Genetic Epidemiology - 1996

78 articles | Last updated: 2025-12-03 14:12:56
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The Fourth Annual Meeting of the International Genetic Epidemiology Society, June 20–22, 1995, Snowbird, Utah
Health and numbers: Basic biostatistical methods, Chap T. Le and James R. Boen. New York: John Wiley & Sons, Inc., 1995, 247 pages, $34.95
Textbook in psychiatric epidemiology, M.T. Tsuang, M. Tohen, and G.E. Zahner, eds. New York: Wiley-Liss, 1995, xii, 483 pages, $59.95
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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Abstracts from the Fifth Annual Meeting of the International Genetic Epidemiology Society
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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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Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders
The family study of otitis media: Design and disease and risk factor profiles
Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state
Two‐stage global search designs for linkage analysis using pairs of affected relatives
Commingling analysis of the distribution of a phenotype conditioned on two marker genotypes: Application to plasma angiotensin-converting enzyme levels
Partitioned association-linkage test: distinguishing “necessary” from “susceptibility” loci
Prediction of linkage phase by parental phenotypes
Improving the robustness of the weighted pairwise correlation test for linkage analysis
Determining linkage and mode of inheritance: Mod scores and other methods
<i>BRCA1</i> R841W: A strong candidate for a common mutation with moderate phenotype
Heterogeneity of familial risk in sarcoidosis
On planning of samples for linkage analysis: Two ways of a sample size reduction
Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992
Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels
Random effects model for meta-analysis of multiple quantitative sibpair linkage studies
The inheritance of factors associated with joint mobility
Validation of family history of breast cancer and identification of the BRCA1 and other syndromes using a population-based cancer registry
Segregation analysis of breast cancer: A comparison of type-dependent age-at-onset versus type-dependent susceptibility models
Maternal exposure to paternal HLA does not explain the postpartum increase in rheumatoid arthritis
General score tests for associations of genetic markers with disease using cases and their parents
Association within twin pairs for a dichotomous trait
Segregation analysis of breast cancer: A comparison of type‐dependent age‐at‐onset versus type‐dependent susceptibility models
Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992
Heterogeneity of familial risk in sarcoidosis
Determining linkage and mode of inheritance: Mod scores and other methods
Maternal exposure to paternal HLA does not explain the postpartum increase in rheumatoid arthritis
Genetic and epidemiological risk factors for a malignant melanoma-predisposing phenotype: The great number of nevi
NewMspI polymorphism at +83 bp of the human apolipoprotein al gene: Association with increased circulating high density lipoprotein cholesterol levels
Genetic analysis of sex and generation differences in plasma lipid, lipoprotein, and apolipoprotein levels in adolescent twins and their parents
Pedigree analysis package vs. MIXD: Fitting the mixed model on a large pedigree
BRCA1 R841W: A strong candidate for a common mutation with moderate phenotype
Apolipoprotein E-η4 allele and familial risk in Alzheimer's disease
Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations
The family study of otitis media: Design and disease and risk factor profiles
Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state
Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment
Prediction of linkage phase by parental phenotypes
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders
Partitioned association‐linkage test: distinguishing “necessary” from “susceptibility” loci
Comparison of methods for survival analysis of dependent data
Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: Results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia
Analysis of case-control/family sampling design
Genetic variation and human disease
On estimation of linkage test power
Segregation analysis of two lung function indices in a random sample of young families: The humboldt family study
Association between family history of cancer and breast cancer defined by estrogen and progesterone receptor status
Familial clustering of obesity and breast cancer
Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy
Commingling analysis of the distribution of a phenotype conditioned on two marker genotypes: Application to plasma angiotensin‐converting enzyme levels
Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci
Univariate analysis of dichotomous or ordinal data from twin pairs: A simulation study comparing structural equation modeling and logistic regression
Two‐stage global search designs for linkage analysis using pairs of affected relatives
On planning of samples for linkage analysis: Two ways of a sample size reduction
Improving the robustness of the weighted pairwise correlation test for linkage analysis
Risk of alcoholism and parental history: Gender differences and a possible reporting bias
Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels
Validation of family history of breast cancer and identification of the BRCA1 and other syndromes using a population‐based cancer registry
Random effects model for meta‐analysis of multiple quantitative sibpair linkage studies
The inheritance of factors associated with joint mobility
Heterogeneous rates for birth defects in Latin America: Hints on causality
Estimating disease risks for individuals with a given family history in different populations with an application to breast cancer