Genetic Epidemiology - 1989

101 articles | Last updated: 2025-12-03 14:12:56
Caucasian
3
White
3
European
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Other
10
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
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Repeated‐measures model for the investigation of temporal trends using longitudinal family studies: Application to systolic blood pressure
Path analysis under generalized marital resemblance: Evaluation of the assumptions underlying the mixed homogamy model by the Monte Carlo method
Proceedings of the Second International Conference on Quantitative Genetics, edited by B.S. Weir, E.J. Eisen, M.M. Goodman, and G. Namkoong, Sunderland, MA: Sinauer Associates Inc., 1988, xii + 724 pa
Estimation of genetic model parameters: Variables correlated with a quantitative phenotype exhibiting major locus inheritance
Robust methods for the detection of genetic linkage for quantitative data from pedigrees
Announcement
Phenotypic effects of apolipoprotein structural variation on lipid profiles. I. APO H and quantitative lipid measures in the healthy women study
Using survival methods to estimate age‐at‐onset distributions for genetic diseases with an application to Huntington disease
Summary measures for evaluating the evidence for linkage
Preface
Acknowledgments
HLA class II typing using oligonucleotide probes
Genetic epidemiology of persistent islet cell antibodies among IDDM patients
Description of amish study data set Amish
Regressive logistic models for ordered and unordered polychotomous traits: Application to affective disorders
Familial analysis of bipolar affective disorder using logistic models
Modelling sibship environment in the regressive logistic model for familial disease
Affective disorders: Evaluation of a three‐allele model accounting for clinical heterogeneity Old Order Amish
Patrick A. P. Moran, 1917–1988: In memorium
Relationship between body mass index, cigarette smoking, and plasma sex steroids in normal male twins
Modeling the age‐of‐onset function in segregation analysis: A causal scheme for leprosy
Predicting intrauterine growth reterdation in sibships while considering maternal and infant covariates
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence Western Europe
Handbook of record linkage: Methods for health and statistical studies, administration, and business, Howard B. Newcombe, Oxford, England: Oxford University Press, 1988, 210 pp, $40.00
Announcement
Cardiovascular risk factors in a french canadian population: Resolution of genetic and familial environmental effects on blood pressure using twins, adoptees, and extensive information on environmenta french canadian population
Criteria for onset critically influence the estimation of familial risk in Alzheimer's disease
On the measurement of susceptibility to genetic factors
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Genetic analysis of IDDM: Summary of GAW5 IDDM results
Testing genetic models for IDDM by the MASC method
Linkage analysis and genetic models for IDDM
Remarks on ascertainment
HLA DR4‐DQw3.1 and 3.2 haplotypes among insulin‐dependent diabetics and their unaffected sibs in the GAW5 data ethnic heterogeneity
Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families
Combined segregation and linkage analysis for IDDM and HLA‐DR under several ascertainment assumptions
Autoimmune thyroid disease in type I diabetic families
Description of the National Institute of Mental Health family study of affective disorders
Description of X‐linkage pedigrees
Toronto‐Rochester depression study of 116 HLA‐typed kindreds
Robustness of the unified model to shared environmental effects in the analysis of dichotomous traits
Performance of linkage analysis under misclassification error when the genetic model is unknown
HLA may be involved in resistance and susceptibility to affective disorders
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Announcement
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Announcement
Restriction fragment polymorphisms of the HLA‐DR, HLA‐DQ, and insulin gene regions in IDDM: The GAW5 data
Immunoglobulin allotyping (Gm, Km) of GAW5 families
Charateristics of a multiplex IDDM sample: Unexplained differences with other samples
Genes predisposing to IDDM in multiplex families
Association and sibpair analysis for the HLA, Gm, Km, and insulin polymorphisms in multiplex IDDM families
Genetic analysis of the affective disorders: Summary of GAW5 Old Order Amish
Linkage data on affective disorders in an epidemiologic context
The incomplete, multiple ascertainment model: Assumptions, applications, and alternative models
Linkage analysis under “random” and “genetic” reduced penetrance
Analysis of the Toronto‐Rochester depression study follow‐up data confirms an HLA‐region gene contribution to susceptibility to affective disorder
Phenylthiocarbamide taste sensitivity revisited: Complete sorting test supports residual family resemblance
Simulation of Huntington's disease onset
The impact of altered fitness on the risk of illness in relatives
Phenotypic effects of apolipoprotein structural variation on lipid profiles: II. Apolipoprotein A‐IV and quantitative lipid measures in the healthy women study
Increased risk for gestational diabetes mellitus associated with insulin receptor and insulin‐like growth factor II restriction fragment length polymorphisms black; Hispanic
Importance of hereditary disease at a Neuropsychiatric Institute in Mexico City
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Major gene polymorphism for human erythrocyte (RBC) thiol methyltransferase (TMT)
Erratum
Announcement
Genetic analysis of IDDM: The GAW5 multiplex family dataset
Segregation analysis of two genetic markers in IDDM families under two‐locus models
Statistical properties of the haplotype relative risk
Genetics of IDDM: Evidence for complex inheritance with HLA
HLA DQβ3.2 identifies subtypes of DR4 + haplotypes permissive for IDDM
HLA and insulin gene associations with IDDM
Age of onset, age at examination, and other covariates in the analysis of family data
Familial correlates of risk: Application to the gershon and goldin NIMH pedigree data
A more powerful robust sib‐pair test of linkage for quantitative traits
Genetic studies on an Alzheimer Clinic population
Erratum
Availability of schizophrenic patients and their families for genetic linkage studies: Findings from the Maryland epidemiology sample
Phenotypic effects of apolipoprotein structural variation on lipid profiles. IV. Apolipoprotein polymorphisms in a small group of black women from the Healthy Women Study Black
On the role of vitamin D binding globulin in glucose homeostasis: Results from the San Luis Valley diabetes study Anglos; Hispanic‐Americans; Dogrib Indians
Segregation analysis of quantitative traits in nuclear families: Comparison of three program packages
HLA and insulin‐dependent diabetes: An overview
Coxsackie B virus assays in IDDM families: The GAW5 data on antibody prevalence
Autoantibodies to pancreatic islet cells and insulin in IDDM families: The GAW5 data
The insulin gene and susceptibility to IDDM
Linkage studies of HLA and insulin gene restriction fragment length polymorphisms in families with IDDM
NIMH collaborative program on the psychobiology of depression: Clinical
Linkage analysis with cohort effects: An application to X‐linkage
Linkage analysis with inbreeding
Utility of the affected sib pair method to detect linkage of a sex‐linked dominant disease with a sex‐linked recessive trait
Affective disorder not linked to HLA
Nonrandom sampling in genetic epidemiology: An implementation of the Hanis‐Chakraborty method for multifactorial analysis
Linkage detection tests under heterogeneity
The distribution of debrisoquine metabolic phenotypes and implications for the suggested association with lung cancer risk
Equivalence of the mixed and regressive models for genetic analysis. I. Continuous traits
Complex segregation analysis for a three‐allele locus: Experience from an analysis of acid phosphatase activity British families
Test of genetic heterogeneity of cleft lip with or without cleft palate as related to race and severity Oriental; Japanese; non-Oriental
Alternative genetic models for the inheritance of the phenylthiocarbamide taste deficiency
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