| The Fourth Annual Meeting of the International Genetic Epidemiology Society, June 20–22, 1995, Snowbird, Utah |
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| Health and numbers: Basic biostatistical methods, Chap T. Le and James R. Boen. New York: John Wiley & Sons, Inc., 1995, 247 pages, $34.95 |
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| Textbook in psychiatric epidemiology, M.T. Tsuang, M. Tohen, and G.E. Zahner, eds. New York: Wiley-Liss, 1995, xii, 483 pages, $59.95 |
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| Effects of atomic radiation: A half-century of studies from Hiroshima and Nagasaki, William J. Schull, New York: Wiley-Liss, Inc., 1995, 397 pages, $45.00 |
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| Announcements |
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| Announcements |
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| Announcement |
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| Masthead |
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| Announcement |
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| Abstracts from the Fifth Annual Meeting of the International Genetic Epidemiology Society |
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| Masthead |
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| Announcements |
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| Etiology and pathogenesis of down syndrome, C.J. Epstein, T. Hassold, I.T. Lott, L. Nadel, and D. Patterson, eds. New York: Wiley-Liss, 1995, 260 pages, $110.00 |
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| Masthead |
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| Masthead |
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| Masthead |
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| Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders |
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| The family study of otitis media: Design and disease and risk factor profiles |
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| Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state |
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| Two‐stage global search designs for linkage analysis using pairs of affected relatives |
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| Commingling analysis of the distribution of a phenotype conditioned on two marker genotypes: Application to plasma angiotensin-converting enzyme levels |
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| Partitioned association-linkage test: distinguishing “necessary” from “susceptibility” loci |
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| Prediction of linkage phase by parental phenotypes |
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| Improving the robustness of the weighted pairwise correlation test for linkage analysis |
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| Determining linkage and mode of inheritance: Mod scores and other methods |
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| <i>BRCA1</i>
R841W: A strong candidate for a common mutation with moderate phenotype |
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| Heterogeneity of familial risk in sarcoidosis |
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| On planning of samples for linkage analysis: Two ways of a sample size reduction |
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| Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992 |
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| Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels |
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| Random effects model for meta-analysis of multiple quantitative sibpair linkage studies |
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| The inheritance of factors associated with joint mobility |
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| Validation of family history of breast cancer and identification of the BRCA1 and other syndromes using a population-based cancer registry |
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| Segregation analysis of breast cancer: A comparison of type-dependent age-at-onset versus type-dependent susceptibility models |
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| Maternal exposure to paternal HLA does not explain the postpartum increase in rheumatoid arthritis |
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| General score tests for associations of genetic markers with disease using cases and their parents |
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| Association within twin pairs for a dichotomous trait |
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| Segregation analysis of breast cancer: A comparison of type‐dependent age‐at‐onset versus type‐dependent susceptibility models |
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| Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992 |
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| Heterogeneity of familial risk in sarcoidosis |
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| Determining linkage and mode of inheritance: Mod scores and other methods |
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| Maternal exposure to paternal HLA does not explain the postpartum increase in rheumatoid arthritis |
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| Genetic and epidemiological risk factors for a malignant melanoma-predisposing phenotype: The great number of nevi |
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| NewMspI polymorphism at +83 bp of the human apolipoprotein al gene: Association with increased circulating high density lipoprotein cholesterol levels |
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| Genetic analysis of sex and generation differences in plasma lipid, lipoprotein, and apolipoprotein levels in adolescent twins and their parents |
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| Pedigree analysis package vs. MIXD: Fitting the mixed model on a large pedigree |
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| BRCA1 R841W: A strong candidate for a common mutation with moderate phenotype |
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| Apolipoprotein E-η4 allele and familial risk in Alzheimer's disease |
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| Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations |
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| The family study of otitis media: Design and disease and risk factor profiles |
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| Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state |
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| Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment |
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| Prediction of linkage phase by parental phenotypes |
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| Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders |
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| Partitioned association‐linkage test: distinguishing “necessary” from “susceptibility” loci |
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| Comparison of methods for survival analysis of dependent data |
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| Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: Results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia |
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| Analysis of case-control/family sampling design |
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| Genetic variation and human disease |
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| On estimation of linkage test power |
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| Segregation analysis of two lung function indices in a random sample of young families: The humboldt family study |
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| Association between family history of cancer and breast cancer defined by estrogen and progesterone receptor status |
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| Familial clustering of obesity and breast cancer |
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| Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy |
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| Commingling analysis of the distribution of a phenotype conditioned on two marker genotypes: Application to plasma angiotensin‐converting enzyme levels |
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| Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci |
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| Univariate analysis of dichotomous or ordinal data from twin pairs: A simulation study comparing structural equation modeling and logistic regression |
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| Two‐stage global search designs for linkage analysis using pairs of affected relatives |
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| On planning of samples for linkage analysis: Two ways of a sample size reduction |
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| Improving the robustness of the weighted pairwise correlation test for linkage analysis |
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| Risk of alcoholism and parental history: Gender differences and a possible reporting bias |
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| Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels |
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| Validation of family history of breast cancer and identification of the BRCA1 and other syndromes using a population‐based cancer registry |
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| Random effects model for meta‐analysis of multiple quantitative sibpair linkage studies |
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| The inheritance of factors associated with joint mobility |
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| Heterogeneous rates for birth defects in Latin America: Hints on causality |
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| Estimating disease risks for individuals with a given family history in different populations with an application to breast cancer |
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