| A tree‐based model for allele‐sharing‐based linkage analysis in human complex diseases |
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| Fine mapping of disease genes via haplotype clustering |
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| A multimarker regression‐based test of linkage for affected sib‐pairs at two linked loci |
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| A novel method to identify gene–gene effects in nuclear families: the MDR‐PDT |
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| Family‐based association test for time‐to‐onset data with time‐dependent differences between the hazard functions |
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| Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak |
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| Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database |
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CEU, CEPH Utah, Finnish, population-specific differences, four-population HapMap data |
| Incorporating endophenotypes into allele‐sharing based linkage tests |
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✓ |
Asian Pacific |
| Validity, efficiency, and robustness of a family‐based test of association |
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| Comparison of methods incorporating quantitative covariates into affected sib pair linkage analysis |
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| Microsatellites versus single‐nucleotide polymorphisms in confidence interval estimation of disease loci |
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| Editorial |
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| A two‐step procedure for constructing confidence intervals of trait loci with application to a rheumatoid arthritis dataset |
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| The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits |
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| Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3 |
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| Summary of contributions to GAW Group 5: Linkage mapping methods, Problem 2 |
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| Fine mapping by linkage and association in nuclear family and case-control designs |
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| Alcoholism and related traits: a summary of Group 13 contributions |
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| Approaches to detecting gene × gene interaction in Genetic Analysis Workshop 14 pedigrees |
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| Genotyping errors, pedigree errors, and missing data |
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| Haplotypes and haplotype-tagging single-nucleotide polymorphism: Presentation Group 8 of Genetic Analysis Workshop 14 |
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| Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels |
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| Summary of contributions to GAW Group 12: Multivariate Methods |
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| Genetic Analysis Workshop 14: Introduction to Workshop Summaries |
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| Linkage mapping methods applied to the COGA data set: Presentation Group 4 of Genetic Analysis Workshop 14 |
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| Dissection of heterogeneous phenotypes for quantitative trait mapping |
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| Association mapping: methodologies, strategies, and issues |
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| Case-control analyses: Geneopardy! |
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| Data mining |
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| Heterogeneity: GAW Group 15 |
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| Parent-of-origin, imprinting, mitochondrial, and X-linked effects in traits related to alcohol dependence: Presentation Group 18 of Genetic Analysis Workshop 14 |
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| Potential bias in generalized estimating equations linkage methods under incomplete information |
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| A sparse marker extension tree algorithm for selecting the best set of haplotype tagging single nucleotide polymorphisms |
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| Multipoint linkage disequilibrium mapping using case-control designs |
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| Estimating the additive genetic effect of the X chromosome |
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| Thanks to editorial reviewers for 2005 |
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| Multicomponent variance estimation for binary traits in family‐based studies |
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| Haplotype interaction analysis of unlinked regions |
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| Maximum likelihood estimation of haplotype effects and haplotype-environment interactions in association studies |
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| Global transmission/disequilibrium tests based on haplotype sharing in multiple candidate genes |
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| Abstracts from the Fourteenth Annual Meeting of the International Genetic Epidemiology Society |
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| Genome scans with gene‐covariate interaction |
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| Localization of breast cancer susceptibility loci by genome‐wide SNP linkage disequilibrium mapping |
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Ashkenazi Jewish; Jewish disease genes |
| Tests for the presence of two linked disease susceptibility genes |
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| Multilocus LD measure and tagging SNP selection with generalized mutual information |
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| Testing association and linkage using affected‐sib‐parent study designs |
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| Genome‐wide identity‐by‐descent sharing among CEPH siblings |
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| Exact family‐based association tests for biallelic data |
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| Multipoint linkage analysis for a very dense set of markers |
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| Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individuals |
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| Correction for Thomas et al., 2004, Genet. Epidemiol. 26:116-124 |
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| Detection of genotyping errors and pseudo‐SNPs via deviations from Hardy‐Weinberg equilibrium |
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| Analysis of case-control studies of genetic and environmental factors with missing genetic information and haplotype-phase ambiguity |
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| Determining joint carrier probabilities of cancer-causing genes using Markov chain Monte Carlo methods |
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| A method for identifying genes related to a quantitative trait, incorporating multiple siblings and missing parents |
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| Asymptotic equivalence between two score tests for haplotype-specific risk in general linear models |
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| Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes |
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| Genetic admixture and asthma‐related phenotypes in Mexican American and Puerto Rican asthmatics |
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✓ |
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✓ |
European ancestry; Europeans; Mexican Americans; Puerto Ricans; Native Americans; ancestrally admixed; ancestrally distinct popula |
| Robust ascertainment‐adjusted parameter estimation |
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| Comparison of population‐ and family‐based methods for genetic association analysis in the presence of interacting loci |
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| A weighted cohort approach for analysing factors modifying disease risks in carriers of high‐risk susceptibility genes |
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| Association testing with Mendel |
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| Two‐level Haseman‐Elston regression for general pedigree data analysis |
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| Characterizing allelic associations from unphased diploid data by graphical modeling |
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| Practical population group assignment with selected informative markers: Characteristics and properties of Bayesian clustering via STRUCTURE |
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✓ |
✓ |
✓ |
European Americans (EAs); African Americans (AAs) |
| Premature death of adult adoptees: Analyses of a case‐cohort sample |
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✓ |
✓ |
Danish adoptees |
| Bayesian modelling of multivariate quantitative traits using seemingly unrelated regressions |
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| Reduction of selection bias in genomewide studies by resampling |
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| Evolutionary‐based grouping of haplotypes in association analysis |
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| Estimation of individual admixture: Analytical and study design considerations |
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| Cytochrome P450 gene polymorphisms and risk of low birth weight |
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| A conditional‐on‐exchangeable‐parental‐genotypes likelihood that remains unbiased at the causal locus under multiple‐affected‐sibling ascertainment |
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| Streamlined analysis of pooled genotype data in SNP‐based association studies |
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| Haplotype sharing transmission/disequilibrium tests that allow for genotyping errors |
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| QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies |
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| Analysis of single‐locus tests to detect gene/disease associations |
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| Response to letter by Veronica J. Vieland and Susan E. Hodge |
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| Accounting for haplotype uncertainty in matched association studies: A comparison of simple and flexible techniques |
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| Characterization of multilocus linkage disequilibrium |
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| New simple tests for age‐at‐onset anticipation: Application to panic disorder |
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| Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: <i>ELAC2</i> and familial early‐onset prostate cancer |
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| Covariate adjustment in family‐based association studies |
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| Erratum |
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| Ascertainment bias in linkage analysis: Comments on Ginsburg et al. |
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