| The impacts of errors in individual genotyping and DNA pooling on association studies |
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| Analysis of SNPs in pooled DNA: A decision theoretic model |
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| Principal component analysis for selection of optimal SNP‐sets that capture intragenic genetic variation |
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| Power estimation of multiple SNP association test of case‐control study and application |
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| Tests for covariate‐associated heterogeneity in <i>IBD</i> allele sharing of affected relatives |
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| Family‐based tests for associating haplotypes with general phenotype data: Application to asthma genetics |
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| Bayesian trio models for association in the presence of genotyping errors |
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| Reducing sample sizes in genome scans: Group sequential study designs with futility stops |
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| Heritability of LDL peak particle diameter in the Quebec Family Study |
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| Sum statistics for the joint detection of multiple disease loci in case‐control association studies with SNP markers |
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| Rank truncated product of <i>P</i>‐values, with application to genomewide association scans |
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| Multipoint linkage disequilibrium mapping for complex diseases |
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| Parameter estimation in ascertainment adjustment in complex diseases |
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| Haplotyping using SIMPLE: Caution on ignoring interference |
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| Adjustment for competing risk in kin‐cohort estimation |
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✓ |
✓ |
Ashkenazi |
| Cleft palate, transforming growth factor alpha gene variants, and maternal exposures: Assessing gene‐environment interactions in case‐parent triads |
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| Estimating the relative recurrence risk ratio using a global cross‐ratio model |
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| Erratum |
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| Recipients of Genetic Epidemiology Best Paper of the Year Award |
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| Reviewer Acknowledgement |
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| Candidate gene association analysis for a quantitative trait, using parent‐offspring trios |
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✓ |
✓ |
ethnic confounding; population stratification bias |
| Score tests for epistasis models on quantitative traits using general pedigree data |
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| Model comparison and the likelihood ratio test in segregation analysis |
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| Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13 |
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| Summary report: Missing data and pedigree and genotyping errors |
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| Group 6: Pleiotropy and multivariate analysis |
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| Data Mining and Computationally intensive methods: Summary of Group 7 contributions to Genetic Analysis Workshop 13 |
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| Modeling and dissection of longitudinal blood pressure and hypertension phenotypes in genetic epidemiological studies |
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| Longitudinal data analysis in pedigree studies |
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| Effects of covariates: A summary of Group 5 contributions |
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| Summary of Group 8: Development and extension of linkage methods |
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| Genetic analysis workshop 13: Summary of analyses of alcohol and cigarette use phenotypes in the Framingham Heart Study |
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| Consistency of genetic analyses in longitudinal data: Observations from the GAW13 Framingham Heart Study data |
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| Genetic Analysis Workshop 13: Introduction to workshop summaries |
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| Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13 |
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| Analysis of twin data ascertained through probands: The double‐entry approach |
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| Abstracts from the Twelfth Annual Meeting of the International Genetic Epidemiology Society |
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| Detecting low‐quality markers using map expanders |
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| Genotype‐based association test for general pedigrees: The genotype‐PDT |
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| Logistic regression of family data from retrospective study designs |
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| Polygenic inheritance of breast cancer: Implications for design of association studies |
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| Improved use of SNP information to detect the role of genes |
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| Linkage disequilibrium assessment via log‐linear modeling of SNP haplotype frequencies |
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| Sample size calculations for population‐ and family‐based case‐control association studies on marker genotypes |
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| Family‐based analysis of MSX1 haplotypes for association with oral clefts |
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| Application of Bayesian spatial statistical methods to analysis of haplotypes effects and gene mapping |
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| Pedigree disequilibrium tests for multilocus haplotypes |
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| Bayesian analysis of multilocus association in quantitative and qualitative traits |
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| Optimal two‐stage genotyping in population‐based association studies |
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| Multipoint linkage disequilibrium mapping approach: Incorporating evidence of linkage and linkage disequilibrium from unlinked region |
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| Finding starting points for Markov chain Monte Carlo analysis of genetic data from large and complex pedigrees |
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✓ |
✓ |
founder populations; Hutterite pedigrees |
| Testing linkage and Gene × Environment interaction: Comparison of different affected sib‐pair methods |
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| Genetic association tests for family data with missing parental genotypes: A comparison |
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| Assessing accuracy in linkage analysis by means of confidence regions |
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| Linkage analysis with sequential imputation |
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| Cleft lip and palate: From origin to treatment, Diego F. Wyszynski. Oxford: Oxford University Press, 2002, 518 pages, 110 British pounds |
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| Analysis of multilocus models of association |
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| Evolutionary‐based association analysis using haplotype data |
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| Adjusting for population heterogeneity: A framework for characterizing statistical information and developing efficient test statistics |
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| Diagnostic tools in linkage analysis for quantitative traits |
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| Contribution of thermolabile methylenetetrahydrofolate reductase variant to total plasma homocysteine levels in healthy men and women. Inter99 (2) |
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| Genetic maps of microsatellite and single‐nucleotide polymorphism markers: Are the distances accurate? |
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| Exploring the “two‐hit hypothesis” in NF2: Tests of two‐hit and three‐hit models of vestibular schwannoma development |
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| Simple method to analyze SNP‐based association studies using DNA pools |
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| A note on genetic variance components in mixed models |
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| Association between lipoprotein lipase (LPL) gene and blood lipids: A common variant for a common trait? |
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| New multivariate test for linkage, with application to pleiotropy: Fuzzy Haseman‐Elston |
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| Candidate‐gene association studies with pedigree data: Controlling for environmental covariates |
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| Optimal designs for estimating penetrance of rare mutations of a disease‐susceptibility gene |
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| Removing phenotypic distribution assumptions from tests of linkage disequilibrium for quantitative traits |
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| Does accounting for gene‐environment (G×E) interaction increase the power to detect the effect of a gene in a multifactorial disease? |
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| Regressive logistic and proportional hazards disease models for within‐family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancer |
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| Variants of developmental genes (<i>TGFA, TGFB3</i>, and <i>MSX1</i>) and their associations with orofacial clefts: A case‐parent triad analysis |
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| A score for Bayesian genome screening |
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| A general class of association tests for family‐based data using weight functions |
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| Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q |
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| Kin‐cohort evaluation of relative risks of genetic variants |
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| Multivariate and multilocus variance components method, based on structural relationships to assess quantitative trait linkage via SEGPATH |
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| Three‐state frailty model for age at onset of dementia and death in Swedish twins |
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✓ |
✓ |
Swedish; Swedish Twin Registry |
| Genetic association tests with age at onset |
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| Book review: Mathematical and statistical methods for genetic analysis |
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| Multipoint affected sibpair linkage methods for localizing susceptibility genes of complex diseases |
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| Power of multifactor dimensionality reduction for detecting gene‐gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity |
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| Limits of fine‐mapping a quantitative trait |
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| Review of proteomics with applications to genetic epidemiology |
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