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