Case–Control and Case‐Only Designs with Genotype and Family History Data: Estimating Relative Risk, Residual Familial Aggregation, and Cumulative Risk
From MaRDI portal
Publication:5473203
Recommendations
- A Frailty‐Model‐Based Approach to Estimating the Age‐Dependent Penetrance Function of Candidate Genes Using Population‐Based Case‐Control Study Designs: An Application to Data on the BRCA1 Gene
- Combined association and aggregation analysis of data from case-control family studies
- Some Biases That May Affect Kin-Cohort Studies for Estimating the Risks from Identified Disease Genes
- Combined association, segregation and aggregation analysis on case-control family data
- Analysis of survival data from case-control family studies
Cites work
- scientific article; zbMATH DE number 3325347 (Why is no real title available?)
- A marginal likelihood approach for estimating penetrance from kin-cohort designs
- A model for association in bivariate life tables and its application in epidemiological studies of familial tendency in chronic disease incidence
- Analysis of Age of Onset Data from Case-Control Family Studies
- Analysis of survival data from case-control family studies
- Bivariate Survival Models Induced by Frailties
- Combined association and aggregation analysis of data from case-control family studies
- Inferences on the Association Parameter in Copula Models for Bivariate Survival Data
- Logistic disease incidence models and case-control studies
- Logistic regression of family data from case-control studies
- Modeling Multivariate Discrete Failure Time Data
- On dependence estimation using correlated failure time data from case-control family studies
- On the simultaneous associativity of F(x,y) and x+y-F(x,y)
- Statistical Inference Procedures for Bivariate Archimedean Copulas
- Weighted Distributions and Size-Biased Sampling with Applications to Wildlife Populations and Human Families
Cited in
(15)- Combining isotonic regression and EM algorithm to predict genetic risk under monotonicity constraint
- The Case‐Only Odds Ratio as a Causal Parameter
- Modeling familial association of ages at onset of disease in the presence of competing risk
- Some Biases That May Affect Kin-Cohort Studies for Estimating the Risks from Identified Disease Genes
- Meta-analysis of family-based and case-control genetic association studies that use the same cases
- Missing genetic information in case-control family data with general semi-parametric shared frailty model
- A Frailty‐Model‐Based Approach to Estimating the Age‐Dependent Penetrance Function of Candidate Genes Using Population‐Based Case‐Control Study Designs: An Application to Data on the BRCA1 Gene
- Effects of violations of assumptions on likelihood methods for estimating the penetrance of an autosomal dominant mutation from kin-cohort studies.
- Analysis of secondary failure time responses in studies with response‐dependent sampling schemes
- Estimation and interpretation of models of absolute risk from epidemiologic data, including family-based studies
- Fully nonparametric estimation of the marginal survival function based on case-control clustered data
- On estimation of the hazard function from population-based case-control studies
- Frailty models for familial risk with application to breast cancer
- A copula model for marked point processes
- Statistical inference on the penetrances of rare genetic mutations based on a case-family design
This page was built for publication: Case–Control and Case‐Only Designs with Genotype and Family History Data: Estimating Relative Risk, Residual Familial Aggregation, and Cumulative Risk
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q5473203)
