Novel Genome-Wide Method for Detecting Selection
Direct Testing of Untyped SNPs Using Multimarker Tags
Improvement of Haplotype Sharing Analysis for Localization of Disease Loci Using Entropy Based Marker Selection
Quantification and Correction of Bias in Tagging SNPs Caused by Insufficient Sample Size and Marker Density by Means of Haplotype-Dropping
Bayesian Meta Analysis of Genetic Association Studies with Different Sets of Markers
Estimating Risks of Common Complex Diseases Across Genetic and Environmental Risk Factors
Using WinZip as a Tool for Analysis of Genetic Data
Ignoring Intermarker Linkage Disequilibrium Induces False-Positive Evidence of Linkage for Consanguineous Pedigrees When Genotype Data is Missing for Any Pedigree Member
Potential of Genomic Control for Pedigree-Based Association of Quantitative Traits
Turbo Genomic Control
A Novel Strategy to Identify Modifier Genes
Efficiency of Multiple Imputation for the Detection of the True Disease Susceptibility Site in Presence of Missing Data
Estimation of the Genotype Relative Risk Using One or Three Pseudocontrols in Family Based Analyses
The Effect of Assortative Mating on the Power of Transmission Disequilibrium Test
Family-Based Association Analysis of Inflammatory Genes' Polymorphisms and Haplotypes in Premature Coronary Artery Disease
Mixed Modeling for Unobservable Phase Haplotype Data
Impact of Genotyping Errors on the Type I Error Rates of Haplotype-Based Association Methods Revisited
Nonparametric Detection of Genes and Their Interaction Influencing the Longitudinal Course of a Phenotype
Influence of Linkage Disequilibrium and Marker Allele Frequency on the Sample Size Needed to Detect Gene-Environment Interaction in Indirect Association Mapping
A Mixture Model Approach for Multiple Testing in Variance Component Linkage Analyses
Estimating Genome-Wide Significance Levels for Association
Assessing the Posterior Odds of a Genuine Association in Whole-Genome Association Scans
Bayesian Shrinkage Priors for Detecting Multiple Causal Variants from Genome-Wide Association Studies
Catching Local Replications
Large Scale Association Studies
Exploiting Gene-Environment Interaction in Genome-Wide Association Scans
Comparison of Methods for Combining Case-Control and Family-Based Association Studies
Correlation Among Agronomic Traits Using Multivariate Analysis
Haplotype-Based Association Studies with Phase-Unknown Multilocus Genotypes
MCMC Methods for Bayesian Variable Selection in Large-Scale Genomic Applications
An MCMC Approach to Copy Number Polymorphism in Nuclear Families