Genetic Epidemiology - 2000

105 articles | Last updated: 2025-12-03 14:12:56
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T A T A T A T A
Genetic epidemiology of breast cancer: Segregation analysis of 389 Icelandic pedigrees
James Van Gundia Neel
Clustering methods applied to allele sharing data
Potential gain in efficiency and power to detect gene-environment interactions by matching in case-control studies
Risk models for familial ovarian and breast cancer
Use of conditional and marginal odds-ratios for analysing familial aggregation of binary data
Frequency and allelic association of common variants in the lipoprotein lipase gene in different ethnic groups: The Wandsworth Heart and Stroke Study different ethnic groups
Family risk score of coronary heart disease (CHD) as a predictor of CHD: the atherosclerosis risk in communities (ARIC) study and The NHLBI Family Heart Study
Linkage analysis of 150 high-risk prostate cancer families at 1q24-25
Effect of physical activity on lipid levels in a population-based sample of men with and without the Arg192 variant of the human paraoxonase gene
Resolution passed by the IGES board of directors: James V. Neel, a visionary leader among leaders
Model-free sib-pair linkage analysis: Combining full-sib and half-sib pairs
Estimation of apolipoprotein E genotype-specific relative mortality risks from the distribution of genotypes in centenarians and middle-aged men: Apolipoprotein E gene is a ?frailty gene,? not a ?long
Familial history of metabolic disorders and the Multiple Metabolic syndrome: The NHLBI family heart study
Toward guidelines for pedigree selection in genetic studies of attention deficit hyperactivity disorder
Two-stage global search designs for linkage analysis II: Including discordant relative pairs in the study
Segregation analysis of IgE levels in 335 French families (EGEA) using different strategies to correct for the ascertainment through a correlated trait (asthma)
Ascertainment bias in the estimation of sibling genetic risk parameters
Score tests for familial correlation in genotyped-proband designs
Implementing a unified approach to family-based tests of association
Ascertainment issues in variance components models
Genetic inheritance of body mass index in African-American and African families African-American; African
Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data
Associations of clinical features in neurofibromatosis 1 (NF1)
A weighted test using both extreme discordant and concordant sib pairs for detecting linkage
Editorial
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer
Getting ready for the tidal wave
Resolution passed by the IGES board of directors: James V. Neel, a visionary leader among leaders
Framework for identifying quantitative trait loci in association studies using structural equation modeling
Power comparison of regression methods to test quantitative traits for association and linkage
Using unaffected child trios to test for transmission distortion
Abstracts from the Ninth Annual Meeting of the International Genetic Epidemiology Society
Evidence of major gene control of cortical bone loss in humans
Associations of clinical features in neurofibromatosis 1 (NF1)
Racial and genetic determinants of plasma factor XIII activity
Cancer incidence for Swedish twins studied by means of bivariate frailty models
Modeling the HLA component in rheumatoid arthritis: Sensitivity to DRB1 allele frequencies
James Van Gundia Neel
Relationship between case-control studies and the transmission/disequilibrium test
Book Review
Estimation of apolipoprotein E genotype‐specific relative mortality risks from the distribution of genotypes in centenarians and middle‐aged men: Apolipoprotein E gene is a “frailty gene,” not a “long
Ascertainment issues in variance components models
Familial history of metabolic disorders and the Multiple Metabolic syndrome: The NHLBI family heart study
A single, sequential, genome-wide test to identify simultaneously all promising areas in a linkage scan
Use of classification trees for association studies
Case-parents design for gene-environment interaction by Schaid
Analysis of longitudinal data from twins
Bias in multipoint linkage analysis arising from map misspecification
Combined linkage and linkage disequilibrium mapping for genome screens
Genetic epidemiology with a capital ?E?
IGES resolution concerning recent allegations against James V. Neel
Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage
Mulitpoint admixture mapping
Familial cancer risks in affected sibships: Results from the Swedish Family-Cancer Database
A Bayesian hierarchical model for allele frequencies
Effect of allelic heterogeneity on the power of the transmission disequilibrium test
Determination of bone mineral density of the hip and spine in human pedigrees by genetic and life-style factors
Apo E genotype, diabetes, and peripheral arterial disease in older men: The Honolulu Asia-Aging Study
Bootstrap confidence intervals for relative risk parameters in affected-sib-pair data
Risk models for familial ovarian and breast cancer
Correcting for ascertainment bias of relative-risk estimates obtained using affected-sib-pair linkage data
Extensive association analysis between the CETP gene and coronary heart disease phenotypes reveals several putative functional polymorphisms and gene-environment interaction
Genetic inheritance of body mass index in African‐American and African families
Power of a score test for quantitative trait linkage analysis of relative pairs
Variance components analysis for pedigree-based censored survival data using generalized linear mixed models (GLMMs) and Gibbs sampling in BUGS
Implementing a unified approach to family‐based tests of association
Least squares estimation of variance components for linkage
Estimation of genetic and environmental components in colorectal and lung cancer and melanoma
Gene-diet interactions and plasma lipoproteins: Role of apolipoprotein E and habitual saturated fat intake
Toward guidelines for pedigree selection in genetic studies of attention deficit hyperactivity disorder
Genetic epidemiology of breast cancer: Segregation analysis of 389 Icelandic pedigrees
Two-stage global search designs for linkage analysis II: Including discordant relative pairs in the study
Score tests for familial correlation in genotyped‐proband designs
Methods for multipoint disease mapping using linkage disequilibrium
Linkage disequilibrium mapping in populations of variable size using the decay of haplotype sharing and a stepwise-mutation model
Potential gain in efficiency and power to detect gene‐environment interactions by matching in case‐control studies
Segregation analysis of IgE levels in 335 French families (EGEA) using different strategies to correct for the ascertainment through a correlated trait (asthma)
Bayesian linkage and segregation analysis: Factoring the problem
Robust transmission regression models for linkage and association
Comparison of allele-sharing statistics for general pedigrees
Circumventing multiple testing: A multilocus Monte Carlo approach to testing for association
Detecting association in a case-control study while correcting for population stratification
Transmission/disequilibrium tests for quantitative traits
Mapping a quantitative trait locus via the EM algorithm and Bayesian classification
A general test of association for complex diseases with variable age of onset
Haseman and Elston revisited
ApoE polymorphism accounts for only part of the genetic variation in quantitative ApoE levels
Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data
Two-stage global search designs for linkage analysis I: Use of the mean statistic for affected sib pairs
Model‐free sib‐pair linkage analysis: Combining full‐sib and half‐sib pairs
Book Review
A Monte Carlo procedure for two-stage tests with correlated data
Clustering methods applied to allele sharing data
Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome
Variance-components QTL linkage analysis of selected and non-normal samples: Conditioning on trait values
An analysis of strategies for discovery of single-nucleotide polymorphisms
Assessing changes in ages at onset over successive generation: An application to breast cancer
Zero-recombinant haplotyping: Applications to fine mapping using SNPs
Robust LOD scores for variance component-based linkage analysis
Evidence for major genes influencing pulmonary function in the NHLBI Family Heart Study
Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: Issues of power and type I error rate
Sampling among haplotype resolutions in a coalescent-based genealogy sampler
Expansion mutation frequency and CGG/GCC repeat polymorphism inFMR1 andFMR2 genes in an Indian population
Ramifications of HLA class I polymorphism and population genetics for vaccine development