| Bayesian models for population‐based case‐control studies when the population is in Hardy‐Weinberg equilibrium |
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| Identifying SNPs predictive of phenotype using random forests |
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| Heterogeneity testing in meta‐analysis of genome searches |
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| Exploiting gene‐environment independence in family‐based case‐control studies: Increased power for detecting associations, interactions and joint effects |
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| Case‐control single‐marker and haplotypic association analysis of pedigree data |
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| New joint covariance- and marginal-based tests for association and linkage for quantitative traits for random and non-random sampling |
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| Estimating haplotype-disease associations with pooled genotype data |
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| Allelic association patterns for a dense SNP map |
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| Two‐Stage sampling designs for gene association studies |
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| Evaluating associations of haplotypes with traits |
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| SNPs, haplotypes, and model selection in a candidate gene region: The SIMPle analysis for multilocus data |
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| Genetic epidemiology and haplotypes |
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| Genotype prediction using a dense map of SNPs |
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✓ |
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| Recipients of Genetic Epidemiology Best Paper of the Year Award |
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| Thanks to Editorial Reviewers for 2004 |
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| Random‐effects Cox proportional hazards model: General variance components methods for time‐to‐event data |
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| Identifying interacting SNPs using Monte Carlo logic regression |
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| How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage |
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| Power and robustness of linkage tests for quantitative traits in general pedigrees |
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| Multipoint linkage mapping using sibpairs: Non-parametric estimation of trait effects with quantitative covariates |
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| Use of unphased multilocus genotype data in indirect association studies |
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| Simultaneous localization of two linked disease susceptibility genes |
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| Thirteenth Annual Meeting of the International Genetic Epidemiology Society |
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| Comparison of prospective and retrospective methods for haplotype inference in case‐control studies |
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| Algorithms for inferring haplotypes |
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| The role of haplotypes in candidate gene studies |
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| An exact maternal-fetal genotype incompatibility (MFG) test |
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| Tag SNP selection for association studies |
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| Robust estimation of critical values for genome scans to detect linkage |
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| A hidden Markov modeling approach for admixture mapping based on case‐control data |
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✓ |
✓ |
"ethnicity", "founding populations of different ethnicity", "admixed populations", "ethnicity relati |
| Haplotype block structures show significant variation among populations |
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✓ |
✓ |
✓ |
European; African |
| Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes |
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| Increased power for case‐control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraints |
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| Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome |
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| Co‐localization of differentially expressed genes and shared susceptibility loci in human autoimmunity |
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| Classifying disease chromosomes arising from multiple founders, with application to fine‐scale haplotype mapping |
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| Assessing genomewide statistical significance in linkage studies |
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| Bounds and normalization of the composite linkage disequilibrium coefficient |
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| The haplotype runs test: The parent‐parent‐affected offspring trio design |
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| Score test for detecting linkage to complex traits in selected samples |
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| Sampling correction in linkage analysis |
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| Assessment of sex‐specific genetic and environmental effects on bone mineral density |
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| Is haplotype block identification useful for association mapping studies? |
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| Case‐control association studies with matching and genomic controlling |
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✓ |
✓ |
race, ethnicity, nationality, ancestry, birthplace |
| Maximum‐likelihood estimation of haplotype frequencies in nuclear families |
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| Haplotype sharing correlation analysis using family data: A comparison with family‐based association test in the presence of allelic heterogeneity |
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| Detecting epistatic interactions contributing to quantitative traits |
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| Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onset |
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| New approach to association testing in case‐parent designs under informative parental missingness |
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| Method for using complete and incomplete trios to identify genes related to a quantitative trait |
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| Power calculations for familial aggregation studies |
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| Information on ancestry from genetic markers |
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| Evaluating bias due to population stratification in case‐control association studies of admixed populations |
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✓ |
✓ |
African Americans; admixed ethnicities; ethnicities; admixed ethnicity |
| Ordered subset analysis in genetic linkage mapping of complex traits |
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| Multivariate linkage analysis of blood pressure and body mass index |
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✓ |
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| Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile‐X |
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| Biostatistical Genetics and Genetic Epidemiology, Edited by Robert Elston, Jane Olson, and Lyle Palmer. Hoboken, NJ: John Wiley & Sons, Inc., 2002, 831 pages, U.S.$415.00 |
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| Quantitative trait linkage analysis by generalized estimating equations: Unification of variance components and Haseman‐Elston regression |
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| Haplotype‐based association analysis in cohort studies of unrelated individuals |
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| Combined association and linkage analysis applied to the <i>APOE</i> locus |
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✓ |
✓ |
Dutch |
| Consanguinity and endogamy in Northern Tunisia and its impact on non‐syndromic deafness |
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| The estimation of sibling genetic risk parameters revisited |
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| Affected‐sib‐pair test for linkage based on constraints for identical‐by‐descent distributions corresponding to disease models with imprinting |
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| Power of non‐parametric linkage analysis in mapping genes contributing to human longevity in long‐lived sib‐pairs |
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| Properties of case/pseudocontrol analysis for genetic association studies: Effects of recombination, ascertainment, and multiple affected offspring |
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| Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene‐gene and gene‐environment interactions, and parent‐of‐origin |
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| Multipoint linkage analysis of quantitative traits on sex‐chromosomes |
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| Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities |
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| Evaluations of maximization procedures for estimating linkage parameters under heterogeneity |
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| Efficient Simulation of <i>P</i> Values for Linkage Analysis |
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| What SNP genotyping errors are most costly for genetic association studies? |
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| Testing for association with a case‐parents design in the presence of genotyping errors |
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| IL10 gene polymorphisms are associated with asthma phenotypes in children |
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✓ |
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| Gamma regression improves Haseman‐Elston and variance components linkage analysis for sib‐pairs |
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| Power of direct vs. indirect haplotyping in association studies |
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| A trisomic transmission disequilibrium test |
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| Conditional multipoint linkage analysis using affected sib pairs: An alternative approach |
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| C.C. Li (1912–2003): His science and his spirit |
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