| Practical information on getting the most from <i>Genetic Epidemiology</i> |
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| Robustness of inference on measured covariates to misspecification of genetic random effects in family studies |
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| On the use of DNA pooling to estimate haplotype frequencies |
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| On a semiparametric test to detect associations between quantitative traits and candidate genes using unrelated individuals |
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| Correcting for nonrandom ascertainment in generalized linear mixed models (GLMMs), fitted using Gibbs sampling |
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| Haplotype sharing analysis with SNPs in candidate genes: the genetic analysis workshop 12 example |
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| Detecting genotype combinations that increase risk for disease: Maternal‐Fetal genotype incompatibility test |
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| Association mapping of complex diseases in linked regions: estimation of genetic effects and feasibility of testing rare variants |
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| On selecting markers for association studies: Patterns of linkage disequilibrium between two and three diallelic loci |
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| “Reply to Olson” |
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| Univariate and multivariate family‐based association analysis of the IL‐13 ARG130GLN polymorphism in the Childhood Asthma Management program |
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| Preferential transmission of type 1 diabetes from parents to offspring: fact or artifact? |
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Caucasoid populations |
| Relative efficiency of ambiguous vs. directly measured haplotype frequencies |
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| “Rejoinder” |
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| Segregation analysis of 389 Icelandic pedigrees with Breast and prostate cancer |
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| Evidence that <i>BCL3</i> plays a role in the etiology of nonsyndromic oral clefts in Brazilian families |
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| Impact of parental relationships in maximum lod score affected sib‐pair method |
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| “Power comparisons for genotypic vs. allelic TDT methods with >2 Alleles” |
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| “Reply to Fallin et al.” |
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| Erratum: Broman KW. 2001. Estimation of Allele Frequencies With Data on Sibships. Genet Epidemiol 20:307–15. |
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| Thanks to editorial reviewers for 2002 |
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| Recipients of genetic epidemiology best paper of the year award |
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| “Mixture models for linkage analysis of affected sibling pairs with covariates” |
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| Regressive threshold model for familial analysis of complex diseases with variable age of onset |
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| Score test for mapping quantitative‐trait loci with sibships of arbitrary size when the dominance effect is not negligible |
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| Comment on “Ascertainment adjustment in complex diseases” |
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| On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles |
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| Ascertainment adjustment in complex diseases |
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| Increase in power of transmission‐disequilibrium tests for quantitative traits |
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| Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2) |
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| Abstracts from the eleventh annual meeting of the International Genetic Epidemiology Society |
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| Rejoinder on “ascertainment adjustment in complex diseases” |
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| Comment on “Ascertainment adjustment in complex diseases” |
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| Hereditary hemochromatosis: detection of C282Y and H63D mutations in <i>HFE</i> gene by means of guthrie cards in population of Czech Republic |
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Central and Western European populations; population of the Czech Republic |
| Association mapping, using a mixture model for complex traits |
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| Fat distribution, menopausal age, and breast cancer risk: a shared preconceptional, maternal/oocyte‐mediated link? |
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| Hand grip strength: A phenotype suitable for identifying genetic variants affecting mid‐ and late‐life physical functioning |
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Danish |
| Genetic determination of biological age in the mennonites of the midwestern United States |
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Mennonites |
| On a general class of conditional tests for family‐based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations |
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| Evidence for a major gene influencing risk of pancreatic cancer |
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| Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1) |
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| Case‐control study of genetic and environmental influences on premature death of adult adoptees |
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| Empirical bayes methods and false discovery rates for microarrays |
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| Design of studies using DNA microarrays |
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| Microarrays and genetic epidemiology: A multipurpose tool for a multifaceted field |
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| Symbolic discriminant analysis of microarray data in autoimmune disease |
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| Mantel statistics to correlate gene expression levels from microarrays with clinical covariates |
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| Role of gene expression microarray analysis in finding complex disease genes |
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| Genetic epidemiology and microarrays |
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| LPL polymorphism predicts stroke risk in men |
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| A note on estimating the posterior density of a quantitative trait locus from a Markov chain Monte Carlo sample |
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| Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis |
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| Truncated product method for combining<i>P</i>‐values |
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| Characteristics of genetic markers and maps for cost‐effective genome screens using diallelic markers |
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| Allele sharing and allelic association I: Sib pair tests with increased power |
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| Professor Cedric B. Smith, pioneer in statistical genetics: Died January 10, 2002, at the age of 84 |
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| A Bayesian partition model for case‐control studies on highly polymorphic candidate genes |
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| Multiple sclerosis recurrence risk for siblings in an isolated population of Central Sardinia, Italy |
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| Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis |
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| Adjusting for population structure in admixed populations |
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| Genetic component to susceptibility to <i>Trichuris trichiura</i>: Evidence from two Asian populations |
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| Unified sampling approach for multipoint linkage disequilibrium mapping of qualitative and quantitative traits |
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| Mapping multiple genes for quantitative or complex traits |
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| Haplotype frequency estimation in patient populations: The effect of departures from Hardy‐Weinberg proportions and collapsing over a locus in the HLA region |
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| Interactions between genetic and reproductive factors in breast cancer risk in a population‐based sample of African‐American families |
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African‐American; ethnic groups; French families |
| The role of genotype in determining the effects of cigarette smoking on pulmonary function |
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| Genotype by smoking interaction for leptin levels in the San Antonio family heart study |
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| Quantification of type I error probabilities for heterogeneity LOD scores |
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| Properties of the transmission‐disequilibrium test in the presence of inbreeding |
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| Mortality differences by APOE genotype estimated from demographic synthesis |
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| Tests for genetic association using family data |
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| Score test for detecting linkage to quantitative traits |
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